Karapınar D - Search Results

1

Coexistence of Gaucher Disease and severe congenital neutropenia.

Kose MD, Canda E, Kağnıcı M, Uçar SK, Onay H, Yıldırım Sozmen E, Karapınar D, Özkınay F, Çoker M. Kose MD, et al. Among authors: karapinar d. Blood Cells Mol Dis. 2019 May;76:1-6. doi: 10.1016/j.bcmd.2018.07.001. Epub 2018 Aug 10. Blood Cells Mol Dis. 2019. PMID: 30473482

2

Evaluation of telomerase mRNA (hTERT) in childhood acute leukemia.

Cogulu O, Kosova B, Karaca E, Gunduz C, Ozkinay F, Aksoylar S, Gulen H, Kantar M, Oniz H, Karapinar D, Cetingul N, Erbay A, Vergin C, Ozkinay C. Cogulu O, et al. Among authors: karapinar d. Leuk Lymphoma. 2004 Dec;45(12):2477-80. doi: 10.1080/10428190400007508. Leuk Lymphoma. 2004. PMID: 15621763

3

Unusual course of an acute lymphoblastic leukemia case with i(9q) as a sole cytogenetic abnormality.

Cogulu O, Karapinar DY, Karaca E, Aydinok Y, Ozkinay F. Cogulu O, et al. Leuk Res. 2006 Nov;30(11):1461-3. doi: 10.1016/j.leukres.2006.02.018. Epub 2006 Mar 24. Leuk Res. 2006. PMID: 16564090

4

The evaluation of hTERT mRNA expression in acute leukemia children and 2 years follow-up of 40 cases.

Cogulu O, Kosova B, Gunduz C, Karaca E, Aksoylar S, Erbay A, Karapinar D, Vergin C, Vural F, Tombuloglu M, Cetingul N, Ozkinay F. Cogulu O, et al. Among authors: karapinar d. Int J Hematol. 2008 Apr;87(3):276-83. doi: 10.1007/s12185-008-0054-y. Epub 2008 Feb 22. Int J Hematol. 2008. PMID: 18293058

5

A further Turkish case of Griscelli syndrome with new RAB27A mutation.

Onay H, Balkan C, Cogulu O, Aydinok Y, Karapinar DY, Ozkinay F. Onay H, et al. J Am Acad Dermatol. 2008 May;58(5 Suppl 1):S115-6. doi: 10.1016/j.jaad.2007.05.002. J Am Acad Dermatol. 2008. PMID: 18489042 No abstract available.

6

Long-term evaluation of chromosomal breakages after radioisotope synovectomy for treatment of target joints in patients with haemophilia.

Kavakli K, Cogulu O, Aydogdu S, Ozkiliç H, Durmaz B, Kirbiyik O, Ozkinay F, Balkan C, Karapinar D, Ay Y. Kavakli K, et al. Among authors: karapinar d. Haemophilia. 2010 May;16(3):474-8. doi: 10.1111/j.1365-2516.2009.02167.x. Epub 2009 Dec 28. Haemophilia. 2010. PMID: 20050929

7

The Association of minor congenital anomalies and childhood cancer.

Durmaz A, Durmaz B, Kadioglu B, Aksoylar S, Karapinar D, Koturoglu G, Orman MN, Ozkinay F, Cogulu O. Durmaz A, et al. Among authors: karapinar d. Pediatr Blood Cancer. 2011 Jul 1;56(7):1098-102. doi: 10.1002/pbc.23049. Epub 2011 Feb 25. Pediatr Blood Cancer. 2011. PMID: 21360657

8

Micronucleus evaluation for determining the chromosomal breakages after radionuclide synovectomy in patients with hemophilia.

Kavakli K, Cogulu O, Karaca E, Durmaz B, Ozkinay F, Aydogdu S, Ozkilic H, Balkan C, Karapinar D, Ay Y. Kavakli K, et al. Among authors: karapinar d. Ann Nucl Med. 2012 Jan;26(1):41-6. doi: 10.1007/s12149-011-0540-9. Epub 2011 Oct 14. Ann Nucl Med. 2012. PMID: 21996780

9

A novel mutation, IVS13+5G>A, in Ellis-van Creveld syndrome associated with haemophagocytic lymphohistiocytosis.

Zeytinoglu M, Aykut A, Hazan F, Torrente I, Akay MC, Karapinar DY, Vergin C, Cogulu O, Ozkinay F. Zeytinoglu M, et al. Clin Dysmorphol. 2013 Oct;22(4):140-142. doi: 10.1097/MCD.0b013e3283633831. Clin Dysmorphol. 2013. PMID: 23924873 No abstract available.

10

Dysbiosis of the Oral Ecosystem in Severe Congenital Neutropenia Patients.

Zaura E, Brandt BW, Buijs MJ, Emingil G, Ergüz M, Karapinar DY, Pekpinarli B, Bao K, Belibasakis GN, Bostanci N. Zaura E, et al. Proteomics Clin Appl. 2020 May;14(3):e1900058. doi: 10.1002/prca.201900058. Epub 2020 Mar 3. Proteomics Clin Appl. 2020. PMID: 32026584 Free PMC article.

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