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European Journal of Haematology
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May 5, 1999
Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence
T Sipahi, F Duru, E Ciftçi, et al.
Thrombosis Research
|
April 27, 2001
Common mutations at the homocysteine metabolism pathway and pediatric stroke
N Akar, E Akar, D Ozel, et al.
Pediatric Hematology and Oncology
|
September 1, 1995
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey
N Akar, T Sipahi, Y Eğin, et al.
Pediatric Hematology and Oncology
|
December 22, 1999
Coexistence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients
N Akar, E Akar, G Deda, et al.
European Journal of Pediatrics
|
January 5, 2002
Is it possible to diagnose Rapunzel syndrome pre-operatively?
A Uçkun, T Sipahi, M Igde, et al.
Archives of Pediatrics & Adolescent Medicine
|
November 14, 2000
Special feature: pathological case of the month. Glycogen storage disease with renal tubular dysfunction (type XI, Fanconi-Bickel syndrome)
F Sahin, T Sipahi, H Doğan, et al.
Thrombosis Research
|
April 27, 2001
The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct
N Akar, T Duman, E Akar, et al.
Haemostasis
|
October 3, 2000
Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct
N Akar, E Yilmaz, E Akar, et al.
Journal of Child Neurology
|
December 11, 1999
Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct
N Akar, E Akar, G Deda, et al.
Pediatric Hematology and Oncology
|
September 16, 2000
Parvovirus B19 infection reminiscent of myelodysplastic syndrome in three children with chronic hemolytic anemia
N Yarali, F Duru, T Sipahi, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
European Journal of Haematology
|
May 5, 1999
Cerebral infarct associated with prothrombin gene G 20210 A variant in a Turkish child with cystic fibrosis: an unusual coexistence
T Sipahi, F Duru, E Ciftçi, et al.
Thrombosis Research
|
April 27, 2001
Common mutations at the homocysteine metabolism pathway and pediatric stroke
N Akar, E Akar, D Ozel, et al.
Pediatric Hematology and Oncology
|
September 1, 1995
Incidence of parvovirus B19 infection among thalassemia major patients from Ankara, Turkey
N Akar, T Sipahi, Y Eğin, et al.
Pediatric Hematology and Oncology
|
December 22, 1999
Coexistence of two prothrombotic mutations, factor V 1691 G-A and prothrombin gene 20210 G-A, and the risk of cerebral infarct in pediatric patients
N Akar, E Akar, G Deda, et al.
European Journal of Pediatrics
|
January 5, 2002
Is it possible to diagnose Rapunzel syndrome pre-operatively?
A Uçkun, T Sipahi, M Igde, et al.
Archives of Pediatrics & Adolescent Medicine
|
November 14, 2000
Special feature: pathological case of the month. Glycogen storage disease with renal tubular dysfunction (type XI, Fanconi-Bickel syndrome)
F Sahin, T Sipahi, H Doğan, et al.
Thrombosis Research
|
April 27, 2001
The alpha2 Gene alleles of the platelet collagen receptor integrin alpha2 beta1 in Turkish children with cerebral infarct
N Akar, T Duman, E Akar, et al.
Haemostasis
|
October 3, 2000
Factor V (His 1299 Arg) in young Turkish patients with cerebral infarct
N Akar, E Yilmaz, E Akar, et al.
Journal of Child Neurology
|
December 11, 1999
Factor V1691 G-A, prothrombin 20210 G-A, and methylenetetrahydrofolate reductase 677 C-T variants in Turkish children with cerebral infarct
N Akar, E Akar, G Deda, et al.
Pediatric Hematology and Oncology
|
September 16, 2000
Parvovirus B19 infection reminiscent of myelodysplastic syndrome in three children with chronic hemolytic anemia
N Yarali, F Duru, T Sipahi, et al.
Page
of 3