Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2011 2
2013 3
2014 13
2015 7
2016 5
2017 1
2018 6
2019 6
2020 6
2021 7
2022 11
2023 2
2024 4

Text availability

Article attribute

Article type

Publication date

Search Results

58 results

Results by year

Filters applied: . Clear all
Page 1
Genetic Forms of Calciopenic Rickets.
Donmez AS, Turkyilmaz A, Cayir A. Donmez AS, et al. Among authors: cayir a. Eurasian J Med. 2022 Dec;54(Suppl1):159-163. doi: 10.5152/eurasianjmed.2022.22322. Eurasian J Med. 2022. PMID: 36655461
Vici syndrome in siblings born to consanguineous parents.
Tasdemir S, Sahin I, Cayır A, Yuce I, Ceylaner S, Tatar A. Tasdemir S, et al. Among authors: cayir a. Am J Med Genet A. 2016 Jan;170A(1):220-5. doi: 10.1002/ajmg.a.37398. Epub 2015 Sep 23. Am J Med Genet A. 2016. PMID: 26395118 Review.
High Fetuin-A Levels in Children with Celiac Disease.
Kurt N, Ozgeris FB, Volkan B, Gul MA, Cayir A. Kurt N, et al. Among authors: cayir a. Eurasian J Med. 2022 Jun;54(2):186-190. doi: 10.5152/eurasianjmed.2022.21293. Eurasian J Med. 2022. PMID: 35703528 Free PMC article.
A Genetic Approach in the Evaluation of Short Stature.
Turkyilmaz A, Donmez AS, Cayir A. Turkyilmaz A, et al. Among authors: cayir a. Eurasian J Med. 2022 Dec;54(Suppl1):179-186. doi: 10.5152/eurasianjmed.2022.22171. Eurasian J Med. 2022. PMID: 36655465
Nationwide Turkish Cohort Study of Hypophosphatemic Rickets.
Şıklar Z, Turan S, Bereket A, Baş F, Güran T, Akberzade A, Abacı A, Demir K, Böber E, Özbek MN, Kara C, Poyrazoğlu Ş, Aydın M, Kardelen A, Tarım Ö, Eren E, Hatipoğlu N, Büyükinan M, Akyürek N, Çetinkaya S, Bayramoğlu E, Selver Eklioğlu B, Uçaktürk A, Abalı S, Gökşen D, Kor Y, Ünal E, Esen İ, Yıldırım R, Akın O, Çayır A, Dilek E, Kırel B, Anık A, Çatlı G, Berberoğlu M. Şıklar Z, et al. Among authors: cayir a. J Clin Res Pediatr Endocrinol. 2020 Jun 3;12(2):150-159. doi: 10.4274/jcrpe.galenos.2019.2019.0098. Epub 2019 Sep 13. J Clin Res Pediatr Endocrinol. 2020. PMID: 31514490 Free PMC article.
A rare cause of primary amenorrhea: LHCGR gene mutations.
Aktar Karakaya A, Çayır A, Unal E, Beştaş A, Ece Solmaz A, Kenan Haspolat Y. Aktar Karakaya A, et al. Among authors: cayir a. Eur J Obstet Gynecol Reprod Biol. 2022 May;272:193-197. doi: 10.1016/j.ejogrb.2022.03.033. Epub 2022 Mar 19. Eur J Obstet Gynecol Reprod Biol. 2022. PMID: 35366614
Catch-up Growth and Discontinuation of Fludrocortisone Treatment in Aldosterone Synthase Deficiency.
Gurpinar Tosun B, Kendir Demirkol Y, Seven Menevse T, Kaygusuz SB, Ozbek MN, Altincik SA, Mammadova J, Cayir A, Doger E, Bayramoglu E, Nalbantoglu O, Yesiltepe Mutlu G, Aghayev A, Turan S, Bereket A, Guran T. Gurpinar Tosun B, et al. Among authors: cayir a. J Clin Endocrinol Metab. 2022 Jan 1;107(1):e106-e117. doi: 10.1210/clinem/dgab619. J Clin Endocrinol Metab. 2022. PMID: 34415991
58 results