138 related articles for article (PubMed ID: 6308176)
1. Nuclear inclusions in oculopharyngeal dystrophy. An ultrastructural study of six cases.
Coquet M; Vallat JM; Vital C; Fournier M; Barat M; Orgogozo JM; Julien J; Loiseau P
J Neurol Sci; 1983 Jul; 60(1):151-6. PubMed ID: 6308176
[TBL] [Abstract][Full Text] [Related]
2. Nuclear inclusions in innervated cultured muscle fibers from patients with oculopharyngeal muscular dystrophy.
Tomé FM; Askanas V; Engel WK; Alvarez RB; Lee CS
Neurology; 1989 Jul; 39(7):926-32. PubMed ID: 2544827
[TBL] [Abstract][Full Text] [Related]
3. [Oculopharyngeal muscular dystrophy specific intranuclear tubulofilamentous inclusions].
Uyama E; Uchino M; Ando M; Chateau D; Tomé FM
Rinsho Shinkeigaku; 1995 Jul; 35(7):817-8. PubMed ID: 8777812
[No Abstract] [Full Text] [Related]
4. Presence of inclusion body myositis-like filaments in oculopharyngeal muscular dystrophy. Ultrastructural study of 10 cases.
Coquet M; Vital C; Julien J
Neuropathol Appl Neurobiol; 1990 Oct; 16(5):393-400. PubMed ID: 2175847
[TBL] [Abstract][Full Text] [Related]
5. Intranuclear inclusions in oculopharyngeal muscular dystrophy among Bukhara Jews.
Blumen SC; Sadeh M; Korczyn AD; Rouche A; Nisipeanu P; Asherov A; Tomé FM
Neurology; 1996 May; 46(5):1324-8. PubMed ID: 8628475
[TBL] [Abstract][Full Text] [Related]
6. Nuclear inclusions in oculopharyngeal dystrophy.
Tomé FM; Fardeau M
Acta Neuropathol; 1980; 49(1):85-7. PubMed ID: 6243839
[TBL] [Abstract][Full Text] [Related]
7. Oculopharyngeal muscular dystrophy: clinical and morphological follow-up study reveals mitochondrial alterations and unique nuclear inclusions in a severe autosomal recessive type.
Schröder JM; Krabbe B; Weis J
Neuropathol Appl Neurobiol; 1995 Feb; 21(1):68-73. PubMed ID: 7770123
[TBL] [Abstract][Full Text] [Related]
8. Morphological changes in muscle fibers in oculopharyngeal muscular dystrophy.
Tomé FM; Chateau D; Helbling-Leclerc A; Fardeau M
Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S63-9. PubMed ID: 9392019
[TBL] [Abstract][Full Text] [Related]
9. Oculopharyngeal muscular dystrophy: recent ultrastructural evidence for mitochondrial abnormalities.
Pratt MF; Meyers PK
Laryngoscope; 1986 Apr; 96(4):368-73. PubMed ID: 3007900
[TBL] [Abstract][Full Text] [Related]
10. Nuclear inclusions in oculopharyngeal muscular dystrophy in Quebec.
Bouchard JP; Gagné F; Tomé FM; Brunet D
Can J Neurol Sci; 1989 Nov; 16(4):446-50. PubMed ID: 2553230
[TBL] [Abstract][Full Text] [Related]
11. Ocular myopathies.
Tomé FM; Fardeau M
Pathol Res Pract; 1985 Jul; 180(1):19-27. PubMed ID: 4034429
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. 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]
14. Intranuclear inclusions in oculopharyngeal dystrophy.
Smith TW; Chad D
Muscle Nerve; 1984 May; 7(4):339-40. PubMed ID: 6328293
[No Abstract] [Full Text] [Related]
15. Oculopharyngeal muscular dystrophy. A case with abnormal mitochondria and "fingerprint" inclusions.
Julien J; Vital C; Vallat JM; Vallat M; Le Blanc M
J Neurol Sci; 1974 Feb; 21(2):165-9. PubMed ID: 4374513
[No Abstract] [Full Text] [Related]
16. Oculopharyngeal muscular dystrophy in Italy.
Meola G; Sansone V; Rotondo G; Tomé FM; Bouchard JP
Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S53-6. PubMed ID: 9392017
[TBL] [Abstract][Full Text] [Related]
17. Structural alterations of the junctional region in extraocular muscle of dystrophic mice. I. Modifications of sole-plate nuclei.
Davidowitz J; Pachter BR; Philips G; Breinin GM
Am J Pathol; 1976 Jan; 82(1):101-10. PubMed ID: 174436
[TBL] [Abstract][Full Text] [Related]
18. [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]
19. Autosomal recessive oculopharyngodistal myopathy in light of distal myopathy with rimmed vacuoles and oculopharyngeal muscular dystrophy.
Uyama E; Uchino M; Chateau D; Tomé FM
Neuromuscul Disord; 1998 Apr; 8(2):119-25. PubMed ID: 9608566
[TBL] [Abstract][Full Text] [Related]
20. Immunolocalization of ubiquitin in muscle biopsies of patients with inclusion body myositis and oculopharyngeal muscular dystrophy.
Askanas V; Serdaroglu P; Engel WK; Alvarez RB
Neurosci Lett; 1991 Sep; 130(1):73-6. PubMed ID: 1660975
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
