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8. Electromyography in patients with lesions of the central motor neuron and the so-called parietal muscular atrophy. Notermans SL, Blokzijl EJ. Psychiatr Neurol Neurochir; 1969 Jan 22; 72(6):557-67. PubMed ID: 5369244 [No Abstract] [Full Text] [Related]
9. The nosology of the spinal muscular atrophies. Emery AE. J Med Genet; 1971 Dec 22; 8(4):481-95. PubMed ID: 4948374 [No Abstract] [Full Text] [Related]
10. Juvenile motor neuron diseases--the sex influence in benign juvenile pseudodystrophic spinal muscular atrophy. Hausmanowa-Petrusewicz I, Borkowska J, Zaremba J. Adv Neurol; 1982 Dec 22; 36():131-7. PubMed ID: 7180679 [No Abstract] [Full Text] [Related]
11. Unilateral spinal muscular atrophy. A case report. Thijsse WJ, Spaans F. Clin Neurol Neurosurg; 1983 Dec 22; 85(2):117-21. PubMed ID: 6309457 [Abstract] [Full Text] [Related]
12. Spinal muscular atrophy. McLeod JG, Williams IM. Minn Med; 1971 Jun 22; 54(6):457-61. PubMed ID: 5559368 [No Abstract] [Full Text] [Related]
13. [Clinical study of muscular atrophy]. Shinoda M. Hokkaido Igaku Zasshi; 1974 Jan 22; 49(1):23-31. PubMed ID: 4376121 [No Abstract] [Full Text] [Related]
14. Electrophysiological estimation of motor units in limb-girdle muscular dystrophy and chronic spinal muscular atrophy. Panayiotopoulos CP, Scarpalezos S. J Neurol Sci; 1975 Jan 22; 24(1):95-107. PubMed ID: 1110376 [No Abstract] [Full Text] [Related]
15. [Clinicopathology of neuromuscular diseases]. Tokuomi H. Rinsho Byori; 1969 Jan 22; 17(1):6-14. PubMed ID: 5814289 [No Abstract] [Full Text] [Related]
16. Progressive proximal spinal and bulbar muscular atrophy of late onset. A sex-linked recessive trait. Kennedy WR, Alter M, Sung JH. Neurology; 1968 Jul 22; 18(7):671-80. PubMed ID: 4233749 [No Abstract] [Full Text] [Related]
17. [Histopathology of neuromuscular and intramuscular nerve fibers in patients with Werdnig-Hoffmann infantile spinal amyotrophy]. Cazzato G, Dall'Olio G. Acta Neurol (Napoli); 1969 Jul 22; 24(2):208-19. PubMed ID: 4247846 [No Abstract] [Full Text] [Related]
18. [Malate dehydrogenase activity in patients with different forms of progressive muscular dystrophy]. Gil'manov VKh. Zh Nevropatol Psikhiatr Im S S Korsakova; 1970 Jul 22; 70(9):1309-12. PubMed ID: 5511109 [No Abstract] [Full Text] [Related]
19. [Contribution of electromyography to the diagnosis of Werdnig-Hoffmann infantile spinal amyotrophy]. Raimbault J, Laget P. Pathol Biol (Paris); 1972 Mar 22; 20(5):287-96. PubMed ID: 4556213 [No Abstract] [Full Text] [Related]
20. A family with Kugelberg-Welander sydrome. Hereditary proximal spinal muscul atrophy--some additional features. Almog C, Tal E. Confin Neurol; 1968 Mar 22; 30(5):313-24. PubMed ID: 5729137 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]