WordNet

any degenerative disorder resulting from inadequate or faulty nutrition
of or relating to or consisting of muscle; "muscular contraction"
having or suggesting great physical power or force; "the muscular and passionate Fifth Symphony"

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Protein profiling reveals energy metabolism and cytoskeletal protein alterations in LMNA mutation carriers.

Magagnotti C, Bachi A, Zerbini G, Fattore E, Fermo I, Riba M, Previtali SC, Ferrari M, Andolfo A, Benedetti S.SourceProMiFa, Protein Microsequencing Facility, Division of Cell Biology and Genetics, San Raffaele Scientific Institute, Milan, Italy.
Biochimica et biophysica acta.Biochim Biophys Acta.2012 Jun;1822(6):970-9. Epub 2012 Feb 3.
Nuclear envelope-related muscular dystrophies, in particular those referred to as laminopathies, are relatively novel and unclear diseases, also considering the increasing number of mutations identified so far in genes of the nuclear envelope. As regard LMNA gene, only tentative relations between ph
PMID 22326558

Taranum S, Vaylann E, Meinke P, Abraham S, Yang L, Neumann S, Karakesisoglou I, Wehnert M, Noegel AA.SourceInstitute for Biochemistry I, Medical Faculty, University of Cologne, Joseph-Stelzmann-Str. 52, 50931 Cologne, Germany; Center for Molecular Medicine Cologne (CMMC) and Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD), Medical Faculty, University of Cologne, Joseph-Stelzmann-Str. 52, 50931 Cologne, Germany.
European journal of cell biology.Eur J Cell Biol.2012 May 1. [Epub ahead of print]
Emery-Dreifuss muscular dystrophy (EDMD) is a late onset-disease characterized by skeletal muscle wasting and heart defects with associated risk of sudden death. The autosomal dominant form of the disease is caused by mutations in the LMNA gene encoding LaminA and C, the X-linked form results from m
PMID 22555292

Ueyama Hidetsugu,Kumamoto Toshihide,Horinouchi Hideo [他],FIJIMOTO Shin,AONO Hiroshi,TSUDA Tomiyasu
Internal medicine 41(7), 532-536, 2002-07-01
… Based on the initial distribution of muscle involvement, clinical phenotypes were divided into four subtypes: limb-girdle type, Miyoshi's type, distal anterior compartment type, or scapuloperoneal type. …
NAID 10009277900

佐藤徹,継健,永田雅良,中沢博江,石原伝幸
医療 41(4), 361-363, 1987
症例は52才の男性で, 主訴は心拡大. 現病歴は, 幼少時より歩行の異常に気付かれ, また右肘関節の伸展が不十分であり, 40才の時心拡大を指摘された. 理学的所見では, 脈拍数45/分と徐脈, 肩甲帯・上腕部・前頸骨筋に筋力低下と筋の萎縮を認め, 頸部前屈に制限があり, 右肘関節に拘縮を認めた. 胸部X-PではCTR 71%と著明な心拡大, 心電図では心室性固有調律であり, 心臓カテーテル検査で …
NAID 130004107051