Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal.
about
Multicenter analysis of glucocerebrosidase mutations in Parkinson's disease.Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's diseaseThe relationship between glucocerebrosidase mutations and Parkinson diseaseLoss of β-glucocerebrosidase activity does not affect alpha-synuclein levels or lysosomal function in neuronal cellsGenetic susceptibility in Parkinson's diseaseGreater risk of parkinsonism associated with non-N370S GBA1 mutationsThe risk of Parkinson's disease in type 1 Gaucher disease.Gaucher disease ascertained through a Parkinson's center: imaging and clinical characterization.Gaucher disease: insights from a rare Mendelian disorder.Glucocerebrosidase mutations are not a common risk factor for Parkinson disease in North Africa.The glucocerobrosidase E326K variant predisposes to Parkinson's disease, but does not cause Gaucher's disease.Glucocerebrosidase mutations in primary parkinsonismThe genetic background of Parkinson's disease: current progress and future prospects.Glucocerebrosidase gene mutations associated with Parkinson's disease: a meta-analysis in a Chinese populationDifferential effects of severe vs mild GBA mutations on Parkinson disease.Progressive decline of glucocerebrosidase in aging and Parkinson's disease.Exploring the link between glucocerebrosidase mutations and parkinsonismGlucocerebrosidase is present in α-synuclein inclusions in Lewy body disorders.Glucocerebrosidase activity in Parkinson's disease with and without GBA mutationsGBA Variants Influence Motor and Non-Motor Features of Parkinson's Disease.Age-specific Parkinson disease risk in GBA mutation carriers: information for genetic counselingThe role of glucocerebrosidase mutations in Parkinson disease and Lewy body disordersGlucocerebrosidase L444P mutation confers genetic risk for Parkinson's disease in central ChinaTranscranial sonography and functional imaging in glucocerebrosidase mutation Parkinson diseaseEmerging pathways in genetic Parkinson's disease: Potential role of ceramide metabolism in Lewy body disease.The association between mutations in the lysosomal protein glucocerebrosidase and parkinsonismA multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies.Glucocerebrosidase involvement in Parkinson disease and other synucleinopathies.α-Synuclein and mitochondrial dysfunction in Parkinson's disease.Mutations in GBA and risk of Parkinson's disease: a meta-analysis based on 25 case-control studies.The association between ß-glucocerebrosidase mutations and parkinsonismParkinson's disease: from genetics to clinical practice.Genetic convergence of Parkinson's disease and lysosomal storage disorders.Association of GBA Mutations and the E326K Polymorphism With Motor and Cognitive Progression in Parkinson Disease.Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.Association of the glucocerebrosidase N370S allele with Parkinson's disease in two separate Chinese Han populations of mainland China.Integrated Genetic Analysis of Racial Differences of Common GBA Variants in Parkinson's Disease: A Meta-Analysis.The Association between E326K of GBA and the Risk of Parkinson's Disease.
P2860
Q24634577-E4FF711B-2E0E-410C-AD03-C7C75B3787FCQ24656668-382CAA2F-667F-4273-BD9F-A89AE62B834BQ28077257-02384100-A8A6-4466-8A18-D8DD590BD531Q28118642-C3E303C5-8F61-4DA4-9F76-FE7D26CE9DF3Q30435626-EA6BA82A-1A0C-48C0-BD67-C4CBB548AE04Q33916685-B56BA80C-0501-4097-A63A-634DCB92DD26Q33919614-B0999198-EC20-4340-92F2-E27E578400EDQ34037141-A0E5A6B8-2D79-4FAF-A09B-E4FDA1C8344DQ34077331-48EF08B7-FAB8-4640-B316-4A54746B69BEQ34267725-5F735F9C-4C21-4C67-9DF9-AA92EC963187Q34398442-8E02A69F-7600-4EB1-ADBC-86F4A00F99AFQ34491177-5AAF500F-8F26-4ABF-9515-F35FAB8C2672Q34513714-6EBB28CD-1A84-4A26-90C4-9D8FF3368BB5Q34764825-42514F1C-A81F-402A-A9B9-519C1FD75455Q35153677-DFDE78FB-CB12-4441-B342-C0E91A32A4CFQ35469684-B6DB64FB-E323-4AC1-B332-AB96150A8547Q35955350-D6959E3D-DF51-4170-8E91-471B18B24ECCQ35960413-6106A172-0F90-4ADE-842D-933C317A35D4Q36041420-1AFC98E3-3656-40F3-9A24-205801A4D1F2Q36234536-7D74DAFC-E022-4EBE-88AA-C71E7F468C70Q36460324-C620058A-F540-440A-8610-C9C87AF6F856Q36486264-B742E703-EA79-4944-BAA4-6E2D70EF0C76Q36513434-B7162E2C-B47E-4185-AA89-96A407EFA1ACQ36595145-CFD88774-EF06-4C77-BD32-F214F28DB348Q37105393-5816A449-F9F7-4BFA-8600-6271BCF7AAE1Q37329304-FD08212D-F0D9-4490-9553-14D88F196A6CQ37346468-F070DF32-2BBB-4382-95EB-11292D769969Q38007465-F252120A-C466-49ED-AC5C-FAB2E525DB44Q38077665-A5A90620-FF56-4488-88CB-21027044A08FQ38107046-529E26B1-A575-4471-B952-B2DD19A4305EQ38118169-FEA1B4FA-18CC-465B-BE90-2DB09ED6D2D7Q38188556-B8E13292-47C1-413E-9CE4-1372B9043649Q38237560-3C6F8BF1-95AC-48A7-9DC1-A0EB41D49882Q40603461-B6503F85-D2A1-4475-AE1B-2C6D70C5BA63Q41677841-3190C053-33A5-47E6-BEC7-0D4F244B3926Q54425209-795CD42D-8110-4BE2-98D9-7FC368E6B481Q55056377-D0D5D0C2-8B1E-48DB-B40C-D1EC5682A020Q55431262-DFE519ED-F14E-4F2B-B324-4819EEBF29E3
P2860
Complete screening for glucocerebrosidase mutations in Parkinson disease patients from Portugal.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 21 December 2007
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Complete screening for glucoce ...... isease patients from Portugal.
@en
Complete screening for glucoce ...... isease patients from Portugal.
@nl
type
label
Complete screening for glucoce ...... isease patients from Portugal.
@en
Complete screening for glucoce ...... isease patients from Portugal.
@nl
prefLabel
Complete screening for glucoce ...... isease patients from Portugal.
@en
Complete screening for glucoce ...... isease patients from Portugal.
@nl
P2093
P2860
P50
P921
P1476
Complete screening for glucoce ...... isease patients from Portugal.
@en
P2093
Ana Morgadinho
Cristina Januario
Ellen Sidransky
Maria Helena Ribeiro
P2860
P304
P356
10.1016/J.NEUROBIOLAGING.2007.11.016
P577
2007-12-21T00:00:00Z