WordNet

make ones way by force; "He muscled his way into the office"
animal tissue consisting predominantly of contractile cells (同)muscular_tissue
one of the contractile organs of the body (同)musculus
authority or power or force (especially when used in a coercive way); "the senators used their muscle to get the party leader to resign"

PrepTutorEJDIC

〈U〉(動物体の組織としての)『筋肉』,筋(きん);〈C〉(体の各部を動かす)筋肉 / 〈U〉力,(特に)筋力,腕力 / 《俗に》(…に)強引に割り込む《+『in on』(『into, through』)+『名』》
筋肉の,筋力のある / 力ずくの

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The first case of Silver-Russell syndrome accompanied by linea alba hernia in China.

Wong KF1, Wong WW, Li BX, Song YZ.
Singapore medical journal.Singapore Med J.2010 Jan;51(1):e9-e11.
A 10-month-old Chinese boy presented with delayed motor development for seven months. Blood and biochemistry investigations revealed no abnormalities. The physical examination showed poor postnatal growth (below -2 standard deviation from the mean at diagnosis), preservation of the occipitofrontal h
PMID 20200765

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation.

Clement E1, Mercuri E, Godfrey C, Smith J, Robb S, Kinali M, Straub V, Bushby K, Manzur A, Talim B, Cowan F, Quinlivan R, Klein A, Longman C, McWilliam R, Topaloglu H, Mein R, Abbs S, North K, Barkovich AJ, Rutherford M, Muntoni F.
Annals of neurology.Ann Neurol.2008 Nov;64(5):573-82. doi: 10.1002/ana.21482.
OBJECTIVE: To assess the range and severity of brain involvement, as assessed by magnetic resonance imaging, in 27 patients with mutations in POMT1 (4), POMT2 (9), POMGnT1 (7), Fukutin (4), or LARGE (3), responsible for muscular dystrophies with abnormal glycosylation of dystroglycan (dystroglycanop
PMID 19067344

Shwachman-Diamond syndrome is associated with structural brain alterations on MRI.

Toiviainen-Salo S1, Mäkitie O, Mannerkoski M, Hämäläinen J, Valanne L, Autti T.
American journal of medical genetics. Part A.Am J Med Genet A.2008 Jun 15;146A(12):1558-64. doi: 10.1002/ajmg.a.32354.
Shwachman-Diamond syndrome (SDS) is an autosomal recessive condition that results from mutations in the SBDS gene, at chromosome 7q11. Main features include exocrine pancreatic failure, neutropenia and skeletal dysplasia. This study investigated brain structures by magnetic resonance imaging (MRI) i
PMID 18478597

Immediate effectiveness of balloon dilatation therapy for patients with dysphagia due to cricopharyngeal dysfunction

Onogi Keiko,Saitoh Eiichi,Kondo Izumi,Ozeki Megumi,Kagaya Hitoshi
Japanese Journal of Comprehensive Rehabilitation Science 5(0), 87-92, 2014
… The amount of residue and the occipitofrontal diameter of the UES were measured before and after dilatation. … However, no significant difference was seen in the occipitofrontal diameter of the upper esophagus after dilatation. …
NAID 130005098627