Works matching DE "NEUROMUSCULAR diseases"
Results: 5000
Central and Peripheral Fatigue in Physical Effort: A Mini-Review.
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- Journal of Exercise Physiology Online, 2019, v. 22, n. 5, p. 220
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- Publication type:
- Article
The Growing Engagement of Emergent Concerned Groups in Political and Economic Life: Lessons from the French Association of Neuromuscular Disease Patients.
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- Science, Technology & Human Values, 2008, v. 33, n. 2, p. 230, doi. 10.1177/0162243907311264
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- Article
Trying Out the Wheelchair: The Mutual Shaping of People and Devices through Adjustment.
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- Science, Technology & Human Values, 2006, v. 31, n. 1, p. 52, doi. 10.1177/0162243905280023
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- Publication type:
- Article
Acute neuromuscular failure acquired in the community: A state-of-the-art review.
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- Revista Mexicana de Neurociencia, 2022, v. 23, n. 2, p. 63, doi. 10.24875/RMN.21000007
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- Article
Síndromes neurológicos paraneoplásicos (Parte II): Sistema Nervioso Periférico y Autonómico.
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- Revista Mexicana de Neurociencia, 2010, v. 11, n. 3, p. 226
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- Publication type:
- Article
The aetiology of chronic vulval pain and entry dyspareunia: a retrospective review of 525 cases.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2017, v. 57, n. 4, p. 446, doi. 10.1111/ajo.12613
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- Article
Successful management of pregnancy-aggravated myasthenic crisis after complete remission of the disease.
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- Australian & New Zealand Journal of Obstetrics & Gynaecology, 2005, v. 45, n. 4, p. 331, doi. 10.1111/j.1479-828X.2005.00423.x
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- Article
FiMec tremor stabilization spoon: design and active stabilization control of two DoF robotic eating devices for hand tremor patients.
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- Medical & Biological Engineering & Computing, 2023, v. 61, n. 10, p. 2757, doi. 10.1007/s11517-023-02886-z
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- Article
Flexible Pressure Sensors for Objective Assessment of Motor Disorders.
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- Advanced Functional Materials, 2020, v. 30, n. 20, p. 1, doi. 10.1002/adfm.201905241
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- Article
Adipogenic potential can be activated during muscle regeneration.
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- Molecular & Cellular Biochemistry, 2007, v. 304, n. 1/2, p. 25, doi. 10.1007/s11010-007-9482-x
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- Publication type:
- Article
Ablation of de novo DNA methyltransferase Dnmt3a in the nervous system leads to neuromuscular defects and shortened lifespan.
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- Developmental Dynamics, 2007, v. 236, n. 6, p. 1663, doi. 10.1002/dvdy.21176
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- Publication type:
- Article
Neuromuscular stimulation causes muscle phenotype‐dependent changes in the expression of the IGFs and their binding proteins in developing slow and fast muscle of chick embryos.
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- Developmental Dynamics, 2006, v. 235, n. 7, p. 1777
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- Publication type:
- Article
Comprehensive quantitative magnetic resonance imaging assessment of skeletal muscle pathophysiology in golden retriever muscular dystrophy: Insights from multicomponent water T2 and extracellular volume fraction.
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- NMR in Biomedicine, 2025, v. 38, n. 1, p. 1, doi. 10.1002/nbm.5278
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- Publication type:
- Article
Probing diffusion of water and metabolites to assess white matter microstructure in Duchenne muscular dystrophy.
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- NMR in Biomedicine, 2024, v. 37, n. 11, p. 1, doi. 10.1002/nbm.5212
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- Publication type:
- Article
Activity During the COVID-19 Pandemic in Children with Cardiac Rhythm Management Devices.
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- Pediatric Cardiology, 2022, v. 43, n. 4, p. 784, doi. 10.1007/s00246-021-02787-8
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- Publication type:
- Article
Diagnostic and Prognostic Value of Cardiovascular Magnetic Resonance in Neuromuscular Cardiomyopathies.
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- Pediatric Cardiology, 2022, v. 43, n. 1, p. 27, doi. 10.1007/s00246-021-02686-y
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- Publication type:
- Article
Natural History of Conduction Abnormalities in a Patient with Kearns-Sayre Syndrome.
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- 2013
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- Publication type:
- Report
A genetic and phenotypic analysis in Spanish spinal muscular atrophy patients with c.399_402del AGAG, the most frequently found subtle mutation in the SMN1 gene (Communicated by Graham R. Taylor).
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- Human Mutation, 2003, v. 22, n. 2, p. 136, doi. 10.1002/humu.10245
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- Article
Determination of SMN1 and SMN2 copy number using TaqMan™ technologyCommunicated by Graham Taylor.
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- Human Mutation, 2003, v. 22, n. 1, p. 74, doi. 10.1002/humu.10221
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- Publication type:
- Article
Determination of SMN1 and SMN2 copy number using TaqMan technology (Communicated by Graham Taylor).
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- Human Mutation, 2003, v. 22, n. 1, p. 74, doi. 10.1002/humu.10221
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- Publication type:
- Article
Functional consequences of an LMNA mutation associated with a new cardiac and non-cardiac phenotype (Communicated by Jacques S. Beckmann).
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- Human Mutation, 2003, v. 21, n. 5, p. 473, doi. 10.1002/humu.10170
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- Publication type:
- Article
Disuse Osteoporosis: Clinical and Mechanistic Insights.
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- Calcified Tissue International, 2022, v. 110, n. 5, p. 592, doi. 10.1007/s00223-021-00836-1
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- Publication type:
- Article
A Systematic Review of the Role of Vitamin D on Neuromuscular Remodelling Following Exercise and Injury.
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- 2016
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- Publication type:
- journal article
Early kidney transplantation improves neurocognitive outcome in patients with severe congenital chronic kidney disease.
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- Transplant International, 2015, v. 28, n. 4, p. 429, doi. 10.1111/tri.12510
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- Article
Expression of the muscular dystrophy-associated caveolin-3<sup>P104L</sup> mutant in adult mouse skeletal muscle specifically alters the Ca<sup>2+</sup> channel function of the dihydropyridine receptor.
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- Pflügers Archiv: European Journal of Physiology, 2008, v. 457, n. 2, p. 361, doi. 10.1007/s00424-008-0528-z
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- Article
Belgian Society of Fundamental and Clinical Physiology and Pharmacology. Abstracts of the Autumn Meeting, 16 November 2002, Gent, Belgium.
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- Pflügers Archiv: European Journal of Physiology, 2003, v. 445, n. 5, p. R1, doi. 10.1007/s00424-002-1005-8
- Publication type:
- Article
Apoptosis in co-cultures of human muscle and rat spinal cord during the formation of the neuromuscular junction.
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- Pflügers Archiv: European Journal of Physiology, 2001, v. 442, n. 7, p. r177
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- Publication type:
- Article
Hereditary motor and sensory neuropathy associated with auditory neuropathy in a Gypsy family.
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- Pflügers Archiv: European Journal of Physiology, 2000, v. 439, n. 7, p. r208, doi. 10.1007/BF03376574
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- Publication type:
- Article
The effects of equinatoxin II on respiration – possible mechanism of the toxin lethality.
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- Pflügers Archiv: European Journal of Physiology, 2000, v. 439, n. 7, p. r129, doi. 10.1007/BF03376545
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- Publication type:
- Article
A selective antisense oligonucleotide against the G93A mutant of the Cu/Zn-SODI mRNA is effective in cell culture.
- Published in:
- 2000
- Publication type:
- Abstract
Neuromuscular hamartoma arising in the brachial plexus.
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- Neuroradiology, 2004, v. 46, n. 3, p. 216, doi. 10.1007/s00234-003-1130-x
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- Publication type:
- Article
Systemic inhibition of bone morphogenetic protein 1.3 as a possible treatment for laminin-related congenital muscular dystrophy.
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- International Orthopaedics, 2025, v. 49, n. 1, p. 45, doi. 10.1007/s00264-024-06389-w
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- Article
Outcomes of dual mobility articulation total hip arthroplasty in ipsilateral residual poliomyelitis.
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- International Orthopaedics, 2022, v. 46, n. 3, p. 489, doi. 10.1007/s00264-021-05222-y
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- Publication type:
- Article
Patient-reported outcomes after primary rotating hinge total knee arthroplasty: a multi-centre clinical cohort study.
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- International Orthopaedics, 2021, v. 45, n. 11, p. 2893, doi. 10.1007/s00264-021-05162-7
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- Publication type:
- Article
The contribution of the scapula to active shoulder motion and self-assessed function in three hundred and fifty two patients prior to elective shoulder surgery.
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- 2018
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- Publication type:
- journal article
Prediction of respiratory function in patients with severe scoliosis on the basis of the novel individualized spino-pelvic index.
- Published in:
- 2018
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- Publication type:
- journal article
The increasing importance of environmental conditions in amyotrophic lateral sclerosis.
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- International Journal of Biometeorology, 2018, v. 62, n. 8, p. 1361, doi. 10.1007/s00484-018-1550-2
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- Publication type:
- Article
Intraoperative chirurgisch-anästhesiologische Probleme und deren Konsequenzen für die Chirurgie.
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- Der Chirurg, 2012, v. 83, n. 7, p. 617, doi. 10.1007/s00104-011-2213-6
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- Article
The Virgin and Child with the Infant St. John the Baptist by Sandro Botticelli (1445–1510): does the child have Pompe disease?
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- Child's Nervous System, 2022, v. 38, n. 7, p. 1267, doi. 10.1007/s00381-022-05537-0
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- Article
Kyphoscoliosis complicating pregnancy: maternal and neonatal outcome.
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- Archives of Gynecology & Obstetrics, 2011, v. 284, n. 2, p. 295, doi. 10.1007/s00404-010-1638-3
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- Publication type:
- Article
Inter-alpha-trypsin inhibitor heavy chain H3 is a potential biomarker for disease activity in myasthenia gravis.
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- Acta Neuropathologica, 2024, v. 147, n. 1, p. 1, doi. 10.1007/s00401-024-02754-6
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- Publication type:
- Article
X-linked myotubular myopathy is associated with epigenetic alterations and is ameliorated by HDAC inhibition.
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- Acta Neuropathologica, 2022, v. 144, n. 3, p. 537, doi. 10.1007/s00401-022-02468-7
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- Publication type:
- Article
AR cooperates with SMAD4 to maintain skeletal muscle homeostasis.
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- Acta Neuropathologica, 2022, v. 143, n. 6, p. 713, doi. 10.1007/s00401-022-02428-1
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- Publication type:
- Article
Intracellular calcium leak as a therapeutic target for RYR1-related myopathies.
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- Acta Neuropathologica, 2020, v. 139, n. 6, p. 1089, doi. 10.1007/s00401-020-02150-w
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- Article
ALS/FTLD: experimental models and reality.
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- Acta Neuropathologica, 2017, v. 133, n. 2, p. 177, doi. 10.1007/s00401-016-1666-6
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- Publication type:
- Article
Glycolytic-to-oxidative fiber-type switch and mTOR signaling activation are early-onset features of SBMA muscle modified by high-fat diet.
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- Acta Neuropathologica, 2016, v. 132, n. 1, p. 127, doi. 10.1007/s00401-016-1550-4
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- Publication type:
- Article
A truncating SOD1 mutation, p.Gly141X, is associated with clinical and pathologic heterogeneity, including frontotemporal lobar degeneration.
- Published in:
- 2015
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- Publication type:
- Report
Pathogenic Ubqln2 gains toxic properties to induce neuron death.
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- Acta Neuropathologica, 2015, v. 129, n. 3, p. 417, doi. 10.1007/s00401-014-1367-y
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- Publication type:
- Article
Mitochondrial fission augments capsaicin-induced axonal degeneration.
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- Acta Neuropathologica, 2015, v. 129, n. 1, p. 81, doi. 10.1007/s00401-014-1354-3
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- Publication type:
- Article
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration.
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- Acta Neuropathologica, 2014, v. 128, n. 3, p. 397, doi. 10.1007/s00401-014-1298-7
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- Publication type:
- Article