Ali Dursun

Natural History, Outcome, and Treatment Efficacy in Children and Adults with Glutaryl-CoA Dehydrogenase Deficiency

Stefan Kölker, Sven F. Garbade, Cheryl R. Greenberg et al. · Pediatric Research · 2006 · 266 citations · Full text

Nutrition, Metabolic Disorder, Pediatric Hematology +8

Biallelic mutations in SNX14 cause a syndromic form of cerebellar atrophy and lysosome-autophagosome dysfunction

Naiara Akizu, Vincent Cantagrel, Maha S. Zaki et al. · Nature Genetics · 2015 · 134 citations · Full text

Cell Autophagy, Mitophagy, Biallelic Mutations +10

Identification of 16 novel mutations in the argininosuccinate synthetase gene and genotype-phenotype correlation in 38 classical citrullinemia patients

Hong‐Zhi Gao, Keiko Kobayashi, Ayako Tabata et al. · Human Mutation · 2003 · 83 citations

Argininosuccinate Synthetase Gene, Classical Citrullinemia Patients, Genetic Disorder +15

Dry Eye Related to Commonly Used New Antidepressants

Emel Koçer, Abdülkadir Koçer, Mustafa Özsütçü et al. · Journal of Clinical Psychopharmacology · 2015 · 77 citations

New Antidepressants, Ophthalmology, Psychiatry +14

Newborn PKU screening in Turkey: at present and organization for future.

İ Özalp, Turgay Coşkun, H. Serap Kalkanoğlu et al. · PubMed · 2001 · 65 citations

Pkenylketonuria Screening, Persistent Hyperphenylalaninemia, Neonatology +19