Çavdarlı B - Search Results

1

Impact of Inflammation-Related Genes on COVID-19: Prospective Study at Turkish Cohort.

Ceylan AC, Çavdarlı B, Ceylan GG, Topçu V, Satılmış SBA, Bektaş ŞG, Kalem AK, Kayaaslan B, Eser F, Kalkan EA, İnan O, Hasanoğlu İ, Yüksel S, Ateş İ, İzdeş S, Güner R, Gündüz CNS. Ceylan AC, et al. Among authors: cavdarli b. Tohoku J Exp Med. 2023 Nov 11;261(3):179-185. doi: 10.1620/tjem.2023.J071. Epub 2023 Aug 25. Tohoku J Exp Med. 2023. PMID: 37635061 Free article.

2

Imerslund-Gräsbeck Syndrome presenting with microangiopathic hemolytic anemia in a child.

Gurlek Gokcebay D, Akpinar Tekgunduz S, Cavdarli B. Gurlek Gokcebay D, et al. Among authors: cavdarli b. Eur J Med Genet. 2020 Jun;63(6):103880. doi: 10.1016/j.ejmg.2020.103880. Epub 2020 Feb 8. Eur J Med Genet. 2020. PMID: 32045704

3

Molecular karyotyping of an isolated partial trisomy 11q patient with additional findings.

Kayhan G, Cavdarli B, Yirmibes Karaoguz M, Percin EF, Oztürk Kaymak A, Biri A, Ergun MA. Kayhan G, et al. Among authors: cavdarli b. Gene. 2013 Jul 25;524(2):355-60. doi: 10.1016/j.gene.2013.04.053. Epub 2013 May 1. Gene. 2013. PMID: 23644025

4

Duplication 4q associated with chronic cholestatic changes in liver biopsy.

Egritas O, Cavdarli B, Dalgic B, Ergun MA, Percin F, Ziegler M, Pohle B, Liehr T. Egritas O, et al. Among authors: cavdarli b. Eur J Med Genet. 2010 Nov-Dec;53(6):411-4. doi: 10.1016/j.ejmg.2010.08.008. Epub 2010 Sep 6. Eur J Med Genet. 2010. PMID: 20826235

5

A novel deletion involving exon 13 of factor VIII gene in a newborn with splenic hematoma.

Gurlek Gokcebay D, Akpinar Tekgunduz S, Sarici D, Uysal Ramadan S, Cavdarli B. Gurlek Gokcebay D, et al. Among authors: cavdarli b. Transfus Apher Sci. 2020 Feb;59(1):102562. doi: 10.1016/j.transci.2019.06.002. Epub 2019 Jun 19. Transfus Apher Sci. 2020. PMID: 31230948

6

A case of Carvajal syndrome associated with cervical neuroblastoma in an 8-year-old girl.

Akdogan N, Incel-Uysal P, Cavdarli B, Topcu V, Yalcin B. Akdogan N, et al. Among authors: cavdarli b. Int J Dermatol. 2019 May;58(5):611-613. doi: 10.1111/ijd.14154. Epub 2018 Aug 6. Int J Dermatol. 2019. PMID: 30079965 No abstract available.

7

Widespread keratosis pilaris in a patient with Noonan syndrome with multiple lentigines.

Purnak S, Topçu V, Çavdarlı B, Kadan E, Yalçın B. Purnak S, et al. Among authors: cavdarli b. Int J Dermatol. 2018 Nov;57(11):e140-e141. doi: 10.1111/ijd.14209. Epub 2018 Aug 27. Int J Dermatol. 2018. PMID: 30152106 No abstract available.

8

Frequency of germline BRCA1/2 mutations and association with clinicopathological characteristics in Turkish women with epithelial ovarian cancer.

Sunar V, Korkmaz V, Topcu V, Cavdarli B, Arik Z, Ozdal B, Ustun YE. Sunar V, et al. Among authors: cavdarli b. Asia Pac J Clin Oncol. 2022 Feb;18(1):84-92. doi: 10.1111/ajco.13520. Epub 2021 Feb 25. Asia Pac J Clin Oncol. 2022. PMID: 33629534

9

The molecular landscape of progressive familial intrahepatic cholestasis in Turkey: Defining the molecular profiles and expanding the variant spectrum.

Bakır A, Topçu V, Çavdarlı B. Bakır A, et al. Among authors: cavdarli b. Ann Hum Genet. 2022 May;86(3):119-126. doi: 10.1111/ahg.12456. Epub 2021 Dec 28. Ann Hum Genet. 2022. PMID: 34961929

10

Contribution of Inherited Variants to Hereditary Cancer Syndrome Predisposition.

Güleç Ceylan G, Arslan Satılmış SB, Çavdarlı B, Semerci Gündüz CN. Güleç Ceylan G, et al. Among authors: cavdarli b. Tohoku J Exp Med. 2022 Nov 22;258(4):319-325. doi: 10.1620/tjem.2022.J087. Epub 2022 Oct 27. Tohoku J Exp Med. 2022. PMID: 36288950 Free article.

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