Kayhan G - Search Results

1

Novel Compound Heterozygous Mutations of TGM1 Gene Identified in a Turkish Collodion Baby Diagnosed with Non-Bullous Congenital Ichthyosiform Erythroderma.

Gülnerman EK, Hanedan N, Akillioglu M, Kayhan G, Adişen E, Erdem Ö, Hirfanoğlu İM, Ergenekon E, Önal EE, Türkyilmaz C, Koç E. Gülnerman EK, et al. Among authors: kayhan g. Ann Dermatol. 2023 Nov;35(Suppl 2):S234-S238. doi: 10.5021/ad.21.134. Ann Dermatol. 2023. PMID: 38061711 Free PMC article.

2

Infraclavicular Catheter in MELAS Syndrome for Analgesic Purposes.

Onay M, Kiremitçi TT, Kayhan GE, Algın Dİ, Güleç MS. Onay M, et al. Among authors: kayhan ge. Neurol India. 2023 Jul-Aug;71(4):764-766. doi: 10.4103/0028-3886.383869. Neurol India. 2023. PMID: 37635512 Free article.

3

Clinical and genetic characteristics of retinoblastoma patients in a single center with four novel RB1 variants.

Vural Ö, Atalay HT, Kayhan G, Tarlan B, Oral M, Okur A, Pınarlı FG, Karadeniz C. Vural Ö, et al. Among authors: kayhan g. Int J Ophthalmol. 2023 Aug 18;16(8):1274-1279. doi: 10.18240/ijo.2023.08.13. eCollection 2023. Int J Ophthalmol. 2023. PMID: 37602348 Free PMC article.

4

Long-term follow-up and novel variant in Suleiman-El-Hattab syndrome: Expanding the genotypic and clinical spectrum of a rare neurodevelopmental disorder.

Sezer A, Kayhan G, Percin FE. Sezer A, et al. Among authors: kayhan g. Eur J Med Genet. 2023 Sep;66(9):104809. doi: 10.1016/j.ejmg.2023.104809. Epub 2023 Jul 19. Eur J Med Genet. 2023. PMID: 37474017

5

Expanding the phenotype and genotype in Thauvin-Robinet-Faivre syndrome: A new patient with a novel variant and additional clinical findings.

Duzenli T, Sezer A, Kayhan G, Arslan AT, Percin FE. Duzenli T, et al. Among authors: kayhan g. Am J Med Genet A. 2023 Aug;191(8):2232-2239. doi: 10.1002/ajmg.a.63300. Epub 2023 May 23. Am J Med Genet A. 2023. PMID: 37218527

6

Cystic hygroma: a single-centre experience.

Özdemir H, Karçaaltıncaba D, Kayhan G, Çalış PT, Tuğ E, Taner MZ, Bayram M, Karaoğuz MY. Özdemir H, et al. Among authors: kayhan g. Singapore Med J. 2023 Apr 25. doi: 10.4103/singaporemedj.SMJ-2020-534. Online ahead of print. Singapore Med J. 2023. PMID: 37171419 Free article. No abstract available.

7

Two distinct syndromic children with T-acute lymphoblastic leukemia: Noonan syndrome and Sotos syndrome.

Kaya Z, Keser E, Atalay E, Kayhan G, Karamercan S, Topuz B, Kirkiz S, Koçak Ü. Kaya Z, et al. Among authors: kayhan g. Leuk Res. 2022 Dec;123:106981. doi: 10.1016/j.leukres.2022.106981. Epub 2022 Oct 22. Leuk Res. 2022. PMID: 36356491 No abstract available.

8

A homozygous missense variant in the WRN gene segregating in a family with progressive pulmonary failure with recurrent spontaneous pneumothorax and interstitial lung disease.

Sezer A, Kayhan G, Gursoy TR, Eyuboglu TS, Percin FE. Sezer A, et al. Among authors: kayhan g. Am J Med Genet A. 2023 Jan;191(1):220-227. doi: 10.1002/ajmg.a.62986. Epub 2022 Oct 10. Am J Med Genet A. 2023. PMID: 36214313

9

Two Cases With Neonatal Cholestasis and Renal Disorders Due to DCDC2 Mutation.

Teker Düztaş D, Sarı S, Eğritaş Gürkan Ö, Kayhan G, Dalgıç A, Dalgıç B. Teker Düztaş D, et al. Among authors: kayhan g. Exp Clin Transplant. 2022 May;20(Suppl 3):115-117. doi: 10.6002/ect.PediatricSymp2022.O37. Exp Clin Transplant. 2022. PMID: 35570614 Free article.

10

A de novo heterozygous HOXA11 variant in a patient with mesomelic dysplasia with urogenital abnormalities.

Sezer A, Perçin FE, Kazan HH, Kayhan G, Akturk M. Sezer A, et al. Among authors: kayhan g. Am J Med Genet A. 2022 Jun;188(6):1890-1895. doi: 10.1002/ajmg.a.62713. Epub 2022 Mar 6. Am J Med Genet A. 2022. PMID: 35253374

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