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5. [Heart muscle involvement in myopathies]. Finsterer J; Stoellberger C; Keller H; Slany J; Mamoli B Wien Med Wochenschr; 1996; 146(9-10):212. PubMed ID: 9012218 [TBL] [Abstract][Full Text] [Related]
6. Oculopharyngeal muscular dystrophy, other ocular myopathies, and progressive external ophthalmoplegia. Rowland LP; Hirano M; DiMauro S; Schon EA Neuromuscul Disord; 1997 Oct; 7 Suppl 1():S15-21. PubMed ID: 9392010 [TBL] [Abstract][Full Text] [Related]
7. [Protein and DNA sequencing analyses of transthyretin in familial amyloidotic polyneuropathy]. Nakazato M Rinsho Shinkeigaku; 1995 Dec; 35(12):1436-7. PubMed ID: 8752422 [TBL] [Abstract][Full Text] [Related]
8. Molecular analysis of the Duchenne muscular dystrophy gene in Spanish individuals: deletion detection and familial diagnosis. Patiño A; Narbona J; García-Delgado M Am J Med Genet; 1995 Nov; 59(2):182-7. PubMed ID: 8588583 [TBL] [Abstract][Full Text] [Related]
9. Muscular dystrophy versus mitochondrial myopathy: the dilemma of the undiagnosed hypotonic child. Allison KR Paediatr Anaesth; 2007 Jan; 17(1):1-6. PubMed ID: 17184424 [No Abstract] [Full Text] [Related]
10. [Rapid screening of the Duchenne muscular dystrophy gene deletion by two multiplex PCR]. Ma S Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1993 Feb; 15(1):74-8. PubMed ID: 8324844 [TBL] [Abstract][Full Text] [Related]
11. [Corino Andrade disease]. Munar-Qués M An R Acad Nac Med (Madr); 1999; 116(3):667-80; discussion 681-2. PubMed ID: 10846584 [TBL] [Abstract][Full Text] [Related]
16. [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]
17. [The other genome: the clinical concept of mitochondrial cytopathies or disorders of pxidative phosphorylation]. Barrera-Ramírez CF; Barragán-Campos HM; Sánchez-Guerrero J; García-Ramos G; Vega-Boada F; Estañol B Rev Invest Clin; 1999; 51(2):121-34. PubMed ID: 10410592 [TBL] [Abstract][Full Text] [Related]
18. Two pathogenic point mutations exist in the authentic mitochondrial genome, not in the nuclear pseudogene. Akanuma J; Muraki K; Komaki H; Nonaka I; Goto Y J Hum Genet; 2000; 45(6):337-41. PubMed ID: 11185741 [TBL] [Abstract][Full Text] [Related]
19. [Analysis of the Duchenne muscular dystrophy gene with PCR analysis in paraffin-embedded tissue. A new diagnostic possibility]. Apold J; Eiken HG; Engebretsen LF; Boman H Tidsskr Nor Laegeforen; 1993 Oct; 113(26):3233-5. PubMed ID: 8236215 [TBL] [Abstract][Full Text] [Related]