Aydin HI - Search Results

1

Coexistence of guanidinoacetate methyltransferase (GAMT) deficiency and neuroleptic malignant syndrome without creatine kinase elevation.

Ayanoğlu M, Korgali E, Sezer T, Aydin HI, Sönmez FM. Ayanoğlu M, et al. Among authors: aydin hi. Brain Dev. 2020 May;42(5):418-420. doi: 10.1016/j.braindev.2020.02.001. Epub 2020 Mar 12. Brain Dev. 2020. PMID: 32173091

2

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

Aydın Hİ, Sönmez FM. Aydın Hİ, et al. Turk J Pediatr. 2019;61(1):92-96. doi: 10.24953/turkjped.2019.01.014. Turk J Pediatr. 2019. PMID: 31559727 Free article.

3

Severe isolated sulfide oxidase deficiency with a novel mutation.

Ergene M, Yarar N, Öncel EP, Sezer T, Çavdarlı B, Ecevit İZ, Aydın Hİ. Ergene M, et al. Among authors: aydin hi. Turk J Pediatr. 2021;63(4):716-720. doi: 10.24953/turkjped.2021.04.021. Turk J Pediatr. 2021. PMID: 34449156 Free article.

4

Creatine Transporter Deficiency in Two Brothers with Autism Spectrum Disorder.

Aydin HI. Aydin HI. Indian Pediatr. 2018 Jan 15;55(1):67-68. Indian Pediatr. 2018. PMID: 29396939

5

Hearing loss in biotinidase deficiency: genotype-phenotype correlation.

Sivri HS, Genç GA, Tokatli A, Dursun A, Coşkun T, Aydin HI, Sennaroğlu L, Belgin E, Jensen K, Wolf B. Sivri HS, et al. Among authors: aydin hi. J Pediatr. 2007 Apr;150(4):439-42. doi: 10.1016/j.jpeds.2007.01.036. J Pediatr. 2007. PMID: 17382128

6

3-phosphoglycerate dehydrogenase deficiency: a case report of a treatable cause of seizures.

Coşkun T, Aydin HI, Kiliç M, Dursun A, Haliloğlu G, Topaloğlu H, Karli-Oğuz K, de Koning TJ. Coşkun T, et al. Among authors: aydin hi. Turk J Pediatr. 2009 Nov-Dec;51(6):587-92. Turk J Pediatr. 2009. PMID: 20196394

7

Genetic Studies in Autism: Correspondence.

Aydin HI. Aydin HI. Indian J Pediatr. 2017 Feb;84(2):170-171. doi: 10.1007/s12098-016-2201-4. Epub 2016 Aug 10. Indian J Pediatr. 2017. PMID: 27506425 No abstract available.

8

Thoracic ectopic kidney in a child: a case report.

Aydin HI, Sarici SU, Alpay F, Gökçay E. Aydin HI, et al. Turk J Pediatr. 2000 Jul-Sep;42(3):253-5. Turk J Pediatr. 2000. PMID: 11105630

9

Molecular and clinical evaluation of Turkish patients with lysinuric protein intolerance.

Güzel-Ozantürk A, Ozgül RK, Unal O, Hişmi B, Aydın Hİ, Sivri S, Tokatlı A, Coşkun T, Aksöz E, Dursun A. Güzel-Ozantürk A, et al. Among authors: aydin hi. Gene. 2013 Jun 1;521(2):293-5. doi: 10.1016/j.gene.2013.03.033. Epub 2013 Mar 28. Gene. 2013. PMID: 23542076

10

Evaluation of bone mineral density in chronic glue sniffers.

Dündaröz MR, Sarici SU, Türkbay T, Baykal B, Kocaoğlu M, Aydin HI, Gökçay E. Dündaröz MR, et al. Among authors: aydin hi. Turk J Pediatr. 2002 Oct-Dec;44(4):326-9. Turk J Pediatr. 2002. PMID: 12458809

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