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The Role of Mitochondrial Copy Number in Neurodegenerative Diseases: Present Insights and Future Directions.
- Published in:
- International Journal of Molecular Sciences, 2024, v. 25, n. 11, p. 6062, doi. 10.3390/ijms25116062
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- 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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- Article
Using the Theory of Planned Behavior and Past Behavior to Explain the Intention to Receive a Seasonal Influenza Vaccine among Family Caregivers of People with Dementia.
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- International Journal of Translational Medicine, 2023, v. 3, n. 2, p. 246, doi. 10.3390/ijtm3020017
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- Article
Neurodegenerative clinical records analyzer: detection of recurrent patterns within clinical records towards the identification of typical signs of neurodegenerative disease history.
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- JLIS.it: Italian Journal of Library, Archives & Information Science, 2023, v. 14, n. 2, p. 20, doi. 10.36253/jlis.it-522
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- Article
Thymic function and survival at advance ages in nursing home residents from Southern Italy.
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- Immunity & Ageing, 2023, v. 20, n. 1, p. 1, doi. 10.1186/s12979-023-00340-0
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- Publication type:
- Article
The Nerve Growth Factor Receptor (NGFR/p75 NTR): A Major Player in Alzheimer's Disease.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 4, p. 3200, doi. 10.3390/ijms24043200
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- Article
Expression and Signaling Pathways of Nerve Growth Factor (NGF) and Pro-NGF in Breast Cancer: A Systematic Review.
- Published in:
- Current Oncology, 2022, v. 29, n. 11, p. 8103, doi. 10.3390/curroncol29110640
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- Article
Calabria as a Genetic Isolate: A Model for the Study of Neurodegenerative Diseases.
- Published in:
- Biomedicines, 2022, v. 10, n. 9, p. 2288, doi. 10.3390/biomedicines10092288
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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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- Article
Amyloid Precursor Protein A713T Mutation in Calabrian Patients with Alzheimer's Disease: A Population Genomics Approach to Estimate Inheritance from a Common Ancestor.
- Published in:
- Biomedicines, 2022, v. 10, n. 1, p. 20, doi. 10.3390/biomedicines10010020
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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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- Case Study
The largest caucasian kindred with dentatorubral-pallidoluysian atrophy: A founder mutation in italy.
- Published in:
- 2019
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- Publication type:
- journal article
NGF controls APP cleavage by downregulating APP phosphorylation at Thr668: relevance for Alzheimer's disease.
- Published in:
- Aging Cell, 2016, v. 15, n. 4, p. 661, doi. 10.1111/acel.12473
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- Publication type:
- Article
Mutation analysis of CHCHD10 in different neurodegenerative diseases.
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- 2015
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- Publication type:
- journal article
The C9orf72 repeat expansion itself is methylated in ALS and FTLD patients.
- Published in:
- Acta Neuropathologica, 2015, v. 129, n. 5, p. 715, doi. 10.1007/s00401-015-1401-8
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- Publication type:
- Article
Hypermethylation of the CpG-island near the C9orf72 G4C2-repeat expansion in FTLD patients.
- Published in:
- Human Molecular Genetics, 2014, v. 23, n. 21, p. 5630, doi. 10.1093/hmg/ddu279
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- Publication type:
- Article
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
A Novel Pathogenic PSEN1 Mutation in a Family with Alzheimer's Disease: Phenotypical and Neuropathological Features.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 25, n. 3, p. 425, doi. 10.3233/JAD-2011-110185
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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
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
Epidemiology of Frontotemporal dementia in southern Italy
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- 2009
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- Publication type:
- Abstract
AβPP A713T Mutation in Late Onset Alzheimer's Disease with Cerebrovascular Lesions.
- Published in:
- 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
P3-220: PS1 polymorphism and a novel PS2 mutation in a patient with late-onset familial Alzheimer's disease
- Published in:
- 2008
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- Publication type:
- Abstract
P3-277: TAU V363I mutation: Pathogenic or not?
- Published in:
- 2008
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- Publication type:
- Abstract
P3-279: A novel progranulin mutation in a large frontotemporal dementia calabrian kindred
- Published in:
- 2008
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- Publication type:
- Abstract
P3-286: Subcortical ischemic vascular dementia: A search for APP gene mutations
- Published in:
- 2008
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- Publication type:
- Abstract
Late onset familial Alzheimer's disease: novel presenilin 2 mutation and PS1 E318G polymorphism.
- Published in:
- Journal of Neurology, 2008, v. 255, n. 4, p. 604, doi. 10.1007/s00415-008-0764-3
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- Publication type:
- Article
Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” Alzheimer’s disease.
- Published in:
- Journal of Neurology, 2007, v. 254, n. 3, p. 391, doi. 10.1007/s00415-006-0373-y
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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.
- Published in:
- BMC Genomics, 2007, v. 8, p. 293, doi. 10.1186/1471-2164-8-293
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- Article
P1-303: Low levels of sRAGE plasma concentration in different types of dementia
- Published in:
- 2006
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- Publication type:
- Abstract
P1-319: Presenilin 2 Ser130Leu mutation in a case of late-onset “sporadic” AD
- Published in:
- 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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- Publication type:
- Abstract
P3-404: Presenilins mutations are frequent in early-onset familial frontotemporal dementia
- Published in:
- 2006
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- Publication type:
- Abstract
P1-303: Low levels of sRAGE plasma concentration in different types of dementia
- 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
P3-193: Genotype-phenotype relationship is lacking in families with PS1-Met146Leu founder mutation
- Published in:
- 2006
- By:
- Publication type:
- Abstract
P3-404: Presenilins mutations are frequent in early-onset familial frontotemporal dementia
- Published in:
- 2006
- By:
- Publication type:
- Abstract
Relation of Apolipoprotein(a) Size to Alzheimer's Disease and Vascular Dementia.
- Published in:
- Dementia & Geriatric Cognitive Disorders, 2004, v. 18, n. 2, p. 189, doi. 10.1159/000079200
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- Publication type:
- Article
Mitochondrial DNA haplogroups and APOE4 allele are non-independent variables in sporadic Alzheimer's disease.
- Published in:
- Human Genetics, 2001, v. 108, n. 3, p. 194, doi. 10.1007/s004390100463
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- Publication type:
- Article