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10. Very severe spinal muscular atrophy (SMA type 0): an expanding clinical phenotype. Dubowitz V Eur J Paediatr Neurol; 1999; 3(2):49-51. PubMed ID: 10700538 [TBL] [Abstract][Full Text] [Related]
11. [Histopathology of neuromuscular and intramuscular nerve fibers in patients with Werdnig-Hoffmann infantile spinal amyotrophy]. Cazzato G; Dall'Olio G Acta Neurol (Napoli); 1969; 24(2):208-19. PubMed ID: 4247846 [No Abstract] [Full Text] [Related]
12. [Ultrastructural findings and characterization of isoenzymes in the muscle in case of Werdnig-Hoffmann disease]. Ferreli A; Cao A; Onnis C Arch De Vecchi Anat Patol; 1967 Dec; 50(3):629-44. PubMed ID: 5634345 [No Abstract] [Full Text] [Related]
18. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy]. Raimbault J; Laget P Pathol Biol (Paris); 1972 Mar; 20(5):287-96. PubMed ID: 4556213 [No Abstract] [Full Text] [Related]
19. [Acute respiratory insufficiency as the initial clinical manifestation of spinal muscular atrophy]. Poets C; Heyer R; von der Hardt H; Walter GF Monatsschr Kinderheilkd; 1990 Mar; 138(3):157-9. PubMed ID: 2352537 [TBL] [Abstract][Full Text] [Related]