Partially denervated and reinnervated muscles in Duchenne muscular dystrophy

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.

Neuromuscular disorders : NMD·2013

Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature.

Clinical neuropathology·2008

Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle's disease: expression and re-expression of glycogen phosphorylase.

Neuromuscular disorders : NMD·2008

Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle.

Neuromuscular disorders : NMD·2005

Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer.

Gene therapy·2003

Forced myofiber regeneration promotes dystrophin gene transfer and improved muscle function despite advanced disease in old dystrophic mice.

Molecular therapy : the journal of the American Society of Gene Therapy·2001

Efficacy of Neuromuscular Electrical Stimulation in Mitigating Muscle Mass Loss: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Muscle & nerve·2026

Serum Neurofilament Light Chain and GFAP in Amyotrophic Lateral Sclerosis on a Commercial ECLIA Platform.

Muscle & nerve·2026

Risk Factors for Exercise-Associated Muscle Cramps: A Systematic Review With Meta-Analysis.

Muscle & nerve·2026

Whole Body Phase Angle as a Promising Marker of Disease Severity in Facioscapulohumeral Muscular Dystrophy.

Muscle & nerve·2026

Priorities for Advancing Palliative Care for Amyotrophic Lateral Sclerosis: A Consensus Report From a Palliative Care for ALS Working Group in the United States.

Muscle & nerve·2026

Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011-2023.

Muscle & nerve·2026

The Role of overdose Folic Acid in Promoting Neuroinflammation, Oxidative Stress, and Apoptosis in SOD1-G93A Mice.

Free radical research·2026

Delayed diagnosis and genetic testing in spinal muscular atrophy: a case series.

Annals of medicine·2026

Clinical Spectrum, Diagnostic Work-up, and Outcomes of Neurolymphomatosis in Lymphoid Malignancies: A 10-Patient Case Series.

Blood and lymphatic cancer : targets and therapy·2026

Clinical, Immunological, and Neuroimaging Characteristics and Outcome Profile of Neurocysticercosis in Children at a Neurology Department in Antananarivo: A Retrospective Observational Study.

Cureus·2026

De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.

Neurology. Genetics·2026

Spatial navigation and the basal forebrain in Alzheimer's disease and other neurodegenerative diseases.

Trends in neurosciences·2026

Related Experiment Videos

Partially denervated and reinnervated muscles in Duchenne muscular dystrophy

Related Concept Videos

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease.

Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature.

Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle's disease: expression and re-expression of glycogen phosphorylase.

Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle.

Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer.

Forced myofiber regeneration promotes dystrophin gene transfer and improved muscle function despite advanced disease in old dystrophic mice.

Efficacy of Neuromuscular Electrical Stimulation in Mitigating Muscle Mass Loss: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.

Serum Neurofilament Light Chain and GFAP in Amyotrophic Lateral Sclerosis on a Commercial ECLIA Platform.

Risk Factors for Exercise-Associated Muscle Cramps: A Systematic Review With Meta-Analysis.

Whole Body Phase Angle as a Promising Marker of Disease Severity in Facioscapulohumeral Muscular Dystrophy.

Priorities for Advancing Palliative Care for Amyotrophic Lateral Sclerosis: A Consensus Report From a Palliative Care for ALS Working Group in the United States.

Military Service and Survival Among Persons With ALS in the U.S. National ALS Registry, 2011-2023.

The Role of overdose Folic Acid in Promoting Neuroinflammation, Oxidative Stress, and Apoptosis in SOD1-G93A Mice.

Delayed diagnosis and genetic testing in spinal muscular atrophy: a case series.

Clinical Spectrum, Diagnostic Work-up, and Outcomes of Neurolymphomatosis in Lymphoid Malignancies: A 10-Patient Case Series.

Clinical, Immunological, and Neuroimaging Characteristics and Outcome Profile of Neurocysticercosis in Children at a Neurology Department in Antananarivo: A Retrospective Observational Study.

De Novo Facioscapulohumeral Muscular Dystrophy: A Severe Subtype Driven by D4Z4 Repeat Contractions.

Spatial navigation and the basal forebrain in Alzheimer's disease and other neurodegenerative diseases.

Related Experiment Videos

Partially denervated and reinnervated muscles in Duchenne muscular dystrophy

Related Concept Videos

Related Articles