145 related articles for article (PubMed ID: 4952838)
1. Two early infantile hereditary cases of progressive muscular atrophy simulating dystrophy, but on a neural basis. 1891.
Werdnig G
Arch Neurol; 1971 Sep; 25(3):276-8. PubMed ID: 4952838
[No Abstract] [Full Text] [Related]
2. 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]
3. Heredofamilial juvenile muscular atrophy simulating muscular dystrophy.
KUGELBERG E; WELANDER L
AMA Arch Neurol Psychiatry; 1956 May; 75(5):500-9. PubMed ID: 13312732
[No Abstract] [Full Text] [Related]
4. [Two cases of familial congenital muscular dystrophy simulating Werdnig-Hoffman-Oppenheim disease].
LEVESQUE J; LEPAGE F; BOESWILLWALD M; GRUNER J
Arch Fr Pediatr; 1956; 13(2):202-7. PubMed ID: 13328196
[No Abstract] [Full Text] [Related]
5. [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]
6. [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]
7. 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]
8. 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]
9. 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]
10. [Infantile spinal muscular atrophy : therapeutic (R)evolution].
Daron A; Delstanche S; Dangouloff T; Servais L
Rev Med Liege; 2019 Feb; 74(2):82-85. PubMed ID: 30793560
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. [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]
13. [Usefulness of ECG in the early diagnosis of infantile spinal muscular dystrophy].
Carboni P; Porro G
Minerva Pediatr; 1988 Jun; 40(6):321-5. PubMed ID: 3185431
[No Abstract] [Full Text] [Related]
14. [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]
15. [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]
16. 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]
17. [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]
18. Familial progressive bulbar-spinal muscular atrophy.
MAGEE KR
Neurology; 1960 Mar; 10():295-305. PubMed ID: 14419783
[No Abstract] [Full Text] [Related]
19. [Progressive infantile spinal muscular atrophy. Report of 12 cases].
Fontana MH; Pörtner MR; Salim PA; Bobek PR; Da Roza PR
Arq Neuropsiquiatr; 1990 Mar; 48(1):26-31. PubMed ID: 2378573
[TBL] [Abstract][Full Text] [Related]
20. An early description of monomelic amyotrophy: An excerpt from the diaries of Dr. Charles I Smith (1830-1880) in Bangalore, Southern India.
Jain S
Neurol India; 2017; 65(1):11-13. PubMed ID: 28084229
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
