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Thrombosis Research
|
March 15, 2001
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan
G Balta, A Gurgey, D K Kudayarov, et al.
American Journal of Hematology
|
July 1, 1990
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes
C Oner, A Gurgey, C Altay, et al.
Pediatric Hematology and Oncology
|
October 1, 1991
High-dose methylprednisolone for the treatment of priapism in childhood leukemia
F Gumruk, G Hiçsónmez, S Ozsoylu, et al.
Pediatric Cardiology
|
January 11, 2003
Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations
A Gurgey, E Ozyurek, F Gümrük, et al.
Acta Haematologica
|
January 1, 1989
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family
A Gurgey, C Altay, M S Beksaç, et al.
The Turkish Journal of Pediatrics
|
January 1, 1996
Neurologic findings of vitamin B12 deficiency: presentation of 7 cases
O Kalayci, M Cetin, B Kirel, et al.
Clinical and Experimental Obstetrics & Gynecology
|
June 10, 2006
High frequency of thrombophilic disorders in women with recurrent fetal miscarriage
L Onderoglu, C Baykal, R A Al, et al.
Hemoglobin
|
January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site
C Altay, A Gurgey, R Oner, et al.
American Journal of Hematology
|
December 1, 1994
High-dose methylprednisolone and VP-16 in treatment of Griscelli syndrome with central nervous system involvement
A Gurgey, T Sayli, M Gunay, et al.
Hemoglobin
|
January 1, 1981
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotes
G Dincol, C Altay, M Aksoy, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 51) with videos related to
Sort By:
Page
of 6
Thrombosis Research
|
March 15, 2001
Evidence for the existence of the PAF acetylhydrolase mutation (Val279Phe) in non-Japanese populations: a preliminary study in Turkey, Azerbaijan, and Kyrgyzstan
G Balta, A Gurgey, D K Kudayarov, et al.
American Journal of Hematology
|
July 1, 1990
Variation in the level of fetal hemoglobin in (delta beta) (0)-thalassemia heterozygotes with different numbers of alpha-globin genes
C Oner, A Gurgey, C Altay, et al.
Pediatric Hematology and Oncology
|
October 1, 1991
High-dose methylprednisolone for the treatment of priapism in childhood leukemia
F Gumruk, G Hiçsónmez, S Ozsoylu, et al.
Pediatric Cardiology
|
January 11, 2003
Thrombosis in children with cardiac pathology: frequency of factor V Leiden and prothrombin G20210A mutations
A Gurgey, E Ozyurek, F Gümrük, et al.
Acta Haematologica
|
January 1, 1989
Hydrops fetalis due to homozygosity for alpha-thalassemia-1, -(alpha)-20.5 kb: the first observation in a Turkish family
A Gurgey, C Altay, M S Beksaç, et al.
The Turkish Journal of Pediatrics
|
January 1, 1996
Neurologic findings of vitamin B12 deficiency: presentation of 7 cases
O Kalayci, M Cetin, B Kirel, et al.
Clinical and Experimental Obstetrics & Gynecology
|
June 10, 2006
High frequency of thrombophilic disorders in women with recurrent fetal miscarriage
L Onderoglu, C Baykal, R A Al, et al.
Hemoglobin
|
January 1, 1991
A mild thalassemia major resulting from a compound heterozygosity for the IVS-II-1 (G----A) mutation and the rare T----C mutation at the polyadenylation site
C Altay, A Gurgey, R Oner, et al.
American Journal of Hematology
|
December 1, 1994
High-dose methylprednisolone and VP-16 in treatment of Griscelli syndrome with central nervous system involvement
A Gurgey, T Sayli, M Gunay, et al.
Hemoglobin
|
January 1, 1981
Clinical and hematological evaluation of two delta 0 beta 0-thalassemia homozygotes
G Dincol, C Altay, M Aksoy, et al.
Page
of 6