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Bone
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January 18, 2011
The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy
Francesca Rossi, Giulia Bellini, Livio Luongo, et al.
American Journal of Hematology
|
November 30, 2018
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function
Maddalena Casale, Aldo Filosa, Alfonso Ragozzino, et al.
Haematologica
|
May 30, 2013
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range
Silverio Perrotta, Daniel P Stiehl, Francesca Punzo, et al.
Blood Cells, Molecules & Diseases
|
May 19, 2019
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses
Andrea Gerardo Russo, Sara Ponticorvo, Immacolata Tartaglione, et al.
Blood
|
January 9, 2019
Luspatercept improves hemoglobin levels and blood transfusion requirements in a study of patients with β-thalassemia
Antonio Piga, Silverio Perrotta, Maria Rita Gamberini, et al.
Italian Journal of Pediatrics
|
March 8, 2024
Healthcare migration in Italian paediatric haematology-oncology centres belonging to AIEOP
Roberto Rondelli, Tamara Belotti, Riccardo Masetti, et al.
Blood Transfusion = Trasfusione Del Sangue
|
February 3, 2017
Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association
Saverio Ladogana, Matteo Maruzzi, Piera Samperi, et al.
Genes
|
August 3, 2019
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
Teresa Giugliano, Claudia Santoro, Annalaura Torella, et al.
European Journal of Endocrinology
|
March 6, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations
Silverio Perrotta, Natascia Di Iorgi, Fulvio Della Ragione, et al.
Annali Dell'Istituto Superiore Di Sanita
|
December 19, 2019
Blood transfusions and adverse acute events: a retrospective study from 214 transfusion-dependent pediatric patients comparing transfused blood components by apheresis or by whole blood
Maria Rosaria De Pascale, Angela Belsito, Linda Sommese, et al.
Page
of 20
Search research articles
Search
Showing results (131-140 of 200) with videos related to
Sort By:
Page
of 20
Bone
|
January 18, 2011
The endovanilloid/endocannabinoid system: a new potential target for osteoporosis therapy
Francesca Rossi, Giulia Bellini, Livio Luongo, et al.
American Journal of Hematology
|
November 30, 2018
Long-term improvement in cardiac magnetic resonance in β-thalassemia major patients treated with deferasirox extends to patients with abnormal baseline cardiac function
Maddalena Casale, Aldo Filosa, Alfonso Ragozzino, et al.
Haematologica
|
May 30, 2013
Congenital erythrocytosis associated with gain-of-function HIF2A gene mutations and erythropoietin levels in the normal range
Silverio Perrotta, Daniel P Stiehl, Francesca Punzo, et al.
Blood Cells, Molecules & Diseases
|
May 19, 2019
No increased cerebrovascular involvement in adult beta-thalassemia by advanced MRI analyses
Andrea Gerardo Russo, Sara Ponticorvo, Immacolata Tartaglione, et al.
Blood
|
January 9, 2019
Luspatercept improves hemoglobin levels and blood transfusion requirements in a study of patients with β-thalassemia
Antonio Piga, Silverio Perrotta, Maria Rita Gamberini, et al.
Italian Journal of Pediatrics
|
March 8, 2024
Healthcare migration in Italian paediatric haematology-oncology centres belonging to AIEOP
Roberto Rondelli, Tamara Belotti, Riccardo Masetti, et al.
Blood Transfusion = Trasfusione Del Sangue
|
February 3, 2017
Diagnosis and management of newly diagnosed childhood autoimmune haemolytic anaemia. Recommendations from the Red Cell Study Group of the Paediatric Haemato-Oncology Italian Association
Saverio Ladogana, Matteo Maruzzi, Piera Samperi, et al.
Genes
|
August 3, 2019
Clinical and Genetic Findings in Children with Neurofibromatosis Type 1, Legius Syndrome, and Other Related Neurocutaneous Disorders
Teresa Giugliano, Claudia Santoro, Annalaura Torella, et al.
European Journal of Endocrinology
|
March 6, 2015
Early-onset central diabetes insipidus is associated with de novo arginine vasopressin-neurophysin II or Wolfram syndrome 1 gene mutations
Silverio Perrotta, Natascia Di Iorgi, Fulvio Della Ragione, et al.
Annali Dell'Istituto Superiore Di Sanita
|
December 19, 2019
Blood transfusions and adverse acute events: a retrospective study from 214 transfusion-dependent pediatric patients comparing transfused blood components by apheresis or by whole blood
Maria Rosaria De Pascale, Angela Belsito, Linda Sommese, et al.
Page
of 20