Halil İbrahim Aydın

Hearing Loss in Biotinidase Deficiency: Genotype-Phenotype Correlation

Hatice Serap Sivri, Gülsüm Aydan Genç, Ayşegül Tokatlı et al. · The Journal of Pediatrics · 2007 · 47 citations

Health Sciences, Physiology, Audiology +6

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 · 29 citations

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

Metabolic Disorder, Intrauterine Growth, Gynecology +23

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

Macarena Cabrera‐Serrano, Laure Caccavelli, Marco Savarese et al. · Brain · 2021 · 28 citations · Full text

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

Bone Disease, Pathology, Bone Metabolism +7