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Pubmed for Handhelds
PUBMED FOR HANDHELDS
Journal Abstract Search
84 related items for PubMed ID: 7085707
1. Orthopaedic management of childhood neuromuscular disease. Part I: Spinal muscular atrophy. Shapiro F, Bresnan MJ. J Bone Joint Surg Am; 1982 Jun; 64(5):785-9. PubMed ID: 7085707 [No Abstract] [Full Text] [Related]
3. Hypertrophic type of peroneal muscular atrophy and spinal muscular atrophy in siblings. Lope ES, del Campo F, Cabello A. Acta Neurol Scand; 1982 Aug; 66(2):237-47. PubMed ID: 7136488 [No Abstract] [Full Text] [Related]
5. An obscure inherited neuropathy characterized by pain and weakness. Isaacs H, Badenhorst M. S Afr Med J; 1977 Aug 06; 52(7):285-8. PubMed ID: 897927 [Abstract] [Full Text] [Related]
6. The orthopaedic aspects of spinal muscular atrophy. Schwentker EP, Gibson DA. J Bone Joint Surg Am; 1976 Jan 06; 58(1):32-8. PubMed ID: 765347 [Abstract] [Full Text] [Related]
8. [Histological changes in peripheral nerves in spinal Werdnig-Hoffmann muscular atrophy]. Drac H. Neuropatol Pol; 1977 Jan 06; 15(1):1-16. PubMed ID: 840382 [No Abstract] [Full Text] [Related]
9. Variability in nerve biopsy findings in a kinship with dominantly inherited Charcot-Marie-Tooth disease. Van Weerden TW, Houthoff HJ, Sie O, Minderhoud JM. Muscle Nerve; 1982 Mar 06; 5(3):185-96. PubMed ID: 7088015 [No Abstract] [Full Text] [Related]
10. [Formation of "onion bulbs" in Charcot-Marie-Tooth and Dejerine-Sottas hypertrophic neuropathies]. Jedrzejowska H, Drac H, Sawicka E. Neuropatol Pol; 1975 Mar 06; 13(1):93-106. PubMed ID: 1118064 [No Abstract] [Full Text] [Related]
13. Juvenile type of distal and segmental muscular atrophy of upper extremities. Sobue I, Saito N, Iida M, Ando K. Ann Neurol; 1978 May 06; 3(5):429-32. PubMed ID: 727722 [Abstract] [Full Text] [Related]
15. Hereditary motor and sensory polyneuropathy (peroneal muscular atrophy). Thomas PK, Calne DB, Stewart G. Ann Hum Genet; 1974 Oct 06; 38(2):111-53. PubMed ID: 4467779 [No Abstract] [Full Text] [Related]