An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype

Francesco Nicita; Federica Graziola; Federico Vigevano; Enrico Bertini; Alessandro Capuano

doi:10.1007/s13760-019-01087-6

An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype

Francesco Nicita, Federica Graziola, Federico Vigevano, Enrico Bertini, Alessandro Capuano

Ospedale Pediatrico Bambino Gesu

Research output: Contribution to journal › Article

Original language	English
Journal	Acta Neurologica Belgica
DOIs	https://doi.org/10.1007/s13760-019-01087-6
Publication status	E-pub ahead of print - Feb 7 2019

Cite this

Nicita, F., Graziola, F., Vigevano, F., Bertini, E., & Capuano, A. (2019). An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype. Acta Neurologica Belgica. https://doi.org/10.1007/s13760-019-01087-6

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title = "An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype",

author = "Francesco Nicita and Federica Graziola and Federico Vigevano and Enrico Bertini and Alessandro Capuano",

year = "2019",

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doi = "10.1007/s13760-019-01087-6",

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T1 - An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype

AU - Nicita, Francesco

AU - Graziola, Federica

AU - Vigevano, Federico

AU - Bertini, Enrico

AU - Capuano, Alessandro

PY - 2019/2/7

Y1 - 2019/2/7

U2 - 10.1007/s13760-019-01087-6

DO - 10.1007/s13760-019-01087-6

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JO - Acta Neurologica Belgica

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10.1007/s13760-019-01087-6

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OSPEDALE BAMBINO GESU' - GENETICA E MALATTIE RARE IN PEDIATRIA

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An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype

Cite this

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Projects

OSPEDALE BAMBINO GESU' - GENETICA E MALATTIE RARE IN PEDIATRIA