«MYOPATHY»に関連する英語の本
以下の図書目録から
myopathyの使いかたを見つけましょう。
myopathyに関する本と英語文献で使われた文脈を提供するための簡単な抜粋文。
1
Congenital Nemaline
Myopathy: A Longitudinal Study
Sammandrag. - Yhteenveto.
Carina Wallgren-Pettersson, 1990
2
Disorders of Voluntary Muscle
Excessive isometric motor activity may be the cause of PCP myopathy as PCP
does not have a direct toxic effect on muscle (Mastaglia, 1992). Chronic toluene
abuse will often produce symmetric weakness with many associated peripheral ...
George Karpati, David Hilton-Jones, Robert C. Griggs, 2001
3
Mayo Clinic Internal Medicine Review
The diagnosis of myopathy is based on the history and physical examination,
increased levels of creatine kinase, and EMG and muscle biopsy results. For
many adults with acquired myopathy, no underlying cause is found. Inflammatory
...
Thomas M. Habermann, 2006
4
Physical Medicine and Rehabilitation: Principles and Practice
Careful observation of gait is very helpful in evaluation of the patient with
myopathy, and a classic pattern of gait progression may be noted in progressive
dystrophic myopathies. One of the earliest features in patients with myopathy is
hyper- ...
Joel A. DeLisa, Bruce M. Gans, Nicholas E. Walsh, 2005
In 50% there was evidence of undiagnosed myopathy (usually muscular
dystrophy).8 The treatment of the hyperkalemic arrest includes administration of
calcium chloride, glucose, insulin, bicarbonate, and hyperventilation, but not
dantrolene.
6
The 5-minute Neurology Consult
There are also uncommon forms of congenital myopathies, including multicore
myopathy, fingerprint body myopathy, congenital fiber type disproportion, and
protein surplus myopathies due to accumulation of abnormal proteins, such as ...
D. Joanne Lynn, Herbert B. Newton, Alexander Rae-Grant, 2004
7
The Molecular and Genetic Basis of Neurologic and ...
Families having a similar clinical presentation have been reported from Middle
Eastern countries, North America, and India with the diagnosis of hereditary
inclusion body myopathy or quadriceps-sparing myopathy. These patients differ
from ...
Nine of the 25 patients developed a clinically apparent myopathy (114). Many
other reports describe otherwise healthy asthmatic patients who remained
quadriplegic days to weeks after simultaneous treatment with corticosteroids and
NMB ...
William C. Wilson, Christopher M. Grande, David B. Hoyt, 2007
9
Drug-induced Diseases: Prevention, Detection, and Management
Symptomatic myopathy associated with interferon therapy for chronic hepatitis C.
Lancet. 1995;345:582. 28. Mastaglia FL. Adverse effects of drug on muscle.
Drugs. 1982;24:304-321. 29. KuntzerT, Bogousslavsky J, Deruaz JP, et al.
James E. Tisdale, Douglas A. Miller, 2010
10
Current Therapy in Equine Medicine
Polysaccharide storage myopathy (PSSM) was first identified in Quarter Horse–
related breeds in 1992 and is characterized by twofold higher glycogen
concentrations and abnormal granular amylase-resistant inclusions in skeletal
muscle.
Norman Edward Robinson, Kim A. Sprayberry, 2009
用語«MYOPATHY»を含むニュース項目
国内外の報道機関が語った内容や、次のニュース項目の文脈から
myopathyという用語がどのように使われているかを調べてみましょう。
Cytoskeleton Protection by Exercise Training
In skeletal muscle, impairment of the DGC results in muscle myopathy (muscle weakness) and fibrosis (accumulation of fibrous protein, ... «The Eagle, 7月 15»
Ultragenyx Pharmaceutical Inc (NASDAQ:RARE)'s CFO & Senior …
Triheptanoin is a medium odd-chain triglyceride of seven-carbon fatty acids. SA-ER is for the treatment of hereditary inclusion body myopathy ... «OctaFinance.com, 7月 15»
A recurrent copy number variation of the NEB triplicate region: only …
Nemaline (rod) myopathy (NM; MIM IDs: NEM1 #609284, NEM2 #256030, NEM3 #161800, NEM4 #609285, NEM5 #605355, NEM6 #609273, ... «Nature.com, 7月 15»
Pathogenic CWF19L1 variants as a novel cause of autosomal …
MYO18B is unlikely to cause ARCA as variants in this gene are associated with lung cancer or linked to Klippel–Feil anomaly and myopathy, ... «Nature.com, 7月 15»
Merck Marks 30-Year Milestone in Commitment to Innovation and …
Myopathy and rhabdomyolysis have been reported. Use with caution in patients at increased risk of myopathy or rhabdomyolysis, such as ... «PharmiWeb.com, 7月 15»
Golf - After nearly losing wife, losing the The Open no big deal for …
She was so ill three months ago with myopathy, a disease where the muscles cease to function, that he feared he might lose her and thoughts ... «Yahoo Eurosport UK, 7月 15»
Altamira Bio buys NIH license & CRADAs to develop ManNac for …
... pathologies associated with abnormal sialylation of tissues, characteristic of Hereditary Inclusion Body Myopathy (HIBM), also known as GNE ... «pharmabiz.com, 7月 15»
Ultragenyx Pharmaceutical Given Average Rating of "Buy" by …
SA-ER is for the treatment of hereditary inclusion body myopathy (HIBM). Receive News & Ratings for Ultragenyx Pharmaceutical Daily - Enter ... «WKRB News, 7月 15»
NAM Patients Benefit from Aggressive Treatment
The vast majority of patients with necrotizing autoimmune myopathy, a subcategory of acquired idiopathic myopathies, needed two-plus ... «MedPage Today, 7月 15»
That's the best I've played, says Aussie Leishman
She was so ill three months ago with myopathy, a disease where the muscles cease to function, that he feared he might lose her and thoughts ... «Yahoo Canada Sports, 7月 15»
