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Haematologica
|
January 1, 2009
The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura
Roberta Palla, Silvia Lavoretano, Rossana Lombardi, et al.
Acta Bio-Medica : Atenei Parmensis
|
December 6, 2023
A prospective guide for clinical implementation of selected OGTT- derived surrogate indices for the evaluation of β- cell function and insulin sensitivity in patients with transfusion-dependent β- thalassaemia
Vincenzo De Sanctis, Ashraf T Soliman, Shahina Daar, et al.
Expert Review of Hematology
|
October 27, 2017
Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia
Vincenzo De Sanctis, Ashraf T Soliman, Heba Elsedfy, et al.
Annals of Hematology
|
September 2, 2008
Factor XI deficiency in Southern Iran: identification of a novel missense mutation
Mehran Karimi, Hamta Jafari, Saba Lahsaeizadeh, et al.
British Journal of Haematology
|
June 3, 2020
Prevalence and mortality in β-thalassaemias due to outbreak of novel coronavirus disease (COVID-19): the nationwide Iranian experience
Mehran Karimi, Sezaneh Haghpanah, Azita Azarkeivan, et al.
Iranian Red Crescent Medical Journal
|
October 1, 2015
Relationship Between Serum Hepcidin and Ferritin Levels in Patients With Thalassemia Major and Intermedia in Southern Iran
Sezaneh Haghpanah, Masoomeh Esmaeilzadeh, Naser Honar, et al.
Acta Bio-Medica : Atenei Parmensis
|
September 14, 2020
Prevalence and severity of Coronavirus disease 2019 (COVID-19) in Transfusion Dependent and Non-Transfusion Dependent β-thalassemia patients and effects of associated comorbidities: an Iranian nationwide study
Mehran Karimi, Sezaneh Haghpanah, Tahereh Zarei, et al.
Blood Cells, Molecules & Diseases
|
April 22, 2019
A retrospective study on clinical manifestations of neonates with FXIII-A deficiency
Majid Naderi, Nader Cohan, Iraj Shahramian, et al.
BMC Infectious Diseases
|
August 3, 2021
Comparison of the clinical features and outcome of children with hemophagocytic lymphohistiocytosis (HLH) secondary to visceral leishmaniasis and primary HLH: a single-center study
Hadi Mottaghipisheh, Kurosh Kalantar, Ali Amanati, et al.
Journal of Pediatric Hematology/Oncology
|
January 26, 2017
Relationship Between Some Single-nucleotide Polymorphism and Response to Hydroxyurea Therapy in Iranian Patients With β-Thalassemia Intermedia
Mehran Karimi, Tahereh Zarei, Sezaneh Haghpanah, et al.
Page
of 32
Search research articles
Search
Showing results (251-260 of 315) with videos related to
Sort By:
Page
of 32
Haematologica
|
January 1, 2009
The first deletion mutation in the TSP1-6 repeat domain of ADAMTS13 in a family with inherited thrombotic thrombocytopenic purpura
Roberta Palla, Silvia Lavoretano, Rossana Lombardi, et al.
Acta Bio-Medica : Atenei Parmensis
|
December 6, 2023
A prospective guide for clinical implementation of selected OGTT- derived surrogate indices for the evaluation of β- cell function and insulin sensitivity in patients with transfusion-dependent β- thalassaemia
Vincenzo De Sanctis, Ashraf T Soliman, Shahina Daar, et al.
Expert Review of Hematology
|
October 27, 2017
Gonadal dysfunction in adult male patients with thalassemia major: an update for clinicians caring for thalassemia
Vincenzo De Sanctis, Ashraf T Soliman, Heba Elsedfy, et al.
Annals of Hematology
|
September 2, 2008
Factor XI deficiency in Southern Iran: identification of a novel missense mutation
Mehran Karimi, Hamta Jafari, Saba Lahsaeizadeh, et al.
British Journal of Haematology
|
June 3, 2020
Prevalence and mortality in β-thalassaemias due to outbreak of novel coronavirus disease (COVID-19): the nationwide Iranian experience
Mehran Karimi, Sezaneh Haghpanah, Azita Azarkeivan, et al.
Iranian Red Crescent Medical Journal
|
October 1, 2015
Relationship Between Serum Hepcidin and Ferritin Levels in Patients With Thalassemia Major and Intermedia in Southern Iran
Sezaneh Haghpanah, Masoomeh Esmaeilzadeh, Naser Honar, et al.
Acta Bio-Medica : Atenei Parmensis
|
September 14, 2020
Prevalence and severity of Coronavirus disease 2019 (COVID-19) in Transfusion Dependent and Non-Transfusion Dependent β-thalassemia patients and effects of associated comorbidities: an Iranian nationwide study
Mehran Karimi, Sezaneh Haghpanah, Tahereh Zarei, et al.
Blood Cells, Molecules & Diseases
|
April 22, 2019
A retrospective study on clinical manifestations of neonates with FXIII-A deficiency
Majid Naderi, Nader Cohan, Iraj Shahramian, et al.
BMC Infectious Diseases
|
August 3, 2021
Comparison of the clinical features and outcome of children with hemophagocytic lymphohistiocytosis (HLH) secondary to visceral leishmaniasis and primary HLH: a single-center study
Hadi Mottaghipisheh, Kurosh Kalantar, Ali Amanati, et al.
Journal of Pediatric Hematology/Oncology
|
January 26, 2017
Relationship Between Some Single-nucleotide Polymorphism and Response to Hydroxyurea Therapy in Iranian Patients With β-Thalassemia Intermedia
Mehran Karimi, Tahereh Zarei, Sezaneh Haghpanah, et al.
Page
of 32