Found: 51
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Examining the presence and nature of delusions in Alzheimer's disease and frontotemporal dementia syndromes.
- Published in:
- 2022
- By:
- Publication type:
- journal article
DNA methylation of the MAPT gene in Parkinson's disease cohorts and modulation by vitamin E In Vitro.
- Published in:
- Movement Disorders, 2014, v. 29, n. 13, p. 1606, doi. 10.1002/mds.25784
- By:
- Publication type:
- Article
Developments in neuroacanthocytosis: expanding the spectrum of choreatic syndromes.
- Published in:
- 2006
- By:
- Publication type:
- journal article
Chorea-acanthocytosis: Clinical and genetic findings in three families from the Arabian peninsula.
- Published in:
- Movement Disorders, 2003, v. 18, n. 4, p. 403, doi. 10.1002/mds.10361
- By:
- Publication type:
- Article
Effect of stress gene-by-environment interactions on hippocampal volumes and cortisol secretion in adolescent girls.
- Published in:
- Australian & New Zealand Journal of Psychiatry, 2019, v. 53, n. 4, p. 316, doi. 10.1177/0004867419827649
- By:
- Publication type:
- Article
The impact of 5-HTTLPR on acute serotonin transporter blockade by escitalopram on emotion processing: Preliminary findings from a randomised, crossover fMRI study.
- Published in:
- Australian & New Zealand Journal of Psychiatry, 2014, v. 48, n. 12, p. 1115, doi. 10.1177/0004867414533837
- By:
- Publication type:
- Article
The contribution of BDNF and 5-HTT polymorphisms and early life stress to the heterogeneity of major depressive disorder: A preliminary study.
- Published in:
- Australian & New Zealand Journal of Psychiatry, 2012, v. 46, n. 1, p. 55, doi. 10.1177/0004867411430878
- By:
- Publication type:
- Article
Reduced glucocerebrosidase activity in monocytes from patients with Parkinson’s disease.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-33921-x
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- Publication type:
- Article
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia.
- Published in:
- Nature Communications, 2016, v. 7, n. 4, p. 11253, doi. 10.1038/ncomms11253
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- Publication type:
- Article
Reply: CYLD variants in frontotemporal dementia associated with severe memory impairment in a Portuguese cohort.
- Published in:
- 2020
- By:
- Publication type:
- letter
CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis.
- Published in:
- 2020
- By:
- Publication type:
- journal article
Blood-Based Transcriptomic Biomarkers Are Predictive of Neurodegeneration Rather Than Alzheimer's Disease.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 19, p. 15011, doi. 10.3390/ijms241915011
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- Publication type:
- Article
Identification of a VPS13A founder mutation in French Canadian families with chorea-acanthocytosis.
- Published in:
- Neurogenetics, 2005, v. 6, n. 3, p. 151, doi. 10.1007/s10048-005-0220-9
- By:
- Publication type:
- Article
Frontotemporal dementia-amyotrophic lateral sclerosis syndrome locus on chromosome 16p12.1-q12.2: genetic, clinical and neuropathological analysis.
- Published in:
- Acta Neuropathologica, 2013, v. 125, n. 4, p. 523, doi. 10.1007/s00401-013-1078-9
- By:
- Publication type:
- Article
Comparison of fluorescent single-strand conformation polymorphism analysis and denaturing high-performance liquid chromatography for detection of EXT1 and EXT2 mutations in hereditary multiple exostoses.
- Published in:
- European Journal of Human Genetics, 2000, v. 8, n. 1, p. 24, doi. 10.1038/sj.ejhg.5200409
- By:
- Publication type:
- Article
Hailey-Hailey Disease: Molecular and Clinical Characterization of Novel Mutations in the ATP2C1 Gene.
- Published in:
- Journal of Investigative Dermatology, 2002, v. 118, n. 2, p. 338, doi. 10.1046/j.0022-202x.2001.01675.x
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- Publication type:
- Article
THE INTEGRATE MODEL OF EMOTION, THINKING AND SELF REGULATION:: AN APPLICATION TO THE "PARADOX OF AGING".
- Published in:
- Journal of Integrative Neuroscience, 2008, v. 7, n. 3, p. 367, doi. 10.1142/S0219635208001939
- By:
- Publication type:
- Article
A GENOTYPE-ENDOPHENOTYPE-PHENOTYPE PATH MODEL OF DEPRESSED MOOD:: INTEGRATING COGNITIVE AND EMOTIONAL MARKERS.
- Published in:
- Journal of Integrative Neuroscience, 2007, v. 6, n. 1, p. 75, doi. 10.1142/S0219635207001398
- By:
- Publication type:
- Article
INTEGRATING OBJECTIVE GENE-BRAIN-BEHAVIOR MARKERS OF PSYCHIATRIC DISORDERS.
- Published in:
- Journal of Integrative Neuroscience, 2007, v. 6, n. 1, p. 1, doi. 10.1142/S0219635207001465
- By:
- Publication type:
- Article
A Polymorphism of the MAOA Gene is Associated with Emotional Brain Markers and Personality Traits on an Antisocial Index.
- Published in:
- Neuropsychopharmacology, 2009, v. 34, n. 7, p. 1797, doi. 10.1038/npp.2009.1
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- Publication type:
- Article
Effects of mutations in the novel FTD‐ALS gene, CYLD, on SFPQ protein: Developing topics.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.047382
- By:
- Publication type:
- Article
Effects of the novel FTD‐ALS gene CYLD on cell death mechanisms: Genetics/atypical and other dementias.
- Published in:
- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2020, v. 16, n. 11, p. 1, doi. 10.1002/alz.045017
- By:
- Publication type:
- Article
Sigma non-opioid intracellular receptor 1 and neurodegeneration: prevalence of mutations and therapeutic implications
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Positional cloning identifies SIGMAR1 gene as a causative locus for FTLD-MND in a large Australian pedigree
- Published in:
- 2011
- By:
- Publication type:
- Abstract
Schizotypal traits across the amyotrophic lateral sclerosis–frontotemporal dementia spectrum: pathomechanistic insights.
- Published in:
- Journal of Neurology, 2022, v. 269, n. 8, p. 4241, doi. 10.1007/s00415-022-11049-3
- By:
- Publication type:
- Article
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41598-020-68848-9
- By:
- Publication type:
- Article
Cerebellar Integrity in the Amyotrophic Lateral Sclerosis - Frontotemporal Dementia Continuum.
- Published in:
- PLoS ONE, 2014, v. 9, n. 8, p. 1, doi. 10.1371/journal.pone.0105632
- By:
- Publication type:
- Article
<i>GSK3B</i> and <i>MAPT</i> Polymorphisms Are Associated with Grey Matter and Intracranial Volume in Healthy Individuals.
- Published in:
- PLoS ONE, 2013, v. 8, n. 8, p. 1, doi. 10.1371/journal.pone.0071750
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- Publication type:
- Article
<i>C9ORF72</i> Repeat Expansion in Australian and Spanish Frontotemporal Dementia Patients.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056899
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- Publication type:
- Article
An Exploration of the Serotonin System in Antisocial Boys with High Levels of Callous-Unemotional Traits.
- Published in:
- PLoS ONE, 2013, v. 8, n. 2, p. 1, doi. 10.1371/journal.pone.0056619
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- Publication type:
- Article
A Role for Transcription Factor GTF2IRD2 in Executive Function in Williams-Beuren Syndrome.
- Published in:
- PLoS ONE, 2012, v. 7, n. 10, p. 1, doi. 10.1371/journal.pone.0047457
- By:
- Publication type:
- Article
Brain derived neurotrophic factor Val66Met polymorphism, the five factor model of personality and hippocampal volume: Implications for depressive illness.
- Published in:
- Human Brain Mapping, 2009, v. 30, n. 4, p. 1246, doi. 10.1002/hbm.20592
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- Publication type:
- Article
A conserved sorting-associated protein is mutant in chorea-acanthocytosis.
- Published in:
- Nature Genetics, 2001, v. 28, n. 2, p. 119, doi. 10.1038/88821
- By:
- Publication type:
- Article
Impact of the HTR3A gene with early life trauma on emotional brain networks and depressed mood.
- Published in:
- Depression & Anxiety (1091-4269), 2010, v. 27, n. 8, p. 752, doi. 10.1002/da.20726
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- Publication type:
- Article
Methylation of the oxytocin receptor gene and oxytocin blood levels in the development of psychopathy.
- Published in:
- Development & Psychopathology, 2014, v. 26, n. 1, p. 33, doi. 10.1017/S0954579413000497
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- Publication type:
- Article
Polymorphisms in the oxytocin receptor gene are associated with the development of psychopathy.
- Published in:
- Development & Psychopathology, 2014, v. 26, n. 1, p. 21, doi. 10.1017/S0954579413000485
- By:
- Publication type:
- Article
Familial Temporal Lobe Epilepsy as a Presenting Feature of Choreoacanthocytosis.
- Published in:
- Epilepsia (Series 4), 2005, v. 46, n. 8, p. 1256, doi. 10.1111/j.1528-1167.2005.65804.x
- By:
- Publication type:
- Article
Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis.
- Published in:
- Acta Neuropathologica Communications, 2017, v. 5, p. 1, doi. 10.1186/s40478-017-0480-2
- By:
- Publication type:
- Article
Rapid in vitro quantification of TDP-43 and FUS mislocalisation for screening of gene variants implicated in frontotemporal dementia and amyotrophic lateral sclerosis.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-94225-1
- By:
- Publication type:
- Article
A Functional Polymorphism of the MAOA Gene Is Associated with Neural Responses to Induced Anger Control.
- Published in:
- Journal of Cognitive Neuroscience, 2014, v. 26, n. 7, p. 1418, doi. 10.1162/jocn_a_00592
- By:
- Publication type:
- Article
Is CHCHD10 Pro34Ser pathogenic for frontotemporal dementia and amyotrophic lateral sclerosis?
- Published in:
- 2015
- By:
- Publication type:
- commentary
Sigma nonopioid intracellular receptor 1 mutations cause frontotemporal lobar degeneration-motor neuron disease.
- Published in:
- Annals of Neurology, 2010, v. 68, n. 5, p. 639, doi. 10.1002/ana.22274
- By:
- Publication type:
- Article
Chorein detection for the diagnosis of chorea?acanthocytosis.
- Published in:
- Annals of Neurology, 2004, v. 56, n. 2, p. 299
- By:
- Publication type:
- Article
McLeod neuroacanthocytosis: genotype and phenotype.
- Published in:
- 2001
- By:
- Publication type:
- journal article
Hailey-Hailey disease is caused by mutations in ATP2C1 encoding a novel Ca[sup 2+] pump.
- Published in:
- Human Molecular Genetics, 2000, v. 9, n. 7, p. 1131, doi. 10.1093/hmg/9.7.1131
- By:
- Publication type:
- Article
Factors That Influence Non-Motor Impairment Across the ALS-FTD Spectrum: Impact of Phenotype, Sex, Age, Onset and Disease Stage.
- Published in:
- Frontiers in Neurology, 2021, v. 12, p. 1, doi. 10.3389/fneur.2021.743688
- By:
- Publication type:
- Article
Role of the Long Non-Coding RNA MAPT-AS1 in Regulation of Microtubule Associated Protein Tau (MAPT) Expression in Parkinson's Disease.
- Published in:
- PLoS ONE, 2016, v. 11, n. 6, p. 1, doi. 10.1371/journal.pone.0157924
- By:
- Publication type:
- Article
Serotonin 1B Receptor Gene (HTR1B) Methylation as a Risk Factor for Callous-Unemotional Traits in Antisocial Boys.
- Published in:
- PLoS ONE, 2015, v. 10, n. 5, p. 1, doi. 10.1371/journal.pone.0126903
- By:
- Publication type:
- Article
Poly‐GA immunohistochemistry is a reliable tool for detecting C9orf72 hexanucleotide repeat expansions.
- Published in:
- Brain Pathology, 2024, v. 34, n. 5, p. 1, doi. 10.1111/bpa.13216
- By:
- Publication type:
- Article