4.5 Article

Frontotemporal Dementia and Chorea Associated with a Compound Heterozygous TREM2 Mutation

Related references

Note: Only part of the references are listed.
Review Geriatrics & Gerontology

A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature

Efthimios Dardiotis et al.

NEUROBIOLOGY OF AGING (2017)

Article Clinical Neurology

Frontotemporal Dementia

Nicholas T. Olney et al.

NEUROLOGIC CLINICS (2017)

Review Biochemistry & Molecular Biology

Genetics of FTLD: overview and what else we can expect from genetic studies

Cyril Pottier et al.

JOURNAL OF NEUROCHEMISTRY (2016)

Article Neurosciences

Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression

Daniel W. Sirkis et al.

ACTA NEUROPATHOLOGICA COMMUNICATIONS (2016)

Article Medicine, General & Internal

Frontotemporal dementia

Jee Bang et al.

LANCET (2015)

Article Clinical Neurology

RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder

Patrick Santens et al.

NEUROLOGY (2015)

Article Multidisciplinary Sciences

The human splicing code reveals new insights into the genetic determinants of disease

Hui Y. Xiong et al.

SCIENCE (2015)

Article Geriatrics & Gerontology

Homozygous TREM2 mutation in a family with atypical frontotemporal dementia

Isabelle Le Ber et al.

NEUROBIOLOGY OF AGING (2014)

Article Geriatrics & Gerontology

Heterozygous TREM2 mutations in frontotemporal dementia

Barbara Borroni et al.

NEUROBIOLOGY OF AGING (2014)

Article Geriatrics & Gerontology

Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes

Mathias Thelen et al.

NEUROBIOLOGY OF AGING (2014)

Article Clinical Neurology

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

Davina J. Hensman Moss et al.

NEUROLOGY (2014)

Article Cell Biology

TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis

Gernot Kleinberger et al.

SCIENCE TRANSLATIONAL MEDICINE (2014)

Review Clinical Neurology

Huntington's disease and Huntington's disease-like syndromes: an overview

Felix Goevert et al.

CURRENT OPINION IN NEUROLOGY (2013)

Article Geriatrics & Gerontology

A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family

Rita Guerreiro et al.

NEUROBIOLOGY OF AGING (2013)

Article Medicine, General & Internal

Variant of TREM2 Associated with the Risk of Alzheimer's Disease

Thorlakur Jonsson et al.

NEW ENGLAND JOURNAL OF MEDICINE (2013)

Article Medicine, General & Internal

TREM2 Variants in Alzheimer's Disease

Rita Guerreiro et al.

NEW ENGLAND JOURNAL OF MEDICINE (2013)

Article Genetics & Heredity

Mutations in TREM2 Lead to Pure Early-Onset Dementia Without Bone Cysts

Eliane Chouery et al.

HUMAN MUTATION (2008)

Article Immunology

Cutting edge: TREM-2 attenuates macrophage activation

Isaiah R. Turnbull et al.

JOURNAL OF IMMUNOLOGY (2006)

Review Cell Biology

Nonsense-mediated mRNA decay: Splicing, translation and mRNP dynamics

LE Maquat

NATURE REVIEWS MOLECULAR CELL BIOLOGY (2004)

Letter Clinical Neurology

An Italian family with Nasu-Hakola disease

A Salmaggi et al.

JOURNAL OF NEUROLOGY (2003)