148 related articles for article (PubMed ID: 13827049)
1. [Interpretation of a familial case of Werdnig-Hoffmann disease].
GEDDA L; ALFIERI A; GENTILE R
Minerva Med; 1959 Dec; 50():4287-93. PubMed ID: 13827049
[No Abstract] [Full Text] [Related]
2. 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]
3. [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]
4. [Oppenheim-Werdnig-Hoffmann disease].
FULLADOSA A; MAGGI R
Arch Pediatr Urug; 1962 Oct; 33():654-5. PubMed ID: 13960221
[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'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]
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. 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]
9. [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]
10. Prenatal prediction of Werdnig-Hoffmann disease using linked polymorphic DNA probes.
Melki J; Abdelhak S; Burlet P; Raclin V; Kaplan J; Spiegel R; Gilgenkrantz S; Philip N; Chauvet ML; Dumez Y
J Med Genet; 1992 Mar; 29(3):171-4. PubMed ID: 1348092
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. [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]
13. [Cerebral agyria-pachygyria in a child with Werdnig-Hoffmann disease].
Cneude F; Sukno S; Boidein F; Dehouck MB; Bourlet A; Vittu G
Rev Neurol (Paris); 1999 Sep; 155(8):589-91. PubMed ID: 10486849
[TBL] [Abstract][Full Text] [Related]
14. [Werdnig-Hoffmann disease].
Perentes E; Donati F
Rev Med Suisse Romande; 1981 Sep; 101(9):685-96. PubMed ID: 7302452
[No Abstract] [Full Text] [Related]
15. Population frequencies of inherited neuromuscular diseases--a world survey.
Emery AE
Neuromuscul Disord; 1991; 1(1):19-29. PubMed ID: 1822774
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. [The men behind the syndrome: Werdnig and Hoffmann. They classified spinal muscular atrophies].
Fogström B; Bui TH
Lakartidningen; 1993 Jan; 90(4):275-6. PubMed ID: 8433609
[No Abstract] [Full Text] [Related]
18. An unusual neurologic problem: Werdnig-Hoffmann disease.
Barden C; Lee R; Parchment Y; Dempsey RM
Crit Care Nurse; 1990; 10(10):60-7. PubMed ID: 2249464
[TBL] [Abstract][Full Text] [Related]
19. Werdnig-Hoffmann disease with congenital hypothyroidism.
Gunes T; Akcakus M; Cetin N; Kurtoğlu S; Kumandaş S
Ann Trop Paediatr; 2003 Dec; 23(4):301-4. PubMed ID: 14738578
[TBL] [Abstract][Full Text] [Related]
20. Werdnig-Hoffmann disease and chronic distal spinal muscular atrophy with apparent autosomal dominant inheritance.
Boylan KB; Cornblath DR
Ann Neurol; 1992 Sep; 32(3):404-7. PubMed ID: 1416812
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
