Halil İbrahim Aydın

Hearing Loss in Biotinidase Deficiency: Genotype-Phenotype Correlation

Gülsüm Aydan Genç, Ayşegül Tokatlı, Ali Dursun et al. · The Journal of Pediatrics · 2007 · 49 citations

Health Professions, Audiology, Genetics +13

Analysis of heart rate variability in children with primary nocturnal enuresis

Mehmet Ruşen Dündaröz, Metin Denli, Mehmet Uzun et al. · International Urology and Nephrology · 2001 · 30 citations

Medicine, Pediatrics, Physiology +8

Adipokine, adropin and endothelin-1 levels in intrauterine growth restricted neonates and their mothers

Halil İbrahim Aydın, Ayla Eser, İkbal Kaygusuz et al. · Journal of Perinatal Medicine · 2015 · 29 citations

Medicine, Obstetrics, Physiology +16

Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis

Macarena Cabrera‐Serrano, Laure Caccavelli, Marco Savarese et al. · Brain · 2021 · 29 citations · Full text

Medicine, Genetics, Molecular Genetics +14

Lack of prolidase causes a bone phenotype both in human and in mouse

Roberta Besio, Silvia Maruelli, Roberta Gioia et al. · Bone · 2014 · 26 citations

Medicine, Craniofacial Biology, Orthopaedic Surgery +8