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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2016/03/02 16:02:17」(JST)

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1. 糖尿病性筋萎縮症および特発性腰仙骨骨神経叢神経障害 diabetic amyotrophy and idiopathic lumbosacral radiculoplexus neuropathy
2. 筋萎縮性側索硬化症およびその他の運動ニューロン疾患の診断 diagnosis of amyotrophic lateral sclerosis and other forms of motor neuron disease
3. 腕神経叢症候群 brachial plexus syndromes
4. 多発神経根症：脊柱管狭窄症、感染症、癌、および炎症性神経根症候群 polyradiculopathy spinal stenosis infectious carcinomatous and inflammatory nerve root syndromes
5. 糖尿病性神経障害の疫学および分類 epidemiology and classification of diabetic neuropathy

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

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

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