26 related articles for article (PubMed ID: 7416238)
1. S100B protein and 4-hydroxynonenal in the spinal cord of wobbler mice.
Corvino V; Businaro R; Geloso MC; Bigini P; Cavallo V; Pompili E; Mennini T; Fumagalli L; Michetti F
Neurochem Res; 2003 Feb; 28(2):341-5. PubMed ID: 12608707
[TBL] [Abstract][Full Text] [Related]
2. Neuron volume in the ventral horn in Wobbler mouse motoneuron disease: a light microscope stereological study.
Dockery P; Tang Y; Morais M; Vacca-Galloway LL
J Anat; 1997 Jul; 191 ( Pt 1)(Pt 1):89-98. PubMed ID: 9279662
[TBL] [Abstract][Full Text] [Related]
3. [A case of Werdnig-Hoffmann disease in a newborn infant].
Guarniere J; Inferrera C; Di Prima C; Barresi G
Pediatria (Napoli); 1977 Dec; 85(4):625-44. PubMed ID: 349495
[No Abstract] [Full Text] [Related]
4. Echocardiography in neurological disorders.
Lintermans JP
Eur J Pediatr; 1987 Jan; 146(1):15-20. PubMed ID: 3556183
[TBL] [Abstract][Full Text] [Related]
5. Animal model of human disease: Werdnig-Hoffmann disease (infantile spinal muscular atrophy).
Leestma JE
Am J Pathol; 1980 Sep; 100(3):821-4. PubMed ID: 7416238
[No Abstract] [Full Text] [Related]
6. [Infantile progressive spinal muscular atrophy. Werdnig-Hoffmann disease].
Mohr W; Olischläger A; Carl H
Med Welt; 1971 Aug; 35():1317-9. PubMed ID: 5564452
[No Abstract] [Full Text] [Related]
7. Animal model of human disease. Infantile spinal muscular atrophy, Werdnig-Hoffman disease. Animal model: Hereditary neuronal abiotrophy in Swedish Lapland dogs.
Sandefeldt E; Cummings JF; de Lahunta A; Björck G; Krook LP
Am J Pathol; 1976 Mar; 82(3):649-52. PubMed ID: 1258980
[No Abstract] [Full Text] [Related]
8. [Histopathology of neuromuscular and intramuscular nerve fibers in patients with Werdnig-Hoffmann infantile spinal amyotrophy].
Cazzato G; Dall'Olio G
Acta Neurol (Napoli); 1969; 24(2):208-19. PubMed ID: 4247846
[No Abstract] [Full Text] [Related]
9. [Progressive muscular spinal atrophy of Werdnig-Hoffmann].
Galimberti A; Graziano L; Airò R
Folia Hered Pathol (Milano); 1968; ():113-26. PubMed ID: 5760545
[No Abstract] [Full Text] [Related]
10. Acute Werdnig-Hoffmann disease: acute infantile spinal muscular atrophy.
Pearn JH; Wilson J
Arch Dis Child; 1973 Jun; 48(6):425-30. PubMed ID: 4712772
[TBL] [Abstract][Full Text] [Related]
11. Sperm tail axoneme alterations in the Wobbler mouse.
Leestma JE; Sepsenwol S
J Reprod Fertil; 1980 Jan; 58(1):267-70. PubMed ID: 7359484
[TBL] [Abstract][Full Text] [Related]
12. An hereditary motor neurone disease with progressive denervation of muscle in the mouse: the mutant 'wobbler'.
Duchen LW; Strich SJ
J Neurol Neurosurg Psychiatry; 1968 Dec; 31(6):535-42. PubMed ID: 5709840
[No Abstract] [Full Text] [Related]
13. Clinical and pathological findings in an unusual infantile motor neurone disease.
Kohn R
J Neurol Neurosurg Psychiatry; 1971 Aug; 34(4):427-31. PubMed ID: 5096555
[TBL] [Abstract][Full Text] [Related]
14. Spinal motor neurones in murine muscular dystrophy and spinal muscular atrophy. A quantitative histological study.
Papapetropoulos TA; Bradley WG
J Neurol Neurosurg Psychiatry; 1972 Feb; 35(1):60-5. PubMed ID: 5026011
[TBL] [Abstract][Full Text] [Related]
15. The wobbler mouse mutant: an animal model of hereditary motor system disease.
Bird MT; Shuttleworth E; Koestner A; Reinglass J
Acta Neuropathol; 1971; 19(1):39-50. PubMed ID: 4107380
[No Abstract] [Full Text] [Related]
16.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
17.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
18.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
19.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]