Classic ataxia-telangiectasia: the phenotype of long-term survivors

OBJECTIVE: Patients with classic ataxia–telangiectasia (A–T) generally die in the second or third decade of life. Clinical descriptions of A–T tend to focus on the symptoms at presentation. However, during the course of the disease, other symptoms and complications emerge. As long-term survivors wit...

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Detalles Bibliográficos
Publicado en:J Neurol
Autores principales: van Os, Nienke J. H., van Deuren, Marcel, Weemaes, Corry M. R., van Gaalen, Judith, Hijdra, Helma, Taylor, Alexander M. R., van de Warrenburg, Bart P. C., Willemsen, Michèl A. A. P.
Formato: Artigo
Lenguaje:Inglês
Publicado: Springer Berlin Heidelberg 2019
Materias:
Original Communication
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC7035236/
https://ncbi.nlm.nih.gov/pubmed/31776720
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00415-019-09641-1
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