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

Text availability

Article attribute

Article type

Publication date

Search Results

99 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Identification of the molecular etiology in rare congenital hemolytic anemias using next-generation sequencing with exome-based copy number variant analysis.
Isik E, Aydinok Y, Albayrak C, Durmus B, Karakas Z, Orhan MF, Sarper N, Aydın S, Unal S, Oymak Y, Karadas N, Turedi A, Albayrak D, Tayfun F, Tugcu D, Karaman S, Tobu M, Unal E, Ozcan A, Unal S, Aksu T, Unuvar A, Bilici M, Azik F, Ay Y, Gelen SA, Zengin E, Albudak E, Eker I, Karakaya T, Cogulu O, Ozkinay F, Atik T. Isik E, et al. Among authors: albayrak c. Eur J Haematol. 2024 Mar 31. doi: 10.1111/ejh.14194. Online ahead of print. Eur J Haematol. 2024. PMID: 38556258
Invasive fungal infections in children with hematologic and malignant diseases.
Ozsevik SN, Sensoy G, Karli A, Albayrak C, Dagdemir A, Belet N, Elli M, Fisgin T, Ozyurek E, Duru F, Albayrak D. Ozsevik SN, et al. Among authors: albayrak c, albayrak d. J Pediatr Hematol Oncol. 2015 Mar;37(2):e69-72. doi: 10.1097/MPH.0000000000000225. J Pediatr Hematol Oncol. 2015. PMID: 25072372
Pancytopenia As the Initial Manifestation of Brucellosis in Children.
Karli A, Sensoy G, Albayrak C, Koken O, Cıraklı S, Belet N, Albayrak D. Karli A, et al. Among authors: albayrak c, albayrak d. Vector Borne Zoonotic Dis. 2015 Sep;15(9):545-9. doi: 10.1089/vbz.2015.1775. Epub 2015 Sep 14. Vector Borne Zoonotic Dis. 2015. PMID: 26367782
Marked overlap of four genetic syndromes with dyskeratosis congenita confounds clinical diagnosis.
Walne AJ, Collopy L, Cardoso S, Ellison A, Plagnol V, Albayrak C, Albayrak D, Kilic SS, Patıroglu T, Akar H, Godfrey K, Carter T, Marafie M, Vora A, Sundin M, Vulliamy T, Tummala H, Dokal I. Walne AJ, et al. Among authors: albayrak c, albayrak d. Haematologica. 2016 Oct;101(10):1180-1189. doi: 10.3324/haematol.2016.147769. Epub 2016 Sep 9. Haematologica. 2016. PMID: 27612988 Free PMC article.
Juvenile Myelomonocytic Leukemia in Turkey: A Retrospective Analysis of Sixty-five Patients.
Tüfekçi Ö, Koçak Ü, Kaya Z, Yenicesu İ, Albayrak C, Albayrak D, Yılmaz Bengoa Ş, Patıroğlu T, Karakükçü M, Ünal E, Ünal İnce E, İleri T, Ertem M, Celkan T, Özdemir GN, Sarper N, Kaçar D, Yaralı N, Özbek NY, Küpesiz A, Karapınar T, Vergin C, Çalışkan Ü, Tokgöz H, Sezgin Evim M, Baytan B, Güneş AM, Yılmaz Karapınar D, Karaman S, Uygun V, Karasu G, Yeşilipek MA, Koç A, Erduran E, Atabay B, Öniz H, Ören H. Tüfekçi Ö, et al. Among authors: albayrak c, albayrak d. Turk J Haematol. 2018 Mar 1;35(1):27-34. doi: 10.4274/tjh.2017.0021. Epub 2017 Feb 9. Turk J Haematol. 2018. PMID: 28179213 Free PMC article.
Factor 8 Gene Mutation Spectrum of 270 Patients with Hemophilia A: Identification of 36 Novel Mutations.
Atik T, Işık E, Onay H, Akgün B, Shamsali M, Kavaklı K, Evim M, Tüysüz G, Özbek NY, Şahin F, Salcıoğlu Z, Albayrak C, Oymak Y, Ünal E, Belen FB, Yılmaz Keskin E, Balkan C, Baytan B, Küpesiz A, Culha V, Tahtakesen Güçer TN, Güneş AM, Özkınay F. Atik T, et al. Among authors: albayrak c. Turk J Haematol. 2020 Aug 28;37(3):145-153. doi: 10.4274/tjh.galenos.2020.2019.0262. Epub 2020 Feb 6. Turk J Haematol. 2020. PMID: 32026663 Free PMC article.
99 results