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2. An autopsy study of a familial oculopharyngeal muscular dystrophy (OPMD) with distal spread and neurogenic involvement. Schmitt HP; Krause KH Muscle Nerve; 1981; 4(4):296-305. PubMed ID: 7254232 [TBL] [Abstract][Full Text] [Related]
3. [Oculopharyngeal muscular dystrophy. Description of a case with involvement of the central nervous system]. Linoli G; Tomelleri G; Ghezzi M Pathologica; 1991; 83(1085):325-34. PubMed ID: 1923632 [TBL] [Abstract][Full Text] [Related]
4. Oculopharyngeal muscular dystrophy in a northern German family linked to chromosome 14q, and presenting carnitine deficiency. Porschke H; Kress W; Reichmann H; Goebel HH; Grimm T Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S57-62. PubMed ID: 9392018 [TBL] [Abstract][Full Text] [Related]
7. Familial oculopharyngeal muscular dystrophy with distal spread. Vita G; Dattola R; Santoro M; Messina C J Neurol; 1983; 230(1):57-64. PubMed ID: 6194273 [TBL] [Abstract][Full Text] [Related]
8. Neurogenic involvement in a case of oculopharyngeal muscular dystrophy. Boukriche Y; Maisonobe T; Masson C Muscle Nerve; 2002 Jan; 25(1):98-101. PubMed ID: 11754191 [TBL] [Abstract][Full Text] [Related]
9. [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]
10. Oculopharyngeal dystrophy: clinicopathological study of an Australian family. Blumbergs PC; Chin D; Burrow D; Burns RJ; Rice JP Clin Exp Neurol; 1983; 19():102-9. PubMed ID: 6568918 [TBL] [Abstract][Full Text] [Related]
11. Oculopharyngeal muscular dystrophy in two unrelated Japanese families. Uyama E; Nohira O; Chateau D; Tokunaga M; Uchino M; Okabe T; Ando M; Tome FM Neurology; 1996 Mar; 46(3):773-8. PubMed ID: 8618681 [TBL] [Abstract][Full Text] [Related]
12. Possible neurogenic factor in muscular dystrophy: its similarity to denervation atrophy. Dastur DK; Razzak ZA J Neurol Neurosurg Psychiatry; 1973 Jun; 36(3):399-410. PubMed ID: 4714102 [TBL] [Abstract][Full Text] [Related]
13. 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]