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2. Oculopharyngeal muscular dystrophy in a Japanese family with a short GCG expansion (GCG)(11) in PABP2 gene. Nagashima T; Kato H; Kase M; Maguchi S; Mizutani Y; Matsuda K; Chuma T; Mano Y; Goto Y; Minami N; Nonaka I; Nagashima K Neuromuscul Disord; 2000 Mar; 10(3):173-7. PubMed ID: 10734263 [TBL] [Abstract][Full Text] [Related]
3. Oculopharyngeal muscular dystrophy in Japan. Uyama E; Nohira O; Tomé FM; Chateau D; Tokunaga M; Ando M; Maki M; Okabe T; Uchino M Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S41-9. PubMed ID: 9392015 [TBL] [Abstract][Full Text] [Related]
4. 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]
12. Miyoshi-type distal muscular dystrophy. Clinical spectrum in 24 Dutch patients. Linssen WH; Notermans NC; Van der Graaf Y; Wokke JH; Van Doorn PA; Höweler CJ; Busch HF; De Jager AE; De Visser M Brain; 1997 Nov; 120 ( Pt 11)():1989-96. PubMed ID: 9397016 [TBL] [Abstract][Full Text] [Related]
13. Early onset muscular dystrophy with autosomal dominant heredity. Report of a family and CT findings of skeletal muscle. Tohyama J; Inagaki M; Nonaka I Brain Dev; 1994; 16(5):402-6. PubMed ID: 7892962 [TBL] [Abstract][Full Text] [Related]
14. Oculopharyngeal muscular dystrophy. An autopsied case from the French-Canadian kindred. Little BW; Perl DP J Neurol Sci; 1982 Feb; 53(2):145-58. PubMed ID: 7057207 [TBL] [Abstract][Full Text] [Related]
15. Oculopharyngeal dystrophy: ultrastructure of muscles distinct from the primary myopathy. Kozachek JW; Wilson FJ Acta Neuropathol; 1982; 57(1):7-12. PubMed ID: 7090744 [TBL] [Abstract][Full Text] [Related]
16. Oculopharyngeal muscular dystrophy and distal myopathy. Intrafamilial difference in the onset and distribution of muscular involvement. Fukuhara N; Kumamoto T; Tsubaki T; Mayuzumi T; Nitta H Acta Neurol Scand; 1982 May; 65(5):458-67. PubMed ID: 7113658 [TBL] [Abstract][Full Text] [Related]
17. Intranuclear inclusions in oculopharyngeal muscular dystrophy contain poly(A) binding protein 2. Becher MW; Kotzuk JA; Davis LE; Bear DG Ann Neurol; 2000 Nov; 48(5):812-5. PubMed ID: 11079550 [TBL] [Abstract][Full Text] [Related]
18. [A case of Fukuyama type congenital muscular dystrophy with progressive changes in brain CT scanning]. Mori K; Saijo T; Hamaguchi H; Tayama M; Kawano N; Hashimoto T; Miyao M No To Hattatsu; 1988; 20(5):418-22. PubMed ID: 3224015 [No Abstract] [Full Text] [Related]
19. 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]
20. Computed tomographic findings in manifesting carriers of Duchenne muscular dystrophy. de Visser M; Verbeeten B Clin Genet; 1985 Mar; 27(3):269-75. PubMed ID: 3987077 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]