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2. Premature atherosclerosis with photomyoclonic epilepsy, deafness, diabetes mellitus, nephropathy, and neurodegenerative disorder in two brothers: a new syndrome? Feigenbaum A; Bergeron C; Richardson R; Wherrett J; Robinson B; Weksberg R Am J Med Genet; 1994 Jan; 49(1):118-24. PubMed ID: 8172238 [TBL] [Abstract][Full Text] [Related]
3. Mitochondrial non-syndromic sensorineural hearing loss: a clinical, audiological and pathological study from Italy, and revision of the literature. Berrettini S; Forli F; Passetti S; Rocchi A; Pollina L; Cecchetti D; Mancuso M; Siciliano G Biosci Rep; 2008 Feb; 28(1):49-59. PubMed ID: 18215147 [TBL] [Abstract][Full Text] [Related]
6. Hearing loss due to the mitochondrial A1555G mutation in Italian families. Casano RA; Bykhovskaya Y; Johnson DF; Hamon M; Torricelli F; Bigozzi M; Fischel-Ghodsian N Am J Med Genet; 1998 Oct; 79(5):388-91. PubMed ID: 9779807 [TBL] [Abstract][Full Text] [Related]
7. [Unknown cause of familial neuromuscular disease with infiltration of cytotoxic/suppressor T cells]. Fukunaga H; Kitajima I; Sonoda Y; Atuchi H Rinsho Shinkeigaku; 1990 Jun; 30(6):654-8. PubMed ID: 2146056 [TBL] [Abstract][Full Text] [Related]
8. Nerve-muscle involvement in a large family with mitochondrial cytopathy: electrophysiological studies. Torbergsen T; Stålberg E; Bless JK Muscle Nerve; 1991 Jan; 14(1):35-41. PubMed ID: 1846937 [TBL] [Abstract][Full Text] [Related]
10. [Infantile form of nemaline (rod inclusion) myopathy]. Berger W; Grisold W; Jellinger K Wien Klin Wochenschr; 1988 Jun; 100(12):407-12. PubMed ID: 2841810 [TBL] [Abstract][Full Text] [Related]
11. The mitochondrial myopathies: 9 case reports and a literature review. Fitzsimons RB Clin Exp Neurol; 1981; 17():185-210. PubMed ID: 7346199 [TBL] [Abstract][Full Text] [Related]
12. Concentric laminated bodies in muscle pathology. Gambarelli D; Hassoun J; Pellissier JF; Berard M; Toga M Pathol Eur; 1974; 9(4):289-96. PubMed ID: 4457782 [TBL] [Abstract][Full Text] [Related]
13. [Contributions to clinical myology. The role of electron microscopy]. Lehmann J Psychiatr Neurol Med Psychol Beih; 1987; 38():108-19. PubMed ID: 2841706 [No Abstract] [Full Text] [Related]
14. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Tamura K; Santa T; Kuroiwa Y Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795 [No Abstract] [Full Text] [Related]
16. [Neuromuscular mitochondriopathy. A morphological expression of disorders of the energy metabolism (author's transl)]. Walter GF Veroff Pathol; 1981; 117():1-111. PubMed ID: 6210998 [No Abstract] [Full Text] [Related]