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23. Suppression of galactosylceramidase (GALC) expression in the twitcher mouse model of globoid cell leukodystrophy (GLD) is caused by nonsense-mediated mRNA decay (NMD). Lee WC; Tsoi YK; Dickey CA; Delucia MW; Dickson DW; Eckman CB Neurobiol Dis; 2006 Aug; 23(2):273-80. PubMed ID: 16759875 [TBL] [Abstract][Full Text] [Related]
24. 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]
25. [From gene to disease; Krabbe disease and galactosylceramidase deficiency]. Kleijer WJ; van Diggelen OP; Halley DJ; van der Ploeg AT; Mancini GM Ned Tijdschr Geneeskd; 2004 Apr; 148(17):826-8. PubMed ID: 15141649 [TBL] [Abstract][Full Text] [Related]
26. Globoid cell leukodystrophy: a family with both late-infantile and adult type. Verdru P; Lammens M; Dom R; Van Elsen A; Carton H Neurology; 1991 Sep; 41(9):1382-4. PubMed ID: 1891085 [TBL] [Abstract][Full Text] [Related]
27. Metabolism of cerebroside sulfate and subcellular distribution of its metabolites in cultured skin fibroblasts from controls, metachromatic leukodystrophy, and globoid cell leukodystrophy. Inui K; Furukawa M; Okada S; Yabuuchi H J Clin Invest; 1988 Feb; 81(2):310-7. PubMed ID: 3339122 [TBL] [Abstract][Full Text] [Related]
28. [Use of fluorescence-labelled cerebroside as a substrate for galactosylceramidase of human skin fibroblasts]. Semeniuk EP; Vidershaĭn GIa Biokhimiia; 1984 Sep; 49(9):1556-60. PubMed ID: 6549145 [TBL] [Abstract][Full Text] [Related]
32. Chemical pathology of krabbe's disease. IV. Studies of galactosylceramide and lactosylceramide BETA-galactosidases in brain, white blood cells and aminotic fluid cells. Svennerholm L; Häkansson G; Vanier MT Acta Paediatr Scand; 1975 Jul; 64(4):649-56. PubMed ID: 1155085 [TBL] [Abstract][Full Text] [Related]
33. Detection of Krabbe disease using tritiated galactosylceramides with medium-chain fatty acids. Parvathy MR; Ben-Yoseph Y; Mitchell DA; Nadler HL J Lab Clin Med; 1987 Dec; 110(6):740-6. PubMed ID: 3681116 [TBL] [Abstract][Full Text] [Related]
34. Krabbe disease--a case report. Roy P; Chidambaranathan S; Ramesh S J Indian Med Assoc; 2005 Oct; 103(10):548-50. PubMed ID: 16498763 [TBL] [Abstract][Full Text] [Related]
35. A case of late variant form of infantile Krabbe disease with a partial deficiency of galactocerebrosidase. Okada S; Kato T; Tanaka H; Takada K; Aramitsu Y Brain Dev; 1988; 10(1):45-6. PubMed ID: 3369670 [TBL] [Abstract][Full Text] [Related]
36. 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]
37. Infantile globoid cell leucodystrophy (Krabbe's disease). Some remarks on clinical, biochemical and sural nerve biopsy findings. Joosten EM; Krijgsman JB; Gabreëls-Festen AA; Gabreëels FJ; Baars PE Neuropadiatrie; 1974 May; 5(2):191-209. PubMed ID: 4407759 [No Abstract] [Full Text] [Related]
39. Use of a fluorescent analogue of galactocerebroside for assay of galactocerebroside beta-galactosidase activity in skin fibroblasts from patients with Krabbe's disease. Okada S; Kato T; Yabuuchi H; Yoshino K; Naoi M; Kiuchi K; Yagi K Clin Chim Acta; 1984 Jan; 136(1):57-63. PubMed ID: 6692566 [TBL] [Abstract][Full Text] [Related]