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Nejat Akar

Showing results (211-220 of 229) with videos related to

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Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 28, 2007
The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolismI Kivilcim Oguzulgen, E Yilmaz, Senay Demirtas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 9, 2005
Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese childrenZehra Aycan, Merih Berberoğlu, Gönül Ocal, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patientsTawhida Y Abdel Ghaffar, Solaf M Elsayed, Mohamed A Sakr, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|September 18, 2015
Hemoglobin H Disease in Turkey: Experience from Eight CentersSelma Ünal, Gönül Oktay, Can Acıpayam, et al.
Pediatric Endocrinology Reviews : PER|February 1, 2008
5 alpha steroid reductase deficiency in TurkeyPelin Bilir Adiyaman, Gonul Ocal, Ergun Cetinkaya, et al.
Pediatric Hematology and Oncology|January 15, 2002
Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndromeZümrüt Uysal, Figen Doğu, A Emin Kürekçi, et al.
Plos One|February 19, 2016
Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling StudyAli Kemal Oğuz, Seda Taşır Yılmaz, Çağdaş Şahap Oygür, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 5, 2015
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiencyBuket Dönmez-Demir, Tiraje Celkan, Nazan Sarper, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndromeAyça T Ergür, Gönül Ocal, Merih Berberoglu, et al.
American Journal of Human Genetics|January 20, 2007
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaMustafa Tekin, Burcu Oztürk Hişmi, Suat Fitoz, et al.
Pageof 23

Showing results (211-220 of 229) with videos related to

Sort By:
Pageof 23
Clinical and Applied Thrombosis/Hemostasis : Official Journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis|December 28, 2007
The role of plasminogen activator inhibitor-1 polymorphism, factor-V-Leiden, and prothrombin-20210 mutations in pulmonary thromboembolismI Kivilcim Oguzulgen, E Yilmaz, Senay Demirtas, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 9, 2005
Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese childrenZehra Aycan, Merih Berberoğlu, Gönül Ocal, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|June 7, 2016
Factor V G1691A (Leiden) is a major etiological factor in Egyptian Budd-Chiari syndrome patientsTawhida Y Abdel Ghaffar, Solaf M Elsayed, Mohamed A Sakr, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology|September 18, 2015
Hemoglobin H Disease in Turkey: Experience from Eight CentersSelma Ünal, Gönül Oktay, Can Acıpayam, et al.
Pediatric Endocrinology Reviews : PER|February 1, 2008
5 alpha steroid reductase deficiency in TurkeyPelin Bilir Adiyaman, Gonul Ocal, Ergun Cetinkaya, et al.
Pediatric Hematology and Oncology|January 15, 2002
Recurrent arterial thrombosis in a child: primary antiphospholipid antibody syndromeZümrüt Uysal, Figen Doğu, A Emin Kürekçi, et al.
Plos One|February 19, 2016
Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling StudyAli Kemal Oğuz, Seda Taşır Yılmaz, Çağdaş Şahap Oygür, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|September 5, 2015
Novel plasminogen gene mutations in Turkish patients with type I plasminogen deficiencyBuket Dönmez-Demir, Tiraje Celkan, Nazan Sarper, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 21, 2008
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndromeAyça T Ergür, Gönül Ocal, Merih Berberoglu, et al.
American Journal of Human Genetics|January 20, 2007
Homozygous mutations in fibroblast growth factor 3 are associated with a new form of syndromic deafness characterized by inner ear agenesis, microtia, and microdontiaMustafa Tekin, Burcu Oztürk Hişmi, Suat Fitoz, et al.
Pageof 23