Hoffmann's syndrome in hypothyroid myopathy. Report of a case in an african [1]

Joint Bone Spine

Volumn 68, Issue 1, 2001, Pages 84-85

  Sidibe, El Hassane ^a   Ndoye Diop, A ^a   Thiam, A ^b   Diagne, P M ^b   Sarr, A ^a   Toure, M ^c   Diop, M ^d  

^a Centre Marc Sankale   (Senegal)

^b Centre Hospitalier Universitaire Dakar   (Senegal)

^c UNIVERSITÉ CHEIKH ANTA DIOP   (Senegal)

^d Institut Du Cancer   (Senegal)

Author keywords

Africa; Hypertrophic myopathy; Myxedema; Primary hypothyroidism

Indexed keywords

CREATINE KINASE; LACTATE DEHYDROGENASE;

ADULT; AFRICA; CASE REPORT; DISSECTING PERIFOLLICULITIS; ELECTROMYOGRAM; ENZYME ASSAY; FEMALE; HUMAN; HYPOTHYROIDISM; LETTER; MUSCLE BIOPSY; MUSCLE HYPERTROPHY; MYXEDEMA;

EID: 0035125830     PISSN: 1297319X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1297-319X(00)00231-1     Document Type: Letter

References (10)

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5. Hypothyroid myopathy. Communication of 4 cases
6. Cardiomyopathy in hypothyroidism. Description of a clinical case
7. Myopathy as the persistently isolated symptomatology of primary autoimmune hypothyroidism
8. Study of some components of the cytoskeleton in muscular disorders with nonspecific cytoplasmic bodies
9. The mitochondrion as a primary side of action of glucocorticoid. The interaction of glucocorticoid receptor with mitochondrial DNA sequences showing partial similarity of the nuclear glucocorticoid repressive element
10. Physiological importance of the T3 mitochondrial pathway. Vaudry H, Tonon MC, Roubos EW, De Loof A, Eds. Trends in comparative endocrinology and neurobiology. From molecular to integrative biology