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Mediterranean Journal of Hematology and Infectious Diseases
|
November 29, 2023
A Multicenter ICET-A Study on Age at Menarche and Menstrual Cycles in Patients with Transfusion-Dependent Thalassemia (TDT) who Started Early Chelation Therapy with Different Chelating Agents
Salvatore Di Maio, Pierluigi Marzuillo, Shahina Daar, et al.
Journal of Pharmacopuncture
|
August 29, 2018
Comparative evaluation of the safety and efficacy of recombinant FVIII in severe hemophilia A patients
Hassan Abolghasemi, Yunes Panahi, Minoo Ahmadinejad, et al.
Pediatric Endocrinology Reviews : PER
|
March 1, 2014
Osteoporosis in thalassemia major: an update and the I-CET 2013 recommendations for surveillance and treatment
Vincenzo De Sanctis, Ashraf T Soliman, Heba Elsedfy, et al.
International Journal of Hematology-Oncology and Stem Cell Research
|
December 9, 2016
Health-Related Quality of Life and Health Utility Values in Beta Thalassemia Major Patients Receiving Different Types of Iron Chelators in Iran
Meysam Seyedifar, Farid Abedin Dorkoosh, Amir Ali Hamidieh, et al.
Hemoglobin
|
June 14, 2019
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia
Thomas R L Klei, Sima Kheradmand Kia, Martijn Veldthuis, et al.
Mediterranean Journal of Hematology and Infectious Diseases
|
March 16, 2017
β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint
Vincenzo De Sanctis, Christos Kattamis, Duran Canatan, et al.
Haematologica
|
January 29, 2008
ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission
Flora Peyvandi, Silvia Lavoretano, Roberta Palla, et al.
Thrombosis and Haemostasis
|
December 15, 2012
Replacement therapy for bleeding episodes in factor VII deficiency. A prospective evaluation
Guglielmo Mariani, Mariasanta Napolitano, Alberto Dolce, et al.
Acta Bio-Medica : Atenei Parmensis
|
May 12, 2022
The The use of oral glucose-lowering agents (GLAs) in β-thalassemia patients with diabetes: Preliminary data from a retrospective study of ICET-A Network
Vincenzo De Sanctis, Ashraf Soliman, Ploutarchos Tzoulis, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 31, 2019
Fibrinogen concentrate for treatment of bleeding and surgical prophylaxis in congenital fibrinogen deficiency patients
Toshko Lissitchkov, Bella Madan, Claudia Djambas Khayat, et al.
Page
of 32
Search research articles
Search
Showing results (281-290 of 315) with videos related to
Sort By:
Page
of 32
Mediterranean Journal of Hematology and Infectious Diseases
|
November 29, 2023
A Multicenter ICET-A Study on Age at Menarche and Menstrual Cycles in Patients with Transfusion-Dependent Thalassemia (TDT) who Started Early Chelation Therapy with Different Chelating Agents
Salvatore Di Maio, Pierluigi Marzuillo, Shahina Daar, et al.
Journal of Pharmacopuncture
|
August 29, 2018
Comparative evaluation of the safety and efficacy of recombinant FVIII in severe hemophilia A patients
Hassan Abolghasemi, Yunes Panahi, Minoo Ahmadinejad, et al.
Pediatric Endocrinology Reviews : PER
|
March 1, 2014
Osteoporosis in thalassemia major: an update and the I-CET 2013 recommendations for surveillance and treatment
Vincenzo De Sanctis, Ashraf T Soliman, Heba Elsedfy, et al.
International Journal of Hematology-Oncology and Stem Cell Research
|
December 9, 2016
Health-Related Quality of Life and Health Utility Values in Beta Thalassemia Major Patients Receiving Different Types of Iron Chelators in Iran
Meysam Seyedifar, Farid Abedin Dorkoosh, Amir Ali Hamidieh, et al.
Hemoglobin
|
June 14, 2019
A Homozygous Mutation on the HBA1 Gene Coding for Hb Charlieu (HBA1: c.320T>C) Together with β-Thalassemia Trait Results in Severe Hemolytic Anemia
Thomas R L Klei, Sima Kheradmand Kia, Martijn Veldthuis, et al.
Mediterranean Journal of Hematology and Infectious Diseases
|
March 16, 2017
β-Thalassemia Distribution in the Old World: an Ancient Disease Seen from a Historical Standpoint
Vincenzo De Sanctis, Christos Kattamis, Duran Canatan, et al.
Haematologica
|
January 29, 2008
ADAMTS13 and anti-ADAMTS13 antibodies as markers for recurrence of acquired thrombotic thrombocytopenic purpura during remission
Flora Peyvandi, Silvia Lavoretano, Roberta Palla, et al.
Thrombosis and Haemostasis
|
December 15, 2012
Replacement therapy for bleeding episodes in factor VII deficiency. A prospective evaluation
Guglielmo Mariani, Mariasanta Napolitano, Alberto Dolce, et al.
Acta Bio-Medica : Atenei Parmensis
|
May 12, 2022
The The use of oral glucose-lowering agents (GLAs) in β-thalassemia patients with diabetes: Preliminary data from a retrospective study of ICET-A Network
Vincenzo De Sanctis, Ashraf Soliman, Ploutarchos Tzoulis, et al.
Journal of Thrombosis and Haemostasis : JTH
|
December 31, 2019
Fibrinogen concentrate for treatment of bleeding and surgical prophylaxis in congenital fibrinogen deficiency patients
Toshko Lissitchkov, Bella Madan, Claudia Djambas Khayat, et al.
Page
of 32