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1,103 results

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Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor gene.
Tanner SM, Li Z, Perko JD, Oner C, Cetin M, Altay C, Yurtsever Z, David KL, Faivre L, Ismail EA, Gräsbeck R, de la Chapelle A. Tanner SM, et al. Among authors: cetin m. Proc Natl Acad Sci U S A. 2005 Mar 15;102(11):4130-3. doi: 10.1073/pnas.0500517102. Epub 2005 Feb 28. Proc Natl Acad Sci U S A. 2005. PMID: 15738392 Free PMC article.
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East.
Tanner SM, Li Z, Bisson R, Acar C, Oner C, Oner R, Cetin M, Abdelaal MA, Ismail EA, Lissens W, Krahe R, Broch H, Gräsbeck R, de la Chapelle A. Tanner SM, et al. Among authors: cetin m. Hum Mutat. 2004 Apr;23(4):327-33. doi: 10.1002/humu.20014. Hum Mutat. 2004. PMID: 15024727
Long term biweekly 1 mg oral vitamin B12 ensures normal hematological parameters, but does not correct all other markers of vitamin B12 deficiency. A study in patients with inherited vitamin B12 deficiency.
Bor MV, Cetin M, Aytaç S, Altay C, Ueland PM, Nexo E. Bor MV, et al. Among authors: cetin m. Haematologica. 2008 Nov;93(11):1755-8. doi: 10.3324/haematol.13122. Epub 2008 Sep 2. Haematologica. 2008. PMID: 18768530 Free article. No abstract available.
Gray platelet syndrome: natural history of a large patient cohort and locus assignment to chromosome 3p.
Gunay-Aygun M, Zivony-Elboum Y, Gumruk F, Geiger D, Cetin M, Khayat M, Kleta R, Kfir N, Anikster Y, Chezar J, Arcos-Burgos M, Shalata A, Stanescu H, Manaster J, Arat M, Edwards H, Freiberg AS, Hart PS, Riney LC, Patzel K, Tanpaiboon P, Markello T, Huizing M, Maric I, Horne M, Kehrel BE, Jurk K, Hansen NF, Cherukuri PF, Jones M, Cruz P, Mullikin JC, Nurden A, White JG, Gahl WA, Falik-Zaccai T. Gunay-Aygun M, et al. Among authors: cetin m. Blood. 2010 Dec 2;116(23):4990-5001. doi: 10.1182/blood-2010-05-286534. Epub 2010 Aug 13. Blood. 2010. PMID: 20709904 Free PMC article.
Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families.
Colakoglu S, Bayhan T, Tavil B, Keskin EY, Cakir V, Gümrük F, Çetin M, Aytaç S, Berber E. Colakoglu S, et al. Among authors: cetin m. Blood Transfus. 2018 Jan;16(1):105-113. doi: 10.2450/2016.0098-16. Epub 2016 Oct 4. Blood Transfus. 2018. PMID: 27723456 Free PMC article. Clinical Trial.
Transcobalamin II Deficiency in Four Cases with Novel Mutations.
Ünal Ş, Rupar T, Yetgin S, Yaralı N, Dursun A, Gürsel T, Çetin M. Ünal Ş, et al. Among authors: cetin m. Turk J Haematol. 2015 Dec;32(4):317-22. doi: 10.4274/tjh.2014.0154. Epub 2015 Apr 27. Turk J Haematol. 2015. PMID: 25914105 Free PMC article.
1,103 results