These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
147 related articles for article (PubMed ID: 14236013)
1. INFANTILE MUSCULAR ATROPHY. A PROSPECTIVE STUDY WITH PARTICULAR REFERENCE TO A SLOWLY PROGRESSIVE VARIETY. DUBOWITZ V Brain; 1964 Dec; 87():707-18. PubMed ID: 14236013 [No Abstract] [Full Text] [Related]
2. [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; 67():745-8. PubMed ID: 14096316 [No Abstract] [Full Text] [Related]
4. [On the morphology, nosological position and pathogenesis of Oppenheim's myotonia congenita and Werdnig-Hoffmann's infantile spinal progressive muscular atrophy]. GEILER G; GEILER G Virchows Arch Pathol Anat Physiol Klin Med; 1962; 335():654-67. PubMed ID: 13897523 [No Abstract] [Full Text] [Related]
5. [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; 44(37):1499. PubMed ID: 14806955 [No Abstract] [Full Text] [Related]
6. Hereditary factors in infantile progressive muscular atrophy; study of 112 cases in 70 families. BRANDT S Am J Dis Child (1911); 1949 Aug; 78(2):226-36. PubMed ID: 18135521 [No Abstract] [Full Text] [Related]
12. [Infantile spinal muscular atrophy. Description of 2 cases of Werdnig-Hoffmann disease]. Priora U; Quaglia P; Vivalda M; Giachino-Amistà MT; Domeneghetti G; Sardi R Minerva Pediatr; 1987 Sep; 39(17-18):709-14. PubMed ID: 3437861 [No Abstract] [Full Text] [Related]
13. [On the problem of spinal muscular atrophy resembling progressive muscular dystrophy (Kugelberg-Welander's juvenile muscular atrophy)]. GOLDSZTAJN M; ZEBROWSKI S Neurol Neurochir Psychiatr Pol; 1962; 12():669-73. PubMed ID: 13948828 [No Abstract] [Full Text] [Related]
14. Contributions to the symptomatology of amyotonia congenita (infantile spinal muscular atrophy). WOHLFART G Acta Med Scand; 1946; 123(5):428-47. PubMed ID: 21026460 [No Abstract] [Full Text] [Related]
15. Distal infantile spinal muscular atrophy associated with paralysis of the diaphragm: a variant of infantile spinal muscular atrophy. Bertini E; Gadisseux JL; Palmieri G; Ricci E; Di Capua M; Ferriere G; Lyon G Am J Med Genet; 1989 Jul; 33(3):328-35. PubMed ID: 2801766 [TBL] [Abstract][Full Text] [Related]
16. CEREBELLO-THALAMO-SPINAL DEGENERATION IN INFANCY: AN UNUSUAL VARIANT OF WERDNIG-HOFFMANN DISEASE. NORMAN RM; KAY JM Arch Dis Child; 1965 Jun; 40(211):302-8. PubMed ID: 14294750 [No Abstract] [Full Text] [Related]
17. Type I spinal muscular atrophy can mimic sensory-motor axonal neuropathy. Anagnostou E; Miller SP; Guiot MC; Karpati G; Simard L; Dilenge ME; Shevell MI J Child Neurol; 2005 Feb; 20(2):147-50. PubMed ID: 15794183 [TBL] [Abstract][Full Text] [Related]
18. Infantile spinal progressive muscular atrophy in twins. POIRIER R; CORBET RC; BUCKWOLD AE Can Med Assoc J; 1951 Oct; 65(4):342-3. PubMed ID: 14879299 [No Abstract] [Full Text] [Related]
19. Course and symptoms of progressive infantile muscular atrophy; a follow-up study of 112 cases in Denmark. BRANDT S Arch Neurol Psychiatry; 1950 Feb; 63(2):218-28. PubMed ID: 15404484 [No Abstract] [Full Text] [Related]