Tokgoz H - Search Results

1

Ophthalmic manifestations in recently diagnosed childhood leukemia.

Bitirgen G, Belviranli S, Caliskan U, Tokgoz H, Ozkagnici A, Zengin N. Bitirgen G, et al. Among authors: tokgoz h. Eur J Ophthalmol. 2016 Jan-Feb;26(1):88-91. doi: 10.5301/ejo.5000647. Epub 2015 Jul 3. Eur J Ophthalmol. 2016. PMID: 26165325

2

Persistent nasal bleeding due to nasal CPAP application in 2 premature newborns successfully treated with topical "Ankaferd blood stopper".

Altunhan H, Annagür A, Tokgöz H, Çaliskan Ü, Örs R. Altunhan H, et al. Among authors: tokgoz h. Clin Appl Thromb Hemost. 2011 Nov-Dec;17(6):E181-2. doi: 10.1177/1076029610394441. Clin Appl Thromb Hemost. 2011. PMID: 22345627 Free article. No abstract available.

3

Successful use of fondaparinux in a child with heparin-induced thrombocytopenia.

Tokgoz H, Caliskan U, Demir M. Tokgoz H, et al. Blood Coagul Fibrinolysis. 2012 Dec;23(8):769-71. doi: 10.1097/MBC.0b013e328358afc9. Blood Coagul Fibrinolysis. 2012. PMID: 22964766

4

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. J Pediatr Hematol Oncol. 2014 Jan;36(1):e39-41. doi: 10.1097/MPH.0b013e3182816074. J Pediatr Hematol Oncol. 2014. PMID: 23389505

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. Pediatr Allergy Immunol. 2013 May;24(3):257-62. doi: 10.1111/pai.12063. Pediatr Allergy Immunol. 2013. PMID: 23590417

6

CD3G gene defects in familial autoimmune thyroiditis.

Gokturk B, Keles S, Kirac M, Artac H, Tokgoz H, Guner SN, Caliskan U, Caliskaner Z, van der Burg M, van Dongen J, Morgan NV, Reisli I. Gokturk B, et al. Among authors: tokgoz h. Scand J Immunol. 2014 Nov;80(5):354-61. doi: 10.1111/sji.12200. Scand J Immunol. 2014. PMID: 24910257 Free article.

7

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. Platelets. 2015;26(8):779-82. doi: 10.3109/09537104.2014.998994. Epub 2015 Mar 3. Platelets. 2015. PMID: 25734216 Free article.

8

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. Platelets. 2015;26(8):805-8. doi: 10.3109/09537104.2015.1041900. Epub 2015 May 13. Platelets. 2015. PMID: 25970554 Free article.

9

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: tokgoz h. Blood Coagul Fibrinolysis. 2016 Sep;27(6):637-44. doi: 10.1097/MBC.0000000000000383. Blood Coagul Fibrinolysis. 2016. PMID: 26340456

10

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: tokgoz h. 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.

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