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4. [Mitochondrial anomalies in oculopharyngeal muscular dystrophy]. de Seze J; Pasquier F; Ruchoux MM; Hurtevent JF; Petit H Rev Neurol (Paris); 1997 Jun; 153(5):335-8. PubMed ID: 9296168 [TBL] [Abstract][Full Text] [Related]
5. Oculopharyngeal muscular dystrophy in France. Fardeau M; Tomé FM Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S30-3. PubMed ID: 9392012 [TBL] [Abstract][Full Text] [Related]
6. Gross mosaic pattern of mitochondrial DNA deletions in skeletal muscle tissues of an individual adult human subject. Zhang C; Liu VW; Nagley P Biochem Biophys Res Commun; 1997 Apr; 233(1):56-60. PubMed ID: 9144395 [TBL] [Abstract][Full Text] [Related]
10. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia. Moslemi AR; Melberg A; Holme E; Oldfors A Ann Neurol; 1996 Nov; 40(5):707-13. PubMed ID: 8957011 [TBL] [Abstract][Full Text] [Related]
11. [Anatomo-clinical study of a Breton family with oculopharyngeal dystrophy]. Goas JY; Leroy JP; Bastard J; Missoum A; Mocquard Y; Volant A Rev Otoneuroophtalmol; 1984; 56(2):213-5. PubMed ID: 6474028 [No Abstract] [Full Text] [Related]
12. Report on the first international symposium on oculopharyngeal muscular dystrophy. Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S2-4. PubMed ID: 9392007 [No Abstract] [Full Text] [Related]
13. [Some questions and comments for the original article entitled "autosomal recessive oculopharyngeal 'muscular dystrophy'"]. Uyama E Rinsho Shinkeigaku; 1992 Jan; 32(1):94-5. PubMed ID: 1628446 [No Abstract] [Full Text] [Related]
14. Increased mitochondrial DNA deletions in the skeletal muscle of myotonic dystrophy. Sahashi K; Tanaka M; Tashiro M; Ohno K; Ibi T; Takahashi A; Ozawa T Gerontology; 1992; 38(1-2):18-29. PubMed ID: 1319380 [TBL] [Abstract][Full Text] [Related]
16. Homozygotes for oculopharyngeal muscular dystrophy have a severe form of the disease. Blumen SC; Brais B; Korczyn AD; Medinsky S; Chapman J; Asherov A; Nisipeanu P; Codère F; Bouchard JP; Fardeau M; Tomé FM; Rouleau GA Ann Neurol; 1999 Jul; 46(1):115-8. PubMed ID: 10401788 [TBL] [Abstract][Full Text] [Related]
17. Mitochondrial abnormalities in oculopharyngeal muscular dystrophy. Sadeh M; Pauzner R; Blatt I; Mouallem M; Farfel Z Muscle Nerve; 1993 Sep; 16(9):982-3. PubMed ID: 8257512 [No Abstract] [Full Text] [Related]
18. Oculopharyngeal muscular dystrophy in Uruguay. Medici M; Pizzarossa C; Skuk D; Yorio D; Emmanuelli G; Mesa R Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S50-2. PubMed ID: 9392016 [TBL] [Abstract][Full Text] [Related]
19. MtDNA deletions in aging and in nonmitochondrial pathologies. Cormio A; Lezza AM; Vecchiet J; Felzani G; Marangi L; Guglielmi FW; Francavilla A; Cantatore P; Gadaleta MN Ann N Y Acad Sci; 2000 Jun; 908():299-301. PubMed ID: 10911970 [No Abstract] [Full Text] [Related]