Search research articles
Contact Us
Filters
Showing results (11-20 of 16) with videos related to
Page
of 2
Sort By:
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 Turkey
Zafer Salcioglu, Deniz Tugcu, Arzu Akcay, et al.
Disease Markers
|
August 5, 2010
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL
Yucel 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.
Page
of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 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 Turkey
Zafer Salcioglu, Deniz Tugcu, Arzu Akcay, et al.
Disease Markers
|
August 5, 2010
Prognostic significance of NOTCH1 and FBXW7 mutations in pediatric T-ALL
Yucel 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.
Page
of 2