126 related articles for article (PubMed ID: 10888370)
1. Ultrastructural analysis and TUNEL demonstrate motor neuron apoptosis in Werdnig-Hoffmann disease.
Simic G; Seso-Simic D; Lucassen PJ; Islam A; Krsnik Z; Cviko A; Jelasic D; Barisic N; Winblad B; Kostovic I; Kruslin B
J Neuropathol Exp Neurol; 2000 May; 59(5):398-407. PubMed ID: 10888370
[TBL] [Abstract][Full Text] [Related]
2. Aberrant glycosylation/phosphorylation in chromatolytic motoneurons of Werdnig-Hoffmann disease.
Chou SM; Wang HS
J Neurol Sci; 1997 Nov; 152(2):198-209. PubMed ID: 9415542
[TBL] [Abstract][Full Text] [Related]
3. A study of cell death in Werdnig Hoffmann disease brain.
Hayashi M; Arai N; Murakami T; Yoshio M; Oda M; Matsuyama H
Neurosci Lett; 1998 Feb; 243(1-3):117-20. PubMed ID: 9535127
[TBL] [Abstract][Full Text] [Related]
4. Adult-onset motor neuron disease and infantile Werdnig-Hoffmann disease (spinal muscular atrophy type 1) in the same family.
Shaw PJ; Ince PG; Goodship J; Burn J; Slade J; Bates D; Medwin DG
Neurology; 1992 Aug; 42(8):1477-80. PubMed ID: 1641139
[TBL] [Abstract][Full Text] [Related]
5. Neuropathological analysis in spinal muscular atrophy type II.
Araki S; Hayashi M; Tamagawa K; Saito M; Kato S; Komori T; Sakakihara Y; Mizutani T; Oda M
Acta Neuropathol; 2003 Nov; 106(5):441-8. PubMed ID: 12898156
[TBL] [Abstract][Full Text] [Related]
6. Downregulation of Bcl-2 proteins in type I spinal muscular atrophy motor neurons during fetal development.
Soler-Botija C; Ferrer I; Alvarez JL; Baiget M; Tizzano EF
J Neuropathol Exp Neurol; 2003 Apr; 62(4):420-6. PubMed ID: 12722834
[TBL] [Abstract][Full Text] [Related]
7. Is Werdnig-Hoffmann disease a pure lower motor neuron disorder?
Towfighi J; Young RS; Ward RM
Acta Neuropathol; 1985; 65(3-4):270-80. PubMed ID: 3976363
[TBL] [Abstract][Full Text] [Related]
8. Large-scale deletions in a Chinese infant associated with a variant form of Werdnig-Hoffmann disease.
Jong YJ; Chang JG; Wu JR
Neurology; 1998 Sep; 51(3):878-9. PubMed ID: 9748047
[TBL] [Abstract][Full Text] [Related]
9. Neuronal death is enhanced and begins during foetal development in type I spinal muscular atrophy spinal cord.
Soler-Botija C; Ferrer I; Gich I; Baiget M; Tizzano EF
Brain; 2002 Jul; 125(Pt 7):1624-34. PubMed ID: 12077011
[TBL] [Abstract][Full Text] [Related]
10. Molecular analysis of candidate genes on chromosome 5q13 in autosomal recessive spinal muscular atrophy: evidence of homozygous deletions of the SMN gene in unaffected individuals.
Hahnen E; Forkert R; Marke C; Rudnik-Schöneborn S; Schönling J; Zerres K; Wirth B
Hum Mol Genet; 1995 Oct; 4(10):1927-33. PubMed ID: 8595417
[TBL] [Abstract][Full Text] [Related]
11. [Motor neuron diseases: a type of programmed cell death?].
Ferrer I
Neurologia; 1996 Dec; 11 Suppl 5():7-13. PubMed ID: 9044576
[TBL] [Abstract][Full Text] [Related]
12. Spinal Muscular Atrophy: Autopsy Based Neuropathological Demonstration.
Thirunavukkarasu B; Gupta K; Bansal A; Dhanasekaran N; Baranwal A
Neurol India; 2020; 68(4):882-885. PubMed ID: 32859833
[TBL] [Abstract][Full Text] [Related]
13. Abnormal motoneuron migration, differentiation, and axon outgrowth in spinal muscular atrophy.
Simic G; Mladinov M; Seso Simic D; Jovanov Milosevic N; Islam A; Pajtak A; Barisic N; Sertic J; Lucassen PJ; Hof PR; Kruslin B
Acta Neuropathol; 2008 Mar; 115(3):313-26. PubMed ID: 18075747
[TBL] [Abstract][Full Text] [Related]
14. Axonal neuropathy and predominance of type II myofibers in infantile spinal muscular atrophy.
Omran H; Ketelsen UP; Heinen F; Sauer M; Rudnik-Schöneborn S; Wirth B; Zerres K; Kratzer W; Korinthenberg R
J Child Neurol; 1998 Jul; 13(7):327-31. PubMed ID: 9701481
[TBL] [Abstract][Full Text] [Related]
15. Proximal and distal motor nerve conduction velocities in Werdnig-Hoffmann disease.
Imai T; Minami R; Nagaoka M; Ishikawa Y; Kameda K; Okabe M; Matsumoto H
Pediatr Neurol; 1990; 6(2):82-6. PubMed ID: 2340034
[TBL] [Abstract][Full Text] [Related]
16. Cytochrome c oxidase deficiency due to a novel SCO2 mutation mimics Werdnig-Hoffmann disease.
Salviati L; Sacconi S; Rasalan MM; Kronn DF; Braun A; Canoll P; Davidson M; Shanske S; Bonilla E; Hays AP; Schon EA; DiMauro S
Arch Neurol; 2002 May; 59(5):862-5. PubMed ID: 12020273
[TBL] [Abstract][Full Text] [Related]
17. Prenatal diagnosis of spinal muscular atrophy type I (Werdnig- hoffmann) by DNA deletion analysis of cultivated amniocytes.
Stipoljev F; Sertić J; Latin V; Rukavina-Stavljenić A; Kurjak A
Croat Med J; 1999 Sep; 40(3):433-7. PubMed ID: 10411975
[TBL] [Abstract][Full Text] [Related]
18. Chronic treatment with lithium does not improve neuromuscular phenotype in a mouse model of severe spinal muscular atrophy.
Dachs E; Piedrafita L; Hereu M; Esquerda JE; Calderó J
Neuroscience; 2013 Oct; 250():417-33. PubMed ID: 23876328
[TBL] [Abstract][Full Text] [Related]
19. Synaptophysin expression in the anterior horn of Werdnig-Hoffmann disease.
Ikemoto A; Hirano A; Matsumoto S; Akiguchi I; Kimura J
J Neurol Sci; 1996 Mar; 136(1-2):94-100. PubMed ID: 8815186
[TBL] [Abstract][Full Text] [Related]
20. Infantile progressive spinal muscular atrophy with ophthalmoplegia and pyramidal symptoms.
Hamano K; Tsukamoto H; Yazawa T; Yoshimura M; Takita H
Pediatr Neurol; 1994 Jun; 10(4):320-4. PubMed ID: 8068160
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
