Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Ahmet Okay Cağlayan"'
Autor:
Hilal Akköprü, Alper Alnak, Zeynep Nur Karadoğan, Ahmet Okay Çağlayan, Mustafa Özçetin, Murat Coşkun
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 33, Iss 1, Pp 14-19 (2023)
Externí odkaz:
https://doaj.org/article/88f72bd0cf4a4be79c52f18d2a251046
Publikováno v:
Psychiatry and Clinical Psychopharmacology, Vol 31, Iss 3, Pp 261-268 (2021)
Externí odkaz:
https://doaj.org/article/098fc880b5484d199961a19b18203602
Autor:
Meral Torun Bayram, Gizem Yildiz, Ahmet Okay Cağlayan, Ayfer Ulgenalp, Sadiye Mehtat Unlu, Alper Soylu, Salih Kavukcu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f0a5f39c5c4d1872f5cc540605456be
https://avesis.deu.edu.tr/publication/details/7f3617ac-5d0c-4289-be42-3cad9af2a7b7/oai
https://avesis.deu.edu.tr/publication/details/7f3617ac-5d0c-4289-be42-3cad9af2a7b7/oai
Autor:
Meral Torun Bayram, Gizem Yildiz, Ahmet Okay Cağlayan, Ayfer Ulgenalp, Sadiye Mehtat Unlu, Alper Soylu, Salih Kavukcu
Publikováno v:
Pediatric nephrology (Berlin, Germany). 38(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e9724dcb3a450a4d696ca53b53f4c0e
https://pubmed.ncbi.nlm.nih.gov/35695963
https://pubmed.ncbi.nlm.nih.gov/35695963
Autor:
Hakan, Gümüş, Stijn, Ghesquiere, Hüseyin, Per, Meda, Kondolot, Kimiyoshi, Ichida, Gamze, Poyrazoğlu, Sefer, Kumandaş, John, Engelen, Munis, Dundar, Ahmet Okay, Cağlayan
Publikováno v:
Developmental medicine and child neurology. 52(9)
Molybdenum cofactor (MoCo) deficiency is a rare autosomal recessive inherited metabolic disorder resulting in the combined deficiency of aldehyde oxidase, xanthine dehydrogenase, and sulfite oxidase. We report a male infant with MoCo deficiency whose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c83375f4327339b8d4a41c6bbf51fb4a
https://pubmed.ncbi.nlm.nih.gov/20573177
https://pubmed.ncbi.nlm.nih.gov/20573177