Author

Halil İbrahim Aydın

Observed names: AYDIN, H.İ., AYDIN, HALİL İBRAHİM, AYDIN, Halil İbrahim, H. I. Aydin, H. Ibrahim Aydin, H. İbrahim Aydın, H.I. Aydin, H.İ Aydı́n, H.İ. Aydın, HALİL İBRAHİM AYDIN, Halil Aydin, Halil I Aydin, Halil I. Aydın, Halil Ibrahim Aydin, Halil Ibrahim Aydın, Halil İBrahim Aydin, Halil İbrahim Aydin, Halil İbrahim Aydi̇n, Halıl Ibrahım Aydın

Institutions: Başkent University, Başkent University Hospital

Observed institutions: Ministry of Education, Culture, Sports, Science and Technology, University of Connecticut, Henry Ford Health, Wayne State University, Başkent University, Henry Ford Hospital, Gülhane Askerî Tıp Akademisi, Başkent University Hospital, Etimesgut Asker Hastanesi, Turgut Özal University, Hacettepe University, UConn Health, Teikyo University

ORCID: 0000-0001-7994-4394

Observed ORCID: 0000-0001-7994-4394

OpenAlex ID: A5011174794

Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters

2009 · F. Hörster, S. F. Garbade, et al. · Journal of Inherited Metabolic Disease · 74

Hearing Loss in Biotinidase Deficiency: Genotype-Phenotype Correlation

2007 · Hatice Serap Kalkanoğlu Sivri, Gülsüm Aydan Genç, et al. · The Journal of Pediatrics · 50

Diagnostic work‐up and management of patients with isolated methylmalonic acidurias in European metabolic centres

2008 · T. Zwickler, M. Lindner, et al. · Journal of Inherited Metabolic Disease · 43

Thoracic ectopic kidney in a child: a case report

2000 · Halil İbrahim Aydın, S. Ümit Sarıcı, et al. · The Turkish Journal of Pediatrics · 40

PDF

NMR-Based Screening for Inborn Errors of Metabolism: Initial Results from a Study on Turkish Neonates

2014 · Sitke Aygen, Ulrich Dürr, et al. · JIMD Reports · 36

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

2015 · Halil Ibrahim Aydin, Ayla Eser, et al. · Journal of Perinatal Medicine · 31

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

2021 · Macarena Cabrera-Serrano, Laure Caccavelli, et al. · Brain · 30

PDF

Analysis of heart rate variability in children with primary nocturnal enuresis

2001 · M. Ruşen Dündaröz, Metin Denli, et al. · International Urology and Nephrology · 30

Two Cases of Ralstonia pickettii Bacteremias in a Pediatric Oncology Unit Requiring Removal of the Port-A-Caths

2005 · Erol Kismet, Abdullah Avni Atay, et al. · Journal of Pediatric Hematology/Oncology · 26

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

2014 · Roberta Besio, Silvia Maruelli, et al. · Bone · 25

Audiologic findings in children with biotinidase deficiency in Turkey

2006 · G.A. Genc, H.S. Sivri-Kalkanoğlu, et al. · International Journal of Pediatric Otorhinolaryngology · 22

Three-Country Snapshot of Ornithine Transcarbamylase Deficiency

2022 · Berna Seker Yilmaz, Julien Baruteau, et al. · Life · 19

PDF

HDR Syndrome (Hypoparathyroidism, Sensorineural Deafness and Renal Disease) Accompanied by Renal Tubular Acidosis and Endocrine Abnormalities

2008 · Abdullah Taslipinar, Levent Kebapcilar, et al. · Internal Medicine · 19

PDF

Henoch-Schönlein Purpura in a Child Following Varicella

2005 · Süleyman Kalman, H. İbrahim Aydın, et al. · Journal of Tropical Pediatrics · 19

Hand and heart, hand in hand: is radiological hand osteoarthritis associated with atherosclerosis?

2013 · Ozlem Cemeroglu, Halil I. Aydın, et al. · International Journal of Rheumatic Diseases · 17

PDF

Meningitis with multidrug-resistant Acinetobacter baumannii treated with ampicillin/sulbactam

2004 · T Kendirli, H.İ Aydı́n, et al. · Journal of Hospital Infection · 16

Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance

2013 · Ayşegül Güzel-Ozantürk, Rıza Köksal Özgül, et al. · Gene · 15

Two novel deletions in hypotonia–cystinuria syndrome

2012 · Luc Régal, Halil Ibrahim Aydin, et al. · Molecular Genetics and Metabolism · 15

Antiannexin V autoantibody in thrombophilic Beh�et?s disease

2004 · M. I. Yilmaz, A. Sengul, et al. · Rheumatology International · 15

Evaluation of bone mineral density in chronic glue sniffers

2002 · M. Ruşen Dündaröz, S. Ümit Sarıcı, et al. · The Turkish Journal of Pediatrics · 15

PDF

A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism

2019 · Halil İbrahim Aydın, Fatma Müjgan Sönmez · The Turkish Journal of Pediatrics · 14

PDF

Bone age in children with nocturnal enuresis

2001 · M. Ruşen Dündaröz, S. Ümit Sarici, et al. · International Urology and Nephrology · 14

A Turkish Case with Molybdenum Cofactor Deficiency

2006 · K. Ichida, H. Ibrahim Aydin, et al. · Nucleosides Nucleotides & Nucleic Acids · 13

A novel mutation in TRMT5 associated with idiopathic non-cirrhotic portal hypertension and hepatopulmonary syndrome: Case report of two siblings

2022 · Khaled Warasnhe, Figen Özçay, et al. · Clinics and Research in Hepatology and Gastroenterology · 12

A Novel Mutation of Na+/Glucose Cotransporter in a Turkish Newborn with Congenital Glucose‐Galactose Malabsorption

2005 · Faysal Gok, Halil I Aydin, et al. · Journal of Pediatric Gastroenterology and Nutrition · 12

Works count: 83

Citation count: 790

H-index: 16

I10-index: 29