Aydin H - Search Results

1

Lymphocytic vacuolization in sialic acid storage disease.

Kuskonmaz B, Unal S, Cördükcü E, Aydin H, Coskun T, Gurgey A, Gumruk F. Kuskonmaz B, et al. Among authors: aydin h. Am J Hematol. 2008 Oct;83(10):821. doi: 10.1002/ajh.21097. Am J Hematol. 2008. PMID: 18050357 Free article. No abstract available.

2

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. J Pediatr. 2007 Apr;150(4):439-42. doi: 10.1016/j.jpeds.2007.01.036. J Pediatr. 2007. PMID: 17382128

3

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

4

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. Gene. 2013 Jun 1;521(2):293-5. doi: 10.1016/j.gene.2013.03.033. Epub 2013 Mar 28. Gene. 2013. PMID: 23542076

5

Audiologic findings in children with biotinidase deficiency in Turkey.

Genc GA, Sivri-Kalkanoğlu HS, Dursun A, Aydin HI, Tokatli A, Sennaroglu L, Belgin E, Wolf B, Coşkun T. Genc GA, et al. Among authors: aydin hi. Int J Pediatr Otorhinolaryngol. 2007 Feb;71(2):333-9. doi: 10.1016/j.ijporl.2006.11.001. Epub 2006 Dec 11. Int J Pediatr Otorhinolaryngol. 2007. PMID: 17161472

6

Two cases of Ralstonia pickettii bacteremias in a pediatric oncology unit requiring removal of the Port-A-Caths.

Kismet E, Atay AA, Demirkaya E, Aydin HI, Aydogan H, Koseoglu V, Gokcay E. Kismet E, et al. Among authors: aydin hi. J Pediatr Hematol Oncol. 2005 Jan;27(1):37-8. doi: 10.1097/01.mph.0000149960.89192.b0. J Pediatr Hematol Oncol. 2005. PMID: 15654276

7

Familial high factor VIII level in a child with necrotizing fasciitis complicating primary varicella infection.

Kurekci AE, Aydin HI, Atay AA, Akar N, Cetan T, Ozcan O, Gokcay E. Kurekci AE, et al. Among authors: aydin hi. Pediatr Hematol Oncol. 2005 Apr-May;22(3):219-22. doi: 10.1080/08880010590921540. Pediatr Hematol Oncol. 2005. PMID: 16020105

8

A Turkish case with molybdenum cofactor deficiency.

Ichida K, Aydin HI, Hosoyamada M, Kalkanoglu HS, Dursun A, Ohno I, Coskun T, Tokatli A, Shibasaki T, Hosoya T. Ichida K, et al. Among authors: aydin hi. Nucleosides Nucleotides Nucleic Acids. 2006;25(9-11):1087-91. doi: 10.1080/15257770600894022. Nucleosides Nucleotides Nucleic Acids. 2006. PMID: 17065069

9

Four novel mutations in the β-galactosidase gene identified in infantile type of GM1 gangliosidosis.

Celtikçi B, Aydın Hİ, Sivri S, Sönmez M, Topçu M, Ozkara HA. Celtikçi B, et al. Clin Biochem. 2012 May;45(7-8):571-4. doi: 10.1016/j.clinbiochem.2011.12.019. Epub 2012 Jan 3. Clin Biochem. 2012. PMID: 22234367

10

Retrospective evaluation of patients with X-linked adrenoleukodystrophy with a wide range of clinical presentations: a single center experience.

Olgac A, Kasapkara ÇS, Derinkuyu B, Yüksel D, Çetinkaya S, Aksoy A, Ceylaner S, Güleray N, Yeşilipek A, Aydın Hİ, Orgun LT, Kılıç M. Olgac A, et al. J Pediatr Endocrinol Metab. 2021 Jun 24;34(9):1169-1179. doi: 10.1515/jpem-2021-0032. Print 2021 Sep 27. J Pediatr Endocrinol Metab. 2021. PMID: 34162029 Clinical Trial.

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