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Nucleic Acid Therapeutics
|
February 11, 2014
Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophy
Maria Sofia Falzarano, Chiara Passarelli, Alessandra Ferlini
Experimental Cell Research
|
January 7, 2014
Biomarkers in rare neuromuscular diseases
Chiara Scotton, Chiara Passarelli, Marcella Neri, et al.
Molecules (Basel, Switzerland)
|
October 13, 2015
Duchenne Muscular Dystrophy: From Diagnosis to Therapy
Maria Sofia Falzarano, Chiara Scotton, Chiara Passarelli, et al.
International Journal of Molecular Medicine
|
June 2, 2010
GSSG-mediated Complex I defect in isolated cardiac mitochondria
Chiara Passarelli, Giulia Tozzi, Anna Pastore, et al.
Human Gene Therapy
|
September 23, 2014
Biodistribution studies of polymeric nanoparticles for drug delivery in mice
Maria Sofia Falzarano, Elena Bassi, Chiara Passarelli, et al.
Clinical and Experimental Rheumatology
|
June 20, 2017
Haematological involvement associated with a mild autoinflammatory phenotype, in two patients carrying the E250K mutation of PSTPIP1
Elena Belelli, Chiara Passarelli, Manuela Pardeo, et al.
Pediatric Diabetes
|
September 14, 2011
All glutathione forms are depleted in blood of obese and type 1 diabetic children
Anna Pastore, Paolo Ciampalini, Giulia Tozzi, et al.
Journal of Molecular Neuroscience : MN
|
July 6, 2021
Clinical and Molecular Aspects of the Neurodevelopmental Disorder Associated with PAK3 Perturbation
Giulia Pascolini, Federica Gaudioso, Chiara Passarelli, et al.
Diagnostics (Basel, Switzerland)
|
December 11, 2025
Adult Onset of Type 2 Familial Hemophagocytic Lymphohistiocytosis After SARS-CoV-2 Vaccination with an Unusual Neurological Onset: The Great Mimic
Flaminia Bellisario, Assunta Bianco, Francesco D'Alo', et al.
The Journal of Rheumatology
|
January 17, 2019
Variable Clinical Phenotypes and Relation of Interferon Signature with Disease Activity in ADA2 Deficiency
Antonella Insalaco, Gian Marco Moneta, Manuela Pardeo, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 45) with videos related to
Sort By:
Page
of 5
Nucleic Acid Therapeutics
|
February 11, 2014
Nanoparticle delivery of antisense oligonucleotides and their application in the exon skipping strategy for Duchenne muscular dystrophy
Maria Sofia Falzarano, Chiara Passarelli, Alessandra Ferlini
Experimental Cell Research
|
January 7, 2014
Biomarkers in rare neuromuscular diseases
Chiara Scotton, Chiara Passarelli, Marcella Neri, et al.
Molecules (Basel, Switzerland)
|
October 13, 2015
Duchenne Muscular Dystrophy: From Diagnosis to Therapy
Maria Sofia Falzarano, Chiara Scotton, Chiara Passarelli, et al.
International Journal of Molecular Medicine
|
June 2, 2010
GSSG-mediated Complex I defect in isolated cardiac mitochondria
Chiara Passarelli, Giulia Tozzi, Anna Pastore, et al.
Human Gene Therapy
|
September 23, 2014
Biodistribution studies of polymeric nanoparticles for drug delivery in mice
Maria Sofia Falzarano, Elena Bassi, Chiara Passarelli, et al.
Clinical and Experimental Rheumatology
|
June 20, 2017
Haematological involvement associated with a mild autoinflammatory phenotype, in two patients carrying the E250K mutation of PSTPIP1
Elena Belelli, Chiara Passarelli, Manuela Pardeo, et al.
Pediatric Diabetes
|
September 14, 2011
All glutathione forms are depleted in blood of obese and type 1 diabetic children
Anna Pastore, Paolo Ciampalini, Giulia Tozzi, et al.
Journal of Molecular Neuroscience : MN
|
July 6, 2021
Clinical and Molecular Aspects of the Neurodevelopmental Disorder Associated with PAK3 Perturbation
Giulia Pascolini, Federica Gaudioso, Chiara Passarelli, et al.
Diagnostics (Basel, Switzerland)
|
December 11, 2025
Adult Onset of Type 2 Familial Hemophagocytic Lymphohistiocytosis After SARS-CoV-2 Vaccination with an Unusual Neurological Onset: The Great Mimic
Flaminia Bellisario, Assunta Bianco, Francesco D'Alo', et al.
The Journal of Rheumatology
|
January 17, 2019
Variable Clinical Phenotypes and Relation of Interferon Signature with Disease Activity in ADA2 Deficiency
Antonella Insalaco, Gian Marco Moneta, Manuela Pardeo, et al.
Page
of 5