Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype - sprookjes - yvandenbroek - TriplyDB

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

http://www.wikidata.org/entity/Q24642852

about

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia Characterization of frontotemporal dementia and/or amyotrophic lateral sclerosis associated with the GGGGCC repeat expansion in C9ORF72 Neuroimaging signatures of frontotemporal dementia genetics: C9ORF72, tau, progranulin and sporadics A harmonized classification system for FTLD-TDP pathology Neuropathology of non-Alzheimer degenerative disorders Molecular Pathological Classification of Neurodegenerative Diseases: Turning towards Precision Medicine Frontotemporal dementia: a bridge between dementia and neuromuscular disease Progranulin: normal function and role in neurodegeneration In vivo signatures of nonfluent/agrammatic primary progressive aphasia caused by FTLD pathology Variation at GRN 3'-UTR rs5848 is not associated with a risk of frontotemporal lobar degeneration in Dutch population.Plasma phosphorylated-TDP-43 protein levels correlate with brain pathology in frontotemporal lobar degeneration.Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration Neuropathological heterogeneity in frontotemporal lobar degeneration with TDP-43 proteinopathy: a quantitative study of 94 cases using principal components analysis Sporadic corticobasal syndrome due to FTLD-TDP.Classification of FTLD-TDP cases into pathological subtypes using antibodies against phosphorylated and non-phosphorylated TDP43.Recent insights into the molecular genetics of dementia The role of transactive response DNA-binding protein-43 in amyotrophic lateral sclerosis and frontotemporal dementia.Asymmetric TDP-43 distribution in primary progressive aphasia with progranulin mutation Survival profiles of patients with frontotemporal dementia and motor neuron disease.FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration.Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration.Elevated expression of TDP-43 in the forebrain of mice is sufficient to cause neurological and pathological phenotypes mimicking FTLD-U.Altered microRNA expression in frontotemporal lobar degeneration with TDP-43 pathology caused by progranulin mutations.TDP-43 proteinopathy and motor neuron disease in chronic traumatic encephalopathy.FET proteins TAF15 and EWS are selective markers that distinguish FTLD with FUS pathology from amyotrophic lateral sclerosis with FUS mutations.Cognitive impairment in lacunar strokes: the SPS3 trial.Imaging correlates of pathology in corticobasal syndrome.Alteration of POLDIP3 splicing associated with loss of function of TDP-43 in tissues affected with ALS TDP-43 subtypes are associated with distinct atrophy patterns in frontotemporal dementia.Does TDP-43 type confer a distinct pattern of atrophy in frontotemporal lobar degeneration?Brain distribution of dipeptide repeat proteins in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9ORF72 TDP-43 in aging and Alzheimer's disease - a review Antemortem differential diagnosis of dementia pathology using structural MRI: Differential-STAND.Evaluation of subcortical pathology and clinical correlations in FTLD-U subtypes.Hippocampal sclerosis in advanced age: clinical and pathological features.Hippocampal sclerosis in the elderly: genetic and pathologic findings, some mimicking Alzheimer disease clinically Motor neuron disease clinically limited to the lower motor neuron is a diffuse TDP-43 proteinopathy.Amyotrophic lateral sclerosis and frontotemporal lobar degeneration: a spectrum of TDP-43 proteinopathies.Brainstem: neglected locus in neurodegenerative diseases.

P2860

Q24600027-B8B7CABC-0531-4FF6-BE0A-E049DCFE775D Q24630288-18FBEB6C-5EDC-4308-B51F-F4C0EB77FB15 Q24630362-1D678803-5604-4D68-BCEB-5F6D20115C7D Q24630756-0CD8C374-686A-4812-A005-B61A7B409B05 Q24657571-912FD096-C34A-45BF-8EA3-BD0D0E92E4BC Q26768648-722EDF87-0849-43E9-8B9B-62140337DF86 Q28081198-93EC93DE-05CC-4086-AD3D-91CCDCE6E7D8 Q28254281-DE122328-B9D0-47BA-B62C-F07F8646524D Q30568992-14824ED4-E735-4043-8E7A-28F2116FDA3F Q33511759-D923446E-E649-435A-8338-9371E8984B2F Q33601762-8F094D10-6B62-49FC-8595-6E579D351E95 Q33685317-01A2027C-D42C-4952-9EAD-B37A8A6B319F Q33694019-595B05FD-DB6B-429E-9BA2-7A887B49B9DA Q33703433-DC6281E6-415D-4B30-B703-0F0914E9AE1D Q33715607-FC0A08C2-4205-4BFB-8BA3-16E107715FE6 Q33830518-B8BEDB46-CD89-41AD-809F-BEA7C3DE71EB Q33847532-94D5A61F-36AC-4068-8E8C-F42D9A39E083 Q33871696-9DA1BC27-7657-41AA-8380-E2838C3D3072 Q33896030-5F992283-A6D4-4FDB-A3F0-91B6CD32A309 Q33922335-9CD8C114-4E80-4385-B1FA-38C74927DECF Q34023599-3B57992C-2D5D-4B4E-8908-D95AE0C71354 Q34028511-488D044E-AD06-4EEE-AFBD-AB846BD5DCB1 Q34044401-6A8BBABB-2739-417D-980B-D648A1905C86 Q34059809-87DE25CC-0601-47B4-B0A3-C7D5B7AE0689 Q34131994-258C07E8-D6CF-4786-B985-0C0BC71B381B Q34209561-99BC77F4-1828-4DB9-BDE4-AD829DB83DAF Q34343910-EB7E5E0D-B42E-4A12-A9C4-0810B7EC2A88 Q34370058-223E952D-63E9-44EA-B984-3A54270BEE8F Q34382817-7D963397-08CD-43D0-A800-CE01CBC1C672 Q34455599-C7542B2D-1485-4DDD-9856-602E1824FC96 Q34455613-DA797C05-E807-4CAF-98AE-A3B34D010331 Q34500097-7A3FA091-420B-40EC-BBB4-9517161C1FC9 Q34566756-1F8379AA-CA12-4C90-8A59-804BABBC5BD9 Q34575415-7CB2EFC4-40DA-4094-A256-AC4ECF5FA025 Q34604146-FBD7768D-9ED6-4486-B901-1C40F537F160 Q34992164-A052451D-7D0C-45CE-B1E2-B567DBEAFB8A Q35022179-33446B9D-9C79-4B85-B756-BF17E8B55AAE Q35075257-07514C1F-D192-4DDC-A096-288E30C3C3C5 Q35092787-20B177EB-D39E-40F1-BA31-F65ACFA90BDF Q35103955-03C38A12-A276-46A5-BBBE-1B05DC987868

P2860

Heterogeneity of ubiquitin pathology in frontotemporal lobar degeneration: classification and relation to clinical phenotype

http://www.wikidata.org/entity/Q24642852

description

2006 nî lūn-bûn

@nan

2006 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի նոյեմբերին հրատարակված գիտական հոդված

@hy

2006年の論文

@ja

2006年論文

@yue

2006年論文

@zh-hant

2006年論文

@zh-hk

2006年論文

@zh-mo

2006年論文

@zh-tw

2006年论文

@wuu

name

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@ast

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@en

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@nl

type

label

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@ast

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@en

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@nl

prefLabel

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@ast

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@en

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@nl

P1433

Q24642852-767FC7E3-AC0C-43EB-BA05-ED83C214817E

P1476

Q24642852-36D2497E-7059-4A72-9448-13428F8493BF

P2093

Q24642852-26C62595-34D0-468C-B51D-424F4B84BF57

Q24642852-38F0F9A5-2A6B-412C-A438-6372796321A8

Q24642852-5B34C5C0-0950-45AF-A9CA-BB491203DFC8

Q24642852-6080296D-2ED9-4AEE-B6FC-7D87AB6C3298

Q24642852-9AC46891-5437-4F7D-8DEE-DC76C3129498

Q24642852-A40ABA22-6D1D-403A-9868-19BEA1E1D506

Q24642852-BF15C6DC-9D0B-4D23-9A64-119D15A6E207

P2860

Q24642852-04443E22-4B90-46A4-A3FD-95DC253658B3

Q24642852-17FDE6B1-16EB-4780-813F-B56526DDC255

Q24642852-2773A520-E83D-4583-85EA-BEFD0D7390E8

Q24642852-2E7BBCAD-AC0C-4839-A331-5EEE3294A705

Q24642852-30E7B913-DA85-4093-BBF7-089FE3EB980E

Q24642852-3D9D5E16-770A-44EE-968E-B23C958B9CBF

Q24642852-41D527C1-10AC-4D93-BD8E-596EAE61CDBD

Q24642852-47570A84-B29A-4E1F-B83F-3FEFB69B03B8

Q24642852-568524BB-D3A3-47B7-9136-DF9F4EDDF8D7

Q24642852-5994AB82-4EA5-45B4-9179-814F86902A53

P2888

Q24642852-A717B34A-F79E-4C3F-9FAE-B8BF9EB3E2A9

P304

Q24642852-E30B012D-B2FA-4FBB-8541-552F17A2A68D

P31

Q24642852-FB7C1767-D936-4AD9-A265-F5633507FC59

P3181

Q24642852-1D074CA2-193F-4799-A197-7F9932197F04

P356

Q24642852-FAD5F7B1-2580-430E-A233-DA92BB21E2AB

P407

Q24642852-663B3201-1B9C-45C7-9D06-A1DA74C9B599

P433

Q24642852-4BA9EEB1-7CCC-4738-AE0A-831E32A2248B

P478

Q24642852-7E77C929-3E61-4299-B68F-E559F3B281B9

P50

Q24642852-88585FB4-83E8-40A3-9EE1-7787B2E328EF

Q24642852-A007EDA7-80B3-42E7-B20B-EBF07FB710BB

P577

Q24642852-EACCE6B6-CD95-4C21-B502-227413B505DE

P5875

Q24642852-EBBE5D5C-4EAC-4905-8676-689D479E8080

P6179

Q24642852-FBB89E0F-167F-4067-A254-65C847E59F8B

P698

Q24642852-9B520BB8-83EE-4FE2-850B-CCB9B391A131

P921

Q24642852-8bb51f49-ca64-48cb-b92f-418cb448ba36

P932

Q24642852-D26A7DA5-0F2D-40EC-9AFD-FB5094872534

P3181

P356

S00401-006-0138-9

P1433

Acta Neuropathologica

P1476

Heterogeneity of ubiquitin pat ...... relation to clinical phenotype

@en

P2093

Atik Baborie

http://www.w3.org/2001/XMLSchema#string

Daniel Du Plessis

http://www.w3.org/2001/XMLSchema#string

David M A Mann

http://www.w3.org/2001/XMLSchema#string

David Neary

http://www.w3.org/2001/XMLSchema#string

Evelyn Jaros

http://www.w3.org/2001/XMLSchema#string

Ian R A Mackenzie

http://www.w3.org/2001/XMLSchema#string

Robert H Perry

http://www.w3.org/2001/XMLSchema#string

P2860

Null mutations in progranulin cause ubiquitin-positive frontotemporal dementia linked to chromosome 17q21

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

Neuropathologic, biochemical, and molecular characterization of the frontotemporal dementias.

Frontal lobe dementia and motor neuron disease.

Survival in frontotemporal dementia.

Clinicopathological correlates in frontotemporal dementia.

Frontotemporal dementia: clinicopathological correlations

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation.

The neuropathology of frontotemporal lobar degeneration with respect to the cytological and biochemical characteristics of tau protein.

P2888

s00401-006-0138-9

P304

539-49

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P3181

533548

http://www.w3.org/2001/XMLSchema#string

P356

10.1007/S00401-006-0138-9

http://www.w3.org/2001/XMLSchema#string

P407

P433

5

http://www.w3.org/2001/XMLSchema#string

P478

112

http://www.w3.org/2001/XMLSchema#string

P50

Stuart Pickering-Brown

P577

2006-11-01T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

6772794

http://www.w3.org/2001/XMLSchema#string

P6179

1011285999

http://www.w3.org/2001/XMLSchema#string

P698

17021754

http://www.w3.org/2001/XMLSchema#string

P921

P932

2668618

http://www.w3.org/2001/XMLSchema#string