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Muscles, atrophy of

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  • Regulation of a notch3-hes1 pathway and protective effect by a tocopherol-omega alkanol chain derivative in muscle atrophy.
  • von Grabowiecki Y1, Licona C1, Palamiuc L1, Abreu P1, Vidimar V1, Coowar D1, Mellitzer G1, Gaiddon C2.
  • The Journal of pharmacology and experimental therapeutics.J Pharmacol Exp Ther.2015 Jan;352(1):23-32. doi: 10.1124/jpet.114.216879. Epub 2014 Oct 17.
  • Muscular atrophy, a physiopathologic process associated with severe human diseases such as amyotrophic lateral sclerosis (ALS) or cancer, has been linked to reactive oxygen species (ROS) production. The Notch pathway plays a role in muscle development and in muscle regeneration upon physical injury.
  • PMID 25326132
  • Intrafamilial Variable Hearing Loss in TRPV4 Induced Spinal Muscular Atrophy.
  • Oonk AM1, Ekker MS2, Huygen PL3, Kunst HP3, Kremer H4, Schelhaas JJ5, Pennings RJ3.
  • The Annals of otology, rhinology, and laryngology.Ann Otol Rhinol Laryngol.2014 Dec;123(12):859-65. doi: 10.1177/0003489414539130. Epub 2014 Jun 24.
  • OBJECTIVE: Mutations in the transient receptor potential vanilloid 4 gene (TRPV4) can induce a great diversity of neuropathies. Together with these neuropathies, hearing loss can occur. This study is focused on providing an audiometric phenotype description of a Dutch family with spinal muscular atr
  • PMID 24963089
  • Evidence for clinical, genetic and biochemical variability in spinal muscular atrophy with progressive myoclonic epilepsy.
  • Dyment DA1, Sell E, Vanstone MR, Smith AC, Garandeau D, Garcia V, Carpentier S, Le Trionnaire E, Sabourdy F, Beaulieu CL, Schwartzentruber JA, McMillan HJ; FORGE Canada Consortium, Majewski J, Bulman DE, Levade T, Boycott KM.
  • Clinical genetics.Clin Genet.2014 Dec;86(6):558-63. doi: 10.1111/cge.12307. Epub 2013 Nov 21.
  • Spinal muscular atrophy with progressive myoclonic epilepsy (SMA-PME) is a recently delineated, autosomal recessive condition caused by rare mutations in the N-acylsphingosine amidohydrolase 1 (acid ceramidase) ASAH1 gene. It is characterized by motor neuron disease followed by progressive myoclonic
  • PMID 24164096


  • 専門医試験をめざす症例問題トレーニング 神経・筋疾患(末梢神経麻痺を含む)
  • 今城 靖明
  • 整形外科 = Orthopedic surgery 66(9), 1008-1012, 2015-08
  • NAID 40020542989
  • 異所性右鎖骨下動脈をともなった真の神経原性胸郭出口症候群の1例
  • 関口 兼司,齋藤 貴徳,横田 一郎,古和 久朋,苅田 典生,戸田 達史
  • 臨床神経学 55(3), 155-159, 2015
  • 症例は7年の経過で緩徐に右手内筋萎縮が進行した65歳女性.C8,Th1神経根支配筋に一致した筋力低下,筋萎縮をみとめ,神経電気診断では下神経幹の軸索障害が示唆された.CTにて異所性右鎖骨下動脈と長大な右C7横突起をみとめ,MRIでは下神経幹の上方への牽引がうたがわれた.術中所見で右C7横突起に付着する線維性索状物が確認され,これを切除したところ症状の進行は停止した.一側上肢筋萎縮をきたす原因疾患の …
  • NAID 130004921322
  • 特発性前骨間神経麻痺と特発性後骨間神経麻痺の病態解明と治療方針確立の試み : 神経痛性筋萎縮症として保存的に治療すべきか否か (特集 Orthopaedic Neurology : 神経内科と整形外科の狭間で)
  • 越智 健介,加藤 博之
  • Brain and nerve : 神経研究の進歩 66(12), 1441-1452, 2014-12
  • NAID 40020289358


amyotrophy [a″mi-ot´ro-fe] a painful condition with wasting and weakness of muscle, commonly involving the deltoid muscle. a·my·ot·ro·phy (ă'mī'ot'rō-fē), Muscular wasting or atrophy. Synonym(s): amyotrophia [G. a-priv. + mys, muscle, + ...
American Association of Neuromuscular & Electrodiagnostic Medicine -A searchable database of common muscle and nerve disorders. ... What is Diabetic Amyotrophy? Diabetic amyotrophy,also known as proximal diabetic ...



拡張検索neuralgic amyotrophy」「scapuloperoneal amyotrophy



  • adj.
  • 筋萎縮性の
  • ex.
amyotrophymuscle atrophymuscular atrophy



muscular atrophymuscle atrophyamyotrophy

neuralgic amyotrophy」



brachial neuritisbrachial plexus neuritisParsonage-Turner syndrome

scapuloperoneal amyotrophy」

  [★] 肩甲腓骨型筋萎縮症