Selective Pyramidal Tract Involvement in Late-Onset Krabbe Disease
Author:
Publisher
Springer Science and Business Media LLC
Subject
Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s12098-019-02972-x.pdf
Reference5 articles.
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2. Duffner PK, Barczykowski A, Kay DM, et al. Later onset phenotypes of Krabbe disease: results of the world-wide registry. Pediatr Neurol. 2012;46:298–306.
3. Hagberg B. Krabbe’s disease: clinical presentation of neurological variants. Neuropediatrics. 1984;15:11–5.
4. Krägeloh-Mann I, Harzer K, Rostásy K, et al. Late onset Krabbe disease due to the new GALC p.Ala543Pro mutation, with intriguingly high residual GALC activity in vitro. Eur J Paediatr Neurol. 2017;21:522–9.
5. Del Bigio MR, Chudley AE, Both FA, Pacin S. Late infantile onset Krabbe disease in siblings with cortical degeneration and absence of cerebral globoid cells. Neuropediatrics. 2004;35:297–301.
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