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...

Täydet tiedot

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Bibliografiset tiedot
Julkaisussa:J Neurol
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Springer Berlin Heidelberg 2019
Aiheet:
Original Communication
Linkit: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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