234 related articles for article (PubMed ID: 24262167)
1. Niemann-Pick's and Gaucher's diseases.
Stern G
Parkinsonism Relat Disord; 2014 Jan; 20 Suppl 1():S143-6. PubMed ID: 24262167
[TBL] [Abstract][Full Text] [Related]
2. Sphingomyelin and glucocerebroside of spleen in cases of Gaucher's and Niemann-Pick's diseases.
Taketomi T; Yamakawa T
Jpn J Exp Med; 1967 Oct; 37(5):505-9. PubMed ID: 5303496
[No Abstract] [Full Text] [Related]
3. Lysosomal trafficking defects link Parkinson's disease with Gaucher's disease.
Wong YC; Krainc D
Mov Disord; 2016 Nov; 31(11):1610-1618. PubMed ID: 27619775
[TBL] [Abstract][Full Text] [Related]
4. Type I Gaucher's disease with homozygous R463C mutation without neurological involvement.
Bolaman Z; Kadikoylu G; Levi E; Barutca S; Temucin K
Haematologia (Budap); 2002; 32(4):487-93. PubMed ID: 12803123
[TBL] [Abstract][Full Text] [Related]
5. A histochemical study of Gaucher's disease and Niemann-Pick's disease.
Lake BD
J R Microsc Soc; 1967 Apr; 86(4):417-25. PubMed ID: 4166487
[No Abstract] [Full Text] [Related]
6. A mutation in the human glucocerebrosidase gene in neuronopathic Gaucher's disease.
Tsuji S; Choudary PV; Martin BM; Stubblefield BK; Mayor JA; Barranger JA; Ginns EI
N Engl J Med; 1987 Mar; 316(10):570-5. PubMed ID: 2880291
[TBL] [Abstract][Full Text] [Related]
7. Emerging links between pediatric lysosomal storage diseases and adult parkinsonism.
Ysselstein D; Shulman JM; Krainc D
Mov Disord; 2019 May; 34(5):614-624. PubMed ID: 30726573
[TBL] [Abstract][Full Text] [Related]
8. [Genetics of Gaucher's disease. Genotype-phenotype correlation].
Alfonso Palacín P; Pocoví M
Med Clin (Barc); 2011 Sep; 137 Suppl 1():17-22. PubMed ID: 22230121
[TBL] [Abstract][Full Text] [Related]
9. Neonatal screening for lysosomal storage disorders: feasibility and incidence from a nationwide study in Austria.
Mechtler TP; Stary S; Metz TF; De Jesús VR; Greber-Platzer S; Pollak A; Herkner KR; Streubel B; Kasper DC
Lancet; 2012 Jan; 379(9813):335-41. PubMed ID: 22133539
[TBL] [Abstract][Full Text] [Related]
10. Gaucher's disease and pregnancy.
Fasouliotis SJ; Ezra Y; Schenker JG
Am J Perinatol; 1998 May; 15(5):311-8. PubMed ID: 9643638
[TBL] [Abstract][Full Text] [Related]
11. Lysosomal storage disorders and Parkinson's disease: Gaucher disease and beyond.
Shachar T; Lo Bianco C; Recchia A; Wiessner C; Raas-Rothschild A; Futerman AH
Mov Disord; 2011 Aug; 26(9):1593-604. PubMed ID: 21618611
[TBL] [Abstract][Full Text] [Related]
12. [Gaucher's disease: pathogenesis, diagnosis and therapy].
Pregun I; Tulassay Z
Orv Hetil; 2004 Sep; 145(37):1883-90. PubMed ID: 15493618
[TBL] [Abstract][Full Text] [Related]
13. Beta-glucocerebrosidase gene locus as a link for Gaucher's disease and familial hypo-alpha-lipoproteinaemia.
Pocovi M; Cenarro A; Civeira F; Torralba MA; Perez-Calvo JI; Mozas P; Giraldo P; Giralt M; Myers RH; Cupples LA; Ordovas JM
Lancet; 1998 Jun; 351(9120):1919-23. PubMed ID: 9654259
[TBL] [Abstract][Full Text] [Related]
14. Impaired trafficking of mutants of lysosomal glucocerebrosidase in Gaucher's disease.
Schmitz M; Alfalah M; Aerts JM; Naim HY; Zimmer KP
Int J Biochem Cell Biol; 2005 Nov; 37(11):2310-20. PubMed ID: 15982918
[TBL] [Abstract][Full Text] [Related]
15. Mutations in the glucocerebrosidase gene and Parkinson's disease in Ashkenazi Jews.
Aharon-Peretz J; Rosenbaum H; Gershoni-Baruch R
N Engl J Med; 2004 Nov; 351(19):1972-7. PubMed ID: 15525722
[TBL] [Abstract][Full Text] [Related]
16. Animal model of Gaucher's disease from targeted disruption of the mouse glucocerebrosidase gene.
Tybulewicz VL; Tremblay ML; LaMarca ME; Willemsen R; Stubblefield BK; Winfield S; Zablocka B; Sidransky E; Martin BM; Huang SP
Nature; 1992 Jun; 357(6377):407-10. PubMed ID: 1594045
[TBL] [Abstract][Full Text] [Related]
17. Measurement of GCase Activity in Cultured Cells.
Shojima Y; Ogata J; Tsunemi T; Imai Y; Hattori N
Methods Mol Biol; 2021; 2322():47-52. PubMed ID: 34043191
[TBL] [Abstract][Full Text] [Related]
18. Parkinson's disease in patients and obligate carriers of Gaucher disease.
Becker JG; Pastores GM; Di Rocco A; Ferraris M; Graber JJ; Sathe S
Parkinsonism Relat Disord; 2013 Jan; 19(1):129-31. PubMed ID: 22940477
[TBL] [Abstract][Full Text] [Related]
19. Do heterozygous mutations of Niemann-Pick type C predispose to late-onset neurodegeneration: a review of the literature.
Schneider SA; Tahirovic S; Hardy J; Strupp M; Bremova-Ertl T
J Neurol; 2021 Jun; 268(6):2055-2064. PubMed ID: 31701332
[TBL] [Abstract][Full Text] [Related]
20. A novel Parkinson's disease risk variant, p. W378R, in the Gaucher's disease GBA gene.
Lubomski M; Hayes M; Kennerson M; Ellis M; Chu S; Blackie J; O'Sullivan JD; Nicholson G
Mov Disord; 2018 Oct; 33(10):1662-1664. PubMed ID: 30216542
[No Abstract] [Full Text] [Related]
[Next] [New Search]
