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Zafer Salcioglu

Showing results (11-20 of 16) with videos related to

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Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 26, 2013
Surgical interventions in childhood rare factor deficiencies: a single-center experience from TurkeyZafer Salcioglu, Deniz Tugcu, Arzu Akcay, et al.
Disease Markers|August 5, 2010
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALLYucel Erbilgin, Muge Sayitoglu, Ozden Hatirnaz, et al.
Atherosclerosis|February 7, 2018
A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry)Meral Kayikcioglu, Lale Tokgozoglu, Mehmet Yilmaz, et al.
Journal of Clinical Lipidology|April 1, 2019
Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)Meral Kayikcioglu, Ozlem Kuman-Tunçel, Sebnem Pirildar, et al.
European Journal of Haematology|October 10, 2018
Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM)Bulent Antmen, Zeynep Karakaş, Mehmet Akif Yeşilipek, et al.
Atherosclerosis|October 2, 2018
What have we learned from Turkish familial hypercholesterolemia registries (A-HIT1 and A-HIT2)?Meral Kayikcioglu, Lale Tokgozoglu, Volkan Dogan, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 26, 2013
Surgical interventions in childhood rare factor deficiencies: a single-center experience from TurkeyZafer Salcioglu, Deniz Tugcu, Arzu Akcay, et al.
Disease Markers|August 5, 2010
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALLYucel Erbilgin, Muge Sayitoglu, Ozden Hatirnaz, et al.
Atherosclerosis|February 7, 2018
A nation-wide survey of patients with homozygous familial hypercholesterolemia phenotype undergoing LDL-apheresis in Turkey (A-HIT 1 registry)Meral Kayikcioglu, Lale Tokgozoglu, Mehmet Yilmaz, et al.
Journal of Clinical Lipidology|April 1, 2019
Clinical management, psychosocial characteristics, and quality of life in patients with homozygous familial hypercholesterolemia undergoing LDL-apheresis in Turkey: Results of a nationwide survey (A-HIT1 registry)Meral Kayikcioglu, Ozlem Kuman-Tunçel, Sebnem Pirildar, et al.
European Journal of Haematology|October 10, 2018
Deferasirox in children with transfusion-dependent thalassemia or sickle cell anemia: A large cohort real-life experience from Turkey (REACH-THEM)Bulent Antmen, Zeynep Karakaş, Mehmet Akif Yeşilipek, et al.
Atherosclerosis|October 2, 2018
What have we learned from Turkish familial hypercholesterolemia registries (A-HIT1 and A-HIT2)?Meral Kayikcioglu, Lale Tokgozoglu, Volkan Dogan, et al.
Pageof 2