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Results: 1-17 |
Results: 17
Evidence for the existence of the PAF acetylhydrolase mutation (Va1279Phe)in non-Japanese populations: A preliminary study in Turkey, Azerbaijan, and Kyrgyzstan
Authors: Balta, G Gurgey, A Kudayarov, DK Tunc, B Altay, C
Citation: G. Balta et al., Evidence for the existence of the PAF acetylhydrolase mutation (Va1279Phe)in non-Japanese populations: A preliminary study in Turkey, Azerbaijan, and Kyrgyzstan, THROMB RES, 101(4), 2001, pp. 231-234
Efficacy of oral vitamin B-12 treatment in children
Authors: Cetin, M Altay, C
Citation: M. Cetin et C. Altay, Efficacy of oral vitamin B-12 treatment in children, J PEDIAT, 139(5), 2001, pp. 754-754
beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G -> A substitution at+22 relative to the beta-globin cap site
Authors: Oner, R Oner, C Birben, E Sozen, M Gumruk, F Gurgey, A Altay, C
Citation: R. Oner et al., beta-Thalassaemia intermedia in a Turkish girl: homozygosity for G -> A substitution at+22 relative to the beta-globin cap site, BR J HAEM, 115(1), 2001, pp. 90-94
Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9
Authors: Demuth, I Wlodarski, M Tipping, AJ Morgan, NV de Winter, JP Thiel, M Grasl, S Schindler, D D'Andrea, AD Altay, C Kayserili, H Zatterale, A Kunze, J Ebell, W Mathew, CG Joenje, H Sperling, K Digweed, M
Citation: I. Demuth et al., Spectrum of mutations in the Fanconi anaemia group G gene, FANCG/XRCC9, EUR J HUM G, 8(11), 2000, pp. 861-868
Molecular characterization of glucose-6-phosphate dehydrogenase deficiencyin Turkey
Authors: Oner, R Gumruk, F Acar, C Oner, C Gurgey, A Altay, C
Citation: R. Oner et al., Molecular characterization of glucose-6-phosphate dehydrogenase deficiencyin Turkey, HAEMATOLOG, 85(3), 2000, pp. 320-321
Molecular analysis of Turkish beta-thalassemia heterozygotes with normal Hb A(2) levels
Authors: Oner, R Birben, E Acar, C Oner, C Kara, A Gumruk, F Gurgey, A Altay, C
Citation: R. Oner et al., Molecular analysis of Turkish beta-thalassemia heterozygotes with normal Hb A(2) levels, HEMOGLOBIN, 24(3), 2000, pp. 195-201
beta-thalassemia intermedia associated with homozygosity for the -87 (C ->T) mutation in a Turkish family
Authors: Gumruk, F Mergen, H Oner, R Ozcebe, O Sayinalp, N Oner, C Gurgey, A Altay, C
Citation: F. Gumruk et al., beta-thalassemia intermedia associated with homozygosity for the -87 (C ->T) mutation in a Turkish family, HEMOGLOBIN, 24(1), 2000, pp. 23-29
The factor V Leiden and prothrombin G20210A mutations in Kirghiz population
Authors: Gurgey, A Kudayarov, DK Tuncer, M Parlak, H Altay, C
Citation: A. Gurgey et al., The factor V Leiden and prothrombin G20210A mutations in Kirghiz population, THROMB HAEM, 84(2), 2000, pp. 356-356
Prevalence of the prothrombin gene G20210A mutation in Azerbaijan
Authors: Togrul, J Rustamov, R Gurgey, A Altay, S Altay, C
Citation: J. Togrul et al., Prevalence of the prothrombin gene G20210A mutation in Azerbaijan, BR J HAEM, 108(4), 2000, pp. 887-888
Association of complementation group and mutation type with clinical outcome in Fanconi anemia
Authors: Faivre, L Guardiola, P Lewis, C Dokal, I Ebell, W Zatterale, Z Altay, C Poole, J Stones, D Kwee, ML van Weel-Sipman, M Havenga, C Morgan, N de Winter, J Digweed, M Savoia, A Pronk, J de Ravel, T Jansen, S Joenje, H Gluckman, E Mathew, CG
Citation: L. Faivre et al., Association of complementation group and mutation type with clinical outcome in Fanconi anemia, BLOOD, 96(13), 2000, pp. 4064-4070
Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient
Authors: Koc, A Oner, R Oner, C Aktas, D Sozen, M Tuncbilek, E Altay, C
Citation: A. Koc et al., Myelodysplastic syndrome (MDS) associated with increased hemoglobin F and trisomy 8: presentation of a patient, HEM CELL TH, 41(4), 1999, pp. 187-189
Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene
Authors: Wijker, M Morgan, NV Herterich, S van Berkel, CGM Tipping, AJ Gross, HJ Gille, JJP Pals, G Savino, M Altay, C Mohan, S Dokal, I Cavenagh, J Marsh, J Van Weel, M Ortega, JJ Schuler, D Samochatova, E Karwacki, M Bekassy, AN Abecasis, M Ebell, W Kwee, ML de Ravel, T Gibson, RA Gluckman, E Arwert, F Joenje, H Savoia, A Hoehn, H Pronk, JC Mathew, CG
Citation: M. Wijker et al., Heterogeneous spectrum of mutations in the Fanconi anaemia group A gene, EUR J HUM G, 7(1), 1999, pp. 52-59
Vitamin B-12 absorption test and oral treatment in 14 children with selective vitamin B-12 malabsorption
Authors: Altay, C Cetin, M
Citation: C. Altay et M. Cetin, Vitamin B-12 absorption test and oral treatment in 14 children with selective vitamin B-12 malabsorption, PED HEM ONC, 16(2), 1999, pp. 159-163
Beta thalassaemia: A report of 20 children
Authors: Onur, O Sivri, A Gumruk, F Altay, C
Citation: O. Onur et al., Beta thalassaemia: A report of 20 children, CLIN RHEUMA, 18(1), 1999, pp. 42-44
Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemia
Authors: Kinik, ST Tuncer, AR Altay, C
Citation: St. Kinik et al., Transferrin receptor on peripheral blood lymphocytes in iron deficiency anaemia, BR J HAEM, 104(3), 1999, pp. 494-498
Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family
Authors: Koc, A Pronk, JC Alikasifoglu, M Joenje, H Altay, C
Citation: A. Koc et al., Variable pathogenicity of exon 43del (FAA) in four Fanconi anaemia patients within a consanguineous family, BR J HAEM, 104(1), 1999, pp. 127-130
The Fanconi anemia group E gene, FANCE, maps to chromosome 6p
Authors: Waisfisz, Q Saar, K Morgan, NV Altay, C Leegwater, PA de Winter, JP Komatsu, K Evans, GR Wegner, RD Reis, A Joenje, H Arwert, F Mathew, CG Pronk, JC Digweed, M
Citation: Q. Waisfisz et al., The Fanconi anemia group E gene, FANCE, maps to chromosome 6p, AM J HU GEN, 64(5), 1999, pp. 1400-1405
Risultati: 1-17 |