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| Prediction of outcome in isolated methylmalonic acidurias: combined use of clinical and biochemical parameters F Hörster, SF Garbade, T Zwickler, HI Aydin, OA Bodamer, AB Burlina, ... Journal of inherited metabolic disease 32 (5), 630-639, 2009 | 87 | 2009 |
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| Hearing loss in biotinidase deficiency: genotype-phenotype correlation HSK Sivri, GA Genç, A Tokatlı, A Dursun, T Coşkun, Hİ Aydın, ... The Journal of pediatrics 150 (4), 439-442, 2007 | 65 | 2007 |
| Engelli çocuklara sahip ailelerin psiko-sosyal durumlarının ve beklentilerinin incelenmesi F Özşenol, B Ünay, Hİ Aydın, R Akın, E Gökçay Gülhane Tıp Dergisi 44 (2), 188-194, 2002 | 40 | 2002 |
| NMR-based screening for inborn errors of metabolism: initial results from a study on Turkish neonates S Aygen, U Dürr, P Hegele, J Kunig, M Spraul, H Schäfer, D Krings, ... JIMD Reports Volume 16, 101-111, 2014 | 39 | 2014 |
| Audiologic findings in children with biotinidase deficiency in Turkey GA Genc, HS Sivri-Kalkanoğlu, A Dursun, HI Aydın, A Tokatlı, ... International journal of pediatric otorhinolaryngology 71 (2), 333-339, 2007 | 39 | 2007 |
| Meningitis with multidrug-resistant Acinetobacter baumannii treated with ampicillin/sulbactam T Kendirli, HI Aydı́n, D Hacı́hamdioğlu, M Gülgün, B Ünay, R Akı́n, ... Journal of Hospital Infection 56 (4), 328, 2004 | 25 | 2004 |
| Biallelic loss-of-function OBSCN variants predispose individuals to severe, recurrent rhabdomyolysis M Cabrera-Serrano, L Caccavelli, M Savarese, A Vihola, M Jokela, ... bioRxiv, 2021 | 20 | 2021 |
| Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance A Güzel-Ozantürk, RK Özgül, Ö Ünal, B Hişmi, Hİ Aydın, S Sivri, A Tokatlı, ... Gene 521 (2), 293-295, 2013 | 17 | 2013 |
| Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosis B Çeltikçi, Hİ Aydın, S Sivri, M Sönmez, M Topçu, HA Özkara Clinical biochemistry 45 (7-8), 571-574, 2012 | 15 | 2012 |
| Morbidity and mortality characteristics of infants hospitalized in the Pediatrics Department of the largest Turkish military hospital in 2001 S Kiliç, S Tezcan, ME Taşçilar, B Çakir, H İbrahim Aydin, M Hasde, ... Military medicine 170 (1), 48-51, 2005 | 14 | 2005 |
| Serum dipeptidyl peptidase-IV: A better screening test for early detection of mucopolysaccharidosis? I Kurt, E Sertoglu, I Okur, S Tapan, M Uyanık, H Kayadıbı, FS Ezgu, ... Clinica Chimica Acta 431, 250-254, 2014 | 13 | 2014 |
| Henoch-Schönlein purpuralı çocuklarda renal tutulum S Kalman, Hİ Aydın, SÜ Sarıcı Cumhuriyet Üniversitesi Tıp Fakültesi Dergisi 25 (3), 123-128, 2003 | 11 | 2003 |
| A novel mutation in two cousins with guanidinoacetate methyltransferase (GAMT) deficiency presented with autism Hİ Aydın, FM Sönmez The Turkish Journal of Pediatrics 61 (1), 92-96, 2019 | 10 | 2019 |
| Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder. HI Aydin Indian Pediatrics 55 (1), 2018 | 10 | 2018 |
| Analysis of DNA damage using the comet assay in infants fed cow’s milk R Dündaröz, H Ulucan, Hİ Aydın, T Güngör, V Baltacı, M Denli, ... Neonatology 84 (2), 135-141, 2003 | 9 | 2003 |
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| Assessing leptin and soluble leptin receptor levels in full-term asymmetric small for gestational age and healthy neonates. Hİ Aydın, E Demirkaya, RS Karadeniz, A Olgun, F Alpay Turkish Journal of Pediatrics 56 (3), 2014 | 5 | 2014 |
