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9. A new polygenic disturbance: cystinuria, leucinuria and spinal muscular atrophy. Radu H, Tanase-Mogoş I, Roşu AM, Killyen I, Ionescu V. J Neurol; 1974; 207(1):73-83. PubMed ID: 4142888 [No Abstract] [Full Text] [Related]
10. Spinal muscular atrophy with autosomal dominant inheritance. Report of a new kindred. Zellweger H, Simpson J, McCormick WF, Ionasescu V. Neurology; 1972 Sep; 22(9):957-63. PubMed ID: 4673381 [No Abstract] [Full Text] [Related]
11. [Tubular aggregates in a case of chronic proximal spinal atrophy]. Werneck LC, Silvado CE, Boer CA. Arq Neuropsiquiatr; 1979 Mar; 37(1):53-60. PubMed ID: 88934 [Abstract] [Full Text] [Related]
12. Letter: Creatine phosphokinase as indicator of adenosine triphosphate activity. Sklar SH, Wigand JS. JAMA; 1973 Dec 17; 226(12):1464-5. PubMed ID: 4800819 [No Abstract] [Full Text] [Related]
13. Neurogenic muscular atrophy of infancy with prolonged survival. The variable course of Werdnig-Hoffmann Disease. Munsat TL, Woods R, Fowler W, Pearson CM. Brain; 1969 Mar 17; 92(1):9-24. PubMed ID: 5774034 [No Abstract] [Full Text] [Related]
20. A comparison of fibre size, fibre type constitution and spatial fibre type distribution in normal human muscle and in muscle from cases of spinal muscular atrophy and from other neuromuscular disorders. Johnson MA, Sideri G, Weightman D, Appleton D. J Neurol Sci; 1973 Dec 17; 20(4):345-61. PubMed ID: 4272515 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]