- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Pelizaeus-Merzbacher disease (PMD): case report ; 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
-
Russi, Sofia
Teixeira, Amanda Regina Farias
Martins, Caroline Sccantamburlo
Ferreira, Jéssica Kayene Souza
Paschoal, Lana Correa
Passos, Maria Lina Giacomino de Almeida
Martins, Marlos Melo
Mendes, Mariana Horst
Neto, Nilson Russi
- DOI
-
10.1055/s-0043-1774599
- URN
-
urn:nbn:de:101:1-2023110211332784646183
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:54 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
- Russi, Sofia
- Teixeira, Amanda Regina Farias
- Martins, Caroline Sccantamburlo
- Ferreira, Jéssica Kayene Souza
- Paschoal, Lana Correa
- Passos, Maria Lina Giacomino de Almeida
- Martins, Marlos Melo
- Mendes, Mariana Horst
- Neto, Nilson Russi
Other Objects (12)
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease
Subcellular trafficking of proteolipid protein (PLP-DM20) and novel mechanisms of ER retention in Pelizaeus-Merzbacher disease
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans
Merzbacher, Elena geb. Merzbacher
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease
Subcellular trafficking of proteolipid protein (PLP-DM20) and novel mechanisms of ER retention in Pelizaeus-Merzbacher disease
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans
Merzbacher, Elena geb. Merzbacher
Pelizaeus Merzbacher disease: dysmyelination versus demyelination
Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Missense mutation of MAL causes a rare leukodystrophy similar to Pelizaeus-Merzbacher disease
Correction to: Exome sequencing reveals a novel PLP1 mutation in a Moroccan family with connatal Pelizaeus-Merzbacher disease: a case report
Correction to: Ketogenic diet ameliorates axonal defects and promotes myelination in Pelizaeus–Merzbacher disease
Genotype–phenotype correlation and natural history analyses in a Chinese cohort with pelizaeus–merzbacher disease
Subcellular trafficking of proteolipid protein (PLP-DM20) and novel mechanisms of ER retention in Pelizaeus-Merzbacher disease
Pelizäus Merzbacher Erkrankung in einem Fall mit Chromosomenanomalie im Bereich des Genorts PLP
Experimentelle Therapie eines Mausmodells für die Pelizaeus-Merzbacher-Erkrankung mit Lonaprisan und Curcumin
Generation and characterization of mice expressing a mutation in the connexin47 protein wich causes Pelizaeus-Merzbacher Like Disease in humans