UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 78

Sortiert nach

Classification and pathology of primary progressive aphasia

Neurology, 2013-11, Vol.81 (21), p.1832

2013

Volltextzugriff (PDF)

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

Brain (London, England : 1878), 2012-03, Vol.135 (Pt 3), p.693-708

2012

Volltextzugriff (PDF)

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships

Brain (London, England : 1878), 2011-09, Vol.134 (9), p.2478-2492

2011

Volltextzugriff (PDF)

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

Annals of neurology, 2013-07, Vol.74 (1), p.128-139

2013

Volltextzugriff (PDF)

Semantic dementia and the left and right temporal lobes

Cortex, 2018-10, Vol.107, p.188-203

2018

Volltextzugriff (PDF)

Partial volume correction in quantitative amyloid imaging

NeuroImage (Orlando, Fla.), 2015-02, Vol.107, p.55-64

2015

Volltextzugriff (PDF)

Working memory, attention, and executive function in Alzheimer’s disease and frontotemporal dementia

Cortex, 2012-04, Vol.48 (4), p.429-446

2012

Volltextzugriff (PDF)

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

Neurology, 2013-05, Vol.80 (20), p.1881

2013

Volltextzugriff (PDF)

Abnormal Cortical Complexity and Thickness Profiles Mapped in Williams Syndrome

The Journal of neuroscience, 2005-04, Vol.25 (16), p.4146-4158

2005

Volltextzugriff (PDF)

Concomitant progressive supranuclear palsy and Lewy body pathology presenting with circumscribed visual memory loss: A clinicopathological case

Brain pathology (Zurich, Switzerland), 2024-07, Vol.34 (4), p.e13219-n/a

2024

Volltextzugriff (PDF)

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

Acta neuropathologica communications, 2013-10, Vol.1 (1), p.68-68, Article 68

2013

Volltextzugriff (PDF)

Examining the language and behavioural profile in FTD and ALS-FTD

Journal of neurology, neurosurgery and psychiatry, 2017-08, Vol.88 (8), p.675

2017

Volltextzugriff (PDF)

Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies

Journal of neuropathology and experimental neurology, 2018-12, Vol.77 (12), p.1101-1114

2018

Volltextzugriff (PDF)

Cognition and behaviour in frontotemporal dementia with and without amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2020-12, Vol.91 (12), p.1304

2020

Volltextzugriff (PDF)

Naming and conceptual understanding in frontotemporal dementia

Cortex, 2019-11, Vol.120, p.22-35

2019

Volltextzugriff (PDF)

Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues

Acta neuropathologica, 2017-12, Vol.134 (6), p.889-904

2017

Volltextzugriff (PDF)

TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

Acta neuropathologica, 2011-12, Vol.122 (6), p.703-713

2011

Volltextzugriff (PDF)

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry

NeuroImage (Orlando, Fla.), 2007-07, Vol.36 (4), p.1096-1109

2007

Volltextzugriff (PDF)

Psychological, surgical, and sociodemographic predictors of pain outcomes after breast cancer surgery: A population-based cohort study

Pain (Amsterdam), 2014-02, Vol.155 (2), p.232-243

2014

Volltextzugriff (PDF)

Semantic dementia, progressive non-fluent aphasia and their association with amyotrophic lateral sclerosis

Journal of neurology, neurosurgery and psychiatry, 2017-08, Vol.88 (8), p.711

2017

Volltextzugriff (PDF)

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2015-11, Vol.16 (7-8), p.497-505

2015

Volltextzugriff (PDF)

Patterns of microglial cell activation in frontotemporal lobar degeneration

Neuropathology and applied neurobiology, 2014-10, Vol.40 (6), p.686-696

2014

Volltextzugriff (PDF)

Association between semantic dementia and progressive supranuclear palsy

Journal of neurology, neurosurgery and psychiatry, 2019-01, Vol.90 (1), p.115

2019

Volltextzugriff (PDF)

1 – 25 von 78

Suche als RSS-Feed

Aktive Filter

ThemaNeurosciences & Neurology

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(75)
Mit Volltextzugriff
(63)

Publikationsform

Artikel
(78)

Sprache

Englisch
(78)
Japanisch
(16)

Erscheinungsjahr

n.n

Thema

14 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Classification and pathology of primary progressive aphasia

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships

Dravet syndrome patient-derived neurons suggest a novel epilepsy mechanism

Semantic dementia and the left and right temporal lobes

Partial volume correction in quantitative amyloid imaging

Working memory, attention, and executive function in Alzheimer’s disease and frontotemporal dementia

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

Abnormal Cortical Complexity and Thickness Profiles Mapped in Williams Syndrome

Concomitant progressive supranuclear palsy and Lewy body pathology presenting with circumscribed visual memory loss: A clinicopathological case

Dipeptide repeat proteins are present in the p62 positive inclusions in patients with frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72

CYLD is a causative gene for frontotemporal dementia - amyotrophic lateral sclerosis

Examining the language and behavioural profile in FTD and ALS-FTD

Loss of Sarcomeric Scaffolding as a Common Baseline Histopathologic Lesion in Titin-Related Myopathies

Cognition and behaviour in frontotemporal dementia with and without amyotrophic lateral sclerosis

Naming and conceptual understanding in frontotemporal dementia

Affected female carriers of MTM1 mutations display a wide spectrum of clinical and pathological involvement: delineating diagnostic clues

Preclinical profile of a dopamine D1 potentiator suggests therapeutic utility in neurological and psychiatric disorders

TDP-43 pathological changes in early onset familial and sporadic Alzheimer’s disease, late onset Alzheimer’s disease and Down’s Syndrome: association with age, hippocampal sclerosis and clinical phenotype

3D pattern of brain abnormalities in Williams syndrome visualized using tensor-based morphometry

Psychological, surgical, and sociodemographic predictors of pain outcomes after breast cancer surgery: A population-based cohort study

Semantic dementia, progressive non-fluent aphasia and their association with amyotrophic lateral sclerosis

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

Patterns of microglial cell activation in frontotemporal lobar degeneration

Association between semantic dementia and progressive supranuclear palsy

Aktive Filter

Suchergebnisse filtern