References
Duffner PK, Barczykowski A, Kay DM, Jalal K, Yan L, Abdelhalim A, Gill S, Gill AL, Carter R (2012) Later onset phenotypes of Krabbe disease: results of the world-wide registry. Pediatr Neurol 46(5):298–306
Abdelhalim AN, Alberico RA, Barczykowski AL, Duffner PK (2014) Patterns of magnetic resonance imaging abnormalities in symptomatic patients with Krabbe disease correspond to phenotype. Pediatr Neurol 50(2):127–134
Yoshimura A, Kibe T, Irahara K, Sakai N, Yokochi K (2016) Predominant corticospinal tract involvement in a late infant with Krabbe disease. Jpn Clin Med 7:23–26
Sehgal R, Sharma S, Sankhyan N, Kumar A, Gulati S (2011) Selective corticospinal tract involvement in late-onset Krabbe disease. Neurology 77(3):e20
Kamate M, Hattiholi V (2011) Predominant corticospinal tract involvement in early-onset Krabbe disease. Pediatr Neurol 44:155–156
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Nicita, F., Graziola, F., Vigevano, F. et al. An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype. Acta Neurol Belg 119, 619–620 (2019). https://doi.org/10.1007/s13760-019-01087-6
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DOI: https://doi.org/10.1007/s13760-019-01087-6