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"Ears of the lynx" sign and thin corpus callosum on MRI in heterozygous SPG11 mutation carriers.
Rattay, Tim W; Schöls, Ludger; Zeltner, Lena; Rohrschneider, Wiltrud K; Ernemann, Ulrike; Lindig, Tobias.
Afiliação
  • Rattay TW; Department of Neurodegenerative Diseases, Center for Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Hoppe-Seyler-Straße 3, 72076, Tübingen, Germany.
  • Schöls L; German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany.
  • Zeltner L; Center for Rare Diseases (ZSE), University of Tübingen, Tübingen, Germany.
  • Rohrschneider WK; Department of Neurodegenerative Diseases, Center for Neurology and Hertie-Institute for Clinical Brain Research, University of Tübingen, Hoppe-Seyler-Straße 3, 72076, Tübingen, Germany. ludger.schoels@uni-tuebingen.de.
  • Ernemann U; German Center of Neurodegenerative Diseases (DZNE), Tübingen, Germany. ludger.schoels@uni-tuebingen.de.
  • Lindig T; Center for Rare Diseases (ZSE), University of Tübingen, Tübingen, Germany. ludger.schoels@uni-tuebingen.de.
J Neurol ; 269(11): 6148-6151, 2022 11.
Article em En | MEDLINE | ID: mdl-35614164
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Lynx Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Paraplegia Espástica Hereditária / Lynx Limite: Animals / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article