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Journal Abstract Search
100 related items for PubMed ID: 13916648
1. [Contribution to the problem of the diagnosis of Werdnig-Hoffman disease]. STEIN W, RYMCZONEK C. Pediatr Pol; 1961 Sep; 36():977-85. PubMed ID: 13916648 [No Abstract] [Full Text] [Related]
9. [CASE OF MYELOPATHIC MUSCULAR ATROPHY THOUGHT AT FIRST TO BE PROGRESSIVE MUSCULAR DYSTROPHY--A VIEW OF THE RELATION BETWEEN KUGELBERG-WELANDER'S MUSCULAR ATROPHY AND WERDNIG-HOFFMANN DISEASE]. FURUKAWA S, MAMIYA S. Nihon Shonika Gakkai Zasshi; 1963 Nov 01; 67():745-8. PubMed ID: 14096316 [No Abstract] [Full Text] [Related]
12. [Werdnig-Hoffmann's infantile progressive muscular atrophy; clinical aspects, pathology, heredity, and relation to Oppenheim's amyotonia congenita and other morbid conditions with laxity of the joints or muscles in children]. BRANDT S. Nord Med; 1950 Sep 15; 44(37):1499. PubMed ID: 14806955 [No Abstract] [Full Text] [Related]
15. [Myatonia congenita Oppenheim, with special reference to its relation to Werdnig-Hoffmann disease]. FUKUYAMA Y. Sogo Igaku; 1961 Oct 15; 18():671-82. PubMed ID: 13895848 [No Abstract] [Full Text] [Related]
16. Cerebellar hypoplasia in Werdnig-Hoffmann disease. NORMAN RM. Arch Dis Child; 1961 Feb 15; 36(185):96-101. PubMed ID: 13729575 [No Abstract] [Full Text] [Related]
17. CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE. NORMAN RM, KAY JM. Arch Dis Child; 1965 Jun 15; 40(211):302-8. PubMed ID: 14294750 [No Abstract] [Full Text] [Related]