51 results on '"Hernández, Isabel"'
Search Results
2. Prioritization of Drug Targets for Neurodegenerative Diseases by Integrating Genetic and Proteomic Data From Brain and Blood
3. Predicting Kidney Failure, Cardiovascular Disease and Death in Advanced CKD Patients
4. Genome-wide association analysis of dementia and its clinical endophenotypes reveal novel loci associated with Alzheimer's disease and three causality networks: The GR@ACE project
5. Exploring APOE genotype effects on Alzheimer's disease risk and amyloid β burden in individuals with subjective cognitive decline: The FundacioACE Healthy Brain Initiative (FACEHBI) study baseline results
6. A unique common ancestor introduced P301L mutation in MAPT gene in frontotemporal dementia patients from Barcelona (Baix Llobregat, Spain)
7. Design of a comprehensive Alzheimer’s disease clinic and research center in Spain to meet critical patient and family needs
8. Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia
9. Genetic screening of Alzheimer's disease genes in Iberian and African samples yields novel mutations in presenilins and APP
10. Lie Theory: Applications to problems in Mathematical Finance and Economics
11. Assessing the role of TUBA4A gene in frontotemporal degeneration
12. Challenges and Opportunities for Clinical Pharmacogenetic Research Studies in Resource-limited Settings: Conclusions From the Council for International Organizations of Medical Sciences–Ibero-American Network of Pharmacogenetics and Pharmacogenomics Meeting
13. Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes
14. Assessing the role of the TREM2 p.R47H variant as a risk factor for Alzheimer's disease and frontotemporal dementia
15. Exploratory analysis of seven Alzheimer's disease genes: disease progression
16. Expansion mutation in C9ORF72 does not influence plasma progranulin levels in frontotemporal dementia
17. Estrogen receptor alpha gene variants are associated with Alzheimer's disease
18. A truncating mutation in Alzheimer's disease inactivates neuroligin-1 synaptic function
19. A RARE GENETIC VARIANT IN THE PLCG2 GENE IS ASSOCIATED WITH A REDUCED RISK OF ALL MAJOR TYPES OF DEMENTIA AND AN INCREASED RISK TO REACH AN EXTREMELY OLD AGE
20. GENOME-WIDE ASSOCIATION STUDY OF ALZHEIMER’S DISEASE (AD) SUSCEPTIBILITY USING THE FUNDACIO ACE GENOME REPOSITORY: THE GR@ACE PROJECT
21. NON-SCHEDULED CONSULTATIONS CAN HELP TO IDENTIFY HIGHLY DEMANDING DEMENTIA PATIENTS
22. CEREBROSPINAL FLUID AND PLASMA LEVELS OF LYSOPHOSPHATIDIC ACIDS (LPAS) ASSOCIATE WITH CEREBROSPINAL FLUID Aβ-42 AND P-TAU
23. Genetic association of complement receptor 1 polymorphism rs3818361 in Alzheimer’s disease
24. P 174 - Placental and mitochondrial Q10 content after CoQ10 supplementation during pregnancy
25. THE SPANISH VERSION OF FACE-NAME ASSOCIATIVE MEMORY EXAM (S-FNAME) PERFORMANCE IS RELATED TO AMYLOID BURDEN IN SUBJECTIVE COGNITIVE DECLINE
26. GENETIC RISK FOR SCHIZOPHRENIA AND PSYCHOSIS IN ALZHEIMER DISEASE
27. EXPLORING APOE GENOTYPE EFFECTS ON AD RISK AND BETA-AMYLOID BURDEN IN INDIVIDUALS WITH SUBJECTIVE COGNITIVE DECLINE: THE FACEHBI STUDY RESULTS
28. RAMCIP PROJECT, A ROBOTIC ASSISTANT TO SUPPORT ALZHEIMER'S DISEASE PATIENTS AT HOME: A NOVEL APPROACH IN CAREGIVING
29. FUNDACIÓ ACE HEALTHY BRAIN INITIATIVE: A STUDY OF COGNITION AND BIOMARKERS IN INDIVIDUALS WITH SUBJECTIVE COGNITIVE DECLINE
30. GENETIC DETERMINANTS OF ALZHEIMER'S DISEASE PROGRESSION: EXPLORATORY ANALYSIS OF INTERNATIONAL GENOMICS OF ALZHEIMER PROJECT (IGAP) GENETIC MARKERS IN MMSE RATE OF DECLINE AND GDS
31. Erratum to “Exploratory analysis of seven Alzheimer's disease genes: disease progression” [Neurobiol. Aging 34 (2013) 1310.e1–1310.e7]
32. ROLE OF PLD3 RARE VARIANTS IN EUROPEAN SPORADIC ALZHEIMER'S DISEASE PATIENTS
33. A PHASE II STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PLASMA REPLACEMENT WITH 5% ALBUMIN IN BETA-AMYLOID PEPTIDE CLEARANCE IN CEREBROSPINAL FLUID, AND ITS EFFECTS IN PATIENTS WITH MILD-MODERATE ALZHEIMER'S DISEASE
34. TOWARD FINE MAPPING AND FUNCTIONAL CHARACTERIZATION OF GENOME-WIDE ASSOCIATION STUDY-IDENTIFIED LOCUS RS74615166 (TRIP4) FOR ALZHEIMER'S DISEASE
35. Identification of misdiagnosed frontotemporal dementia using apolioprotein genotype and linear discriminant analysis
36. Molecular evaluation of the ubiquitin 2 gene PXX domain in familial frontotemporal dementia patients
37. ATP5H/KCTD2 locus and Alzheimer's disease: An etiological link between key brain functions and dementia
38. Exploratory analysis of seven confirmed risk factors for Alzheimer's disease with disease progression
39. Longitudinal neuroimaging analysis in Alzheimer's disease after plasma exchange with 5% Grifols albumin (Albutein®)
40. Results of a phase II study of plasma exchange with 5 percent albumin (Albutein®) in Alzheimer's disease patients
41. “Open House” Screening Program to Identify Cognitive Impairment Among Community-Dwelling Middle-Aged/Elderly People
42. Neuroimage in Alzheimer's disease: Results after plasma exchange with Human Albumin Grifols®
43. Role of Dihydrofolate Reductase in Atherosclerosis
44. An Angiotensin-Converting Enzyme (ACE) polymorphism is associated with intracerebral hemorrhage recurrences in Cerebral Amyloid Angiopathy patients
45. Estrogen receptor alpha (ESR1) gene variants are associated to Alzheimer's disease in Spanish population
46. Molecular analysis of GOLPH2 gene SNPs in Alzheimer's disease
47. P4-355: An exploratory study of the potential utility of plasma exchange with 5 percent human albumin Grifols ® in the treatment of Alzheimer's disease (AD)
48. P3-259: GAB2 gene does not modify Alzheimer's risk in Spanish APOE E4 carriers
49. P2-269: Brain SPET quantification in incipient Alzheimer (DAT) dementia: Comparison between SPM and neurogam
50. Cardiovascular effects of angiotensin II and vasopressin in intact awake rats
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