First Brazilian case of rare mitochondrial myopathy and ataxia associated to MSTO1 variants
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
First Brazilian case of rare mitochondrial myopathy and ataxia associated to MSTO1 variants ; volume:81 ; number:S 01 ; year:2023 ; 01
Konferenz: SBN Conference 2022; 2022-11-09; Expo United Curitiba
Arquivos de neuro-psiquiatria ; 81, Heft S 01 (2023), 01
- Contributor
-
Torres, Mateus Oliveira
Filho, José Marcos Vieira Albuquerque
Valeriano, Katrine Freitas
Maranhão, Caroline Corrêa
Cyrino, Lorena Raulik
Cajado, Bryan Silva Marques
Aragão, Marcelo Melo
Fonseca, Alulin Tacio Quadros Monteiro
Pinho, Ricardo Silva
- DOI
-
10.1055/s-0043-1774511
- URN
-
urn:nbn:de:101:1-2023110211160059054140
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:56 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Torres, Mateus Oliveira
- Filho, José Marcos Vieira Albuquerque
- Valeriano, Katrine Freitas
- Maranhão, Caroline Corrêa
- Cyrino, Lorena Raulik
- Cajado, Bryan Silva Marques
- Aragão, Marcelo Melo
- Fonseca, Alulin Tacio Quadros Monteiro
- Pinho, Ricardo Silva
Other Objects (12)
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
MSTO 1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
Hepatic mitochondrial dysfunction in Friedreich Ataxia
Mitochondrial myopathy presenting as fibromyalgia: a case report
A case report of mitochondrial myopathy with membranous nephropathy
Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
Myopathy reversion in mice after restauration of mitochondrial complex I
Exploring mitochondrial biomarkers for Friedreich's ataxia: a multifaceted approach
Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy
Salvaging hope: Is increasing NAD + a key to treating mitochondrial myopathy?
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
MSTO 1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
Hepatic mitochondrial dysfunction in Friedreich Ataxia
Mitochondrial myopathy presenting as fibromyalgia: a case report
A case report of mitochondrial myopathy with membranous nephropathy
Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
Myopathy reversion in mice after restauration of mitochondrial complex I
Exploring mitochondrial biomarkers for Friedreich's ataxia: a multifaceted approach
Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy
Salvaging hope: Is increasing NAD + a key to treating mitochondrial myopathy?
MSTO1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
MSTO 1 is a cytoplasmic pro‐mitochondrial fusion protein, whose mutation induces myopathy and ataxia in humans
Hepatic mitochondrial dysfunction in Friedreich Ataxia
Mitochondrial myopathy presenting as fibromyalgia: a case report
A case report of mitochondrial myopathy with membranous nephropathy
Altered skeletal muscle (mitochondrial) properties in patients with mitochondrial DNA single deletion myopathy
Nemaline myopathy in Brazilian patients: clinical, muscle imaging and molecular characterization
A coordinated multiorgan metabolic response contributes to human mitochondrial myopathy
Myopathy reversion in mice after restauration of mitochondrial complex I
Exploring mitochondrial biomarkers for Friedreich's ataxia: a multifaceted approach
Pathological findings with vacuoles in anti-mitochondrial antibody-positive inflammatory myopathy