Format
Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 355

1.

Gaucher's disease: the best laid schemes of mice and men.

Sidransky E, Ginns EI.

Baillieres Clin Haematol. 1997 Dec;10(4):725-37. Review.

PMID:
9497860
2.

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, et al.

Nature. 1992 Jun 4;357(6377):407-10.

PMID:
1594045
3.

Gaucher's disease: clinical features and natural history.

Cox TM, Schofield JP.

Baillieres Clin Haematol. 1997 Dec;10(4):657-89. Review.

PMID:
9497857
4.

Gaucher's disease: a review for the internist and hepatologist.

Niederau C, Häussinger D.

Hepatogastroenterology. 2000 Jul-Aug;47(34):984-97. Review.

PMID:
11020862
5.

Generation of a conditional knockout of murine glucocerebrosidase: utility for the study of Gaucher disease.

Sinclair GB, Jevon G, Colobong KE, Randall DR, Choy FY, Clarke LA.

Mol Genet Metab. 2007 Feb;90(2):148-56. Epub 2006 Oct 31.

PMID:
17079175
6.

Enzymic differentiation of neurologic and nonneurologic forms of Gaucher's disease.

Glew RH, Daniels LB, Clark LS, Hoyer SW.

J Neuropathol Exp Neurol. 1982 Nov;41(6):630-41.

PMID:
6813430
7.

[Gene therapy of Gaucher's and Fabry's diseases: current status and prospects].

Fabrega S, Lehn P.

J Soc Biol. 2002;196(2):175-81. Review. French.

PMID:
12360746
8.

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 5;316(10):570-5.

PMID:
2880291
9.

A case of nonneurologic Gaucher's disease that biochemically resembles the neurologic types.

Glew RH, Gopalan V, Hubbell CA, Beutler E, Geil JD, Lee RE.

J Neuropathol Exp Neurol. 1991 Mar;50(2):108-17.

PMID:
1672707
10.

[Gaucher disease: diagnosis and treatment].

Fumić K, Stavljenić-Rukavina A, Mrsić M, Potocki K.

Acta Med Croatica. 2004;58(5):353-8. Review. Croatian.

PMID:
15756799
11.

Gene transfer and bone marrow transplantation with special reference to Gaucher's disease.

Karlsson S, Correll PH, Xu L.

Bone Marrow Transplant. 1993;11 Suppl 1:124-7.

PMID:
8448536
12.

Genotypic heterogeneity and phenotypic variation among patients with type 2 Gaucher's disease.

Tayebi N, Reissner KJ, Lau EK, Stubblefield BK, Klineburgess AC, Martin BM, Sidransky E.

Pediatr Res. 1998 May;43(5):571-8.

PMID:
9585001
13.

Immunohistochemical and ultrastructural features of Gaucher's cells--five case reports.

Bogoeva B, Petrusevska G.

Acta Med Croatica. 2001;55(3):131-4.

PMID:
11852732
14.

An immunoelectron microscopic study of glucocerebrosidase in type 1 Gaucher's disease spleen.

Willemsen R, van Dongen JM, Aerts JM, Schram AW, Tager JM, Goudsmit R, Reuser AJ.

Ultrastruct Pathol. 1988 Sep-Oct;12(5):471-8.

PMID:
3194992
15.

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.

PMID:
12803123
16.

[Update on Gaucher's disease].

Virgolini L, Silvestri F, Baccarani M.

Minerva Med. 1993 Mar;84(3):81-7. Review. Italian.

PMID:
8492969
17.

Type 2 Gaucher disease with hydrops fetalis in an Ashkenazi Jewish family resulting from a novel recombinant allele and a rare splice junction mutation in the glucocerebrosidase locus.

Reissner K, Tayebi N, Stubblefield BK, Koprivica V, Blitzer M, Holleran W, Cowan T, Almashanu S, Maddalena A, Karson EM, Sidransky E.

Mol Genet Metab. 1998 Apr;63(4):281-8.

PMID:
9635296
18.

Production of glucocerebrosidase with terminal mannose glycans for enzyme replacement therapy of Gaucher's disease using a plant cell system.

Shaaltiel Y, Bartfeld D, Hashmueli S, Baum G, Brill-Almon E, Galili G, Dym O, Boldin-Adamsky SA, Silman I, Sussman JL, Futerman AH, Aviezer D.

Plant Biotechnol J. 2007 Sep;5(5):579-90. Epub 2007 May 24.

19.

Gaucher's disease: studies of gene transfer to haematopoietic cells.

Barranger JA, Rice EO, Dunigan J, Sansieri C, Takiyama N, Beeler M, Lancia J, Lucot S, Scheirer-Fochler S, Mohney T, Swaney W, Bahnson A, Ball E.

Baillieres Clin Haematol. 1997 Dec;10(4):765-78. Review.

PMID:
9497863
20.

[Neurological manifestations of type 1 Gaucher's disease: Is a revision of disease classification needed?].

Chérin P, Sedel F, Mignot C, Schupbach M, Gourfinkel-An I, Verny M, Baumann N.

Rev Neurol (Paris). 2006 Nov;162(11):1076-83. French.

PMID:
17086144

Supplemental Content

Support Center