4.7 Article

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions

相关参考文献

注意:仅列出部分参考文献,下载原文获取全部文献信息。
Letter Clinical Neurology

A harmonized classification system for FTLD-TDP pathology

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2011)

Article Biochemistry & Molecular Biology

Cellular toxicity of expanded RNA repeats: focus on RNA foci

Marzena Wojciechowska et al.

HUMAN MOLECULAR GENETICS (2011)

Review Clinical Neurology

Clinical, genetic and pathological heterogeneity of frontotemporal dementia: a review

Harro Seelaar et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)

Article Clinical Neurology

Clinical, neuroimaging and neuropathological features of a new chromosome 9p-linked FTD-ALS family

Adam L. Boxer et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2011)

Article Clinical Neurology

Predicting survival in frontotemporal dementia with motor neuron disease

E. A. Coon et al.

NEUROLOGY (2011)

Review Clinical Neurology

Classification of primary progressive aphasia and its variants

M. L. Gorno-Tempini et al.

NEUROLOGY (2011)

Article Clinical Neurology

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Hannu Laaksovirta et al.

LANCET NEUROLOGY (2010)

Article Multidisciplinary Sciences

Mutations of optineurin in amyotrophic lateral sclerosis

Hirofumi Maruyama et al.

NATURE (2010)

Article Genetics & Heredity

Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP43 inclusions

Vivianna M. Van Deerlin et al.

NATURE GENETICS (2010)

Article Neurosciences

Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Jane O. Johnson et al.

NEURON (2010)

Article Clinical Neurology

Semantic dementia combined with motor neuron disease

Sook Hui Kim et al.

JOURNAL OF CLINICAL NEUROSCIENCE (2009)

Article Multidisciplinary Sciences

Mutations in the FUS/TLS Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis

T. J. Kwiatkowski et al.

SCIENCE (2009)

Article Clinical Neurology

Distinct genetic forms of frontotemporal dementia

H. Seelaar et al.

NEUROLOGY (2008)

Article Multidisciplinary Sciences

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

Jemeen Sreedharan et al.

SCIENCE (2008)

Article Pathology

TDP-43 in familial and sporadic frontotemporal lobar degeneration with ubiquitin inclusions

Nigel J. Cairns et al.

AMERICAN JOURNAL OF PATHOLOGY (2007)

Review Clinical Neurology

Hereditary frontotemporal dementia caused by Tau gene mutations

John van Swieten et al.

BRAIN PATHOLOGY (2007)

Review Biochemistry & Molecular Biology

Genetics of familial and sporadic amyotrophic lateral sclerosis

Francois Gros-Louis et al.

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE (2006)

Article Multidisciplinary Sciences

Ubiquitinated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis

Manuela Neumann et al.

SCIENCE (2006)

Article Clinical Neurology

Comparison of family histories in FTLD subtypes and related tauopathies

JS Goldman et al.

NEUROLOGY (2005)

Article Clinical Neurology

Familial motor neurone disease with dementia: phenotypic variation and cerebellar pathology

TM Polvikoski et al.

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY (2003)

Article Clinical Neurology

The overlap of amyotrophic lateral sclerosis and frontotemporal dementia

C Lomen-Hoerth et al.

NEUROLOGY (2002)

Article Clinical Neurology

The prevalence of frontotemporal dementia

E Ratnavalli et al.

NEUROLOGY (2002)

Review Medicine, General & Internal

Medical progress: Amyotrophic lateral sclerosis.

LP Rowland et al.

NEW ENGLAND JOURNAL OF MEDICINE (2001)