Detalhe da pesquisa
1.
Non-Ceruloplasmin Copper Identifies a Subtype of Alzheimer's Disease (CuAD): Characterization of the Cognitive Profile and Case of a CuAD Patient Carrying an RGS7 Stop-Loss Variant.
Int J Mol Sci
; 24(7)2023 Mar 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-37047347
2.
Explorative genetic association study of GSTT2B copy number variant in complex disease risks.
Ann Hum Biol
; 43(3): 279-84, 2016 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-26207597
3.
Altered metal metabolism in patients with HCV-related cirrhosis and hepatic encephalopathy.
Metab Brain Dis
; 30(6): 1445-52, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26307419
4.
In silico investigation of the ATP7B gene: insights from functional prediction of non-synonymous substitution to protein structure.
Biometals
; 27(1): 53-64, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24253677
5.
Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer's Disease: a Genetic Study of ATP7B Frequency.
Mol Neurobiol
; 54(1): 671-681, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26758278
6.
Association Between Serum Ceruloplasmin Specific Activity and Risk of Alzheimer's Disease.
J Alzheimers Dis
; 50(4): 1181-9, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26836154
7.
Meta-analysis study on the role of bone-derived neurotrophic factor Val66Met polymorphism in Parkinson's disease.
Rejuvenation Res
; 18(1): 40-7, 2015 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-25431370
8.
Zinc in Alzheimer's Disease: A Meta-Analysis of Serum, Plasma, and Cerebrospinal Fluid Studies.
J Alzheimers Dis
; 46(1): 75-87, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25697706
9.
Val66Met BDNF gene polymorphism influences human motor cortex plasticity in acute stroke.
Brain Stimul
; 8(1): 92-6, 2015.
Artigo
em Inglês
| MEDLINE | ID: mdl-25241287
10.
Intronic rs2147363 variant in ATP7B transcription factor-binding site associated with Alzheimer's disease.
J Alzheimers Dis
; 37(2): 453-9, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23948886
11.
Linkage disequilibrium and haplotype analysis of the ATP7B gene in Alzheimer's disease.
Rejuvenation Res
; 16(1): 3-10, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22950421
12.
Fe and Cu do not differ in Parkinson's disease: a replication study plus meta-analysis.
Neurobiol Aging
; 34(2): 632-3, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22738721
13.
ATP7B variants as modulators of copper dyshomeostasis in Alzheimer's disease.
Neuromolecular Med
; 15(3): 515-22, 2013 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-23760784
14.
Copper in Alzheimer's disease: a meta-analysis of serum, plasma, and cerebrospinal fluid studies.
J Alzheimers Dis
; 30(4): 981-4, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22475798
15.
Association of K832R and R952K SNPs of Wilson's disease gene with Alzheimer's disease.
J Alzheimers Dis
; 29(4): 913-9, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22356903
16.
Erratum to: Non-Ceruloplasmin Copper Distincts Subtypes in Alzheimer's Disease: a Genetic Study of ATP7B Frequency.
Mol Neurobiol
; 54(1): 682-683, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26819212
17.
Effects of hemochromatosis and transferrin gene mutations on iron dyshomeostasis, liver dysfunction and on the risk of Alzheimer's disease.
Neurobiol Aging
; 33(8): 1633-41, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-21514009
18.
Copper in Alzheimer's disease: a meta-analysis of serum,plasma, and cerebrospinal fluid studies.
J Alzheimers Dis
; 24(1): 175-85, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21187586
19.
Association between the c. 2495 A>G ATP7B Polymorphism and Sporadic Alzheimer's Disease.
Int J Alzheimers Dis
; 2011: 973692, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21760992
20.
Copper status abnormalities and how to measure them in neurodegenerative disorders.
Recent Pat CNS Drug Discov
; 5(3): 182-94, 2010 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-20726837