276 related articles for article (PubMed ID: 13312732)
1. 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]
2. [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]
3. [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]
4. [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]
5. Limb-girdle muscular dystrophy or spinal muscular atrophy: a source of diagnostic confusion?
Pogue R; Jackson T; Sayli B; Curtis A; Bushby KM
J Med Genet; 1997 Nov; 34(11):958-9. PubMed ID: 9391899
[No Abstract] [Full Text] [Related]
6. Infantile progressive muscular atrophy; value of muscle biopsy in the diagnosis of and its differentiation from muscular dystrophy.
ROSENBERG HS; McADAMS AJ
AMA Arch Pathol; 1954 Dec; 58(6):604-12. PubMed ID: 13217576
[No Abstract] [Full Text] [Related]
7. Differentiation of Becker muscular dystrophy from limb-girdle muscular dystrophy and Kugelberg-Welander disease using a cDNA probe.
Laing NG; Mears ME; Thomas HE; Chandler DC; Layton MG; Goldblatt J; Kakulas BA
Med J Aust; 1990 Mar; 152(5):270-1. PubMed ID: 2255288
[TBL] [Abstract][Full Text] [Related]
8. [Histopathology of precocious infantile myopathy].
LEY RA
Schweiz Arch Neurol Psychiatr; 1954; 73(1-2):490-2. PubMed ID: 13195597
[No Abstract] [Full Text] [Related]
9. 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]
10. [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]
11. [Incidence of spinal muscular atrophy and Duchenne's muscular dystrophy in the juvenile population of central Slovakia].
Kvasnicová M; Styková J; Hudec P
Bratisl Lek Listy; 1994 Feb; 95(2):78-82. PubMed ID: 7922631
[TBL] [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. Spinal and bulbar muscular atrophy without tongue atrophy.
Sugawara M; Kato K; Watanabe S; Toyoshima I
Eur Neurol; 2001; 45(3):185-6. PubMed ID: 11306865
[No Abstract] [Full Text] [Related]
14. [A CASE OF PROXIMAL SPINAL MUSCULAR ATROPHY SIMULATING MUSCULAR DYSTROPHY].
OTSUKI S; TERAO A; YOKOYAMA S; SHIRAHIGE I
No To Shinkei; 1963 Oct; 15():917-23. PubMed ID: 14052947
[No Abstract] [Full Text] [Related]
15. Muscular dystrophy or spinal muscular atrophy?
Topaloglu H; Renda Y; Kale G; Gucuyener K
Lancet; 1989 Apr; 1(8644):960-1. PubMed ID: 2565450
[No Abstract] [Full Text] [Related]
16. Spinal muscular atrophy: some easy clues to diagnosis.
Gupta PC; Ahuja B; Dhamija K; Mullick DN
Indian Pediatr; 1989 Oct; 26(10):977-80. PubMed ID: 2630460
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. Hereditary proximal spinal muscular atrophy, a clinical entity simulating progressive muscular dystrophy.
WOHLFART G; FEX J; ELIASSON S
Acta Psychiatr Neurol Scand; 1955; 30(1-2):395-406. PubMed ID: 13301901
[No Abstract] [Full Text] [Related]
20. [Plasma alpha/beta lipoprotein coefficient in the diagnosis of progressive muscular dystrophy].
Islamova IB
Lab Delo; 1989; (10):34-5. PubMed ID: 2481069
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
