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Neurogenetics Branch,
National Institute of Neurological Disorders and Stroke,
Neurogenetics Branch, National Institute of Neurological Disorders and Stroke
Carlo Rinaldi has not added Biography.
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A candidate gene for autoimmune myasthenia gravis.
Neurology Jul, 2012 | Pubmed ID: 22744667
Insulinlike growth factor (IGF)-1 administration ameliorates disease manifestations in a mouse model of spinal and bulbar muscular atrophy.
Molecular medicine (Cambridge, Mass.) Dec, 2012 | Pubmed ID: 22952056
Cowchock syndrome is associated with a mutation in apoptosis-inducing factor.
American journal of human genetics Dec, 2012 | Pubmed ID: 23217327
Hereditary spastic paraplegia type 43 (SPG43) is caused by mutation in C19orf12.
Human mutation Oct, 2013 | Pubmed ID: 23857908
Muscle matters in Kennedy's disease.
Neuron Apr, 2014 | Pubmed ID: 24742452
Ataxia with oculomotor apraxia type 2 fibroblasts exhibit increased susceptibility to oxidative DNA damage.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia Sep, 2014 | Pubmed ID: 24814856
Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat.
Neuromuscular disorders : NMD Nov, 2014 | Pubmed ID: 25047668
Mutation in CPT1C Associated With Pure Autosomal Dominant Spastic Paraplegia.
JAMA neurology May, 2015 | Pubmed ID: 25751282
Targeted Molecular Therapies for SBMA.
Journal of molecular neuroscience : MN Mar, 2016 | Pubmed ID: 26576772
MiR-298 Counteracts Mutant Androgen Receptor Toxicity in Spinal and Bulbar Muscular Atrophy.
Molecular therapy : the journal of the American Society of Gene Therapy 05, 2016 | Pubmed ID: 26755334
From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
Molecular and cellular endocrinology Apr, 2018 | Pubmed ID: 28688959
Beyond motor neurons: expanding the clinical spectrum in Kennedy's disease.
Journal of neurology, neurosurgery, and psychiatry Aug, 2018 | Pubmed ID: 29353237
National Institutes of Health
University of Oxford
Naemeh Pourshafie1,
Philip R. Lee2,
Ke-lian Chen1,
George G. Harmison1,
Laura C. Bott1,3,
Kenneth H. Fischbeck1,
Carlo Rinaldi1,4
1Neurogenetics Branch, National Institute of Neurological Disorders and Stroke, National Institutes of Health,
2Section on Nervous System Development and Plasticity, The Eunice Kennedy Shriver National Institute of Child and Human Development, National Institutes of Health,
3Department of Molecular Biosciences, Rice Institute for Biomedical Research, Northwestern University,
4Department of Physiology, Anatomy and Genetics, University of Oxford
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