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Blood
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September 6, 2005
Human mesenchymal stem cells modulate B-cell functions
Anna Corcione, Federica Benvenuto, Elisa Ferretti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2022
Beyond canvas: behavioral onset of rfc1-expansion disease in an Italian family-causal or casual?
Fabiana Colucci, Daniela Di Bella, Chiara Pisciotta, et al.
Giornale Italiano Di Cardiologia (2006)
|
March 14, 2018
[Latest news and perspectives in cardiogenetics]
Michele Malagù, Fatima Zaraket, Francesca Gualandi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 19, 2016
PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian Family
Marialuisa Quadri, Simone Olgiati, Mariachiara Sensi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 13, 2009
Blood stream infections in allogeneic hematopoietic stem cell transplant recipients: reemergence of Gram-negative rods and increasing antibiotic resistance
Malgorzata Mikulska, Valerio Del Bono, Anna Maria Raiola, et al.
BMC Medical Genetics
|
June 7, 2013
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report
Elena Martoni, Stefania Petrini, Cecilia Trabanelli, et al.
Cardiology
|
May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome
Francesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Neuromuscular Disorders : NMD
|
September 11, 2007
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
Marcella Neri, Silvia Torelli, Sue Brown, et al.
Neuromuscular Disorders : NMD
|
August 17, 2010
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation
Giorgio Tasca, Massimiliano Mirabella, Aldobrando Broccolini, et al.
Hemoglobin
|
April 28, 2016
A Family with γ-Thalassemia and High Hb A2 Levels
Giulia Parmeggiani, Francesca Gualandi, Rita Selvatici, et al.
Page
of 17
Search research articles
Search
Showing results (51-60 of 169) with videos related to
Sort By:
Page
of 17
Blood
|
September 6, 2005
Human mesenchymal stem cells modulate B-cell functions
Anna Corcione, Federica Benvenuto, Elisa Ferretti, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
May 18, 2022
Beyond canvas: behavioral onset of rfc1-expansion disease in an Italian family-causal or casual?
Fabiana Colucci, Daniela Di Bella, Chiara Pisciotta, et al.
Giornale Italiano Di Cardiologia (2006)
|
March 14, 2018
[Latest news and perspectives in cardiogenetics]
Michele Malagù, Fatima Zaraket, Francesca Gualandi, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
March 19, 2016
PRKRA Mutation Causing Early-Onset Generalized Dystonia-Parkinsonism (DYT16) in an Italian Family
Marialuisa Quadri, Simone Olgiati, Mariachiara Sensi, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation
|
January 13, 2009
Blood stream infections in allogeneic hematopoietic stem cell transplant recipients: reemergence of Gram-negative rods and increasing antibiotic resistance
Malgorzata Mikulska, Valerio Del Bono, Anna Maria Raiola, et al.
BMC Medical Genetics
|
June 7, 2013
Characterization of a rare case of Ullrich congenital muscular dystrophy due to truncating mutations within the COL6A1 gene C-terminal domain: a case report
Elena Martoni, Stefania Petrini, Cecilia Trabanelli, et al.
Cardiology
|
May 12, 2017
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome
Francesca Gualandi, Fatima Zaraket, Michele Malagù, et al.
Neuromuscular Disorders : NMD
|
September 11, 2007
Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human
Marcella Neri, Silvia Torelli, Sue Brown, et al.
Neuromuscular Disorders : NMD
|
August 17, 2010
An Italian case of hereditary myopathy with early respiratory failure (HMERF) not associated with the titin kinase domain R279W mutation
Giorgio Tasca, Massimiliano Mirabella, Aldobrando Broccolini, et al.
Hemoglobin
|
April 28, 2016
A Family with γ-Thalassemia and High Hb A2 Levels
Giulia Parmeggiani, Francesca Gualandi, Rita Selvatici, et al.
Page
of 17