- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Infantile neuroaxonal dystrophy (INAD): a 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
-
Antonio, Fernanda Ferrão
Benevides, Maria Luiza
Elias, Paula Thais Bandeira
Sommavilla, Larisse Souza
Falcão, Ana Carolina Piauilino
Castellano, Isabelle Salgado
Schmutzler, Katia Maria Ribeiro
Coan, Ana Carolina
Teixeira, Karine Couto Sarmento
- DOI
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10.1055/s-0043-1774580
- URN
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urn:nbn:de:101:1-2023110211291973811046
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:55 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
- Antonio, Fernanda Ferrão
- Benevides, Maria Luiza
- Elias, Paula Thais Bandeira
- Sommavilla, Larisse Souza
- Falcão, Ana Carolina Piauilino
- Castellano, Isabelle Salgado
- Schmutzler, Katia Maria Ribeiro
- Coan, Ana Carolina
- Teixeira, Karine Couto Sarmento
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Fundus flavimaculatus-like in myotonic dystrophy: a case report
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Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Confined placental mosaicism of Duchenne muscular dystrophy: a case report
Surgical correction of hyperlordosis in facioscapulohumeral muscular dystrophy: A case report
Steinert's myotonic dystrophy: a case report
The natural history of infantile neuroaxonal dystrophy
The infantile neuroaxonal dystrophy rating scale (INAD-RS)
Infantile neuroaxonal dystrophy associated with seizures in a patient from a teaching hospital in southern Brazil: case report
GNB1-Related Rod-Cone Dystrophy: A Case Report
Concurrence of myotonic dystrophy and epilepsy: a case report
Fundus flavimaculatus-like in myotonic dystrophy: a case report
Cervical congenital infantile fibrosarcoma: a case report
A case report of infantile cystic nephroblastoma
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Confined placental mosaicism of Duchenne muscular dystrophy: a case report