Found: 57
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Proteinuria in neuronal intranuclear inclusion disease.
- Published in:
- Neurology & Clinical Neuroscience, 2018, v. 6, n. 2, p. 51, doi. 10.1111/ncn3.12182
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- Publication type:
- Article
Techniques for the neurological examination of taxane-induced neuropathy.
- Published in:
- Breast Cancer (13406868), 2004, v. 11, n. 1, p. 86, doi. 10.1007/BF02968009
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- Publication type:
- Article
Mechanism of taxane neurotoxicity.
- Published in:
- Breast Cancer (13406868), 2004, v. 11, n. 1, p. 82, doi. 10.1007/BF02968008
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- Publication type:
- Article
Muscular atrophy of caveolin-3--deficient mice is rescued by myostatin inhibition.
- Published in:
- Journal of Clinical Investigation, 2006, v. 116, n. 11, p. 2924, doi. 10.1172/JCI28520
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- Publication type:
- Article
Atelocollagen-mediated systemic administration of myostatin-targeting siRNA improves muscular atrophy in caveolin-3-deficient mice.
- Published in:
- Development, Growth & Differentiation, 2011, v. 53, n. 1, p. 48, doi. 10.1111/j.1440-169X.2010.01221.x
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- Publication type:
- Article
Alterations of ATG4A and LC3B in neurons derived from Alzheimer's disease patients.
- Published in:
- Genes to Cells, 2023, v. 28, n. 4, p. 319, doi. 10.1111/gtc.13010
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- Publication type:
- Article
Becker Muscular Dystrophy Accompanied by Anti-HMGCR Antibody-positive Immune-mediated Necrotizing Myopathy.
- Published in:
- Internal Medicine, 2023, v. 62, n. 9, p. 1345, doi. 10.2169/internalmedicine.0202-22
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- Publication type:
- Article
A Novel PRPS1 Mutation in a Japanese Patient with CMTX5 .
- Published in:
- Internal Medicine, 2022, v. 61, n. 11, p. 1749, doi. 10.2169/internalmedicine.8029-21
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- Publication type:
- Article
Maximal Multistage Shuttle Run Test-induced Myalgia in a Patient with Muscle Phosphorylase B Kinase Deficiency.
- Published in:
- Internal Medicine, 2022, v. 61, n. 8, p. 1241, doi. 10.2169/internalmedicine.8137-21
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- Publication type:
- Article
Development of sensory neuropathy in streptozotocin‐induced diabetic mice.
- Published in:
- Brain & Behavior, 2013, v. 3, n. 1, p. 35, doi. 10.1002/brb3.111
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- Publication type:
- Article
Calcium dysregulation contributes to neurodegeneration in FTLD patient iPSC-derived neurons.
- Published in:
- Scientific Reports, 2016, p. 34904, doi. 10.1038/srep34904
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- Publication type:
- Article
Biochemical and pathological changes result from mutated Caveolin-3 in muscle.
- Published in:
- Skeletal Muscle, 2018, v. 8, n. 1, p. N.PAG, doi. 10.1186/s13395-018-0173-y
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- Publication type:
- Article
The Inhibitory Core of the Myostatin Prodomain: Its Interaction with Both Type I and II Membrane Receptors, and Potential to Treat Muscle Atrophy.
- Published in:
- PLoS ONE, 2015, v. 10, n. 7, p. 1, doi. 10.1371/journal.pone.0133713
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- Publication type:
- Article
<i>SLC25A13</i> Gene Analysis in Citrin Deficiency: Sixteen Novel Mutations in East Asian Patients, and the Mutation Distribution in a Large Pediatric Cohort in China.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0074544
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- Publication type:
- Article
Local Applications of Myostatin-siRNA with Atelocollagen Increase Skeletal Muscle Mass and Recovery of Muscle Function
- Published in:
- PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064719
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- Publication type:
- Article
A novel method to measure sensory nerve conduction of the posterior antebrachial cutaneous nerve.
- Published in:
- Muscle & Nerve, 2022, v. 66, n. 2, p. 202, doi. 10.1002/mus.27645
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- Publication type:
- Article
Acute inflammatory demyelinating polyneuropathy following Ciguatera poisoning.
- Published in:
- Muscle & Nerve, 2022, v. 65, n. 4, p. E16, doi. 10.1002/mus.27486
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- Publication type:
- Article
Anatomical variations of the superficial branch of the radial nerve and the dorsal branch of the ulnar nerve: A detailed electrophysiological study.
- Published in:
- 2021
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- Publication type:
- journal article
Variations in the distal branches of the superficial fibular sensory nerve.
- Published in:
- 2017
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- Publication type:
- journal article
Whole plantar nerve conduction study with disposable strip electrodes.
- Published in:
- 2016
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- Publication type:
- journal article
A novel method to measure sensory nerve conduction of the supraclavicular nerve.
- Published in:
- Muscle & Nerve, 2014, v. 50, n. 6, p. 1005, doi. 10.1002/mus.24335
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- Publication type:
- Article
Magnetic resonance imaging diagnosis of panniculitis in dermatomyositis.
- Published in:
- Muscle & Nerve, 2010, v. 41, n. 1, p. 151, doi. 10.1002/mus.21537
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- Publication type:
- Article
Tongue fasciculations in chronic inflammatory demyelinating polyradiculoneuropathy.
- Published in:
- Muscle & Nerve, 2008, v. 38, n. 4, p. 1341, doi. 10.1002/mus.21108
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- Publication type:
- Article
Simple and novel method to measure distal sensory nerve conduction of the medial plantar nerve.
- Published in:
- Muscle & Nerve, 2007, v. 36, n. 3, p. 307, doi. 10.1002/mus.20814
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- Publication type:
- Article
Full-length dystrophin cDNA transfer into skeletal muscle of adult mdx mice by electroporation.
- Published in:
- Muscle & Nerve, 2003, v. 27, n. 2, p. 237, doi. 10.1002/mus.10283
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- Publication type:
- Article
Slow-Myofiber Commitment by Semaphorin 3A Secreted from Myogenic Stem Cells.
- Published in:
- Stem Cells, 2017, v. 35, n. 7, p. 1815, doi. 10.1002/stem.2639
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- Publication type:
- Article
Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists.
- Published in:
- Neurology & Clinical Neuroscience, 2019, v. 7, n. 1, p. 3, doi. 10.1111/ncn3.12223
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- Publication type:
- Article
A simplified and sensitive method to identify Alzheimer's disease biomarker candidates using patient-derived induced pluripotent stem cells (iPSCs).
- Published in:
- Journal of Biochemistry, 2017, v. 162, n. 6, p. 391, doi. 10.1093/jb/mvx058
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- Publication type:
- Article
Transgenic expression of a myostatin inhibitor derived from follistatin increases skeletal muscle mass and ameliorates dystrophic pathology in mdx mice.
- Published in:
- FASEB Journal, 2008, v. 22, n. 2, p. 477, doi. 10.1096/fj.07-8673com
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- Publication type:
- Article
A low amyloidogenic E61K transthyretin mutation may cause familial amyloid polyneuropathy.
- Published in:
- Journal of Neurochemistry, 2021, v. 156, n. 6, p. 957, doi. 10.1111/jnc.15162
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- Publication type:
- Article
Schwann cells contribute to neurodegeneration in transthyretin amyloidosis.
- Published in:
- Journal of Neurochemistry, 2015, v. 134, n. 1, p. 66, doi. 10.1111/jnc.13068
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- Publication type:
- Article
Fukuyama-type congenital muscular dystrophy (FCMD) and α-dystroglycanopathy.
- Published in:
- Congenital Anomalies, 2003, v. 43, n. 2, p. 97, doi. 10.1111/j.1741-4520.2003.tb01033.x
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- Publication type:
- Article
Involvement of Wnt4 signaling during myogenic proliferation and differentiation of skeletal muscle.
- Published in:
- Developmental Dynamics, 2007, v. 236, n. 10, p. 2800, doi. 10.1002/dvdy.21327
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- Publication type:
- Article
Endoplasmic reticulum stress response in P104L mutant caveolin-3 transgenic mice.
- Published in:
- Human Molecular Genetics, 2011, v. 20, n. 15, p. 2975, doi. 10.1093/hmg/ddr201
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- Publication type:
- Article
Spuriously Large Subcortex Infarct due to Confluent Smaller Lesions: A Diffusion-Weighted MRI/CT Study.
- Published in:
- European Neurology, 2005, v. 54, n. 3, p. 161, doi. 10.1159/000090106
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- Publication type:
- Article
Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists.
- Published in:
- Journal of Dermatology, 2019, v. 46, n. 1, p. e1, doi. 10.1111/1346-8138.14604
- By:
- Publication type:
- Article
VEGF 164 gene transfer by electroporation improves diabetic sensory neuropathy in mice.
- Published in:
- Journal of Gene Medicine, 2006, v. 8, n. 6, p. 773, doi. 10.1002/jgm.893
- By:
- Publication type:
- Article
Social problems in daily life of patients with dementia.
- Published in:
- Geriatrics & Gerontology International, 2019, v. 19, n. 2, p. 113, doi. 10.1111/ggi.13554
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- Publication type:
- Article
Temporal lobe epilepsy associated with GAD autoimmunity.
- Published in:
- 2017
- By:
- Publication type:
- Letter
Treatment consensus for management of polymyositis and dermatomyositis among rheumatologists, neurologists and dermatologists.
- Published in:
- Modern Rheumatology, 2019, v. 29, n. 1, p. 1, doi. 10.1080/14397595.2018.1521185
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- Publication type:
- Article
Current status and problems of driving in elderly with cognitive decline in Okayama.
- Published in:
- Kawasaki Medical Journal, 2023, v. 49, p. 69, doi. 10.11482/KMJ-E202349069
- By:
- Publication type:
- Article
Clinical value of abnormal median-normal sural sensory response pattern for the early diagnosis of acute oropharyngeal palsy: a comparison of recent and previous cases.
- Published in:
- Kawasaki Medical Journal, 2021, v. 47, p. 21, doi. 10.11482/KMJ-E202147021
- By:
- Publication type:
- Article
Overexpression of P104L mutant caveolin-3 in mice develops hypertrophic cardiomyopathy with enhanced contractility in association with increased endothelial nitric oxide synthase activity.
- Published in:
- Human Molecular Genetics, 2004, v. 13, n. 2, p. 151, doi. 10.1093/hmg/ddh014
- By:
- Publication type:
- Article
Fukutin is required for maintenance of muscle integrity, cortical histiogenesis and normal eye development.
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 12, p. 1449, doi. 10.1093/hmg/ddg153
- By:
- Publication type:
- Article
Transgenic mice expressing mutant caveolin-3 show severe myopathy associated with increased nNOS activity.
- Published in:
- Human Molecular Genetics, 2001, v. 10, n. 3, p. 173, doi. 10.1093/hmg/10.3.173
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- Publication type:
- Article
Bone marrow transplantation improves outcome in a mouse model of congenital muscular dystrophy
- Published in:
- FEBS Letters, 2006, v. 580, n. 18, p. 4463, doi. 10.1016/j.febslet.2006.07.015
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- Publication type:
- Article
Muscular dystrophy associated with β-dystroglycan deficiency.
- Published in:
- Annals of Neurology, 1996, v. 40, n. 6, p. 925, doi. 10.1002/ana.410400617
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- Publication type:
- Article
Clinical heterogeneity of adhalin deficiency.
- Published in:
- 1996
- By:
- Publication type:
- journal article
Inherited amyloid polyneuropathy type IV (gelsolin variant) in a Japanese family.
- Published in:
- Annals of Neurology, 1993, v. 33, n. 1, p. 57, doi. 10.1002/ana.410330110
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- Publication type:
- Article
Haplotype analysis in gelsoiin-related amyloidosis reveals independent origin of identical mutation (G654A) of gelsolin in Finland and Japan.
- Published in:
- Human Mutation, 1995, v. 6, n. 1, p. 60, doi. 10.1002/humu.1380060112
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- Publication type:
- Article