4.7 Article

Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics

Related references

Note: Only part of the references are listed.
Review Clinical Neurology

Neuropathological background of phenotypical variability in frontotemporal dementia

Keith A. Josephs et al.

ACTA NEUROPATHOLOGICA (2011)

Letter Clinical Neurology

A harmonized classification system for FTLD-TDP pathology

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (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

Brain perfusion patterns in familial frontotemporal lobar degeneration

H. Seelaar et al.

NEUROLOGY (2011)

Article Multidisciplinary Sciences

Impaired Structural Motor Connectome in Amyotrophic Lateral Sclerosis

Esther Verstraete et al.

PLOS ONE (2011)

Article Clinical Neurology

In vivo detection of neuropathologic changes in presymptomatic MAPT mutation carriers: A PET and MRI study

Michie Miyoshi et al.

PARKINSONISM & RELATED DISORDERS (2010)

Editorial Material Clinical Neurology

Nomenclature for neuropathologic subtypes of frontotemporal lobar degeneration: consensus recommendations

Ian R. A. Mackenzie et al.

ACTA NEUROPATHOLOGICA (2009)

Article Geriatrics & Gerontology

Prominent phenotypic variability associated with mutations in Progranulin

Brendan J. Kelley et al.

NEUROBIOLOGY OF AGING (2009)

Review Clinical Neurology

Frontotemporal dementia and related disorders: Deciphering the enigma

Keith A. Josephs

ANNALS OF NEUROLOGY (2008)

Article Clinical Neurology

Corticobasal syndrome associated with the A9D Progranulin mutation

Salvatore Spina et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2007)

Article Clinical Neurology

Clinical-pathologic study of biomarkers in FTDP-17 (PPND family with N279K tau mutation)

Zoe Arvanitakis et al.

PARKINSONISM & RELATED DISORDERS (2007)

Article Clinical Neurology

Progranulin mutations in primary progressive aphasia - The PPA1 and PPA3 families

Marsel Mesulam et al.

ARCHIVES OF NEUROLOGY (2007)

Article Biochemistry & Molecular Biology

Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration

Jennifer Gass et al.

HUMAN MOLECULAR GENETICS (2006)

Article Clinical Neurology

Magnetic resonance imaging signatures of tissue pathology in frontotemporal dementia

JL Whitwell et al.

ARCHIVES OF NEUROLOGY (2005)

Article Neurosciences

Unified segmentation

J Ashburner et al.

NEUROIMAGE (2005)

Article Computer Science, Interdisciplinary Applications

Segmentation of brain MR images through a hidden Markov random field model and the expectation-maximization algorithm

YY Zhang et al.

IEEE TRANSACTIONS ON MEDICAL IMAGING (2001)

Article Clinical Neurology

Tau gene mutation K257T causes a tauopathy similar to Pick's disease

C Rizzini et al.

JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY (2000)

Article Neurosciences

Voxel-based morphometry - The methods

J Ashburner et al.

NEUROIMAGE (2000)