- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
1 Online-Ressource.
- Sprache
-
Englisch
- Erschienen in
-
LINC complex alterations are a key feature of sporadic and familial ALS/FTD ; volume:12 ; number:1 ; day:25 ; month:4 ; year:2024 ; pages:1-16 ; date:12.2024
Acta Neuropathologica Communications ; 12, Heft 1 (25.4.2024), 1-16, 12.2024
- Urheber
-
Sirtori, Riccardo
Gregoire, Michelle J.
Potts, Emily M.
Collins, Alicia
Donatelli, Liviana
Fallini, Claudia
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1186/s40478-024-01778-z
- URN
-
urn:nbn:de:101:1-2407120728339.980491538816
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:49 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Sirtori, Riccardo
- Gregoire, Michelle J.
- Potts, Emily M.
- Collins, Alicia
- Donatelli, Liviana
- Fallini, Claudia
- SpringerLink (Online service)
Ähnliche Objekte (12)
Molecular mechanisms and biomarkers of familial FTD/ALS
Differences Between Familial and Sporadic Celiac Disease
A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma
FTD
Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): a qualitative study
Vascular dysfunction in sporadic bvFTD: white matter hyperintensity and peripheral vascular biomarkers
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements
Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas
Imaging Familial and Sporadic Neurodegenerative Disorders Associated with Parkinsonism
Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma
Defining the overlap between sporadic and attenuated familial adenoma risk
Molecular mechanisms and biomarkers of familial FTD/ALS
Differences Between Familial and Sporadic Celiac Disease
A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma
FTD
Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): a qualitative study
Vascular dysfunction in sporadic bvFTD: white matter hyperintensity and peripheral vascular biomarkers
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements
Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas
Imaging Familial and Sporadic Neurodegenerative Disorders Associated with Parkinsonism
Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma
Defining the overlap between sporadic and attenuated familial adenoma risk
Molecular mechanisms and biomarkers of familial FTD/ALS
Differences Between Familial and Sporadic Celiac Disease
A familial FTD associated with C9orf72 repeat expansion and dysplastic gangliocytoma
FTD
Exploring experiences and needs of spousal carers of people with behavioural variant frontotemporal dementia (bvFTD) including those with familial FTD (fFTD): a qualitative study
Vascular dysfunction in sporadic bvFTD: white matter hyperintensity and peripheral vascular biomarkers
"Familial" versus "sporadic" intellectual disability: contribution of subtelomeric rearrangements
Genomic profiling distinguishes familial multiple and sporadic multiple meningiomas
Imaging Familial and Sporadic Neurodegenerative Disorders Associated with Parkinsonism
Sporadic and Familial Acute Myeloid Leukemia with CEBPA Mutations
Analysis of SDHAF3 in familial and sporadic pheochromocytoma and paraganglioma