Metrikler
Yayın
161
Açık Erişim
4
BM Sürdürülebilir Kalkınma Amaçları
Eğitim Bilgileri
2016 - 2020
2016 - 2020Lisans
İstanbul Üniversitesi, Açık ve Uzaktan Eğitim Fakültesi, Açık Öğretim Programları, Türkiye
2006 - 2010
2006 - 2010Tıpta Uzmanlık
İstanbul Üniversitesi, Nöroloji, Türkiye
2000 - 2006
2000 - 2006Doktora
Hacettepe Üniversitesi, Tıp Fakültesi, Türkiye
Yaptığı Tezler
2010
2010Tıpta Uzmanlık
Okülofaringodistal Miyopatinin Klinik ve Genetik Özelliklerinin Belirlenmesi
İstanbul Üniversitesi, Nöroloji Anabilim Dalı, Nöromüsküler Hastalıklar Bilim Dalı
Yabancı Diller
B2 Orta Üstü
B2 Orta ÜstüAlmanca
Araştırma Alanları
Tıp
Sağlık Bilimleri
Dahili Tıp Bilimleri
Nöroloji
Akademik Ünvanlar / Görevler
2021 - Devam Ediyor
2021 - Devam EdiyorProf. Dr.
İstanbul Üniversitesi, İstanbul Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
2015 - 2021
2015 - 2021Doç. Dr.
İstanbul Üniversitesi, İstanbul Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü
2009 - 2009
2009 - 2009Araştırma Görevlisi
Newcastle College
Akademi Dışı Deneyim
2011 - 2012
2011 - 2012Uzman Doktor
Başkale Devlet Hastanesi, Uzman Doktor
Makaleler
Tümü (88)
SCI-E, SSCI, AHCI (83)
SCI-E, SSCI, AHCI, ESCI (87)
ESCI (2)
Scopus (86)
TRDizin (11)
2025
20251. Kyphoscoliosis peptidase deficiency-induced myofibrillar degeneration, focal depletion of mitochondria, and protein aggregation: A true myofibrillar myopathy?
DURMUŞ TEKÇE H., Clemen C. S., ÖNAY UÇAR E., Hofmann A., Schlotzer-Schrehardt U., MERTOĞLU KAMALI E., et al.
JOURNAL OF NEUROMUSCULAR DISEASES
, 2025 (SCI-Expanded, Scopus)
2025
20252. Eculizumab as a Rescue Therapy in Prolonged Myasthenic Crisis in the Intensive Care Unit: A Case Series
Durmus H., Çakar A., Gülşen Parman Y.
Neurocritical Care
, cilt.42, sa.3, ss.1099-1101, 2025 (SCI-Expanded)
2025
20253. Five-Year Results With Patisiran for Hereditary Transthyretin Amyloidosis With Polyneuropathy: A Randomized Clinical Trial With Open-Label Extension
Adams D., Wixner J., Polydefkis M., Berk J. L., Conceição I. M., Dispenzieri A., et al.
JAMA Neurology
, cilt.82, sa.3, ss.228-236, 2025 (SCI-Expanded)
2024
20244. Current insights in ultra-rare adenylosuccinate synthetase 1 myopathy – meeting report on the First Clinical and Scientific Conference. 3 June 2024, National Centre for Advancing Translational Science, Rockville, Maryland, the United States of America
Rybalka E., Park H. J., Nalini A., Baskar D., Polavarapu K., Durmus H., et al.
Orphanet Journal of Rare Diseases
, cilt.19, sa.1, 2024 (SCI-Expanded)
2024
20245. Thymic gene expression analysis reveals a potential link between HIF-1A and Th17/Treg imbalance in thymoma associated myasthenia gravis
Altınönder İ., Kaya M., Yentür S. P., Çakar A., Durmuş H., Yegen G., et al.
Journal of Neuroinflammation
, cilt.21, sa.1, 2024 (SCI-Expanded)
2024
20246. Eculizumab Versus Rituximab for Refractory Antiacetylcholine Receptor Antibody-Positive Generalized Myasthenia Gravis: A Single-Center Experience
DURMUŞ TEKÇE H., ÇAKAR A., Parman Y. G.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.2024, 2024 (SCI-Expanded)
2024
20247. In vitro modulation of T cells in myasthenia gravis by low-dose IL-2
Çebi M., Çakar A., Durmuş H., Akan O., Aysal F., Parman Y., et al.
European Journal of Immunology
, cilt.54, sa.11, 2024 (SCI-Expanded)
2024
20248. Detection of gene variants associated with recessive limb–girdle muscular weakness and Pompe disease in a global cohort of patients through the application of next-generation sequencing analysis
Bevilacqua J. A., Al-Salti A. M., Al Madani A., Alves da Fonseca A., Durmus H., Chai J., et al.
Frontiers in Genetics
, cilt.15, 2024 (SCI-Expanded)
2024
20249. Disease activity in chronic inflammatory demyelinating polyneuropathy: association between circulating B-cell subsets, cytokine levels, and clinical outcomes
Ozdag Acarli A. N., Tuzun E., Sanli E., Koral G., Akbayir E., Cakar A., et al.
CLINICAL AND EXPERIMENTAL IMMUNOLOGY
, cilt.215, sa.1, ss.65-78, 2024 (SCI-Expanded)
2023
202310. Data from the European registry for patients with McArdle disease (EUROMAC): functional status and social participation
Karazi W., Scalco R. S., Stemmerik M. G., Løkken N., Lucia A., Santalla A., et al.
Orphanet Journal of Rare Diseases
, cilt.18, sa.1, 2023 (SCI-Expanded)
2023
202311. Phenotypic features of RETREG1-related hereditary sensory autonomic neuropathy
Çakar A., Bagırova G., Durmuş H., Uyguner O., Parman Y.
Journal of the Peripheral Nervous System
, cilt.28, sa.3, ss.351-358, 2023 (SCI-Expanded)
2023
202312. Thymoma patients with or without myasthenia gravis have increased Th17 cells, IL-17 production and ICOS expression
Cebi M., Cakar A., Erdogdu E., Durmus-Tekce H., Yegen G., Ozkan B., et al.
JOURNAL OF NEUROIMMUNOLOGY
, 2023 (SCI-Expanded)
2023
202313. Expert opinion on the diagnostic odyssey and management of late-onset Pompe disease: a neurologist's perspective
ERDEM ÖZDAMAR S., KOÇ A. F., Durmus Tekce H., Kotan D., Ekmekci A. H., ŞENGÜN İ. Ş., et al.
Frontiers in Neurology
, cilt.14, 2023 (SCI-Expanded)
2023
202314. A novel homozygous loss-of-function variant in SOD1 causing progressive spastic tetraplegia and axial hypotonia
Çakar A., Pekbilir E., CEYLANER S., Durmuş H., Battaloğlu E., Şahin U., et al.
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration
, cilt.24, sa.5-6, ss.535-538, 2023 (SCI-Expanded)
2022
202215. Disease activity in chronic inflammatory demyelinating polyneuropathy: A comparative study of clinical and skin biopsy markers
Acarli A. N. O., Unverengil G., Sirin N. G., Cakar A., Durmus H., Parman Y.
MUSCLE & NERVE
, cilt.66, sa.6, ss.736-743, 2022 (SCI-Expanded)
2022
202216. Desmin Knock-Out Cardiomyopathy: A Heart on the Verge of Metabolic Crisis
Elsnicova B., Hornikova D., Tibenska V., Kolar D., Tlapakova T., Schmid B., et al.
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES
, cilt.23, sa.19, 2022 (SCI-Expanded)
2022
202217. Investigation of a Novel Recessive Mutation in Acetylcholine Receptor Epsilon-Subunit with Slow-Channel Kinetics Causing Congenital Myasthenia Reveals Subunit-Specific Contribution of Cys-Loop Length to Receptor Activation
Shen X., Shen S., Zhao Y., Di L., Durmus H., Deymeer F., et al.
ANNALS OF NEUROLOGY
, cilt.92, 2022 (SCI-Expanded)
2022
202218. Clinical and genetic characteristics of Emery-Dreifuss muscular dystrophy patients from Turkey: 30 years longitudinal follow-up study.
Yunisova G., CEYLANER S., Oflazer P., Deymeer F., Parman Y. G., Durmus H.
Neuromuscular disorders : NMD
, cilt.32, sa.9, ss.718-727, 2022 (SCI-Expanded)
2022
202219. Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (canvas): an important cause of late-onset ataxia with unique clinical features
ÇAKAR A., Sahin E., Tezel S., Candayan A., Samanci B., BATTALOĞLU E., et al.
ACTA NEUROLOGICA BELGICA
, cilt.122, sa.4, ss.939-945, 2022 (SCI-Expanded)
2022
202220. AN EXPLORATORY STUDY OF COGNITIVE INVOLVEMENT IN HEREDITARY ATTRV
Durmus H., Cakar A., Demirci H., Parman Y.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.27, 2022 (SCI-Expanded)
2022
202221. Phenotypical spectrum of SACS variants: Neuromuscular perspective of a complex neurodegenerative disorder
Cakar A., Inci M., Acarli A. N. O., Comu S., Candayan A., BATTALOĞLU E., et al.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.145, ss.619-626, 2022 (SCI-Expanded)
2022
202222. Lumbar Spinal Stenosis: A Rare Presentation of Hereditary Transthyretin Amyloidosis
Cakar A., Atmaca M. M., Kotan D., Durmus H., Deymeer F., Oflazer P., et al.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.59, sa.1, ss.77-79, 2022 (SCI-Expanded)
2021
202123. An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis
Durmus H., Cakar A., Demirci H., ALAYLIOĞLU M., GEZEN AK D., DURSUN E., et al.
ACTA NEUROLOGICA SCANDINAVICA
, cilt.144, sa.6, ss.640-646, 2021 (SCI-Expanded)
2021
202124. Rare slow channel congenital myasthenic syndromes without repetitive compound muscle action potential and dramatic response to low dose fluoxetine
Durmus H., Sticht H., Ceylaner S., Hashemolhosseini S., Deymeer F.
ACTA NEUROLOGICA BELGICA
, cilt.121, sa.6, ss.1755-1760, 2021 (SCI-Expanded)
2021
202125. Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort
Candayan A., Çakar A., Yunisova G., Özdağ Acarlı A. N., Atkinson D., Topaloğlu P., et al.
NEUROLOGY-GENETICS
, cilt.7, sa.5, 2021 (SCI-Expanded)
2021
202126. Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (Canvas) is an important cause of late-onset ataxia
Cakar A., Sahin E., Tezel S., Candayan A., Samanci B., BATTALOĞLU E., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.26, sa.3, ss.364, 2021 (SCI-Expanded)
2021
202127. Episodic psychosis, ataxia, motor neuropathy with pyramidal signs (PAMP sydrome) caused by a novel mutation in ADPRHL2 (AHR3)
Durmus H., Mertoglu E., Sticht H., Ceylaner S., Kulaksizoglu I. B., Hashemolhosseini S., et al.
NEUROLOGICAL SCIENCES
, cilt.42, sa.9, ss.3871-3878, 2021 (SCI-Expanded, Scopus)
2021
202128. The Complex Genetic Landscape of Hereditary Ataxias in Turkey and Implications in Clinical Practice
Vural A., Simsir G., Tekgul S., Kocoglu C., Akcimen F., Kartal E., et al.
MOVEMENT DISORDERS
, cilt.36, ss.1676-1688, 2021 (SCI-Expanded)
2021
202129. Diaphragmatic dysfunction at the first visit to a chest diseases outpatient clinic in 500 patients with amyotrophic lateral sclerosis
Pihtili A., Bingol Z., Durmus H., Parman Y., Kiyan E.
MUSCLE & NERVE
, cilt.63, ss.683-689, 2021 (SCI-Expanded)
2021
202130. SOD1 Mutation: A Single Center Experience
ÇAKAR A., DURMUŞ TEKÇE H., PARMAN F. Y.
NEUROLOGY
, sa.15, 2021 (SCI-Expanded)
2021
202131. Late-onset TK2-Deficiency Patients from Turkey
DURMUŞ TEKÇE H., ÇAKAR A., PARMAN F. Y.
NEUROLOGY
, sa.15, 2021 (SCI-Expanded)
2021
202132. Genotypic and phenotypic features of mutations in the HINT1 gene among Turkish patients with hereditary axonal neuropathy
Acarli A. O., Cakar A., Candayan A., Durmus H., Ceylaner S., Matur Z., et al.
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM
, cilt.26, sa.1, ss.124-125, 2021 (SCI-Expanded)
2020
202033. Data from the European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC)
Scalco R. S., Lucia A., Santalla A., Martinuzzi A., Vavla M., Reni G., et al.
ORPHANET JOURNAL OF RARE DISEASES
, cilt.15, sa.1, 2020 (SCI-Expanded)
2020
202034. Cognition of the mothers of patients with Duchenne muscular dystrophy.
Demirci H., Durmus H., Toksoy G., Uslu A., Parman Y., Hanagasi H. A.
Muscle & nerve
, cilt.62, sa.6, ss.710-716, 2020 (SCI-Expanded, Scopus)
2020
202035. The treatment effect on peripheral B cell markers in antibody positive myasthenia gravis patients
YILMAZ V., TÜZÜN E., DURMUŞ TEKÇE H., Oflazer P., Aysal F., Parman Y., et al.
JOURNAL OF NEUROIMMUNOLOGY
, cilt.349, 2020 (SCI-Expanded)
2020
202036. Correlations between radiographic spinopelvic parameters and health-related quality of life: A prospective evaluation of 37 patients with facioscapulohumeral muscular dystrophy
Bayram S., Kendirci A. Ş., Karalar Ş., Durmuş Tekçe H., Parman F. Y., Akgül T., et al.
Clinical Neurology and Neurosurgery
, cilt.198, 2020 (SCI-Expanded)
2020
202037. Sequential targeted exome sequencing of 1001 patients affected by unexplained limb-girdle weakness
Toepf A., Johnson K., Bates A., Phillips L., Chao K. R., England E. M., et al.
GENETICS IN MEDICINE
, cilt.22, sa.9, ss.1478-1488, 2020 (SCI-Expanded)
2020
202038. Revisiting the complex architecture of ALS in Turkey: Expanding genotypes, shared phenotypes, molecular networks, and a public variant database
Tunca C., Seker T., Akcimen F., Coskun C., Bayraktar E., Palvadeau R., et al.
HUMAN MUTATION
, cilt.41, sa.8, 2020 (SCI-Expanded)
2020
202039. Four Individuals with a Homozygous Mutation in Exon 1f of thePLECGene and Associated Myasthenic Features
Mroczek M., DURMUŞ TEKÇE H., Topf A., Parman Y., Straub V.
GENES
, cilt.11, sa.7, 2020 (SCI-Expanded)
2020
202040. EVALUATION OF REPETITIVE NERVE STIMULATION WITH DIFFERENT STIMULATION FREQUENCIES IN PATIENTS WITH MYASTHENIA GRAVIS
Sirin N. G., KOCASOY ORHAN E., Oguz Akarsu E., DURMUŞ TEKÇE H., Deymeer F., BASLO M. B.
JOURNAL OF ISTANBUL FACULTY OF MEDICINE-ISTANBUL TIP FAKULTESI DERGISI
, cilt.83, sa.3, ss.197-203, 2020 (ESCI)
2020
202041. CD4+ T Cells of Myasthenia Gravis Patients Are Characterized by Increased IL-21, IL-4, and IL-17A Productions and Higher Presence of PD-1 and ICOS
Cebi M., DURMUŞ TEKÇE H., Aysal F., ÖZKAN B., Gul G. E., ÇAKAR A., et al.
Frontiers in Immunology
, cilt.11, 2020 (SCI-Expanded)
2020
202042. Expanding the disease phenotype of ADSSL1-associated myopathy in non-Korean patients
Mroczek M., DURMUŞ TEKÇE H., Bijarnia-Mahay S., Topf A., Ghaoui R., Bryen S., et al.
NEUROMUSCULAR DISORDERS
, cilt.30, sa.4, ss.310-314, 2020 (SCI-Expanded)
2020
202043. Late-onset generalized myasthenia gravis: clinical features, treatment, and outcome
Yildiz Celik S., DURMUŞ TEKÇE H., YILMAZ V., SARUHAN DİRESKENELİ G., Gulsen Parman Y., Serdaroglu Oflazer P., et al.
ACTA NEUROLOGICA BELGICA
, cilt.120, sa.1, ss.133-140, 2020 (SCI-Expanded)
2019
201944. A Val30Met sporadic familial amyloid polyneuropathy case with atypical presentation: upper limb onset of symptoms
Sahin E., Cakar A., Durmus-Tekce H., Parman Y.
ACTA NEUROLOGICA BELGICA
, cilt.119, sa.4, ss.627-628, 2019 (SCI-Expanded)
2019
201945. A novel homozygous FBXO38 variant causes an early-onset distal hereditary motor neuronopathy type IID.
Akcimen F., Vural A., Durmus H., Cakar A., Houlden H., Parman Y. G., et al.
Journal of human genetics
, cilt.64, sa.11, ss.1141-1144, 2019 (SCI-Expanded)
2019
201946. The first biallelic missense mutation in the FXN gene in a consanguineous Turkish family with Charcot-Marie-Tooth-like phenotype
Candayan A., Yunisova G., Cakar A., Durmus H., Basak A. N., Parman Y., et al.
NEUROGENETICS
, 2019 (SCI-Expanded)
2019
201947. Relation of HLA-DRB1 to IgG4 autoantibody and cytokine production in muscle-specific tyrosine kinase myasthenia gravis (MuSK-MG).
ÇEBI M., DURMUŞ H., YILMAZ V., YENTÜR S. P., AYSAL F., OFLAZER P., et al.
Clinical and experimental immunology
, cilt.197, ss.214-221, 2019 (SCI-Expanded)
2019
201948. Mutation spectrum of 260 dystrophinopathy patients from Turkey and important highlights for genetic counseling
Toksoy G., Durmus H., Aghayev A., Bagirova G., Rustemoglu B. S., Basaran S., et al.
NEUROMUSCULAR DISORDERS
, sa.8, ss.601-613, 2019 (SCI-Expanded)
2019
201949. Familial Amyloid Polyneuropathy
Cakar A., Durmus-Tekce H., Parman Y.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, cilt.56, sa.2, ss.150-156, 2019 (SCI-Expanded)
2019
201950. Extending the clinical and mutational spectrum of TRIM32-related myopathies in a non-Hutterite population
Johnson K., De Ridder W., Topf A., Bertoli M., Phillips L., De Jonghe P., et al.
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
, cilt.90, sa.4, ss.490-493, 2019 (SCI-Expanded)
2018
201851. Repetitive nerve stimulation and jitter measurement with disposable concentric needle electrode in newly diagnosed myasthenia gravis patients
Sirin N. G., Orhan E., Durmus H., Deymeer F., Baslo M. B.
NEUROPHYSIOLOGIE CLINIQUE-CLINICAL NEUROPHYSIOLOGY
, cilt.48, sa.5, ss.261-267, 2018 (SCI-Expanded)
2018
201852. Increased costimulatory molecule expression of thymic and peripheral B cells and a sensitivity to IL-21 in myasthenia gravis
Hocaoglu M., Durmus H., Ozkan B., Yentur S. P., Dogan O., Parman Y., et al.
JOURNAL OF NEUROIMMUNOLOGY
, cilt.323, ss.36-42, 2018 (SCI-Expanded)
2018
201853. Detection of variants in dystroglycanopathy-associated genes through the application of targeted whole-exome sequencing analysis to a large cohort of patients with unexplained limb-girdle muscle weakness
Johnson K., Bertoli M., Phillips L., Topf A., Van den Bergh P., Vissing J., et al.
SKELETAL MUSCLE
, cilt.8, 2018 (SCI-Expanded)
2018
201854. Congenital myasthenic syndromes in Turkey: Clinical clues and prognosis with long term follow-up
Durmus H., SHEN X., Serdaroglu-Oflazer P., Kara B., Parman-Gulsen Y., Ozdemir C., et al.
NEUROMUSCULAR DISORDERS
, cilt.28, sa.4, ss.315-322, 2018 (SCI-Expanded)
2018
201855. A database for screening and registering late onset Pompe disease in Turkey
GOKYIGIT M. C., Ekmekci H., Durmus H., Karll N., Koseoglu E., AYSAL F., et al.
NEUROMUSCULAR DISORDERS
, cilt.28, sa.3, ss.262-267, 2018 (SCI-Expanded)
2018
201856. Mutations causing congenital myasthenia reveal principal coupling pathway in the acetylcholine receptor epsilon-subunit
SHEN X., BRENGMAN J. M., SHEN S., Durmus H., PREETHISH-KUMAR V., Yuceyar N., et al.
JCI INSIGHT
, cilt.3, sa.2, 2018 (SCI-Expanded)
2017
201757. Myophosphorylase (PYGM) mutations determined by next generation sequencing in a cohort from Turkey with McArdle disease
Inal-Gultekin G., Toptas-Hekimoglu B., Gormez Z., Gelisin O., Durmus H., ERGUNER B., et al.
NEUROMUSCULAR DISORDERS
, cilt.27, sa.11, ss.997-1008, 2017 (SCI-Expanded, Scopus)
2017
201758. Elevated IL-4 and IFN-γ Levels in Muscle Tissue of Patients with Dermatomyositis
Giris M., Durmus H., Yetimler B., Tasli H., Parman Y., Tuzun E.
IN VIVO
, sa.4, ss.657-660, 2017 (SCI-Expanded)
2017
201759. MUSCLE MAGNETIC RESONANCE IMAGING IN SPINAL MUSCULAR ATROPHY TYPE 3: SELECTIVE AND PROGRESSIVE INVOLVEMENT
Durmus H., Yilmaz R. S., Gulsen-Parman Y., Oflazer-Serdaroglu P., CUTTINI M., Dursun M., et al.
MUSCLE & NERVE
, cilt.55, sa.5, ss.651-656, 2017 (SCI-Expanded)
2017
201760. Jitter measurement using a concentric needle in 133 patients with myasthenia gravis: A retrospective analysis
Sirin N. G., Orhan E. K., Durmus H., Oflazer P., Parman Y., Oge A. E., et al.
Journal of Neurological Sciences
, cilt.34, sa.3, ss.207-214, 2017 (SCI-Expanded)
2016
201661. Neuromuscular endplate pathology in recessive desminopathies: Lessons from man and mice
Durmus H., Ayhan O., CIRAK S., Deymeer F., Parman Y., FRANKE A., et al.
NEUROLOGY
, sa.8, ss.799-805, 2016 (SCI-Expanded)
2016
201662. Genotypic and phenotypic presentation of transthyretin-related familial amyloid polyneuropathy (TTR-FAP) in Turkey.
Durmus-Tekce H., MATUR Z., Atmaca M. M., Poda M., Cakar A., ULAS U. H., et al.
Neuromuscular disorders : NMD
, cilt.26, sa.7, ss.441-6, 2016 (SCI-Expanded)
2016
201663. Genetic heterogeneity within the HLA region in three distinct clinical subgroups of myasthenia gravis.
Saruhan-Direskeneli G., HUGHES T., Yilmaz V., Durmus H., ADLER A., Alahgholi-Hajibehzad M., et al.
Clinical immunology (Orlando, Fla.)
, ss.81-8, 2016 (SCI-Expanded)
2016
201664. Titin antibodies in "seronegative" myasthenia gravis--A new role for an old antigen.
Stergiou C., Lazaridis K., Zouvelou V., Tzartos J., Mantegazza R., Antozzi C., et al.
Journal of neuroimmunology
, cilt.292, ss.108-15, 2016 (SCI-Expanded)
2016
201665. Myasthenia gravis after botulinum toxin type A injection Botulinum toksin tip A enjeksiyonu sonrası açığa çıkan myasthenia gravis olgusu
Tekce H., Deymeer F., Serdaroglu P. O., Parman Y.
Turk Noroloji Dergisi
, cilt.22, sa.3, ss.143-144, 2016 (Scopus)
2016
201666. Vocal Cord Paralysis and Hypercapnic Respiratory Failure in a Patient with Familial Amyloidotic Polyneuropathy
PIHTILI A., Bingol Z., Durmus H., Parman Y., Kiyan E.
INTERNAL MEDICINE
, sa.13, ss.1783-1786, 2016 (SCI-Expanded)
2015
201567. Reduced muscle mitochondrial enzyme activity in MuSK-immunized mice.
Ozkok E., Durmus H., Yetimler B., Tasli H., TRAKAS N., Ulusoy C. A., et al.
Clinical neuropathology
, cilt.34, sa.6, ss.359-63, 2015 (SCI-Expanded)
2015
201568. MuSK autoantibodies in myasthenia gravis detected by cell based assay--A multinational study.
Tsonis A. I., Zisimopoulou P., Lazaridis K., Tzartos J., Matsigkou E., Zouvelou V., et al.
Journal of neuroimmunology
, cilt.284, ss.10-7, 2015 (SCI-Expanded)
2015
201569. Differential cytokine changes in patients with myasthenia gravis with antibodies against AChR and MuSK
Yilmaz V., Oflazer P., AYSAL F., Durmus H., Poulas K., Yentur S. P., et al.
PLoS ONE
, cilt.10, sa.4, 2015 (SCI-Expanded)
2015
201570. Regulatory function of CD4+CD25++ T cells in patients with myasthenia gravis is associated with phenotypic changes and STAT5 signaling: 1,25-Dihydroxyvitamin D3 modulates the suppressor activity.
Alahgholi-Hajibehzad M., Oflazer P., Aysal F., Durmus H., Gulsen-Parman Y., MARX A., et al.
Journal of neuroimmunology
, cilt.281, ss.51-60, 2015 (SCI-Expanded)
2015
201571. The distinct genetic pattern of ALS in Turkey and novel mutations
Ozoguz A., Uyan O., Birdal G., Iskender C., Kartal E., Lahut S., et al.
Neurobiology of Aging
, cilt.36, sa.4, 2015 (SCI-Expanded)
2015
201572. Prevalence of Parkinson's disease in Baskale, Turkey: a population based study
Durmus H., Gökalp M. A., Hanagasi H. A.
NEUROLOGICAL SCIENCES
, cilt.36, sa.3, ss.411-413, 2015 (SCI-Expanded)
2014
201473. Association between restless leg syndrom and slow coronary flow
ERDEN I., ERDEN E. C., Durmus H., Tibilli H., TABAKCI M., KALKAN M. E., et al.
ANADOLU KARDIYOLOJI DERGISI-THE ANATOLIAN JOURNAL OF CARDIOLOGY
, cilt.14, sa.7, ss.612-616, 2014 (SCI-Expanded)
2014
201474. Facial and Skeletal Muscle Magnetic Resonance Imaging in Oculopharyngodistal Myopathy
DURMUŞ TEKÇE H., Dursun M., Sencer S., Deymeer F., Oflazer-Serdaroglu P.
TURKISH JOURNAL OF NEUROLOGY
, cilt.20, sa.4, ss.121-125, 2014 (ESCI)
2014
201475. A comprehensive analysis of the epidemiology and clinical characteristics of anti-LRP4 in myasthenia gravis
ZISIMOPOULOU P., EVANGELAKOU P., TZARTOS J., LAZARIDIS K., ZOUVELOU V., MANTEGAZZA R., et al.
Journal of Autoimmunity
, cilt.52, ss.139-145, 2014 (SCI-Expanded)
2013
201376. Prevalence of Parkinson's disease in Baskale, Turkey: A population-based study
Durmus H., Gokalp M. A., Hanagasi H. A.
MOVEMENT DISORDERS
, cilt.28, 2013 (SCI-Expanded)
2013
201377. Comparative clinical characteristics of early- and adult-onset multiple sclerosis patients with seizures
Durmus H., Kurtuncu M., Tuzun E., Pehlivan M., Akman-Demir G., Yapici Z., et al.
Acta Neurologica Belgica
, cilt.113, sa.4, ss.421-426, 2013 (SCI-Expanded)
2011
201178. Autoantibodies to neuronal surface antigens in thyroid antibody-positive and -negative limbic encephalitis
Tuzun E., Erdag E., Durmus H., Brenner T., Turkoglu R., Kurtuncu M., et al.
NEUROLOGY INDIA
, cilt.59, sa.1, ss.47-50, 2011 (SCI-Expanded)
2010
201079. SLEEP RELATED BREATHING DISORDERS AND LUNG FUNCTION IN PATIENTS WITH OCULOPHARYNGODISTAL MYOPATHY
Memis U., Kiyan E., Durmus H., Oflazer P.
RESPIROLOGY
, cilt.15, ss.106, 2010 (SCI-Expanded)
2010
201080. Unihemispheric acute disseminated encephalomyelitis: A case report Tek hemisferi tutan akut dissemine ensefalomiyelit: Olgu sunumu
Durmus H., TURKOGLU R., Tuzun E.
Noropsikiyatri Arsivi
, cilt.47, sa.2, ss.166-168, 2010 (SCI-Expanded)
2010
201081. Amphiphysin Autoimmunity: Associated Neurological Syndromes and Tumors in The Turkish Population
Tuzun E., Bebek N., Icoz S., Durmus H., Kurtuncu M., Gurses C., et al.
JOURNAL OF NEUROLOGICAL SCIENCES-TURKISH
, cilt.27, sa.2, ss.121-126, 2010 (SCI-Expanded)
2010
201082. Long-term follow-up in patients with congenital myasthenic syndrome due to CHAT mutations
Schara U., Christen H., Durmus H., Hietala M., Krabetz K., Rodolico C., et al.
EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY
, cilt.14, sa.4, ss.326-333, 2010 (SCI-Expanded)
2010
201083. Sensorimotor neuropathy associated with endometrioid endometrial carcinoma
Durmus H., Tuzun E., Icoz S., Akman-Demir G., Parman Y.
European Journal of Obstetrics and Gynecology and Reproductive Biology
, cilt.150, sa.2, ss.216-217, 2010 (SCI-Expanded)
2010
201084. Enhanced IL-6 Production in Aquaporin-4 Antibody Positive Neuromyelitis Optica Patients
Icoz S., Tuzun E., Kurtuncu M., Durmus H., Mutlu M., Eraksoy M., et al.
INTERNATIONAL JOURNAL OF NEUROSCIENCE
, sa.1, ss.71-75, 2010 (SCI-Expanded)
2009
200985. Primary cerebral lymphoma with a 5-year remission to single-agent corticosteroids
Kurtuncu M., Tuzun E., Durmus H., Mutlu M., Akman-Demir G., Eraksoy M.
Leukemia and Lymphoma
, cilt.50, sa.9, ss.1552-1553, 2009 (SCI-Expanded)
2009
200986. Antinuclear antibodies in juvenile myoclonic epilepsy
Altindag E., Icoz S., Tuzun E., Durmus H., Uludokumaci A., Demir G. A., et al.
Journal of Neurological Sciences
, cilt.26, sa.1, ss.43-48, 2009 (Scopus)
2009
200987. Pregnancy-Induced Atypic Demyelinating Inflammatory Disease
Durmus H., Tuzun E., Kurtuncu M., Mutlu M., Demir G. A., Eraksoy M.
NOROPSIKIYATRI ARSIVI-ARCHIVES OF NEUROPSYCHIATRY
, sa.2, ss.80-83, 2009 (SCI-Expanded)
2009
200988. Development of multiple sclerosis in patients with optic neuritis: Analysis of predictive factors
Durmuş Tekçe H., Kürtüncü M., Tüzün E., Akalın B. E., Mutlu M., Akman Demir G., et al.
TURK NOROLOJI DERGISI , cilt.15, sa.3, ss.119-123, 2009 (Hakemli Dergi)
Hakemli Bilimsel Toplantılarda Yayımlanmış Bildiriler
2024
20241. GENETIC LANDSCAPE OF CHARCOT-MARIE-TOOTH DISEASE IN TURKIYE: DISTINCT DISTRIBUTION, RARE PHENOTYPES, AND NOVEL VARIANTS
Çakar A., Candayan A., Bagirova G., Uyguner Z. O., Ceylaner S., Durmuş Tekçe H., et al.
Annual Meeting of the Peripheral-Nerve-Society (PNS), Montreal, Kanada, 22 - 25 Haziran 2024, cilt.29, ss.11, (Özet Bildiri)
2022
20222. Long-term follow-up of five families from Turkey with UBQLN2 variants
Durmus H., ÇAKAR A., Aysal F., Ertas M., Basak N., Parman Y.
21st Annual Meeting of the Northeast-Amyotrophic-Lateral-Sclerosis-Consortium (NEALS), Florida, Amerika Birleşik Devletleri, 1 - 03 Kasım 2022, (Özet Bildiri)
2022
20223. Correlations Between Radiographic Spinopelvic Parameters And Health-Related Quality Of Life: A Prospective Evaluation Of 37 Patients With Facioscapulohumeral Muscular Dystrophy
BAYRAM S., KENDİRCİ A. Ş., KARALAR Ş., DURMUŞ TEKÇE H., PARMAN F. Y., AKGÜL T., et al.
23nd EFORT Congress, Lisbon, Portekiz, 22 - 24 Haziran 2022, cilt.23, (Tam Metin Bildiri)
2022
20224. GNE miyopatisinde solunumsal problemler
Dikmen B., Pıhtılı A., Kıyan E., Parman F. Y., Durmuş Tekçe H.
Türk Toraks Derneği 25. Yıllık Kongresi, Antalya, Türkiye, 24 - 28 Mayıs 2022, ss.896, (Özet Bildiri)
2022
20225. An Exploratory Study of Cognitive Involvement in Hereditary Transthyretin Amyloidosis
Durmus H., ÇAKAR A., Demirci H., Parman F. Y.
Annual Meeting of the American-Academy-of-Neurology, Washington, Amerika Birleşik Devletleri, 2 - 07 Nisan 2022, (Özet Bildiri)
2021
20216. YAYGIN HİPERPİGMENTASYON İLE BAŞVURAN BİR DERMATOMİYOZİT OLGUSU
GEZEGEN H., ALTINKAYNAK M., ÇAKAR A., DURMUŞ TEKÇE H., AKPINAR T. S., PARMAN F. Y.
57. Ulusal nöroloji kongresi, Antalya, Türkiye, 27 Kasım 2021, (Özet Bildiri)
2021
20217. Pandemi Öncesi ve Pandemi Döneminde Guillain-Barré Sendromunun Klinik ve Elektrofizyolojik Özellikleri: Çok Merkezli İstanbul Çalışması
Taşdemir V., Şirin İnan N. G., Çakar A., Çulha A., Soysal A., Elmalı Yazıcı A. D., et al.
57. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 27 Kasım - 01 Aralık 2021, (Yayınlanmadı)
2021
20218. Effects of immunosuppressive treatment on thymocyte maturation in Myasthenia Gravis patiens
Yentür S. P., Durmuş Tekçe H., Erdoğdu E., Yegen G., Yılmaz V., Özkan B., et al.
European Congress of Immunology, Belgrade, Sırbistan, 1 - 04 Eylül 2021, ss.78, (Özet Bildiri)
2021
20219. Expanding the phenotypical spectrum of SACS mutation: A Single Center Experience
ÇAKAR A., İNCİ M., ÖZDAĞ ACARLI A. N., DURMUŞ TEKÇE H., PARMAN F. Y.
Virtual Annual Meeting of the American-Academy-of-Neurology, ELECTR NETWORK, 17 - 22 Nisan 2021, (Özet Bildiri)
2021
202110. Cognitive involvement in transthyretin-related familial amyloid polyneuropathy (TTR-FAP)
DURMUŞ TEKÇE H., ÇAKAR A., Demirci H., PARMAN F. Y.
Virtual Annual Meeting of the American-Academy-of-Neurology, ELECTR NETWORK, 17 - 22 Nisan 2021, (Özet Bildiri)
2020
202011. Cognitive involvement in ATTR amyloidosis (TTR-FAP)
DURMUŞ TEKÇE H., ÇAKAR A., Demirci H., Alaylioglu M., GEZEN AK D., DURSUN E., et al.
Virtual Conference of Peripheral-Nerve-Society, ELECTR NETWORK, 01 Ocak 2020, ss.527, (Özet Bildiri)
2020
202012. Clinical features of a homozygous missense mutation in the FXN gene resulting in a Charcot-Marie-Tooth-like phenotype
ÇAKAR A., Candayan A., Yunisova G., Battaloglu E., DURMUŞ TEKÇE H., PARMAN F. Y.
Virtual Conference of Peripheral-Nerve-Society, ELECTR NETWORK, 01 Ocak 2020, ss.490, (Özet Bildiri)
2020
202013. Episodic psychosis, ataxia, motor neuropathy caused by a novel mutation in ADPRHL2
DURMUŞ TEKÇE H., Hashemolhosseini S., CEYLANER S., PARMAN F. Y.
Virtual Conference of Peripheral-Nerve-Society, ELECTR NETWORK, 01 Ocak 2020, ss.558, (Özet Bildiri)
2020
202014. 3 individuals with mutation in exon 1f of PLEC and myasthenic phenotype
Mroczek M., Durmus H., Topf A., Duff J., Parman Y., Straub V.
6th Congress of the European-Academy-of-Neurology (EAN), ELECTR NETWORK, 23 - 26 Mayıs 2020, cilt.27, ss.1151, (Özet Bildiri)
2020
202015. Clinical And Genetic Characteristics of Bethlem Myopathy Patients from Turkey
Yunisova G., Ceylaner S., Deymeer F., Oflazer P., Durmus H., Parman Y.
6th Congress of the European-Academy-of-Neurology (EAN), ELECTR NETWORK, 23 - 26 Mayıs 2020, cilt.27, ss.1158, (Özet Bildiri)
2020
202016. EPISODIC PSYCHOSIS, ATAXIA, MOTOR NEUROPATHY CAUSED BY A NOVEL MUTATION IN ADPRHL2
DURMUŞ TEKÇE H., Sticht H., Ceylaner S., Hashemolhosseini S., Parmn Y.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)
2020
202017. Circulating B Cell Subsets and Cytokine Gene Expression Levels in Peripheral Blood and Skin Biopsy in Chronic Inflammatory Demyelinating Polyneuropathy
Acarli A. N. O., Yilmaz V., Sirin N. G., ÇAKAR A., Soysal A., Aysal F., et al.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, (Özet Bildiri)
2020
202018. Clinical and genetic features of SPG11: A Single Center Experience
Cakar A., Gezegen H., Tunca C., Bayraktar E., Basak N., Durmus-Tekce H., et al.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)
2020
202019. Studying Clinical and Genetic Characteristics of Emery-Dreifuss Muscular Dystrophy
Yunisova G., Oflazer P., Deymeer F., ÇAKAR A., PARMAN F. Y., DURMUŞ TEKÇE H.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, cilt.94, (Özet Bildiri)
2020
202020. Skin Biopsy as a Biomarker in Chronic Inflammatory Demyelinating Polyneuropathy
Parman Y., Acarli A. N. O., ÜNVERENGİL G., Sirin N. G., ÇAKAR A., DURMUŞ TEKÇE H.
Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 25 Nisan - 01 Mayıs 2020, (Özet Bildiri)
2019
201921. Antibodies Against Peripheral Nerve Antigens in Chronic Inflammatory Demyelinating Polyradiculoneuropathy in a Turkish Cohort
ÖZDAĞ ACARLI A. N., VURAL A., YILMAZ V., Şirin N., DURMUŞ TEKÇE H., SARUHAN DİRESKENELİ G., et al.
2019 PNS (Peripheral Nerve Society) Annual Meeting, Cenova, İtalya, 21 - 26 Haziran 2019
2019
201922. GNE MYOPATHY in TURKEY: CLINICAL FEATURES AND NOVEL MUTATIONS
Durmus H., Ceylaner S., Parman F. Y., Deymeer F., Serdaroglu P.
71st Annual Meeting of the American-Academy-of-Neurology (AAN), Pennsylvania, Amerika Birleşik Devletleri, 4 - 10 Mayıs 2019, cilt.92, (Özet Bildiri)
2019
201923. Autosomal Recessive Charcot-Marie-Tooth Disease in Turkey
Parman Y., Cakar A., Candayan A., Akcay H. I., Yunisova G., Ulukan Ç., et al.
71st Annual Meeting of the American-Academy-of-Neurology (AAN), Pennsylvania, Amerika Birleşik Devletleri, 4 - 10 Mayıs 2019, cilt.92, (Özet Bildiri)
2018
201824. Congenital myasthenic syndromes due to impaired principal coupling pathway in the epsilon-subunit of muscle acetylcholine receptor
Shen X., Selcen D., Brengman J., Shen S., Durmus H., Preethish-Kumar V., et al.
23rd International Annual Congress of the World-Muscle-Society (WMS), Mendoza, Arjantin, 2 - 06 Ekim 2018, cilt.28, (Özet Bildiri)
2018
201825. Clinical and Genetic Features in X-Linked Charcot-Marie-Tooth Neuropathy (CMT-X) Patients from Turkey
Parman Y., Durmus H., Candayan A., Akcay H. I., Yunisova G., Ulukan Ç., et al.
70th Annual Meeting of the American-Academy-of-Neurology (AAN), Los-Angeles, Şili, 21 - 27 Nisan 2018, cilt.90, (Özet Bildiri)
2018
201826. Congenital Myasthenic Syndromes (CMS) Due to Impaired Principal Coupling Pathway in the. Subunit of Muscle Acetylcholine Receptor (AChR)
Shen X., Brengman J., Shen S., Durmus H., Preethish-Kumar V., Yuceyar N., et al.
70th Annual Meeting of the American-Academy-of-Neurology (AAN), Los-Angeles, Şili, 21 - 27 Nisan 2018, cilt.90, (Özet Bildiri)
2018
201827. Klinik Fasilitasyonun Eşlik Ettiği Myasthenia Gravis: Olgu Serisi
ATMACA M. M., DURMUŞ TEKÇE H., KOCASOY ORHAN E., BASLO M. B., DEYMEER F.
34.Ulusal Klinik Nörofizyoloji EEG-EMG Kongresi, Türkiye, 4 - 08 Nisan 2018
2017
201728. GENOTYPIC AND PHENOTYPIC PRESENTATION OF TRANSTHYRETIN- RELATED FAMILIAL AMYLOID POLYNEUROPATHY (TTR-FAP) IN TURKEY
Durmus H., Cakar A., Sahin E., Matur Z., Poda M., Altunoglu U., et al.
Peripheral-Nerve-Society Meeting, Sitges, İspanya, 8 - 12 Temmuz 2017, cilt.22, ss.276-277, (Özet Bildiri)
2017
201729. Congenital myasthenic syndromes in Turkey
Durmus H., Kara B., Parman Y., Oflazer P., Deymeer F.
3rd Congress of the European-Academy-of-Neurology, Amsterdam, Hollanda, 01 Haziran 2017, cilt.24, ss.500, (Özet Bildiri)
2016
201630. PAROKSİSMAL DİZARTRİ VE ATAKSİ ATAKLARIYLA BAŞVURAN LEPTOMENİNGEAL TUTULUMLA GİDEN MEME KANSERİ OLGUSU
Uygun Ö., Sezgin M., Durmuş Tekçe H., Baykan B.
52. ULUSAL NÖROLOJİ KONGRESİ, Antalya, Türkiye, 25 Kasım - 01 Aralık 2016, ss.97-98, (Özet Bildiri)
2016
201631. CHARCOT-MARIE-TOOTH DISEASE IN TURKEY: CLINICAL AND GENETIC FINDINGS FROM A SINGLE-CENTRE EXPERIENCE
Akcay H., Durmus H., Deymeer F., Oflazer-Serdaroglu P., Sivaci M., Candayan A., et al.
Inflammatory Neuropathy Consortium and GBS 100 Centenary Symposium and Ceilidh, Glasgow, Birleşik Krallık, 21 - 24 Haziran 2016, cilt.21, ss.230-231, (Özet Bildiri)
2016
201632. Clinical and Genetic Heterogeneity in Charcot-Marie-Tooth Neuropathy Type 2 Patients from Turkey
Durmus H., Akcay H. I., Sivaci M., Serdaroglu P., Deymeer F., Battaloglu E., et al.
68th Annual Meeting of the American-Academy-of-Neurology (AAN), Vancouver, Kanada, 15 - 21 Nisan 2016, cilt.86, (Özet Bildiri)
2016
201633. Clinical and Genetic Heterogeneity in Familial ALS Patients from Turkey
Durmus H., Sezgin M., Samanci B., Ozoguz A., Deymeer F., Serdaroglu P., et al.
68th Annual Meeting of the American-Academy-of-Neurology (AAN), Vancouver, Kanada, 15 - 21 Nisan 2016, (Özet Bildiri)
2015
201534. TÜRK TOPLUMUNDA EN SIK RASTLANILAN MİYOFOSFORİLAZ (PYGM) MUTASYONLARI: MCARDLE HASTALIĞININ GENETİK TANISI İÇİN YENİ NESİL DİZİLEME
İNAL GÜLTEKİN G., TOPTAŞ HEKİMOĞLU B., GÖRMEZ Z., DURMUŞ TEKÇE H., SAĞIROĞLU M. Ş., DEMİRCİ H., et al.
51. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 27 Kasım - 03 Aralık 2015, (Özet Bildiri)
2015
201535. Genotypic and phenotypic presentation of Glu89Gln mutation in Turkey
DURMUŞ TEKÇE H., MATUR Z., ATMACA M. M., PODA M., ÇAKAR A., SERDAROĞLU OFLAZER P., et al.
First European Congress on Hereditary ATTR amyloidosis, Fransa, 2 - 03 Kasım 2015
2015
201536. Evaluation of maximum oxygen utilization in McArdle patients before and after exercise training
Gelisin O., Durmus H., Yakal S., Kasikcioglu E., Parman Y., Deymeer F., et al.
20th International Congress of the World-Muscle-Society, Brighton, Birleşik Krallık, 30 Eylül - 04 Ekim 2015, cilt.25, (Özet Bildiri)
2015
201537. Myophosphorylase (PYGM) mutations in Turkish patients with McArdle disease: A next generation sequencing study
Gultekin G. I., Hekimoglu B. T., Gormez Z., Durmus H., Demirci H., Sagiroglu M., et al.
20th International Congress of the World-Muscle-Society, Brighton, İngiltere, 30 Eylül - 04 Ekim 2015, (Özet Bildiri)
2015
201538. CLINICAL AND GENETIC CHARACTERISTICS OF 20 ALS PATIENTS FROM TURKEY WITH SOD1 MUTATIONS
Samanci B., Durmus H., Ozoguz A., Oflazer-Serdaroglu P., Deymeer F., Basak A. N., et al.
Biennial Meeting of the Peripheral-Nerve-Society, Quebec, Kanada, 27 Haziran - 02 Temmuz 2015, ss.224-225, (Özet Bildiri)
2015
201539. GENETIC SURVEY OF A LARGE COHORT OF CMT PATIENTS FROM TURKEY REVEALED EQUAL FREQUENCIES OF CMT1A DUPLICATION AND HNPP DELETION
Ozes B., Sivaci M., Akyuz K., Durmus H., Deymeer F., Oflazoglu P., et al.
Biennial Meeting of the Peripheral-Nerve-Society, Quebec, Kanada, 27 Haziran - 02 Temmuz 2015, cilt.20, ss.205, (Özet Bildiri)
2015
201540. Reduced muscle mitochondrial enzyme activity in MuSK-immunized mice
Durmus H., Ozkok E., Yetimler B., Tuzun E.
1st Congress of the European-Academy-of-Neurology, Berlin, Almanya, 20 - 23 Haziran 2015, cilt.22, ss.720
2015
201541. Ocular myasthenia gravis
Uyar T., Durmus H., Parman Y., Serdaroglu-Oflazer P., Saruhan-Direskeneli G., Deymeer F.
1st Congress of the European-Academy-of-Neurology, Berlin, Almanya, 20 - 23 Haziran 2015, cilt.22, ss.720, (Özet Bildiri)
2015
201542. Myasthenia gravis hastalarının elektrofizyolojik incelemelerine retrospektif bir bakış
ŞİRİN N. G., KOCASOY ORHAN E., DURMUŞ TEKÇE H., BASLO M. B., DEYMEER F.
31. ulusal klinik nörofizyoloji EEG-EMG kongresi, Türkiye, 8 - 12 Nisan 2015
2014
201443. İ.T.F. NÖROLOJİ ANABİLİM DALINDA İZLENEN AMYOTROFİK LATERAL SKLEROZ HASTALARININ GENETİK VE KLİNİK ÖZELLİKLER AÇISINDAN İNCELENMESİ
Sezgin M., Samancı B., Durmuş Tekçe H., Özoğuz A., Oflazer Serdaoğlu P., Deymeer F., et al.
50. Ulusal Nöroloji Kongresi, Antalya, Türkiye, 22 Kasım - 26 Aralık 2014, ss.90-91, (Özet Bildiri)
2014
201444. Differential cytokine changes in myasthenia gravis patients with antibodies against AChR and Musk
Yilmaz V., Oflazer P., Aysal F., Durmus H., Poulos K., Parman Y., et al.
12th International Congress of Neuroimmunology (ISNI), Mainz, Almanya, 9 - 13 Kasım 2014, cilt.275, ss.212-213, (Özet Bildiri)
2014
201445. Late-onset non-thymomatous generalized myasthenia gravis
Yildiz-Celik S., Durmus H., Hajibehzad M., Yilmaz V., Oflazer-Serdaroglu P., Parman Y., et al.
19th International Congress of the World-Muscle-Society, Berlin, Almanya, 7 - 11 Ekim 2014, cilt.24, ss.842, (Özet Bildiri)
2014
201446. Dramatic improvement after injection augmentation in oculopharyngodistal myopathy
Ozcan O., Durmus H., Tarhan O., Polat Z., Deymeer F., Parman Y., et al.
19th International Congress of the World-Muscle-Society, Berlin, Almanya, 7 - 11 Ekim 2014, cilt.24, ss.796, (Özet Bildiri)
2014
201447. Exome sequencing vs phenotype directed gene screening in CMT patients from Turkey
Sivaci M., Parman Y., Gonzaga-Jauregui C., Pehlivan D., Durmus H., Deymeer F., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201448. Clinical and genetic features of patients with MNGIE: cohort at the department of neurology, Istanbul Faculty of Medicine
Cakar A., Durmus H., Gunduz T., Deymeer F., Parman Y., Oflazer-Serdaroglu P.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.21, ss.519, (Özet Bildiri)
2014
201449. Genotypic and phenotypic presentation of TTR-FAP in Turkey
Durmus H., Matur Z., Atmaca M. M., PODA M., Oflazer-Serdaroglu P., Deymeer F., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201450. Exome sequencing vs. phenotype directed gene screening in CMT patients from Turkey
Sivaci M., Parman Y., Gonzaga-Jauregui C., Pehlivan D., Durmus H., Deymeer F., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.21, ss.209, (Özet Bildiri)
2014
201451. Whole exome sequencing analysis in recessive hereditary spastic paraplegia patients from Turkey
Ozes B., Gonzalez M., Durmus H., Deymeer F., Oflazoglu P., Zuechner S., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201452. Genotypic and phenotypic presentation of TTR-FAP in Turkey
Durmus H., Matur Z., Atmaca M. M., Poda M., Oflazer-Serdaroglu P., Deymeer F., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.21, ss.137, (Özet Bildiri)
2014
201453. The distinct genetic pattern of ALS in Turkey
Ozoguz A., Uyan O., Birdal G., Iskender C., Omur O., Lahut S., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201454. Clinical and genetic features of the patients with MNGIE: cohort at the department of neurology, Istanbul Faculty of Medicine
Cakar A., Durmus H., Gunduz T., Deymeer F., Parman Y., Oflazer-Serdaroglu P.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201455. The distinct genetic pattern of ALS in Turkey
Ozoguz A., Uyan O., Birdal G., Iskender C., Omur O., Lahut S., et al.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.21, ss.63, (Özet Bildiri)
2014
201456. Tafamidis treatment in a patient with transthyretin amyloidosis due to domino liver transplantation
Matur Z., Atmaca M. M., Durmus H., Parman Y.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.21, ss.543, (Özet Bildiri)
2014
201457. Tafamidis treatment in a patient with transthyretin amyloidosis due to domino liver transplantation
Matur Z., Atmaca M. M., Durmus H., Parman Y.
Joint Congress of European Neurology, İstanbul, Türkiye, 31 Mayıs - 03 Haziran 2014, cilt.261, (Özet Bildiri)
2014
201458. Genotype-Phenotype Evaluation In 476 Turkish Dystrophinopathy Patients
Durmuş H., GEYİK F., ERGINEL-UENALTUNA N., PODA M., Çakar A., Altınkaya A., et al.
The 66th AAN Annual Meeting, Philadelphia, Amerika Birleşik Devletleri, 26 Nisan 2014 - 03 Mayıs 0215, ss.96, (Tam Metin Bildiri)
2013
201359. Clinical and Genetic Characteristics of Five Turkish Families with UBQLN2 Mutations
Durmus H., Ozoguz A., Deymeer F., Serdaroglu P., Aysal F., Ertas M., et al.
65th Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 16 - 23 Mart 2013, cilt.80, (Özet Bildiri)
2013
201360. Distribution and Severity of Weakness in Patients with Polymyositis and Dermatomyositis: Different Pathophysiology, Different Affected Muscle Groups
Durmus H., Deymeer F., Parman Y., Serdaroglu P.
65th Annual Meeting of the American-Academy-of-Neurology (AAN), California, Amerika Birleşik Devletleri, 16 - 23 Mart 2013, cilt.80, (Özet Bildiri)
2012
201261. IN-HOSPITAL STROKE RECURRENCE OF ACUTE ISCEMIC STROKE
Durmuş Tekçe H., Yeşilot N., Tuncay R., Çoban O., Zarkobahar S.
21.European Stroke Conference, Lisbon, Portekiz, 22 - 24 Mayıs 2012, ss.651-652, (Özet Bildiri)
2012
201262. Using whole exome sequencing to identify the mutation causing oculopharyngodistal myopathy
Wagner M., Laval S., Mueller J., Durmus H., Serdaroglu-Oflazer P., Lochmueller H.
United Kingdom Neuromuscular Translational Research Conference, Newcastle-Upon-Tyne, Birleşik Krallık, 22 - 23 Mart 2012, cilt.22, (Özet Bildiri)
2012
201263. Clinical Features of the "Optineurin" Mutation in familial FTD and ALS
Cikrikcili U., Durmus H., Basak N., Gunel M., GÜRVİT İ. H., Matur Z., et al.
8th International Conference on Frontotemporal Dementias, Manchester, Birleşik Krallık, 5 - 07 Eylül 2012, cilt.33, ss.231, (Özet Bildiri)
2010
201064. Oculopharyngodistal Myopathy Is a Distinct Entity - Clinical and Genetic Characterization of 40 Turkish OPDM Patients
Durmus H., Laval S. H., Deymeer F., Parman Y., Kiyan E., Gokyigit M., et al.
62nd Annual Meeting of the American-Academy-of-Neurology, Toronto, Kanada, 10 - 17 Nisan 2010, (Özet Bildiri)
2008
200865. Anti-neuronal antibodies in Hashimoto's thyroiditis patients with central nervous system involvement
Durmuş H., Icoez S., Tuezuen E., Kuertuencue M., Hanagasi H. A., Bebek N., et al.
18th Meeting of the European-Neurological-Society, Nice, Fransa, 7 - 11 Haziran 2008, ss.139, (Özet Bildiri)
2008
200866. Syndrome of transient headache and neurological deficits with cerebrospinal fluid lymphocytosis: is it auto-immune?
KURTUNCU M., TUZUN E., ICOZ S., Baslo B., KAYA D., DURMUS H., et al.
18th Meeting of the European-Neurological-Society, Nice, Fransa, 7 - 11 Haziran 2008, cilt.255, ss.216-217, (Özet Bildiri)
2007
200767. Demographic and clinical statistics of multiple sclerosis and demyelinating diseases in an outpatients clinic, Istanbul Faculty of Medicine
Kurtuncu M., Peldivan M., Durmus H., Mutlu M., Yesilot N., Korkmaz F., et al.
23rd Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis/12th Annual Conference of Rehabilitation in MS, Prague, Çek Cumhuriyeti, 11 - 14 Ekim 2007
2007
200768. Epileptic seizures in multiple sclerosis
Durmus H., Kurtuncu M., Matur Z., Pehlivan M., Mutlu M., Yapici Z., et al.
23rd Congress of the European-Committee-for-Treatment-and-Research-in-Multiple-Sclerosis/12th Annual Conference of Rehabilitation in MS, Prague, Çek Cumhuriyeti, 11 - 14 Ekim 2007, cilt.13
2007
200769. Devic's neuromyelitis optica: a prospective study
Eraksoy M., Akman-Demir G., Kurtuncu M., Yapici Z., Mutlu M., Topcular B., et al.
17th Meeting of the European-Neurological-Society, Rhodes, Yunanistan, 16 - 20 Haziran 2007, ss.36
2007
200770. The use of IFNB-1 b therapy before and after 16 years ofage in children with multiple sclerosis: a prospective follow-up
Eraksoy M., Akinan-Demir G., Yapici Z., Kurtuncu M., Mutlu M., Topcular B., et al.
17th Meeting of the European-Neurological-Society, Rhodes, Yunanistan, 16 - 20 Haziran 2007, ss.39
Kitaplar
2020
20201. Familial Amiloid Polinöropati - Dünya ve Türkiye Deneyimi Yeni Gelişmeler Işığında Transtiretin İlişkili Ailevi Amiloid Polinöropatisi
ÇAKAR A., DURMUŞ TEKÇE H., DEYMEER F., OFLAZER P., PARMAN F. Y.
Nadir Hastalıklar Pompe, Fabry ve TTR-FAP, Hilmi Uysal, Editör, Palme Yayınevi, Ankara, ss.177-190, 2020
2015
20152. Konjenital Miyopatiler
DURMUŞ TEKÇE H.
ÇOCUK VE ERGENDE NÖROLOJİK HASTALIKLARA YAKLAŞIMREHBER KİTABI, Ayşın DerventSemih AytaÖzlem ÇokarDerya Uludüz, Editör, Türk Nöroloji Derneği, ss.259-262, 2015
2015
20153. Juvenil Myastenia Gravis
DURMUŞ TEKÇE H., DEYMEER F.
ÇOCUK VE ERGENDE NÖROLOJİK HASTALIKLARAYAKLAŞIM REHBER KİTABI, Ayşın DerventSemih AytaÖzlem ÇokarDerya Uludüz, Editör, Türk Nöroloji Derneği, ss.320-324, 2015
Desteklenen Projeler
2019 - 2023
2019 - 2023Kontraktürle seyreden nöromüsküler hastalıklara neden olabilecek yeni genlerin araştırılması: Genom ve Tüm Ekzom Çalışması
Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi
DURMUŞ TEKÇE H. (Yürütücü), YUNISOVA G., PARMAN F. Y.
2018 - 2019
2018 - 2019Kontraktürlü Miyopatilerin Klinik ve Genetik Özelliklerinin Belirlenmesi
Yükseköğretim Kurumları Destekli Proje , BAP Doktora
DURMUŞ TEKÇE H. (Yürütücü), YUNISOVA G., PARMAN F. Y.
2017 - 2017
2017 - 2017Cytokine Production in Myasthenia Gravis Patients
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
YILMAZ V. (Yürütücü), DEYMEER F., OFLAZER P., SARUHAN DİRESKENELİ G., DURMUŞ TEKÇE H., TÜZÜN E., et al.
2017 - 2017
2017 - 201732 novel pathogenic sequence variants in 253 DMD/BMD patients from Turkey
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
TOKSOY G. (Yürütücü), BAGİROVA G., ALTUNOĞLU U., PARMAN F. Y., UYGUNER Z. O., OFLAZER Z. P., et al.
2016 - 2017
2016 - 2017Myasthenia gravisde otoantikor üretimini düzenleyen mekanizmaların periferik kan ve timus B hücrelerinde incelenmesi
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
SARUHAN DİRESKENELİ G. (Yürütücü), DURMUŞ TEKÇE H., HOCAOĞLU M., ALTINTAŞ F.
2016 - 2017
2016 - 2017Kasa Özgü Kinaza Karşı Otoantikorlarla Gelişen Myasthenia Gravis (MuSK-MG) de HLA İlişkisinin Otoantikor İzotiplerine Etkisi
Yükseköğretim Kurumları Destekli Proje , BAP Y.Lisans
SARUHAN DİRESKENELİ G. (Yürütücü), ÇEBİ M., DURMUŞ TEKÇE H.
2016 - 2016
2016 - 2016Myasthenia gravis'de CD4 efektör ve regulatör T hücre ortak kültürlerinde sitokin üretimi ve IL-21'in etkisi
Yükseköğretim Kurumları Destekli Proje , BAP Diğer
SARUHAN DİRESKENELİ G. (Yürütücü), DURMUŞ TEKÇE H.
2013 - 2015
2013 - 2015Türk toplumunda miyofosforilaz enzim eksikliğinin (McArdle hastalığı) moleküler ve fenotipik karakterizasyonu
Yükseköğretim Kurumları Destekli Proje , BAP Araştırma Projesi
İNAL GÜLTEKİN G. (Yürütücü), ÖZTÜRK O., DURMUŞ TEKÇE H., PARMAN F. Y.
Bilimsel Yayınlarda Hakemlikler
Ekim 2018
Ekim 2018Orphanet Journal of Rare Diseases Editorial Office
Diğer Dergiler
Atıflar
Toplam Atıf Sayısı (WOS): 702
h-indeksi (WOS): 13
Jüri Üyelikleri
Mayıs-2023
Mayıs 2023