Isolated semitendinosus involvement in the initial stages of limb-girdle muscular dystrophy 2L

Neuromuscular Disorders

Volumn 24, Issue 12, 2014, Pages 1118-1119

  Tasca, Giorgio ^a   Evilä, Anni ^b   Pane, Marika ^c   Monforte, Mauro ^c   Graziano, Alessandra ^c   Hackman, Peter ^b   Mercuri, Eugenio ^c   Udd, Bjarne ^b,d,e  

^a BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^b UNIVERSITY OF HELSINKI   (Finland)

^c CATHOLIC UNIVERSITY   (Italy)

^d TAMPERE UNIVERSITY OF TECHNOLOGY   (Finland)

^e VAASA CENTRAL HOSPITAL   (Finland)

Author keywords

Anoctamin 5; LGMD2L; Muscle MRI; Semitendinosus

Indexed keywords

CREATINE KINASE; ANO5 PROTEIN, HUMAN; CHLORIDE CHANNEL;

ADOLESCENT; ANOCTAMIN 5 GENE; ARTICLE; CASE REPORT; CREATINE KINASE BLOOD LEVEL; FATIGUE; GASTROCNEMIUS MUSCLE; GENE; GENE MUTATION; GENE SEQUENCE; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; IMAGE ANALYSIS; LEG MUSCLE; LIMB GIRDLE MUSCULAR DYSTROPHY; LIMB GIRDLE MUSCULAR DYSTROPHY 2L; MALE; MUSCLE BIOPSY; MUSCLE CRAMP; MUSCLE DISEASE; MUSCLE NECROSIS; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PELVIC MUSCLE; PHENOTYPE; SEMITENDINOUS MUSCLE; SKELETAL MUSCLE; THIGH; DISEASE COURSE; GENETICS; LEG; PATHOLOGY; PELVIS;

ADOLESCENT; CHLORIDE CHANNELS; DISEASE PROGRESSION; HUMANS; LEG; MAGNETIC RESONANCE IMAGING; MALE; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES, LIMB-GIRDLE; PELVIS; PHENOTYPE;

EID: 84919422287     PISSN: 09608966     EISSN: 18732364     Source Type: Journal    
DOI: 10.1016/j.nmd.2014.06.442     Document Type: Article

References (3)

1. Fischer D., Kley R.A., Strach K., et al. Distinct muscle imaging patterns in myofibrillar myopathies. Neurology 2008, 71:758-765.
2. Palmio J., Evila A., Chapon F., et al. Hereditary myopathy with early respiratory failure: occurrence in various populations. J Neurol Neurosurg Psychiatry 2014, 85:345-353.
3. Sarkozy A., Deschauer M., Carlier R.Y., et al. Muscle MRI findings in limb girdle muscular dystrophy type 2L. Neuromuscul Disord 2012, 22(Suppl. 2):S122-S129.