168 related articles for article (PubMed ID: 13103782)
1. 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]
2. [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]
3. [Course of infantile spinal amyotrophy].
FURTADO D
Rev Neurol (Paris); 1958 Jun; 98(6):742-9. PubMed ID: 13615091
[No Abstract] [Full Text] [Related]
4. [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]
5. 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]
6. [Werdnig-Hoffmann-Oppenheim's spinal amyotonic-amyotrophic syndrome].
DE MEDEIROS J
Pediatr Prat; 1956 Apr; 27(4):111-34. PubMed ID: 13335312
[No Abstract] [Full Text] [Related]
7. [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]
8. 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]
9. [The hypotonic child].
WALTON JN
Acta Paediatr Belg; 1958; 12(4):141-50. PubMed ID: 13626584
[No Abstract] [Full Text] [Related]
10. 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]
11. [Myatonia congenita Oppenheim, with special reference to its relation to Werdnig-Hoffmann disease].
FUKUYAMA Y
Sogo Igaku; 1961 Oct; 18():671-82. PubMed ID: 13895848
[No Abstract] [Full Text] [Related]
12. [Urinary amino acids in progressive muscular dystrophy and amyotonia congenita].
BAUZA C
Arch Pediatr Urug; 1959 Dec; 30():749-55. PubMed ID: 13797772
[No Abstract] [Full Text] [Related]
13. [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]
14. [A case of infantile muscular atrophy (amyotonia congenita) with hyperplasia of the pituitary eosinophilic cells].
SALAS M; ESPARZA H
Bol Med Hosp Infant Mex; 1960 Aug; 17():637-47. PubMed ID: 13745560
[No Abstract] [Full Text] [Related]
15. Amyotonia congenita syndrome, with the report of a case of Werdnig-Hoffmann disease.
SINGH R; PRASAD R; MATHUR GP; KALRA K
Indian J Pediatr; 1963 Apr; 30():118-21. PubMed ID: 13977661
[No Abstract] [Full Text] [Related]
16. Amyotonia congenita.
Bennett EJ; Dalal FY; Schmidt GB
Middle East J Anaesthesiol; 1974 Jun; 4(2):111-7. PubMed ID: 4480604
[No Abstract] [Full Text] [Related]
17. Studies in disorders of muscle. IX. Glycogen storage disease primarily affecting skeletal muscle and clinically resembling amyotonia congenita.
KRIVIT W; POLGLASE WJ; GUNN FD; TYLER FH
Pediatrics; 1953 Aug; 12(2):165-77. PubMed ID: 13088189
[No Abstract] [Full Text] [Related]
18. ELECTROMYOGRAM IN THE DIFFERENTIAL DIAGNOSIS OF THE "FLOPPY" INFANT.
MARINACCI AA
Bull Los Angel Neuro Soc; 1964 Jun; 29():70-5. PubMed ID: 14169954
[No Abstract] [Full Text] [Related]
19. [Oppenheim-Werdnig-Hoffmann disease].
FULLADOSA A; MAGGI R
Arch Pediatr Urug; 1962 Oct; 33():654-5. PubMed ID: 13960221
[No Abstract] [Full Text] [Related]
20. Muscular hypotonia in infancy; diagnosis and differentiation.
ZELLWEGER HU; SMITH JW; CUSMINSKY M
Rev Can Biol; 1962; 21():599-612. PubMed ID: 14003443
[No Abstract] [Full Text] [Related]
[Next] [New Search]
