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P4-115: Frontotemporal degeneration with ubiquinated inclusions: A case report of a family with corticobasal syndrome and prominent parietal degeneration

Alzheimer's & dementia, 2006-07, Vol.2 (3), p.S549-S549

2006

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Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.709-722

2012

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The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

Brain (London, England : 1878), 2006-11, Vol.129 (11), p.3081-3090

2006

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CLINICAL DETAILS OF THE ILE213LEU PSEN1 MUTATION IN A FAMILY WITH EARLY ONSET FAMILIAL ALZHEIMER DISEASE

Alzheimer's & dementia, 2019-07, Vol.15 (7), p.P289-P289

2019

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P1‐137: CLINICAL DETAILS OF THE ILE213LEU PSEN1 MUTATION IN A FAMILY WITH EARLY ONSET FAMILIAL ALZHEIMER DISEASE

Alzheimer's & dementia, 2019-07, Vol.15 (7S_Part_5), p.P289-P289

2019

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Genomic study of a large family with complex neurological phenotype including hearing loss, imbalance and action tremor

Neurobiology of aging, 2022-05, Vol.113, p.137-142

2022

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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Nature, 2006-08, Vol.442 (7105), p.916-919

2006

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Personal value of Alzheimer's disease biomarker testing and result disclosure from the patient and care partner perspective

Alzheimer's & dementia : translational research & clinical interventions, 2024-04, Vol.10 (2), p.e12463-n/a

2024

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What patients and caregivers do with knowledge of Alzheimer’s disease CSF test results: Findings from the IMPACT‐AD BC study

Alzheimer's & dementia, 2022-12, Vol.18 (S5), p.n/a

2022

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P1‐134: Neurobehavioral characterization of adult‐onset alexander's disease: A family study

Alzheimer's & dementia, 2015-07, Vol.11 (7S_Part_8), p.P393-P393

2015

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Canadian Patient and Care Partner Perspectives on Diagnostic Biomarker Testing for Alzheimer's Disease

Canadian geriatrics journal CGJ, 2023-06, Vol.26 (2), p.318-318

2023

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A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

Brain (London, England : 1878), 2006-04, Vol.129 (4), p.853-867

2006

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Neurobehavioral characterization of adult-onset alexander's disease: A family study

Alzheimer's & dementia, 2015-07, Vol.11 (7), p.P393-P393

2015

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Converging approaches to understanding early onset familial Alzheimer disease: A First Nation study

SAGE open medicine, 2015-01, Vol.3, p.2050312115621766-2050312115621766

2015

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Early-onset familial Alzheimer's disease and the definition of family: Experience with an indigenous community

Alzheimer's & dementia, 2012-07, Vol.8 (4), p.P667-P667

2012

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P4‐099: Early‐onset familial Alzheimer's disease and the definition of family: Experience with an indigenous community

Alzheimer's & dementia, 2012-07, Vol.8 (4S_Part_18), p.P667-P667

2012

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An Assessment of Genetic Counseling Services for Individuals with Multiple Sclerosis

Journal of genetic counseling, 2015-02, Vol.24 (1), p.46-57

2015

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Neuroethics, confidentiality, and a cultural imperative in early onset Alzheimer disease: a case study with a First Nation population

Philosophy, ethics, and humanities in medicine : PEHM, 2013-10, Vol.8 (1), p.15-15, Article 15

2013

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Genetic Counseling for Early-onset Familial Alzheimer Disease in Large Aboriginal Kindred from a Remote Community in British Columbia: Unique Challenges and Possible Solutions

Journal of genetic counseling, 2011-04, Vol.20 (2), p.136-142

2011

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O1‐07‐04: Genetic counseling for early onset familial Alzheimer's disease in a large aboriginal kindred from a remote community in northern British Columbia: Unique challenges and possible solutions

Alzheimer's & dementia, 2009-07, Vol.5 (4S_Part_3), p.P90-P90

2009

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Genetic counseling for early onset familial Alzheimer's disease in a large aboriginal kindred from a remote community in northern British Columbia: Unique challenges and possible solutions

Alzheimer's & dementia, 2009-07, Vol.5 (4), p.P90-P90

2009

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A novel PS1 gene mutation in a large Aboriginal kindred

Canadian journal of neurological sciences, 2010-05, Vol.37 (3), p.359

2010

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P4-115: Frontotemporal degeneration with ubiquinated inclusions: A case report of a family with corticobasal syndrome and prominent parietal degeneration

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene

CLINICAL DETAILS OF THE ILE213LEU PSEN1 MUTATION IN A FAMILY WITH EARLY ONSET FAMILIAL ALZHEIMER DISEASE

P1‐137: CLINICAL DETAILS OF THE ILE213LEU PSEN1 MUTATION IN A FAMILY WITH EARLY ONSET FAMILIAL ALZHEIMER DISEASE

Genomic study of a large family with complex neurological phenotype including hearing loss, imbalance and action tremor

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Personal value of Alzheimer's disease biomarker testing and result disclosure from the patient and care partner perspective

What patients and caregivers do with knowledge of Alzheimer’s disease CSF test results: Findings from the IMPACT‐AD BC study

Brain Health PRO: An Interactive, Online, Educational Program for Dementia

P1‐134: Neurobehavioral characterization of adult‐onset alexander's disease: A family study

Canadian Patient and Care Partner Perspectives on Diagnostic Biomarker Testing for Alzheimer's Disease

A family with tau-negative frontotemporal dementia and neuronal intranuclear inclusions linked to chromosome 17

The Brain Health Support Program: A web‐based interactive platform to increase dementia literacy and awareness regarding lifestyle factors in at‐risk individuals

The Brain Health Support Program: A web‐based interactive platform to increase dementia literacy and awareness regarding lifestyle factors in at‐risk individuals: Advancing clinical trial design and methods in a digital age

Neurobehavioral characterization of adult-onset alexander's disease: A family study

Converging approaches to understanding early onset familial Alzheimer disease: A First Nation study

Early-onset familial Alzheimer's disease and the definition of family: Experience with an indigenous community

P4‐099: Early‐onset familial Alzheimer's disease and the definition of family: Experience with an indigenous community

An Assessment of Genetic Counseling Services for Individuals with Multiple Sclerosis

Neuroethics, confidentiality, and a cultural imperative in early onset Alzheimer disease: a case study with a First Nation population

Genetic Counseling for Early-onset Familial Alzheimer Disease in Large Aboriginal Kindred from a Remote Community in British Columbia: Unique Challenges and Possible Solutions

O1‐07‐04: Genetic counseling for early onset familial Alzheimer's disease in a large aboriginal kindred from a remote community in northern British Columbia: Unique challenges and possible solutions

Genetic counseling for early onset familial Alzheimer's disease in a large aboriginal kindred from a remote community in northern British Columbia: Unique challenges and possible solutions

A novel PS1 gene mutation in a large Aboriginal kindred

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