Phenotypic signatures of genetic frontotemporal dementia
Phenotypic signatures of genetic frontotemporal dementia : Current Opinion in Neurology
Phenotypic signatures of genetic frontotemporal dementia : Current Opinion in Neurology Log in …
Phenotypic signatures of genetic frontotemporal dementia : Current Opinion in Neurology Log in …
Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration
Relating clinical symptoms to neuroanatomical profiles of brain damage and ultimately to
tissue pathology is a key challenge in the field of neurodegenerative disease and …
tissue pathology is a key challenge in the field of neurodegenerative disease and …
Clinical and neuropathologic heterogeneity of c9FTD/ALS associated with hexanucleotide repeat expansion in C9ORF72
ME Murray, M DeJesus-Hernandez, NJ Rutherford… - Acta …, 2011 - Springer
Frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS) are part of a
disease spectrum associated with TDP-43 pathology. Strong evidence supporting this is the …
disease spectrum associated with TDP-43 pathology. Strong evidence supporting this is the …
The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships
JS Snowden, JC Thompson, CL Stopford… - Brain, 2011 - academic.oup.com
Accuracy of clinical diagnosis of dementia is increasingly important for therapeutic and
scientific investigations. In this study, we examine diagnostic accuracy in a consecutive …
scientific investigations. In this study, we examine diagnostic accuracy in a consecutive …
On the development of markers for pathological TDP-43 in amyotrophic lateral sclerosis with and without dementia
F Geser, D Prvulovic, L O'Dwyer, O Hardiman… - Progress in …, 2011 - Elsevier
Pathological 43-kDa transactive response sequence DNA-binding protein (TDP-43) has
been recognized as the major disease protein in amyotrophic lateral sclerosis (ALS) …
been recognized as the major disease protein in amyotrophic lateral sclerosis (ALS) …
Semantic dementia: a specific network-opathy
PD Fletcher, JD Warren - Journal of Molecular Neuroscience, 2011 - Springer
Semantic dementia (SD) is a unique syndrome in the frontotemporal lobar degeneration
spectrum. Typically presenting as a progressive, fluent anomic aphasia, SD is the …
spectrum. Typically presenting as a progressive, fluent anomic aphasia, SD is the …
Misfolded superoxide dismutase-1 in sporadic and familial Amyotrophic Lateral Sclerosis
K Forsberg - 2011 - diva-portal.org
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative syndrome of unknown
etiology that most commonly affects people in middle and high age. The hallmark of ALS is a …
etiology that most commonly affects people in middle and high age. The hallmark of ALS is a …
Frontotemporal Lobar Degeneration
J Schlachetzki - Advanced Understanding of Neurodegenerative …, 2011 - books.google.com
Frontotemporal lobar degeneration (FTLD) comprises diseases with a very diverging
spectrum in regards to clinical presentation, genetics, and neuropathology. In 1892 Arnold …
spectrum in regards to clinical presentation, genetics, and neuropathology. In 1892 Arnold …
教育講演5 前頭側頭葉変性症(FTLD) の概念と分類update
中野今治 - 臨床神経学, 2011 - jstage.jst.go.jp
抄録 FTLD is a neuroanatomical disease concept defined only by the presence of
degeneration of the frontal and temporal lobes regardless of the underlying …
degeneration of the frontal and temporal lobes regardless of the underlying …