Arslan AB - Search Results

1

Novel findings, mini-review and dysmorphological characterization of 16p13.11 microduplication syndrome.

Arslan AB, Zamani AG, Yıldırım MS. Arslan AB, et al. Int J Dev Neurosci. 2022 Jun;82(4):289-294. doi: 10.1002/jdn.10188. Epub 2022 May 24. Int J Dev Neurosci. 2022. PMID: 35470466 Review.

2

A Novel Pathogenic Variant of the CFTR Gene in a Patient with Cystic Fibrosis Phenotype-c.4096A > T.

Arslan AB, Zamani AG, Pekcan S, Yıldırım MS. Arslan AB, et al. J Pediatr Genet. 2020 Mar;9(1):40-43. doi: 10.1055/s-0039-1694964. Epub 2019 Aug 28. J Pediatr Genet. 2020. PMID: 31976142 Free PMC article.

3

Interchromosomal effect: Report of a father and son, bearing different translocations of the same chromosome, and a review of the current literature.

Yıldırım MS, Arslan AB, Zamani AG. Yıldırım MS, et al. Among authors: arslan ab. Andrologia. 2021 Feb;53(1):e13805. doi: 10.1111/and.13805. Epub 2020 Aug 30. Andrologia. 2021. PMID: 32862490 Review.

4

Henoch-Schönlein purpura-related intestinal perforation: a steroid complication?

Yavuz H, Arslan A. Yavuz H, et al. Pediatr Int. 2001 Aug;43(4):423-5. doi: 10.1046/j.1442-200x.2001.01417.x. Pediatr Int. 2001. PMID: 11472592 No abstract available.

5

Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory distress syndrome.

Demirçubuk AG, Coşkun MY, Demiryürek Ş, Dokuyucu R, Öztuzcu S, Taviloğlu ZŞ, Arslan A, Sivaslı E. Demirçubuk AG, et al. Pediatr Pulmonol. 2013 Oct;48(10):976-80. doi: 10.1002/ppul.22759. Epub 2013 Jan 28. Pediatr Pulmonol. 2013. PMID: 23359565

6

GJB2 and mitochondrial A1555G gene mutations in nonsyndromic profound hearing loss and carrier frequencies in healthy individuals.

Baysal E, Bayazit YA, Ceylaner S, Alatas N, Donmez B, Ceylaner G, San I, Korkmaz B, Yilmaz A, Menevse A, Altunyay S, Gunduz B, Goksu N, Arslan A, Ekmekci A. Baysal E, et al. J Genet. 2008 Apr;87(1):53-7. doi: 10.1007/s12041-008-0007-5. J Genet. 2008. PMID: 18560174

7

ACE gene polymorphism in premature neonates with respiratory distress syndrome.

Yimenicioglu S, Oztuzcu S, Sivasli E, Igci M, Igci YZ, Demiryürek S, Ozkara E, Gogebakan B, Arslan A, Coskun MY. Yimenicioglu S, et al. Genet Test Mol Biomarkers. 2011 Dec;15(12):867-70. doi: 10.1089/gtmb.2011.0060. Epub 2011 Jul 12. Genet Test Mol Biomarkers. 2011. PMID: 21749216

8

Effects of single nucleotide polymorphisms in K(ATP) channel genes on type 2 diabetes in a Turkish population.

Gonen MS, Arikoglu H, Erkoc Kaya D, Ozdemir H, Ipekci SH, Arslan A, Kayis SA, Gogebakan B. Gonen MS, et al. Arch Med Res. 2012 May;43(4):317-23. doi: 10.1016/j.arcmed.2012.06.001. Epub 2012 Jun 13. Arch Med Res. 2012. PMID: 22704848

9

Vaginal clear cell adenocarcinoma in an infant.

Yavuz H, Arslan A, Avşaz AF. Yavuz H, et al. Pediatr Hematol Oncol. 1996 Nov-Dec;13(6):577-80. doi: 10.3109/08880019609030875. Pediatr Hematol Oncol. 1996. PMID: 8940743

10

Radiological case of the month. Autosomal recessive osteopetrosis.

Yavuz H, Caliskan O, Bozkir A, Arslan A, Koc H, Wood BP. Yavuz H, et al. Am J Dis Child. 1992 Nov;146(11):1309-10. Am J Dis Child. 1992. PMID: 1415067 No abstract available.

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