Dirim, A. B. Et Al. 2023. Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.. Clinical rheumatology , vol.42, no.2 , 597-606.

Dirim, A. B., Kalayci, T., Safak, S., Garayeva, N., Gultekin, B., Hurdogan, O., ... Solakoglu, S.(2023). Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.. Clinical rheumatology , vol.42, no.2, 597-606.

Dirim, Ahmet Et Al. "Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.," Clinical rheumatology , vol.42, no.2, 597-606, 2023

Dirim, Ahmet B. Et Al. "Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.." Clinical rheumatology , vol.42, no.2, pp.597-606, 2023

Dirim, A. B. Et Al. (2023) . "Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.." Clinical rheumatology , vol.42, no.2, pp.597-606.

@article{article, author={Ahmet Burak DİRİM Et Al. }, title={Heme oxygenase-1 deficiency as an extremely rare cause of AA-type renal amyloidosis: Expanding the clinical features and review of the literature.}, journal={Clinical rheumatology}, year=2023, pages={597-606} }