Multimarker synaptic protein cerebrospinal fluid panels reflect TDP-43 pathology and cognitive performance in a pathological cohort of frontotemporal lobar degeneration

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1750-1326

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Multimarker synaptic protein cerebrospinal fluid panels reflect TDP-43 pathology and cognitive performance in a pathological cohort of frontotemporal lobar degeneration ; volume:17 ; number:1 ; day:8 ; month:4 ; year:2022 ; pages:1-12 ; date:12.2022
Molecular neurodegeneration ; 17, Heft 1 (8.4.2022), 1-12, 12.2022

Creator: Cervantes González, Alba
Irwin, David J.
Alcolea, Daniel
McMillan, Corey T.
Chen-Plotkin, Alice
Wolk, David
Sirisi, Sònia
Dols-Icardo, Oriol
Querol-Vilaseca, Marta
Illán-Gala, Ignacio
Santos-Santos, Miguel Angel
Fortea, Juan
Lee, Edward B.
Trojanowski, John Q.
Grossman, Murray
Lleó, Alberto
Belbin, Olivia

Contributor: SpringerLink (Online service)

DOI: 10.1186/s13024-022-00534-y

URN: urn:nbn:de:101:1-2022062521270998958938

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:38 AM CEST

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Associated

Cervantes González, Alba
Irwin, David J.
Alcolea, Daniel
McMillan, Corey T.
Chen-Plotkin, Alice
Wolk, David
Sirisi, Sònia
Dols-Icardo, Oriol
Querol-Vilaseca, Marta
Illán-Gala, Ignacio
Santos-Santos, Miguel Angel
Fortea, Juan
Lee, Edward B.
Trojanowski, John Q.
Grossman, Murray
Lleó, Alberto
Belbin, Olivia
SpringerLink (Online service)

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Multimarker synaptic protein cerebrospinal fluid panels reflect TDP-43 pathology and cognitive performance in a pathological cohort of frontotemporal lobar degeneration

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Other Objects (12)

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TDP-43 pathology in the retina of patients with frontotemporal lobar degeneration

Delusions in frontotemporal lobar degeneration

Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis

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Apraxia phenotypes and frontotemporal lobar degeneration

Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

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Delusions in frontotemporal lobar degeneration

Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration

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Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis

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Apraxia phenotypes and frontotemporal lobar degeneration

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Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations

TDP-43 as a possible biomarker for frontotemporal lobar degeneration: a systematic review of existing antibodies

Diagnostic value of cerebrospinal fluid tau, neurofilament, and progranulin in definite frontotemporal lobar degeneration

In vivo staging of frontotemporal lobar degeneration TDP-43 type C pathology

TDP-43 pathology in the retina of patients with frontotemporal lobar degeneration

Delusions in frontotemporal lobar degeneration

Neuron loss and degeneration in the progression of TDP-43 in frontotemporal lobar degeneration

FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration

Distinct TDP-43 inclusion morphologies in frontotemporal lobar degeneration with and without amyotrophic lateral sclerosis

Frontotemporal Lobar Degeneration: A Clinical Approach

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