Caliskan U - Search Results

1

Spectrum of the mutations in Bernard-Soulier syndrome.

Savoia A, Kunishima S, De Rocco D, Zieger B, Rand ML, Pujol-Moix N, Caliskan U, Tokgoz H, Pecci A, Noris P, Srivastava A, Ward C, Morel-Kopp MC, Alessi MC, Bellucci S, Beurrier P, de Maistre E, Favier R, Hézard N, Hurtaud-Roux MF, Latger-Cannard V, Lavenu-Bombled C, Proulle V, Meunier S, Négrier C, Nurden A, Randrianaivo H, Fabris F, Platokouki H, Rosenberg N, HadjKacem B, Heller PG, Karimi M, Balduini CL, Pastore A, Lanza F. Savoia A, et al. Among authors: caliskan u. Hum Mutat. 2014 Sep;35(9):1033-45. doi: 10.1002/humu.22607. Epub 2014 Jul 15. Hum Mutat. 2014. PMID: 24934643 Review.

2

Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann's thrombasthenia.

Tokgoz H, Torun Ozkan D, Caliskan U, Akar N. Tokgoz H, et al. Among authors: caliskan u. Platelets. 2015;26(8):779-82. doi: 10.3109/09537104.2014.998994. Epub 2015 Mar 3. Platelets. 2015. PMID: 25734216 Free article.

3

Essential thrombocythemia with Mpl W515 K mutation in a child presenting with Budd-Chiari syndrome.

Tokgoz H, Caliskan U, Yüksekkaya HA, Kucukkaya R. Tokgoz H, et al. Among authors: caliskan u. Platelets. 2015;26(8):805-8. doi: 10.3109/09537104.2015.1041900. Epub 2015 May 13. Platelets. 2015. PMID: 25970554 Free article.

4

Three Novel Calreticulin Mutations in Two Turkish Patients.

Hançer VS, Tokgöz H, Güvenç S, Çalışkan Ü, Büyükdoğan M. Hançer VS, et al. Among authors: caliskan u. Turk J Haematol. 2017 Dec 1;34(4):360-361. doi: 10.4274/tjh.2017.0146. Epub 2017 Jul 27. Turk J Haematol. 2017. PMID: 28747287 Free PMC article. No abstract available.

5

Variable presentation of primary immune deficiency: two cases with CD3 gamma deficiency presenting with only autoimmunity.

Tokgoz H, Caliskan U, Keles S, Reisli I, Guiu IS, Morgan NV. Tokgoz H, et al. Among authors: caliskan u. Pediatr Allergy Immunol. 2013 May;24(3):257-62. doi: 10.1111/pai.12063. Pediatr Allergy Immunol. 2013. PMID: 23590417

6

Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations.

Gultekin ND, Yilmaz FH, Tokgoz H, Tarakci N, Caliskan U. Gultekin ND, et al. Among authors: caliskan u. Indian Pediatr. 2019 Feb 15;56(2):143-144. Indian Pediatr. 2019. PMID: 30819996 Free article.

7

Spontaneous rupture of the spleen in a patient with systemic lupus erythematosus initially presented as Evans syndrome.

Tokgoz H, Caliskan U, Atas B, Ozbek O, Tavil B. Tokgoz H, et al. Among authors: caliskan u. J Pediatr Hematol Oncol. 2014 Jan;36(1):e39-41. doi: 10.1097/MPH.0b013e3182816074. J Pediatr Hematol Oncol. 2014. PMID: 23389505

8

Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiency.

Dönmez-Demir B, Celkan T, Sarper N, Deda G, İnce E, Çalişkan Ü, Öztürk G, Karagün B, Küpesiz A, Tokgöz H, Akar N, Özdağ H. Dönmez-Demir B, et al. Among authors: caliskan u. Blood Coagul Fibrinolysis. 2016 Sep;27(6):637-44. doi: 10.1097/MBC.0000000000000383. Blood Coagul Fibrinolysis. 2016. PMID: 26340456

9

Successful prophylactic use of recombinant activated factor VII (rFVIIa) in a patient with congenital FVII deficiency and inhibitors to FVII.

Tokgoz H, Caliskan U, Lavigne-Lissalde G, Giansily-Blaizot M. Tokgoz H, et al. Among authors: caliskan u. Haemophilia. 2012 Jan;18(1):e25-7. doi: 10.1111/j.1365-2516.2011.02666.x. Epub 2011 Oct 4. Haemophilia. 2012. PMID: 21973016 No abstract available.

10

Traumatic hyphema in a patient with severe hemophilia A: Clinical features and management.

Belviranli S, Ozkagnici A, Tokgoz H, Bitirgen G, Caliskan U. Belviranli S, et al. Among authors: caliskan u. Eur J Ophthalmol. 2021 Mar;31(2):NP106-NP108. doi: 10.1177/1120672119856515. Epub 2019 Jun 12. Eur J Ophthalmol. 2021. PMID: 31187640

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