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3. [Follow-up examination of children with spinal muscular atrophy of the Werdning-Hoffmann type; at the same time a critical contribution to the problem of amyotonia congenita Oppenheim]. KIRCHHOF JK; MULLER F Nervenarzt; 1958 Apr; 29(4):158-67. PubMed ID: 13552903 [No Abstract] [Full Text] [Related]
4. [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]
5. The relationship between progressive muscular atrophy of spinal origin and amyotonia congenita. AREY JB; BAIRD HW AMA Am J Dis Child; 1953 Nov; 86(5):619-20; discussion, 620-1. PubMed ID: 13103782 [No Abstract] [Full Text] [Related]
6. Nuclear myelopathies of childhood. ARONSON SM; VOLK BW Bull N Y Acad Med; 1956 Sep; 32(9):692-4. PubMed ID: 13356109 [No Abstract] [Full Text] [Related]
7. [Muscle diseases in children: with special reference to progressive muscular dystrophy, amyotonia, myohypertonia and myoasthenia]. CORTESE-VERROTTI I Pediatria (Napoli); 1956; 64(2):341-7. PubMed ID: 13335311 [No Abstract] [Full Text] [Related]
8. Case reports of progressive infantile muscular atrophy (Werdnig-Hoffmann) in fraternal twins. LEYRER RH AMA Am J Dis Child; 1954 Nov; 88(5):604-5. PubMed ID: 13206380 [No Abstract] [Full Text] [Related]
9. [Anatomo-clinical comparative studies on amyotonia congenita, on Werdnig-Hoffmann, disease and on arthrogryposis multiplex congenita]. DE CORDOVA A; SOSA BENS D; SALAS PANISELLO F Rev Cubana Pediatr; 1954 Apr; 26(4):231-50. PubMed ID: 13186343 [No Abstract] [Full Text] [Related]
11. [Catamnestic inquiries in conditions of hypertonia in early childhood. With a critical contribution to the differential diagnosis of infantile spinal progressive muscular atrophy (Werdnig-Hoffman disease--myatonia congenital Oppenheilm)]. HORSTMANN W Z Kinderheilkd; 1959; 82():649-67. PubMed ID: 13848453 [No Abstract] [Full Text] [Related]
13. [CLINICAL CONTRIBUTION TO THE STUDY OF WERDNIG-HOFFMANN MUSCULAR AMYOTROPHY]. CIULLA M Boll Soc Med Chir Cremona; 1963; 17():141-8. PubMed ID: 14109627 [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. [Electromyographical studies in myopathies and related diseases]. PERLSTEIN MA; TURNER M; ELAM H Arch Argent Pediatr; 1961 Apr; 55():168-81. PubMed ID: 13734441 [No Abstract] [Full Text] [Related]
20. 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 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]