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Showing results (571-580 of 638) with videos related to

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Neuromuscular Disorders : NMD|June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe diseaseMarco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Journal of Neurology|May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophyDaniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
Genes|October 31, 2018
Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic PatientsTeresa Giugliano, Marco Savarese, Arcomaria Garofalo, et al.
Neuromuscular Disorders : NMD|July 17, 2010
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophyElena Mazzone, Diego Martinelli, Angela Berardinelli, et al.
Current Issues in Molecular Biology|May 15, 2023
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)Paola De Filippi, Edoardo Errichiello, Antonio Toscano, et al.
Immunity|November 17, 2016
Transcriptional Landscape of Human Tissue Lymphocytes Unveils Uniqueness of Tumor-Infiltrating T Regulatory CellsMarco De Simone, Alberto Arrigoni, Grazisa Rossetti, et al.
Orphanet Journal of Rare Diseases|September 28, 2018
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional studyGuja Astrea, Alessandro Romano, Corrado Angelini, et al.
Plos One|June 25, 2021
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow upGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
Neurology|July 8, 2011
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort studyE Mazzone, G Vasco, M P Sormani, et al.
Neuromuscular Disorders : NMD|June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric settingE S Mazzone, S Messina, G Vasco, et al.
Pageof 64

Showing results (571-580 of 638) with videos related to

Sort By:
Pageof 64
Neuromuscular Disorders : NMD|June 9, 2018
Targeted gene panel screening is an effective tool to identify undiagnosed late onset Pompe diseaseMarco Savarese, Annalaura Torella, Olimpia Musumeci, et al.
Journal of Neurology|May 5, 2022
Genetic modifiers of upper limb function in Duchenne muscular dystrophyDaniele Sabbatini, Aurora Fusto, Sara Vianello, et al.
Genes|October 31, 2018
Copy Number Variants Account for a Tiny Fraction of Undiagnosed Myopathic PatientsTeresa Giugliano, Marco Savarese, Arcomaria Garofalo, et al.
Neuromuscular Disorders : NMD|July 17, 2010
North Star Ambulatory Assessment, 6-minute walk test and timed items in ambulant boys with Duchenne muscular dystrophyElena Mazzone, Diego Martinelli, Angela Berardinelli, et al.
Current Issues in Molecular Biology|May 15, 2023
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD)Paola De Filippi, Edoardo Errichiello, Antonio Toscano, et al.
Immunity|November 17, 2016
Transcriptional Landscape of Human Tissue Lymphocytes Unveils Uniqueness of Tumor-Infiltrating T Regulatory CellsMarco De Simone, Alberto Arrigoni, Grazisa Rossetti, et al.
Orphanet Journal of Rare Diseases|September 28, 2018
Broad phenotypic spectrum and genotype-phenotype correlations in GMPPB-related dystroglycanopathies: an Italian cross-sectional studyGuja Astrea, Alessandro Romano, Corrado Angelini, et al.
Plos One|June 25, 2021
North Star Ambulatory Assessment changes in ambulant Duchenne boys amenable to skip exons 44, 45, 51, and 53: A 3 year follow upGiorgia Coratti, Marika Pane, Claudia Brogna, et al.
Neurology|July 8, 2011
Functional changes in Duchenne muscular dystrophy: a 12-month longitudinal cohort studyE Mazzone, G Vasco, M P Sormani, et al.
Neuromuscular Disorders : NMD|June 26, 2009
Reliability of the North Star Ambulatory Assessment in a multicentric settingE S Mazzone, S Messina, G Vasco, et al.
Pageof 64