298 related articles for article (PubMed ID: 9005874)
1. Adult-onset Krabbe's disease in siblings with novel mutations in the galactocerebrosidase gene.
Bernardini GL; Herrera DG; Carson D; DeGasperi R; Gama Sosa MA; Kolodny EH; Trifiletti R
Ann Neurol; 1997 Jan; 41(1):111-4. PubMed ID: 9005874
[TBL] [Abstract][Full Text] [Related]
2. Molecular basis of globoid cell leukodystrophy in Irish setters.
McGraw RA; Carmichael KP
Vet J; 2006 Mar; 171(2):370-2. PubMed ID: 16490723
[TBL] [Abstract][Full Text] [Related]
3. Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging.
Bajaj NP; Waldman A; Orrell R; Wood NW; Bhatia KP
J Neurol Neurosurg Psychiatry; 2002 May; 72(5):635-8. PubMed ID: 11971051
[TBL] [Abstract][Full Text] [Related]
4. Generation of a mouse with low galactocerebrosidase activity by gene targeting: a new model of globoid cell leukodystrophy (Krabbe disease).
Luzi P; Rafi MA; Zaka M; Curtis M; Vanier MT; Wenger DA
Mol Genet Metab; 2001 Jul; 73(3):211-23. PubMed ID: 11461188
[TBL] [Abstract][Full Text] [Related]
5. Globoid cell leukodystrophy (Krabbe's disease): update.
Suzuki K
J Child Neurol; 2003 Sep; 18(9):595-603. PubMed ID: 14572137
[TBL] [Abstract][Full Text] [Related]
6. Genetic galactocerebrosidase deficiency (globoid cell leukodystrophy, Krabbe disease) in rhesus monkeys (Macaca mulatta).
Baskin GB; Ratterree M; Davison BB; Falkenstein KP; Clarke MR; England JD; Vanier MT; Luzi P; Rafi MA; Wenger DA
Lab Anim Sci; 1998 Oct; 48(5):476-82. PubMed ID: 10090061
[TBL] [Abstract][Full Text] [Related]
7. Multiple mutations in the GALC gene in a patient with adult-onset Krabbe disease.
Luzi P; Rafi MA; Wenger DA
Ann Neurol; 1996 Jul; 40(1):116-9. PubMed ID: 8687180
[TBL] [Abstract][Full Text] [Related]
8. A single mutation in the GALC gene is responsible for the majority of late onset Krabbe disease patients in the Catania (Sicily, Italy) region.
Lissens W; Arena A; Seneca S; Rafi M; Sorge G; Liebaers I; Wenger D; Fiumara A
Hum Mutat; 2007 Jul; 28(7):742. PubMed ID: 17579360
[TBL] [Abstract][Full Text] [Related]
9. Molecular genetics of Krabbe disease (globoid cell leukodystrophy): diagnostic and clinical implications.
Wenger DA; Rafi MA; Luzi P
Hum Mutat; 1997; 10(4):268-79. PubMed ID: 9338580
[TBL] [Abstract][Full Text] [Related]
10. Isolated pyramidal tract impairment in the central nervous system of adult-onset Krabbe disease with novel mutations in the GALC gene.
Tokushige S; Sonoo T; Maekawa R; Shirota Y; Hanajima R; Terao Y; Matsumoto H; Hossain MA; Sakai N; Shiio Y
Brain Dev; 2013 Jun; 35(6):579-81. PubMed ID: 22959700
[TBL] [Abstract][Full Text] [Related]
11. Molecular basis of late-life globoid cell leukodystrophy.
De Gasperi R; Gama Sosa MA; Sartorato E; Battistini S; Raghavan S; Kolodny EH
Hum Mutat; 1999; 14(3):256-62. PubMed ID: 10477434
[TBL] [Abstract][Full Text] [Related]
12. [Isolated spastic paraparesis disclosing Krabbe disease in adult age].
Bataillard M; Richard P; Rumbach L; Vanier MT; Truttmann M
Rev Neurol (Paris); 1997 Jun; 153(5):347-50. PubMed ID: 9296171
[TBL] [Abstract][Full Text] [Related]
13. Late-onset globoid cell leucodystrophy (Krabbe's disease). Clinical and genetic delineation of two forms and their relation to the early-infantile form.
Loonen MC; Van Diggelen OP; Janse HC; Kleijer WJ; Arts WF
Neuropediatrics; 1985 Aug; 16(3):137-42. PubMed ID: 4047347
[TBL] [Abstract][Full Text] [Related]
14. AAV-mediated expression of galactocerebrosidase in brain results in attenuated symptoms and extended life span in murine models of globoid cell leukodystrophy.
Rafi MA; Zhi Rao H; Passini MA; Curtis M; Vanier MT; Zaka M; Luzi P; Wolfe JH; Wenger DA
Mol Ther; 2005 May; 11(5):734-44. PubMed ID: 15851012
[TBL] [Abstract][Full Text] [Related]
15. Beyond Krabbe's disease: The potential contribution of galactosylceramidase deficiency to neuronal vulnerability in late-onset synucleinopathies.
Marshall MS; Bongarzone ER
J Neurosci Res; 2016 Nov; 94(11):1328-32. PubMed ID: 27638614
[TBL] [Abstract][Full Text] [Related]
16. [Biochemical diagnosis of globoid cell leukodystrophy (Krabbe's disease)].
Tsvetkova IV; Zolotukhina TV; Rozenfel'd RA
Vopr Med Khim; 1985; 31(2):128-30. PubMed ID: 2860752
[TBL] [Abstract][Full Text] [Related]
17. Krabbe's disease (globoid cell leukodystrophy): report of the first family in Thailand.
Chiemchanya S; Visudhiphan P; Chiuahriun S
J Med Assoc Thai; 1976 Dec; 59(12):567-70. PubMed ID: 1010968
[No Abstract] [Full Text] [Related]
18. [Krabbe's disease--globoid cell leukodystrophy].
Andersen JB
Ugeskr Laeger; 1997 Feb; 159(7):927-32. PubMed ID: 9054082
[TBL] [Abstract][Full Text] [Related]
19. Pathogenesis of leukodystrophy for Krabbe disease: molecular mechanism and clinical treatment.
Sakai N
Brain Dev; 2009 Aug; 31(7):485-7. PubMed ID: 19332366
[TBL] [Abstract][Full Text] [Related]
20. Somatic cell genetic analysis of the galactocerebrosidase gene: lack of complementation in human Krabbe disease/twitcher mouse cell hybrids.
Skiba MC; Lyerla TA; Konola JT; Raghavan S
J Neurosci Res; 1990 Dec; 27(4):472-8. PubMed ID: 2079710
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
