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British Journal of Haematology
|
April 29, 2025
Underlying disease is the main risk factor in post-splenectomy complication risk: Data from a national database
Maddalena Casale, Raffaella Colombatti, Manuela Balocco, et al.
Cancer
|
February 24, 2022
Phase 2 study for nonmetastatic extremity high-grade osteosarcoma in pediatric and adolescent and young adult patients with a risk-adapted strategy based on ABCB1/P-glycoprotein expression: An Italian Sarcoma Group trial (ISG/OS-2)
Emanuela Palmerini, Cristina Meazza, Angela Tamburini, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
May 18, 2021
Association of Immune Thrombocytopenia and Celiac Disease in Children: A Retrospective Case Control Study
Angela Guarina, Maddalena Marinoni, Giuseppe Lassandro, et al.
British Journal of Haematology
|
May 26, 2021
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned
Vania Munaretto, Vincenzo Voi, Giovanni Palazzi, et al.
Nature Medicine
|
January 22, 2019
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia
Sarah Marktel, Samantha Scaramuzza, Maria Pia Cicalese, et al.
The New England Journal of Medicine
|
March 27, 2020
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia
M Domenica Cappellini, Vip Viprakasit, Ali T Taher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2024
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Journal of Cellular and Molecular Medicine
|
March 31, 2022
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry
Ibrahim El-Battrawy, Filomena Longo, Iván J Núñez Gil, et al.
American Journal of Hematology
|
December 3, 2021
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection
Filomena Longo, Barbara Gianesin, Vincenzo Voi, et al.
Human Mutation
|
October 12, 2013
Genetic basis of congenital erythrocytosis: mutation update and online databases
Celeste Bento, Melanie J Percy, Betty Gardie, et al.
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Search research articles
Search
Showing results (191-200 of 200) with videos related to
Sort By:
Page
of 20
You have reached the last page of results.
This site can display upto 200 results.
British Journal of Haematology
|
April 29, 2025
Underlying disease is the main risk factor in post-splenectomy complication risk: Data from a national database
Maddalena Casale, Raffaella Colombatti, Manuela Balocco, et al.
Cancer
|
February 24, 2022
Phase 2 study for nonmetastatic extremity high-grade osteosarcoma in pediatric and adolescent and young adult patients with a risk-adapted strategy based on ABCB1/P-glycoprotein expression: An Italian Sarcoma Group trial (ISG/OS-2)
Emanuela Palmerini, Cristina Meazza, Angela Tamburini, et al.
Turkish Journal of Haematology : Official Journal of Turkish Society of Haematology
|
May 18, 2021
Association of Immune Thrombocytopenia and Celiac Disease in Children: A Retrospective Case Control Study
Angela Guarina, Maddalena Marinoni, Giuseppe Lassandro, et al.
British Journal of Haematology
|
May 26, 2021
Acute events in children with sickle cell disease in Italy during the COVID-19 pandemic: useful lessons learned
Vania Munaretto, Vincenzo Voi, Giovanni Palazzi, et al.
Nature Medicine
|
January 22, 2019
Intrabone hematopoietic stem cell gene therapy for adult and pediatric patients affected by transfusion-dependent ß-thalassemia
Sarah Marktel, Samantha Scaramuzza, Maria Pia Cicalese, et al.
The New England Journal of Medicine
|
March 27, 2020
A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia
M Domenica Cappellini, Vip Viprakasit, Ali T Taher, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
August 14, 2024
Heterozygosity for loss-of-function variants in LZTR1 is associated with isolated multiple café-au-lait macules
Gioia Mastromoro, Claudia Santoro, Marialetizia Motta, et al.
Journal of Cellular and Molecular Medicine
|
March 31, 2022
Thalassaemia is paradoxically associated with a reduced risk of in-hospital complications and mortality in COVID-19: Data from an international registry
Ibrahim El-Battrawy, Filomena Longo, Iván J Núñez Gil, et al.
American Journal of Hematology
|
December 3, 2021
Italian patients with hemoglobinopathies exhibit a 5-fold increase in age-standardized lethality due to SARS-CoV-2 infection
Filomena Longo, Barbara Gianesin, Vincenzo Voi, et al.
Human Mutation
|
October 12, 2013
Genetic basis of congenital erythrocytosis: mutation update and online databases
Celeste Bento, Melanie J Percy, Betty Gardie, et al.
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