Related references
Note: Only part of the references are listed.A novel mutation in TREM2 gene causing Nasu-Hakola disease and review of the literature
Efthimios Dardiotis et al.
NEUROBIOLOGY OF AGING (2017)
Frontotemporal Dementia
Nicholas T. Olney et al.
NEUROLOGIC CLINICS (2017)
Genetics of FTLD: overview and what else we can expect from genetic studies
Cyril Pottier et al.
JOURNAL OF NEUROCHEMISTRY (2016)
Rare TREM2 variants associated with Alzheimer's disease display reduced cell surface expression
Daniel W. Sirkis et al.
ACTA NEUROPATHOLOGICA COMMUNICATIONS (2016)
The role of TREM2 R47H as a risk factor for Alzheimer's disease, frontotemporal lobar degeneration, amyotrophic lateral sclerosis, and Parkinson's disease
Christina M. Lill et al.
ALZHEIMERS & DEMENTIA (2015)
RNF216 mutations as a novel cause of autosomal recessive Huntington-like disorder
Patrick Santens et al.
NEUROLOGY (2015)
The human splicing code reveals new insights into the genetic determinants of disease
Hui Y. Xiong et al.
SCIENCE (2015)
Homozygous TREM2 mutation in a family with atypical frontotemporal dementia
Isabelle Le Ber et al.
NEUROBIOLOGY OF AGING (2014)
Heterozygous TREM2 mutations in frontotemporal dementia
Barbara Borroni et al.
NEUROBIOLOGY OF AGING (2014)
Investigating the role of rare heterozygous TREM2 variants in Alzheimer's disease and frontotemporal dementia
Elise Cuyvers et al.
NEUROBIOLOGY OF AGING (2014)
Investigation of the role of rare TREM2 variants in frontotemporal dementia subtypes
Mathias Thelen et al.
NEUROBIOLOGY OF AGING (2014)
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies
Davina J. Hensman Moss et al.
NEUROLOGY (2014)
TREM2 mutations implicated in neurodegeneration impair cell surface transport and phagocytosis
Gernot Kleinberger et al.
SCIENCE TRANSLATIONAL MEDICINE (2014)
Huntington's disease and Huntington's disease-like syndromes: an overview
Felix Goevert et al.
CURRENT OPINION IN NEUROLOGY (2013)
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer's disease
Margarita Giraldo et al.
NEUROBIOLOGY OF AGING (2013)
A novel compound heterozygous mutation in TREM2 found in a Turkish frontotemporal dementia-like family
Rita Guerreiro et al.
NEUROBIOLOGY OF AGING (2013)
Variant of TREM2 Associated with the Risk of Alzheimer's Disease
Thorlakur Jonsson et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
TREM2 Variants in Alzheimer's Disease
Rita Guerreiro et al.
NEW ENGLAND JOURNAL OF MEDICINE (2013)
Using Exome Sequencing to Reveal Mutations in TREM2 Presenting as a Frontotemporal Dementia-like Syndrome Without Bone Involvement
Rita Joao Guerreiro et al.
JAMA NEUROLOGY (2013)
Optimal Plasma Progranulin Cutoff Value for Predicting Null Progranulin Mutations in Neurodegenerative Diseases: A Multicenter Italian Study
Roberta Ghidoni et al.
NEURODEGENERATIVE DISEASES (2012)
Mutations in TREM2 Lead to Pure Early-Onset Dementia Without Bone Cysts
Eliane Chouery et al.
HUMAN MUTATION (2008)
Cutting edge: TREM-2 attenuates macrophage activation
Isaiah R. Turnbull et al.
JOURNAL OF IMMUNOLOGY (2006)
Nonsense-mediated mRNA decay: Splicing, translation and mRNP dynamics
LE Maquat
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2004)
An Italian family with Nasu-Hakola disease
A Salmaggi et al.
JOURNAL OF NEUROLOGY (2003)
Mutations in two genes encoding different subunits of a receptor signaling complex result in an identical disease phenotype
J Paloneva et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2002)
CNS manifestations of Nasu-Hakola disease - A frontal dementia with bone cysts
J Paloneva et al.
NEUROLOGY (2001)
Cutting edge: Inflammatory responses can be triggered by TREM-1, a novel receptor expressed on neutrophils and monocytes
A Bouchon et al.
JOURNAL OF IMMUNOLOGY (2000)