Muscle magnetic resonance imaging abnormalities in X-linked myopathy with excessive autophagy

Muscle and Nerve

Volumn 52, Issue 4, 2015, Pages 673-680

  Mercier, Sandra ^a,b,c   Magot, Armelle ^b,c   Caillon, Florence ^b   Isidor, Bertrand ^a,b   David, Albert ^a,b   Ferrer, Xavier ^d   Vital, Anne ^d   Coquet, Michelle ^d   Penttilä, Sini ^e   Udd, Bjarne ^e,f,g   Mussini, Jean Marie ^b   Pereon, Yann ^b,c  

^a Hopital Mere Enfant CHU de Nantes   (France)

^b HÔTEL DIEU   (France)

^c UNIVERSITÉ DE NANTES   (France)

^d BORDEAUX UNIVERSITY HOSPITAL   (France)

^e TAMPERE UNIVERSITY OF TECHNOLOGY   (Finland)

^f FOLKHÄLSAN INSTITUTE OF GENETICS   (Finland)

^g VAASA CENTRAL HOSPITAL   (Finland)

Author keywords

Excessive autophagy; Muscle MRI; Myopathy; VMA21; XMEA

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; GENE MUTATION; GENETIC SCREENING; HUMAN; HUMAN TISSUE; MALE; MUSCLE BIOPSY; MUSCLE WEAKNESS; MYOPATHY; NUCLEAR MAGNETIC RESONANCE IMAGING; PELVIC GIRDLE; PRIORITY JOURNAL; RECTUS FEMORIS MUSCLE; THIGH; X CHROMOSOME LINKED DISORDER; X LINKED MYOPATHY WITH EXCESSIVE AUTOPHAGY; AUTOPHAGY; BIOPSY; GENETICS; MUTATION; PATHOLOGY; SKELETAL MUSCLE; ULTRASTRUCTURE;

PROTON TRANSPORTING ADENOSINE TRIPHOSPHATE SYNTHASE; VMA21 PROTEIN, HUMAN;

ADOLESCENT; ADULT; AUTOPHAGY; BIOPSY; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MUSCLE, SKELETAL; MUTATION; MYOPATHIES, STRUCTURAL, CONGENITAL; VACUOLAR PROTON-TRANSLOCATING ATPASES;

EID: 84942192403     PISSN: 0148639X     EISSN: 10974598     Source Type: Journal    
DOI: 10.1002/mus.24664     Document Type: Article

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