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N Akar

Showing results (21-30 of 87) with videos related to

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Pediatric Hematology and Oncology|July 1, 1993
Desferrioxamine and urinary zinc excretion in beta-thalassemia majorZ Uysal, N Akar, S Kemahli, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 1990
Ultrastructural changes in the mucosa of the small intestine in patients with geophagia (Prasad's syndrome)A Arcasoy, N Akar, U Ors, et al.
American Journal of Hematology|April 1, 1995
Discrimination of Hb D Los Angeles (B121 Glu-Gln) and Hb Beograd (B121 Glu-Val) by dual restriction enzyme analysisN Akar, A Ozden, E Akar, et al.
Thrombosis Research|April 27, 2001
Common mutations at the homocysteine metabolism pathway and pediatric strokeN Akar, E Akar, D Ozel, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 24, 2001
Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemiaD Tekin, S Yavuzer, M Tekin, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysisF Yalçinkaya, N Tümer, N Akar, et al.
Bratislavske Lekarske Listy|June 28, 2018
Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemiaD F Akin, D A Oner, E Kurekci, et al.
Pediatric Hematology and Oncology|September 1, 1995
p53 codon 213 (A-G) polymorphism in a Turkish populationI Ilhan, S Erekul, S Ateşalp, et al.
Angiology|May 29, 2000
Prothrombin gene 20210 G-->A and Factor V Arg 506 to Gln mutation in a patient with Buerger's disease--a case reportF Avcu, N Akar, E Akar, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same PatientZ L Uysal, N Akar, Ş Cin, et al.
Pageof 9

Showing results (21-30 of 87) with videos related to

Sort By:
Pageof 9
Pediatric Hematology and Oncology|July 1, 1993
Desferrioxamine and urinary zinc excretion in beta-thalassemia majorZ Uysal, N Akar, S Kemahli, et al.
Journal of Pediatric Gastroenterology and Nutrition|August 1, 1990
Ultrastructural changes in the mucosa of the small intestine in patients with geophagia (Prasad's syndrome)A Arcasoy, N Akar, U Ors, et al.
American Journal of Hematology|April 1, 1995
Discrimination of Hb D Los Angeles (B121 Glu-Gln) and Hb Beograd (B121 Glu-Val) by dual restriction enzyme analysisN Akar, A Ozden, E Akar, et al.
Thrombosis Research|April 27, 2001
Common mutations at the homocysteine metabolism pathway and pediatric strokeN Akar, E Akar, D Ozel, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|February 24, 2001
Possible effects of antioxidant status on increased platelet aggregation in childhood iron-deficiency anemiaD Tekin, S Yavuzer, M Tekin, et al.
Pediatric Nephrology (Berlin, Germany)|August 1, 1995
Tuberculous osteomyelitis: an unusual case of tuberculous infection in a child undergoing continuous ambulatory peritoneal dialysisF Yalçinkaya, N Tümer, N Akar, et al.
Bratislavske Lekarske Listy|June 28, 2018
Determination of CEBPA mutations by next generation sequencing in pediatric acute leukemiaD F Akin, D A Oner, E Kurekci, et al.
Pediatric Hematology and Oncology|September 1, 1995
p53 codon 213 (A-G) polymorphism in a Turkish populationI Ilhan, S Erekul, S Ateşalp, et al.
Angiology|May 29, 2000
Prothrombin gene 20210 G-->A and Factor V Arg 506 to Gln mutation in a patient with Buerger's disease--a case reportF Avcu, N Akar, E Akar, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
Homozygous ß-Thalassemia (FCS8-AA) and Hereditary Spherocytosis in the Same PatientZ L Uysal, N Akar, Ş Cin, et al.
Pageof 9