Calpain 3 Deficiency in Quail Eater's Disease [3]

Annals of Neurology

Volumn 55, Issue 1, 2004, Pages 146-147

  Musumeci, Olimpia ^a   Aguennouz, Mohammed ^a   Cagliani, Rachele ^b   Comi, Giacomo Pietro ^b   Ciranni, Anna ^a   Rodolico, Carmelo ^a   Messina, Corrado ^a   Vita, Giuseppe ^a   Toscano, Antonio ^a  

^a UNIVERSITY OF MESSINA   (Italy)

^b UNIVERSITY OF MILAN   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CALPAIN; CALPAIN 3;

ADULT; ANIMAL; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; FEMALE; FOOD POISONING; HUMAN; IMMUNOHISTOCHEMISTRY; LETTER; MALE; MEAT; METABOLISM; MUSCLE BIOPSY; MUSCLE CRAMP; MUSCLE INJURY; MUSCLE STIFFNESS; MYALGIA; MYOGLOBINURIA; NONHUMAN; NUTRITIONAL DEFICIENCY; PATHOGENESIS; PATHOLOGY; PATHOPHYSIOLOGY; PRIORITY JOURNAL; QUAIL; QUAIL EATER DISEASE; RHABDOMYOLYSIS; SKELETAL MUSCLE; WESTERN BLOTTING;

ADULT; ANIMALS; BLOTTING, WESTERN; CALPAIN; FEMALE; HUMANS; IMMUNOHISTOCHEMISTRY; ISOENZYMES; MALE; MEAT; MUSCLE PROTEINS; MUSCLE, SKELETAL; QUAIL; RHABDOMYOLYSIS;

EID: 0346688754     PISSN: 03645134     EISSN: None     Source Type: Journal    
DOI: 10.1002/ana.10821     Document Type: Letter

References (4)

1. Papadimitriou A, Hadjigeorgiou GM, Tsairis P, et al. Myoglobinuria due to quail poisoning. Eur Neurol 1996;36:142-145.
2. Aparicio R, Onate JM, Arizcun A, et al. [Epidemic rhabdomyolysis due to the eating of quail. A clinical, epidemiological and experimental study]. Med Clin (Barc) 1999;112:143-146.
3. Anderson LV, Harrison RM, Pogue R, et al. Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies). Neuromuscul Disord 2000;10:553-559.
4. Hackman P, Vihola A, Haravuori H, et al. Tibial muscular dystrophy is a titinopathy caused by mutations in TTN, the gene encoding the giant skeletal-muscle protein titin. Am J Hum Genet 2002; 71:492-500.