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8. [Distal spinal-muscular atrophy 1 (DSMA1 or SMARD1)]. Kaindl AM; Guenther UP; Rudnik-Schöneborn S; Varon R; Zerres K; Gressens P; Schuelke M; Hubner C; von Au K Arch Pediatr; 2008 Oct; 15(10):1568-72. PubMed ID: 18804971 [TBL] [Abstract][Full Text] [Related]
9. Characteristic clinical findings in some neurogenic myopathies and in some myogenic myopathies causing muscular weakness, hypotonia and atrophy in infancy and early childhood. Gamstorp I Birth Defects Orig Artic Ser; 1971 Feb; 7(2):72-81. PubMed ID: 5173129 [TBL] [Abstract][Full Text] [Related]
10. [Role of complex studies in the diagnosis of spinal amyotrophy in young children]. Zhurba LT; Timonina OV; Aingorn ED; Koroleva IA; Avakian GN Zh Nevropatol Psikhiatr Im S S Korsakova; 1979; 79(10):1342-5. PubMed ID: 494907 [TBL] [Abstract][Full Text] [Related]
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13. The ultrastructure of peripheral nerve, motor end-plate and skeletal muscle in patients suffering from spinal muscular atrophy with respiratory distress type 1 (SMARD1). Diers A; Kaczinski M; Grohmann K; Hübner C; Stoltenburg-Didinger G Acta Neuropathol; 2005 Sep; 110(3):289-97. PubMed ID: 16025284 [TBL] [Abstract][Full Text] [Related]