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Muscle Weakness

1659  relevant articles (88 outcomes, 85 trials/studies) found for this Disease

Description: A vague complaint of debility, fatigue, or exhaustion attributable to weakness of various muscles. The weakness can be characterized as subacute or chronic, often progressive, and is a manifestation of many muscle and neuromuscular diseases. (From Wyngaarden et al., Cecil Textbook of Medicine, 19th ed, p2251)

Also Known As:
Muscular Weakness; Muscle Weaknesses; Muscular Weaknesses; Weakness, Muscle; Weakness, Muscular; Weaknesses, Muscle; Weaknesses, Muscular

Relationship Network

Disease Context: Research Results

Related Diseases

1. Pain (Aches)
2. Ophthalmoplegia (External Ophthalmoplegia)
3. Atrophy
4. Fatigue
5. Dermatomyositis (Dermatopolymyositis)

Experts

1. Herzog, Walter: 3 articles (11/2005 - 03/2005)
2. Longino, David: 2 articles (11/2005 - 03/2005)
3. Frank, Cy: 2 articles (11/2005 - 11/2005)
4. Drummond, A D: 1 article (05/2008)
5. Williamson, R M: 1 article (05/2008)
6. Rothwell, M P: 1 article (05/2008)
7. Silverdale, M A: 1 article (05/2008)
8. Maddali, Madan Mohan: 1 article (10/2007)
9. Justiniano, Maria: 1 article (10/2007)
10. Mathew, Jotish: 1 article (10/2007)

Drugs and Biologics

Drugs and Important Biological Agents (IBA) related to Muscle Weakness:
1. Prednisolone (Predate)FDA LinkGeneric
2. AntibodiesIBA
3. EnzymesIBA
4. Intravenous Immunoglobulins (IVIG)FDA Link
5. Immunoglobulins (Immunoglobulin)IBA
05/01/1999 - "After an administration of 25 g/day of human gamma-immunoglobulin for 5 days, conduction block as well as F-wave abnormalities in the left median and left ulnar nerve were improved, yet no improvement of muscle weakness was seen. "
07/01/2002 - "A treatment by corticoid and secondary intravenous immune globulins because of corticoid-resistance of the dermatopolymyositis and oesophagus injury led to a significant improvement of the cutaneous signs and of the muscular weakness. "
01/01/2007 - "The intravenously administered immunoglobulin (IVIG) treatment that she received several times over a 3-year period relieved her clinical symptoms of muscle weakness and sensory disturbances, but these symptoms had worsened thereafter despite further IVIG treatment. "
10/24/2000 - "BACKGROUND: Immunoglobulin (Ig) administration induces remyelination in the Theiler's virus model of MS. METHODS: A randomized, double-blinded, placebo-controlled trial of IV immunoglobulin (IVIg) was performed in patients with MS who had persistent muscle weakness that had been stable for between 4 and 18 months to determine whether this would improve muscle strength (primary outcome: isometric muscle strength). "
02/01/2008 - "Autosomal recessive spinal muscular atrophy with respiratory distress type 1 (SMARD1), recently referred to as distal spinal muscular atrophy 1 (DSMA1; MIM#604320) and also known as distal hereditary motor neuropathy type 6 (dHMN6 or HMN6), results from mutations in the IGHMBP2 gene on chromosome 11q13.3 encoding the immunoglobulin micro-binding protein 2. In contrast to the infantile spinal muscular atrophy type 1 (SMA1; Werdnig-Hoffmann disease) with weakness predominantly of proximal muscles and bell-shaped thorax deformities due to intercostal muscle atrophy, infants with distal spinal muscular atrophy 1 usually present with distal muscle weakness, foot deformities, and sudden respiratory failure due to diaphragmatic paralysis that often requires urgent intubation. "
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6. MethylprednisoloneFDA LinkGeneric
7. Cyclophosphamide (Cytoxan)FDA LinkGeneric
8. PotassiumIBA
9. Acetylcholine (Acetylcholine Chloride)FDA Link
10. OxygenIBA

Therapies and Procedures

1. Plasmapheresis
2. Drug Therapy (Chemotherapy)
3. Parathyroidectomy
4. Aftercare (After-Treatment)
5. Thymectomy

Best Treatments:
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