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Characterization of nigrostriatal dysfunction in spinocerebellar ataxia 17.
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- Movement Disorders, 2006, v. 21, n. 6, p. 872, doi. 10.1002/mds.20827
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- Publication type:
- Article
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.
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- Human Genetics, 2001, v. 108, n. 3, p. 194, doi. 10.1007/s004390100463
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- Publication type:
- Article
PSEN1 and PRNP Gene Mutations Co-occurrence Makes Onset Very Early in a Family with FTD Phenotype.
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- Journal of Alzheimer's Disease, 2011, v. 24, n. 3, p. 415, doi. 10.3233/JAD-2011-101890
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- Publication type:
- Article
AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions.
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- Journal of Alzheimer's Disease, 2009, v. 17, n. 2, p. 383, doi. 10.3233/JAD-2009-1061
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- Publication type:
- Article
Antimicrobial Peptides (AMPs) in the Pathogenesis of Alzheimer's Disease: Implications for Diagnosis and Treatment.
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- Antibiotics (2079-6382), 2022, v. 11, n. 6, p. 726, doi. 10.3390/antibiotics11060726
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- Publication type:
- Article
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients.
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- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5630, doi. 10.1093/hmg/ddu279
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- Publication type:
- Article
Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
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- Human Molecular Genetics, 2013, v. 22, n. 7, p. 1417, doi. 10.1093/hmg/dds558
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- Publication type:
- Article
The Nerve Growth Factor Receptor (NGFR/p75 NTR): A Major Player in Alzheimer's Disease.
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- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3200, doi. 10.3390/ijms24043200
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- Publication type:
- Article
Rare Amyloid Precursor Protein Point Mutations Recapitulate Worldwide Migration and Admixture in Healthy Individuals: Implications for the Study of Neurodegeneration.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 15871, doi. 10.3390/ijms232415871
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- Publication type:
- Article
Mutations in Prion Protein Gene: Pathogenic Mechanisms in C-Terminal vs. N-Terminal Domain, a Review.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 14, p. 3606, doi. 10.3390/ijms20143606
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- Publication type:
- Article
The mitochondrial DNA control region shows genetically correlated levels of heteroplasmy in leukocytes of centenarians and their offspring.
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- BMC Genomics, 2007, v. 8, p. 293, doi. 10.1186/1471-2164-8-293
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- Publication type:
- Article
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.
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- Acta Neuropathologica, 2015, v. 129, n. 5, p. 715, doi. 10.1007/s00401-015-1401-8
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- Publication type:
- Article
Manic depressive illness in a founder population.
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- European Journal of Human Genetics, 2003, v. 11, n. 8, p. 597, doi. 10.1038/sj.ejhg.5201001
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- Publication type:
- Article
Clinical Perception and Treatment Options for Behavioral and Psychological Symptoms of Dementia (BPSD) in Italy.
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- Frontiers in Psychiatry, 2022, v. 13, p. 1, doi. 10.3389/fpsyt.2022.843088
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- Publication type:
- Article
SHORT-TERM RESPONSE IS NOT PREDICTIVE OF LONG-TERM RESPONSE TO ACETYLCHOLINESTERASE INHIBITORS IN OLD AGE SUBJECTS WITH ALZHEIMER’S DISEASE: A ‘REAL WORLD’ STUDY.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, p. P1234, doi. 10.1016/j.jalz.2017.07.435
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- Publication type:
- Article
Epidemiology of Frontotemporal dementia in southern Italy
- Published in:
- 2009
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- Publication type:
- Abstract
P3-286: Subcortical ischemic vascular dementia: A search for APP gene mutations
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- 2008
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- Publication type:
- Abstract
P3-277: TAU V363I mutation: Pathogenic or not?
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- 2008
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- Abstract
P3-258: Further evidence of genetic association between SORL1 and Alzheimer's disease
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- 2008
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- Publication type:
- Abstract
P3-220: PS1 polymorphism and a novel PS2 mutation in a patient with late-onset familial Alzheimer's disease
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- 2008
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- Publication type:
- Abstract
P3-404: Presenilins mutations are frequent in early-onset familial frontotemporal dementia
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- 2006
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- Publication type:
- Abstract
P3-193: Genotype-phenotype relationship is lacking in families with PS1-Met146Leu founder mutation
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- 2006
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- Abstract
P2-405: Achei efficacy in familial Alzheimer’s disease
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- 2006
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- Publication type:
- Abstract
P1-329: Presenilin-1 mutation E318G in Italian population: Genetic screening and effect on beta amyloid metabolism in human fibroblasts
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- 2006
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- Publication type:
- Abstract
P1-319: Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” AD
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- 2006
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- Publication type:
- Abstract
P1-303: Low levels of sRAGE plasma concentration in different types of dementia
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- 2006
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- Publication type:
- Abstract
O2-02-06: Results of fine mapping of a late-onset Alzheimer disease locus on chromosome 12: Linkage and association studies
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- 2006
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- Publication type:
- Abstract
P3-404: Presenilins mutations are frequent in early-onset familial frontotemporal dementia
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-193: Genotype-phenotype relationship is lacking in families with PS1-Met146Leu founder mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P2-405: Achei efficacy in familial Alzheimer’s disease
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-329: Presenilin-1 mutation E318G in Italian population: Genetic screening and effect on beta amyloid metabolism in human fibroblasts
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-319: Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” AD
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P1-303: Low levels of sRAGE plasma concentration in different types of dementia
- Published in:
- 2006
- By:
- Publication type:
- Abstract
O2-02-06: Results of fine mapping of a late-onset Alzheimer disease locus on chromosome 12: Linkage and association studies
- Published in:
- 2006
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- Publication type:
- Abstract
Angela R.: a familial Alzheimer's disease case in the days of Auguste D.
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- Journal of Neurology, 2016, v. 263, n. 12, p. 2494, doi. 10.1007/s00415-016-8294-x
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- Publication type:
- Article
Influence of controlled encoding and retrieval facilitation on memory performance in patients with different profiles of mild cognitive impairment.
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- Journal of Neurology, 2015, v. 262, n. 4, p. 938, doi. 10.1007/s00415-015-7662-2
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- Publication type:
- Article
Are we...social enough? Use of social media among members of the Italian Society of Neurology for the study of dementia.
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- Neurological Sciences, 2024, v. 45, n. 8, p. 4027, doi. 10.1007/s10072-024-07550-4
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- Publication type:
- Article
Correction to: Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG‑PET presentation in spinocerebellar ataxia 17: a case report.
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- 2024
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- Publication type:
- Correction Notice
Cognitive dysfunction, social behavior disorder, cerebellar ataxia, and atypical brain FDG-PET presentation in spinocerebellar ataxia 17: a case report.
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- Neurological Sciences, 2024, v. 45, n. 6, p. 2877, doi. 10.1007/s10072-024-07453-4
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- Publication type:
- Article
Accuracy of the clinical diagnosis of dementia with Lewy bodies (DLB) among the Italian Dementia Centers: a study by the Italian DLB study group (DLB-SINdem).
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- 2022
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- Publication type:
- journal article
Somatic comorbidities and Alzheimer's disease treatment.
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- Neurological Sciences, 2013, v. 34, n. 9, p. 1581, doi. 10.1007/s10072-013-1290-3
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- Publication type:
- Article
Position paper of the Italian Society for the study of Dementias (Sindem) on the proposal of a new Lexicon on Alzheimer disease.
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- Neurological Sciences, 2012, v. 33, n. 1, p. 201, doi. 10.1007/s10072-011-0825-8
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- Publication type:
- Article
Novel MAPT Val75Ala mutation and PSEN2 Arg62Hys in two siblings with frontotemporal dementia.
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- Neurological Sciences, 2010, v. 31, n. 1, p. 65, doi. 10.1007/s10072-009-0132-9
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- Publication type:
- Article
Neuropsychiatric or Behavioral and Psychological Symptoms of Dementia (BPSD): Focus on Prevalence and Natural History in Alzheimer's Disease and Frontotemporal Dementia.
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- Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.832199
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- Publication type:
- Article
Evidence for an Alzheimer disease susceptibility locus on chromosome 12 and for further locus heterogeneity.
- Published in:
- 1998
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- Publication type:
- journal article
Somatic Point Mutations in mtDNA Control Region Are Influenced by Genetic Background and Associated with Healthy Aging: A GEHA Study.
- Published in:
- PLoS ONE, 2010, v. 5, n. 10, p. 1, doi. 10.1371/journal.pone.0013395
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- Publication type:
- Article
The Shortening of Leukocyte Telomere Length Contributes to Alzheimer's Disease: Further Evidence from Late-Onset Familial and Sporadic Cases.
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- Biology (2079-7737), 2023, v. 12, n. 10, p. 1286, doi. 10.3390/biology12101286
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- Publication type:
- Article
A Novel Mutation (D395A) in Valosin-Containing Protein Gene Is Associated With Early Onset Frontotemporal Dementia in an Italian Family.
- Published in:
- 2021
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- Publication type:
- Case Study
Clinical manifestations of highly prevalent corticosteroid-binding globulin mutations in a village in southern Italy.
- Published in:
- 2011
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- Publication type:
- journal article
Guidelines for the diagnosis of dementia and Alzheimer's disease.
- Published in:
- Neurological Sciences, 2000, v. 21, n. 4, p. 187
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- Publication type:
- Article