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Online information and support for carers of people with young-onset dementia: A multi-site randomised controlled pilot study.
- Published in:
- 2019
- By:
- Publication type:
- journal article
Differential impairment of cerebrospinal fluid synaptic biomarkers in the genetic forms of frontotemporal dementia.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-01042-3
- By:
- Publication type:
- Article
Cognitive composites for genetic frontotemporal dementia: GENFI-Cog.
- Published in:
- Alzheimer's Research & Therapy, 2022, v. 14, n. 1, p. 1, doi. 10.1186/s13195-022-00958-0
- By:
- Publication type:
- Article
The Revised Self-Monitoring Scale detects early impairment of social cognition in genetic frontotemporal dementia within the GENFI cohort.
- Published in:
- Alzheimer's Research & Therapy, 2021, v. 13, p. 1, doi. 10.1186/s13195-021-00865-w
- By:
- Publication type:
- Article
Aβ and tau prion-like activities decline with longevity in the Alzheimer's disease human brain.
- Published in:
- Science Translational Medicine, 2019, v. 11, n. 490, p. N.PAG, doi. 10.1126/scitranslmed.aat8462
- By:
- Publication type:
- Article
The gene for Best's macular dystrophy is located at 11q13 in a Swedish family.
- Published in:
- Clinical Genetics, 1992, v. 42, n. 3, p. 156, doi. 10.1111/j.1399-0004.1992.tb03229.x
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- Publication type:
- Article
Gene-variant specific effects of plasma amyloid-β levels in Swedish autosomal dominant Alzheimer disease.
- Published in:
- Alzheimer's Research & Therapy, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13195-024-01574-w
- By:
- Publication type:
- Article
A systematic review of progranulin concentrations in biofluids in over 7,000 people—assessing the pathogenicity of GRN mutations and other influencing factors.
- Published in:
- Alzheimer's Research & Therapy, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13195-024-01420-z
- By:
- Publication type:
- Article
Genetic mapping using fluorescent quantification of allele frequencies in pooled DNA loaded by solid support.
- Published in:
- Clinical Genetics, 1997, v. 51, n. 3, p. 145, doi. 10.1111/j.1399-0004.1997.tb02444.x
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- Publication type:
- Article
Conformation‐specific antibodies against multiple amyloid protofibril species from a single amyloid immunogen.
- Published in:
- Journal of Cellular & Molecular Medicine, 2019, v. 23, n. 3, p. 2103, doi. 10.1111/jcmm.14119
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- Publication type:
- Article
Differences in proliferation rate between CADASIL and control vascular smooth muscle cells are related to increased TGFβ expression.
- Published in:
- Journal of Cellular & Molecular Medicine, 2018, v. 22, n. 6, p. 3016, doi. 10.1111/jcmm.13534
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- Publication type:
- Article
Ethical aspects of undergoing a predictive genetic testing for Huntington's disease.
- Published in:
- 2013
- By:
- Publication type:
- Journal Article
DTI changes of thalamic subregions in genetic frontotemporal dementia: findings from the GENFI cohort.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.082484
- By:
- Publication type:
- Article
Altered enzymatic activity and allele frequency of OMI/HTRA2 in Alzheimer's disease.
- Published in:
- FASEB Journal, 2011, v. 25, n. 4, p. 1345, doi. 10.1096/fj.10-163402
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- Publication type:
- Article
Complex genetic counselling and prenatal analysis in a woman with external ophthalmoplegia and deleted mtDNA.
- Published in:
- Prenatal Diagnosis, 2000, v. 20, n. 5, p. 426, doi. 10.1002/(SICI)1097-0223(200005)20:5<426::AID-PD845>3.0.CO;2-K
- By:
- Publication type:
- Article
The CBI‐R detects early behavioural impairment in genetic frontotemporal dementia.
- Published in:
- Annals of Clinical & Translational Neurology, 2022, v. 9, n. 5, p. 644, doi. 10.1002/acn3.51544
- By:
- Publication type:
- Article
Plasma metabolomics of presymptomatic PSEN1‐H163Y mutation carriers: a pilot study.
- Published in:
- Annals of Clinical & Translational Neurology, 2021, v. 8, n. 3, p. 579, doi. 10.1002/acn3.51296
- By:
- Publication type:
- Article
Novel CSF biomarkers in genetic frontotemporal dementia identified by proteomics.
- Published in:
- Annals of Clinical & Translational Neurology, 2019, v. 6, n. 4, p. 698, doi. 10.1002/acn3.745
- By:
- Publication type:
- Article
Poly(GP), neurofilament and grey matter deficits in <italic>C9orf72</italic> expansion carriers.
- Published in:
- Annals of Clinical & Translational Neurology, 2018, v. 5, n. 5, p. 583, doi. 10.1002/acn3.559
- By:
- Publication type:
- Article
Neurofilament light chain: a biomarker for genetic frontotemporal dementia.
- Published in:
- Annals of Clinical & Translational Neurology, 2016, v. 3, n. 8, p. 623, doi. 10.1002/acn3.325
- By:
- Publication type:
- Article
Identification and description of three families with familial Alzheimer disease that segregate variants in the SORL1 gene.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0441-9
- By:
- Publication type:
- Article
Autophagic and lysosomal defects in human tauopathies: analysis of post-mortem brain from patients with familial Alzheimer disease, corticobasal degeneration and progressive supranuclear palsy.
- Published in:
- Acta Neuropathologica Communications, 2016, v. 4, p. 1, doi. 10.1186/s40478-016-0292-9
- By:
- Publication type:
- Article
Amyloid β-Peptide Increases Mitochondria-Endoplasmic Reticulum Contact Altering Mitochondrial Function and Autophagosome Formation in Alzheimer's Disease-Related Models.
- Published in:
- Cells (2073-4409), 2020, v. 9, n. 12, p. 2552, doi. 10.3390/cells9122552
- By:
- Publication type:
- Article
Decreased Global EEG Synchronization in Amyloid Positive Mild Cognitive Impairment and Alzheimer's Disease Patients—Relationship to APOE ε4.
- Published in:
- Brain Sciences (2076-3425), 2021, v. 11, n. 10, p. 1359, doi. 10.3390/brainsci11101359
- By:
- Publication type:
- Article
The effects of different familial Alzheimer's disease mutations on APP processing in vivo.
- Published in:
- Alzheimer's Research & Therapy, 2017, v. 9, p. 1, doi. 10.1186/s13195-017-0234-1
- By:
- Publication type:
- Article
Novel progranulin mutations with reduced serum-progranulin levels in frontotemporal lobar degeneration.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 11, p. 1260, doi. 10.1038/ejhg.2013.37
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- Publication type:
- Article
The PSEN1 I143T mutation in a Swedish family with Alzheimer's disease: clinical report and quantification of Aβ in different brain regions.
- Published in:
- European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1202, doi. 10.1038/ejhg.2010.107
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- Publication type:
- Article
Expanded high-resolution genetic study of 109 Swedish families with Alzheimer's disease.
- Published in:
- European Journal of Human Genetics, 2008, v. 16, n. 2, p. 202, doi. 10.1038/sj.ejhg.5201946
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- Publication type:
- Article
The use of grid computing to drive data-intensive genetic research.
- Published in:
- European Journal of Human Genetics, 2007, v. 15, n. 6, p. 694, doi. 10.1038/sj.ejhg.5201815
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- Publication type:
- Article
Stratifying the Presymptomatic Phase of Genetic Frontotemporal Dementia by Serum NfL and pNfH: A Longitudinal Multicentre Study.
- Published in:
- Annals of Neurology, 2022, v. 91, n. 1, p. 33, doi. 10.1002/ana.26265
- By:
- Publication type:
- Article
Faster Cortical Thinning and Surface Area Loss in Presymptomatic and Symptomatic C9orf72 Repeat Expansion Adult Carriers.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Mitochondrial dysfunction in a transgenic mouse model expressing human amyloid precursor protein ( APP) with the Arctic mutation.
- Published in:
- Journal of Neurochemistry, 2016, v. 136, n. 3, p. 497, doi. 10.1111/jnc.13410
- By:
- Publication type:
- Article
Comparison of arterial spin labeling registration strategies in the multi-center GENetic frontotemporal dementia initiative (GENFI).
- Published in:
- 2018
- By:
- Publication type:
- journal article
Deleterious ABCA7 mutations and transcript rescue mechanisms in early onset Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2017, v. 134, n. 3, p. 475, doi. 10.1007/s00401-017-1714-x
- By:
- Publication type:
- Article
A comprehensive study of the genetic impact of rare variants in SORL1 in European early-onset Alzheimer's disease.
- Published in:
- Acta Neuropathologica, 2016, v. 132, n. 2, p. 213, doi. 10.1007/s00401-016-1566-9
- By:
- Publication type:
- Article
Neuropathological characterization of two siblings carrying the MAPT S305S mutation demonstrates features resembling argyrophilic grain disease.
- Published in:
- 2014
- By:
- Publication type:
- Letter
The APOE ε4 Allele Affects Cognitive Functions Differently in Carriers of APP Mutations Compared to Carriers of PSEN1 Mutations in Autosomal-Dominant Alzheimer's Disease.
- Published in:
- Genes, 2021, v. 12, n. 12, p. 1954, doi. 10.3390/genes12121954
- By:
- Publication type:
- Article
Overall and domain-specific life satisfaction when living with familial Alzheimer's disease risk: A quantitative approach.
- Published in:
- Nursing & Health Sciences, 2017, v. 19, n. 4, p. 452, doi. 10.1111/nhs.12365
- By:
- Publication type:
- Article
Putative risk alleles for LATE‐NC with hippocampal sclerosis in population‐representative autopsy cohorts.
- Published in:
- Brain Pathology, 2020, v. 30, n. 2, p. 364, doi. 10.1111/bpa.12773
- By:
- Publication type:
- Article
Alzheimers sykdom og genetikk.
- Published in:
- Journal of the Norwegian Medical Association / Tidsskrift for Den Norske Laegeforening, 2013, n. 14, p. 1449, doi. 10.4045/tidsskr.12.0873
- By:
- Publication type:
- Article
Cryo-EM structures of amyloid-β filaments with the Arctic mutation (E22G) from human and mouse brains.
- Published in:
- Acta Neuropathologica, 2023, v. 145, n. 3, p. 325, doi. 10.1007/s00401-022-02533-1
- By:
- Publication type:
- Article
The Obesity Related Gene, FTO, Interacts with APOE, and is Associated with Alzheimer's Disease Risk: A Prospective Cohort Study.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 23, n. 3, p. 461, doi. 10.3233/JAD-2010-101068
- By:
- Publication type:
- Article
Linkage to the 8p21.1 Region Including the CLU Gene in Age at Onset Stratified Alzheimer's Disease Families.
- Published in:
- Journal of Alzheimer's Disease, 2011, v. 23, n. 1, p. 13, doi. 10.3233/JAD-2010-101359
- By:
- Publication type:
- Article
The obesity related gene, FTO, interacts with APOE, and is associated with Alzheimer's disease risk: a prospective cohort study.
- Published in:
- 2011
- By:
- Publication type:
- journal article
Novel TARDBP mutations in Nordic ALS patients.
- Published in:
- Journal of Human Genetics, 2012, v. 57, n. 5, p. 316, doi. 10.1038/jhg.2012.24
- By:
- Publication type:
- Article
Linkage to 20p13 including the ANGPT4 gene in families with mixed Alzheimer's disease and vascular dementia.
- Published in:
- Journal of Human Genetics, 2010, v. 55, n. 10, p. 649, doi. 10.1038/jhg.2010.79
- By:
- Publication type:
- Article
APOE ε4 influences cognitive decline positively in APP and negatively in PSEN1 mutation carriers with autosomal‐dominant Alzheimer's disease.
- Published in:
- European Journal of Neurology, 2022, v. 29, n. 12, p. 3580, doi. 10.1111/ene.15536
- By:
- Publication type:
- Article
Tracking reactive astrogliosis in autosomal dominant and sporadic Alzheimer's disease with multi-modal PET and plasma GFAP.
- Published in:
- Molecular Neurodegeneration, 2023, v. 18, n. 1, p. 1, doi. 10.1186/s13024-023-00647-y
- By:
- Publication type:
- Article
The meaning of living close to a person with Alzheimer disease.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Altered levels of CSF proteins in patients with FTD, presymptomatic mutation carriers and non-carriers.
- Published in:
- Translational Neurodegeneration, 2020, v. 9, n. 1, p. 1, doi. 10.1186/s40035-020-00198-y
- By:
- Publication type:
- Article