Early progression of Krabbe disease in patients with symptom onset between 0 and 5 months-Reference-Cited by-同舟云学术

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Early progression of Krabbe disease in patients with symptom onset between 0 and 5 months

Published:2019-02-18 Issue:1 Volume:14 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Beltran-Quintero Maria L.,Bascou Nicholas A.,Poe Michele D.,Wenger David A.,Saavedra-Matiz Carlos A.,Nichols Matthew J.,Escolar Maria L.

Funder

National Institutes of Health

The Legacy of Angels Foundation

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-019-1018-4.pdf

Reference48 articles.

1. Wenger DA, Rafi MA, Luzi P, et al. Krabbe disease: genetic aspects and progress toward therapy. Mol Genet Metab. 2000;70:1–9.

2. Zafeiriou DI, Anastasiou AL, Michelakaki EM, Augoustidou-Savvopoulou PA, Katzos GS, Kontopoulos EE. Early-infantile Krabbe disease: deceptively normal magnetic resonance imaging and serial neurophysiological studies. Brain and Development. 1997;19(7):488–91.

3. Wraith JE. The clinical presentation of lysosomal storage disorders. Acta Neurol Taiwanica. 2004 Sep;13(3):101–6.

4. Suzuki K. Globoid cell leukodystrophy (Krabbe’s disease): update. J Child Neurol. 2003;18(9):595–603.

5. Hagberg B, Sourander P, Svennerholm L. Diagnosis of Krabbe’s infantile leucodystrophy. J Neurol Neurosurg Psychiatry. 1963;26:195–8.

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