Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
1619-7089
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Amyotrophic lateral sclerosis with SOD1 mutations shows distinct brain metabolic changes ; day:25 ; month:1 ; year:2022 ; pages:1-9
European journal of nuclear medicine and molecular imaging ; (25.1.2022), 1-9
- Urheber
-
Canosa, Antonio
Calvo, Andrea
Moglia, Cristina
Vasta, Rosario
Palumbo, Francesca
Solero, Luca
Pede, Francesca Di
Cabras, Sara
Arena, Vincenzo
Zocco, Grazia
Casale, Federico
Brunetti, Maura
Sbaiz, Luca
Gallone, Salvatore
Grassano, Maurizio
Manera, Umberto
Pagani, Marco
Chiò, Adriano
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1007/s00259-021-05668-7
- URN
-
urn:nbn:de:101:1-2022050519100282289767
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:22 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
- Canosa, Antonio
- Calvo, Andrea
- Moglia, Cristina
- Vasta, Rosario
- Palumbo, Francesca
- Solero, Luca
- Pede, Francesca Di
- Cabras, Sara
- Arena, Vincenzo
- Zocco, Grazia
- Casale, Federico
- Brunetti, Maura
- Sbaiz, Luca
- Gallone, Salvatore
- Grassano, Maurizio
- Manera, Umberto
- Pagani, Marco
- Chiò, Adriano
- SpringerLink (Online service)
Ähnliche Objekte (12)
Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation
Protease-resistant SOD1 aggregates in amyotrophic lateral sclerosis demonstrated by paraffin-embedded tissue (PET) blot
Changes in Cerebrospinal Fluid Concentrations of Selenium Species Induced by Tofersen Administration in Subjects with Amyotrophic Lateral Sclerosis Carrying SOD1 Gene Mutations
Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling
Amyotrophic lateral sclerosis
Variability in SOD1-associated amyotrophic lateral sclerosis: geographic patterns, clinical heterogeneity, molecular alterations, and therapeutic implications
A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations
SIRT1 overexpression ameliorates a mouse model of SOD1-linked amyotrophic lateral sclerosis via HSF1/HSP70i chaperone system
Superoxide Dismutase 1 Folding Stability as a Target for Molecular Tweezers in SOD1‐Related Amyotrophic Lateral Sclerosis
Correction to: Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with Molecular modelling
Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation
Protease-resistant SOD1 aggregates in amyotrophic lateral sclerosis demonstrated by paraffin-embedded tissue (PET) blot
Changes in Cerebrospinal Fluid Concentrations of Selenium Species Induced by Tofersen Administration in Subjects with Amyotrophic Lateral Sclerosis Carrying SOD1 Gene Mutations
Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling
Amyotrophic lateral sclerosis
Variability in SOD1-associated amyotrophic lateral sclerosis: geographic patterns, clinical heterogeneity, molecular alterations, and therapeutic implications
A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations
SIRT1 overexpression ameliorates a mouse model of SOD1-linked amyotrophic lateral sclerosis via HSF1/HSP70i chaperone system
Superoxide Dismutase 1 Folding Stability as a Target for Molecular Tweezers in SOD1‐Related Amyotrophic Lateral Sclerosis
Correction to: Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with Molecular modelling
Pathological Modification of TDP-43 in Amyotrophic Lateral Sclerosis with SOD1 Mutations
Misfolded SOD1 pathology in sporadic Amyotrophic Lateral Sclerosis
Widespread CNS pathology in amyotrophic lateral sclerosis homozygous for the D90A SOD1 mutation
Protease-resistant SOD1 aggregates in amyotrophic lateral sclerosis demonstrated by paraffin-embedded tissue (PET) blot
Changes in Cerebrospinal Fluid Concentrations of Selenium Species Induced by Tofersen Administration in Subjects with Amyotrophic Lateral Sclerosis Carrying SOD1 Gene Mutations
Molecular mechanisms underlying the impact of mutations in SOD1 on its conformational properties associated with amyotrophic lateral sclerosis as revealed with molecular modelling
Amyotrophic lateral sclerosis
Variability in SOD1-associated amyotrophic lateral sclerosis: geographic patterns, clinical heterogeneity, molecular alterations, and therapeutic implications
A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations
SIRT1 overexpression ameliorates a mouse model of SOD1-linked amyotrophic lateral sclerosis via HSF1/HSP70i chaperone system
Superoxide Dismutase 1 Folding Stability as a Target for Molecular Tweezers in SOD1‐Related Amyotrophic Lateral Sclerosis