Kırbıyık Ö - Search Results

1

Can a hand radiograph indicate a special diagnosis in a child with chronic kidney disease? Questions.

Soyaltın E, Kasap-Demir B, Alparslan C, Arslansoyu-Çamlar S, Öncel EP, Kırbıyık Ö, Alaygut D, Yavaşcan Ö, Türe G, Mutlubaş F. Soyaltın E, et al. Among authors: kirbiyik o. Pediatr Nephrol. 2018 May;33(5):799-800. doi: 10.1007/s00467-017-3740-2. Epub 2017 Jul 12. Pediatr Nephrol. 2018. PMID: 28702761 No abstract available.

2

Can a hand radiograph indicate a special diagnosis in a child with chronic kidney disease? Answers.

Soyaltın E, Kasap-Demir B, Alparslan C, Arslansoyu-Çamlar S, Öncel EP, Kırbıyık Ö, Alaygut D, Yavaşcan Ö, Türe G, Mutlubaş F. Soyaltın E, et al. Among authors: kirbiyik o. Pediatr Nephrol. 2018 May;33(5):801-803. doi: 10.1007/s00467-017-3742-0. Epub 2017 Jul 24. Pediatr Nephrol. 2018. PMID: 28741273 No abstract available.

3

The Clinical and Molecular Characteristics of Molybdenum Cofactor Deficiency Due to MOCS2 Mutations.

Arican P, Gencpinar P, Kirbiyik O, Bozkaya Yilmaz S, Ersen A, Oztekin O, Olgac Dundar N. Arican P, et al. Among authors: kirbiyik o. Pediatr Neurol. 2019 Oct;99:55-59. doi: 10.1016/j.pediatrneurol.2019.04.021. Epub 2019 May 3. Pediatr Neurol. 2019. PMID: 31201073 Review.

4

The Efficiency of SNP-Based Microarrays in the Detection of Copy-Neutral Events at 15q11.2 and 11p15.5 Loci.

Ozyilmaz B, Kirbiyik O, Ozdemir TR, Kaya OO, Kutbay YB, Erdogan KM, Guvenc MS, Koc A. Ozyilmaz B, et al. Among authors: kirbiyik o. J Pediatr Genet. 2020 Mar;9(1):9-18. doi: 10.1055/s-0039-1698420. Epub 2019 Oct 16. J Pediatr Genet. 2020. PMID: 31976138 Free PMC article.

5

Variant ataxia-telangiectasia in a child presenting with laryngeal dystonia.

Arıcan P, Dündar NO, Kırbıyık Ö, Çavusoğlu D, Yılmaz SB, Gençpınar P. Arıcan P, et al. Among authors: kirbiyik o. Turk J Pediatr. 2020;62(3):491-494. doi: 10.24953/turkjped.2020.03.019. Turk J Pediatr. 2020. PMID: 32558426 Free article.

6

QF-PCR in invasive prenatal diagnosis: a single-center experience in Turkey.

Özer Kaya Ö, Koç A, Özdemir TR, Kirbiyik Ö, Özyilmaz B, Özeren M, Öztekin DC, Taner CE, Kutbay YB. Özer Kaya Ö, et al. Among authors: kirbiyik o. Turk J Med Sci. 2017 Feb 27;47(1):142-147. doi: 10.3906/sag-1511-157. Turk J Med Sci. 2017. PMID: 28263482 Free article.

7

Seckel syndrome with Morgagni hernia.

Onder A, Cogulu O, Ekmekci A, Pariltay E, Kirbiyik O, Ozkinay F. Onder A, et al. Among authors: kirbiyik o. Clin Dysmorphol. 2007 Jul;16(3):209-210. doi: 10.1097/MCD.0b013e3281c9b08e. Clin Dysmorphol. 2007. PMID: 17551341

8

Spinal muscular atrophy with respiratory distress type 1 (SMARD1): a rare cause of hypotonia, diaphragmatic weakness, and respiratory failure in infants.

Pekuz S, Güzin Y, Sarıtaş S, Kırbıyık Ö, Ünalp A, Yılmaz Ü. Pekuz S, et al. Among authors: kirbiyik o. Turk J Pediatr. 2022;64(2):364-374. doi: 10.24953/turkjped.2020.2012. Turk J Pediatr. 2022. PMID: 35611426 Free article.

9

Experiences in microarray-based evaluation of developmental disabilities and congenital anomalies.

Ozyilmaz B, Kirbiyik O, Koc A, Ozdemir TR, Kaya OO, Guvenc MS, Erdoğan KM, Kutbay YB. Ozyilmaz B, et al. Among authors: kirbiyik o. Clin Genet. 2017 Oct;92(4):372-379. doi: 10.1111/cge.12978. Epub 2017 Mar 30. Clin Genet. 2017. PMID: 28128450

10

Two Cases with Ring Chromosome 13 at either End of the Phenotypic Spectrum.

Çakmaklı S, Çankaya T, Gürsoy S, Koç A, Kırbıyık Ö, Kılıçarslan ÖA, Özer E, Erçal D, Bozkaya ÖG. Çakmaklı S, et al. Among authors: kirbiyik o. Cytogenet Genome Res. 2017;153(4):175-180. doi: 10.1159/000486775. Epub 2018 Mar 9. Cytogenet Genome Res. 2017. PMID: 29518772 Review.

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