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6. The significance of target fibers: a clinicopathologic review of 100 patients with neurogenic atrophy. Kovarsky J; Schochet SS; McCormick WF Am J Clin Pathol; 1973 Jun; 59(6):790-7. PubMed ID: 4122677 [No Abstract] [Full Text] [Related]
7. 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]
8. A unique case of reducing body myopathy. Nomizu S; Person DA; Saito C; Lockett LJ Muscle Nerve; 1992 Apr; 15(4):463-6. PubMed ID: 1314327 [TBL] [Abstract][Full Text] [Related]
9. Ultrastructural changes in human muscle fibres in disease. Papadimitriou JM; Mastaglia FL J Submicrosc Cytol; 1982 Jul; 14(3):525-51. PubMed ID: 6757457 [No Abstract] [Full Text] [Related]
10. A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line. Pellegrini G; Barbieri S; Moggio M; Cheldi A; Scarlato G; Minetti C Neuropediatrics; 1985 Aug; 16(3):162-6. PubMed ID: 4047349 [TBL] [Abstract][Full Text] [Related]
11. Myopathy associated with linear scleroderma. A histochemical and electron microscopic study. Stern LZ; Payne CM; Alvarez JT; Hannapel LK Neurology; 1975 Feb; 25(2):114-9. PubMed ID: 163451 [TBL] [Abstract][Full Text] [Related]
12. Fine structure of prenatal and early postnatal dystrophic mouse muscle. Platzer AC; Powell JA J Neurol Sci; 1975 Jan; 24(1):109-26. PubMed ID: 1110369 [No Abstract] [Full Text] [Related]
13. [Ultrastructural characteristics of tubular aggregates in human skeletal muscles]. Babakova LL; Kolomenskaia EA; Kuz'min NV; Pozdniakov OM Arkh Patol; 1974; 36(4):50-6. PubMed ID: 4457084 [No Abstract] [Full Text] [Related]
15. Autosomal dominant neuromuscular disease with cylindrical spirals. Taratuto AL; Matteucci M; Barreiro C; Saccolitti M; Sevlever G Neuromuscul Disord; 1991; 1(6):433-41. PubMed ID: 1822355 [TBL] [Abstract][Full Text] [Related]
16. Follow-up studies in a case of unusual congenital myopathy, suggestive of nemaline type. Gibbels E; Kellermann K; Schädlich HJ; Adams R; Haupt WF Acta Neuropathol; 1992; 83(4):371-8. PubMed ID: 1575014 [TBL] [Abstract][Full Text] [Related]
17. Neuronal changes of hypokalemic myopathy. A light- and electron-microscopic study on muscle biopsy. Hashimoto S; Akai F; Semba E; Sakatani K; Hiruma S; Nagaoka M; Hukuda K; Imada A J Neurol Sci; 1980 Jan; 44(2-3):169-79. PubMed ID: 7354366 [TBL] [Abstract][Full Text] [Related]
18. A new familial congenital myopathy in children with desmin and dystrophin reacting plaques. Fidziańska A; Ryniewicz B; Barcikowska M; Goebel HH J Neurol Sci; 1995 Jul; 131(1):88-95. PubMed ID: 7561954 [TBL] [Abstract][Full Text] [Related]
19. The syndrome of 'continuous muscle-fibre activity' cured: further studies. Isaacs H; Heffron JJ J Neurol Neurosurg Psychiatry; 1974 Nov; 37(11):1231-5. PubMed ID: 4281819 [TBL] [Abstract][Full Text] [Related]