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Journal Abstract Search
183 related items for PubMed ID: 494907
1. [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 [Abstract] [Full Text] [Related]
2. [Charcot-Marie neural amyotrophy (review)]. Savchenko IuN. Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1718-22. PubMed ID: 6098115 [No Abstract] [Full Text] [Related]
4. Peripheral motor and sensory neuropathy of early childhood, simulating Werdnig-Hoffmann disease. Goebel HH, Zeman W, DeMyer W. Neuropadiatrie; 1976 May; 7(2):182-95. PubMed ID: 183171 [Abstract] [Full Text] [Related]
5. [Polymorphism of hereditary atypical spinal amyotrophy in adults]. Dubinskaia EE, Popov'ian MD, Reshetov GN. Zh Nevropatol Psikhiatr Im S S Korsakova; 1987 May; 87(3):334-8. PubMed ID: 3577523 [Abstract] [Full Text] [Related]
6. [Spinal facioscapulo-peroneal (or facioscapulo-crural) muscular atrophy and facioscapulo-peroneal muscular dystrophy]. Kazakov VM, Skoromets AA, Mikhaĭlov EP, Barantsevich ER. Zh Nevropatol Psikhiatr Im S S Korsakova; 1986 May; 86(5):662-7. PubMed ID: 3739474 [Abstract] [Full Text] [Related]
7. [Chronic distal spinal amyotrophy or spinal forms of Charcot-Marie disease. A report on six sporadic adult cases (author's transl)]. Serratrice G, Gastaut JL. Rev Neurol (Paris); 1979 May; 135(11):815-26. PubMed ID: 555021 [Abstract] [Full Text] [Related]
8. 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 [Abstract] [Full Text] [Related]
9. [Family with progressive myelopathic muscular atrophy with proximal distribution and onset in adulthood]. Mapelli G. Riv Patol Nerv Ment; 1983 Feb; 104(4):159-70. PubMed ID: 6681331 [Abstract] [Full Text] [Related]
10. 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 Feb; 72(6):557-67. PubMed ID: 5369244 [No Abstract] [Full Text] [Related]
11. Sensory ganglioneuropathy in infantile spinal muscular atrophy. Light and electronmicroscopic findings in two cases. Probst A, Ulrich J, Bischoff A, Boltshauser E. Neuropediatrics; 1981 Aug; 12(3):215-31. PubMed ID: 7290343 [Abstract] [Full Text] [Related]
12. [For the anatomo-clinical diagnosis of primary muscular dystrophy of neonatal onset: apropos of a case]. Bruni G, Zalla PG. Arch De Vecchi Anat Patol; 1968 Mar; 51(1):435-45. PubMed ID: 5737308 [No Abstract] [Full Text] [Related]
13. [Myocardial lesions in several forms of progressive muscular atrophy]. Popov'ian MD, Dubinskaia EE, Proshina OV, Tul'skaia MP, Loginova LA. Zh Nevropatol Psikhiatr Im S S Korsakova; 1984 Mar; 84(3):330-5. PubMed ID: 6720172 [Abstract] [Full Text] [Related]
14. Infantile neuronal degeneration masquerading as Werdnig-Hoffmann disease. Steiman GS, Rorke LB, Brown MJ. Ann Neurol; 1980 Sep; 8(3):317-24. PubMed ID: 7436375 [Abstract] [Full Text] [Related]
15. Amyotrophy in Shy-Drager syndrome. Montagna P, Martinelli P, Rizzuto N, Salviati A, Rasi F, Lugaresi E. Acta Neurol Belg; 1983 Sep; 83(3):142-57. PubMed ID: 6613517 [Abstract] [Full Text] [Related]
16. [Clinical study of muscular atrophy]. Shinoda M. Hokkaido Igaku Zasshi; 1974 Jan; 49(1):23-31. PubMed ID: 4376121 [No Abstract] [Full Text] [Related]
17. Juvenile type of distal and segmental muscular atrophy of upper extremities. Sobue I, Saito N, Iida M, Ando K. Ann Neurol; 1978 May; 3(5):429-32. PubMed ID: 727722 [Abstract] [Full Text] [Related]
18. [Value of myometric findings in the morphological differential diagnosis of neuromuscular disorders (author's transl)]. Pongratz D. Microsc Acta Suppl; 1980 May; Suppl 4():38-43. PubMed ID: 6931279 [Abstract] [Full Text] [Related]