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Van Der Bergh PY, Hadden RD, Bouche P, et al. European Federation of Neurological Societies\/Peripheral Nerve Society guideline on management of chronic inflammatory demyelinating polyradiculoneuropathy: report of a joint task force of the European Federation of Neurological Societies and the Peripheral Nerve Society. Eur J Neurol 17: 356-363, 2010."},{"key":"2","unstructured":"2. Suzuki Y. Globoid cell leucodystrophy (Krabbe's disease): deficiency of galactocerebroside beta-galactosidase. Proc Natl Acad Sci 66: 302-309, 1970."},{"key":"3","unstructured":"3. Wegener DA, Suzuki K, Suzuki Y, et al. Galactosylceramide lipidosis: globoid cell leukodystrophy (Krabbe disease). In: The Metabolic & Molecular Basis of Inherited Disease. 8th ed. Scriver R, Beaudet AL, Sly WS, et al., Eds. McGraw-Hill, New York, 2001: 3669-3694."},{"key":"4","doi-asserted-by":"crossref","unstructured":"4. Hossain MA, Otomo T, Saito S, et al. 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Krabbe disease in adults: phenotypic and genotypic update from a series of 11 cases and a review. J Inherit Metab Dis 36: 859-868, 2013."},{"key":"9","unstructured":"9. Sakai N. Pathogenesis of leukodystrophy for Krabbe disease: molecular mechanism and clinical treatment. Brain Dev 31: 485-487, 2009."},{"key":"10","doi-asserted-by":"crossref","unstructured":"10. Kondo Y, Wenger AD, Gallo V, Duncan ID. Galactocerebrosidase-deficient oligodendrocytes maintain stable central myelin by exogenous replacement of the missing enzyme mice. Proc Natl Acad Sci 102: 18670-18675, 2005.","DOI":"10.1073\/pnas.0506473102"},{"key":"11","unstructured":"11. Goebel HH, Harzer K, Emst JP, Bohl J, Klein H. Late-onset globoid cell leukodystrophy: unusual ultrastructual pathology and subtotal \u03b2-galactocerebrosidase deficiency. J Child Neurol 5: 299-307, 1990."},{"key":"12","doi-asserted-by":"crossref","unstructured":"12. Mamada N, Nakamagoe K, Shioya A, et al. Adult-onset Krabbe disease presenting as acute hemiparesis and progressive demyelination detected by diffusion-weighted imaging. J Neurol Sci 367: 326-328, 2016.","DOI":"10.1016\/j.jns.2016.06.026"},{"key":"13","doi-asserted-by":"crossref","unstructured":"13. Rachana D, Biswaroop C, Sheffali G, et al. Leukodystrophy presenting as acute-onset polyradiculoneuropathy. Pediatr Neurol 50: 616-618, 2014.","DOI":"10.1016\/j.pediatrneurol.2014.01.028"},{"key":"14","unstructured":"14. Iannaccone S, Nemni R, Fazio R, Quattrini A, Lacerenza M, Smirne S. Polyneuropathy with antibodies to sulphatide and decreased level of arylsulphatase A. J Neurol 240: 260-261, 1993."},{"key":"15","doi-asserted-by":"crossref","unstructured":"15. Eric RS, Jeanne MFP, Hope AS, et al. Innate immune activation in the pathogenesis of a murine model of globoid cell leukodystrophy. Am J Pathol 184: 382-396, 2014.","DOI":"10.1016\/j.ajpath.2013.10.011"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. 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