Mitochondrial cytopathy (MERRF) without ragged-red fibers;Un cas de cytopathie mitochondriale (MERRF) sans « fibres rouges déchiquetées » au début de l'évolution

Revue Neurologique

Volumn 157, Issue 4, 2001, Pages 427-429

  Gignoux, L ^a   Maisonobe, T ^b   Laforet, P ^a   Lombes A ^a   Lyon Caen, O ^c   Fontaine, B ^d  

^a Fédération de Neurologie des Prs Agid ^*  (France)

^b Laboratoire de Neuropathologie du Pr Hauw

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d HÔPITAL NEUROLOGIQUE   (France)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; CLINICAL ARTICLE; CLINICAL FEATURE; CONFERENCE PAPER; DIAGNOSTIC ERROR; FAMILY HISTORY; FEMALE; HISTOPATHOLOGY; HUMAN; MALE; MERRF SYNDROME; MOLECULAR BIOLOGY; MUSCLE BIOPSY; ONSET AGE; RESPIRATORY CHAIN;

ADULT; BIOPSY; DIAGNOSIS, DIFFERENTIAL; ELECTRON TRANSPORT COMPLEX IV; FOLLOW-UP STUDIES; HUMANS; MALE; MERRF SYNDROME; MUSCLE FIBERS, FAST-TWITCH; MUSCLE, SKELETAL; SUCCINATE DEHYDROGENASE;

EID: 0034973268     PISSN: 00353787     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Conference Paper

References (8)

1. Myoclonus epilepsy and ragged-red fibers (MERRF)
2. Mitochondrial myopathies
3. Phenotypic heterogeneity in families with the myoclonic epilepsy and ragged-red fiber disease point mutation in mitochondrial DNA
4. Single muscle fiber analysis of myoclonus epilepsy with ragged-red fibers
5. Molecular analysis of the muscle pathology associated with mitochondrial DNA deletions
6. Case record of the Massachusetts General Hospital. Case 39-1998
7. Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations