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2. An unusual case of late-infantile onset Krabbe disease with selective bilateral corticospinal tract involvement, peripheral demyelinating neuropathy, and mild phenotype. Nicita F; Graziola F; Vigevano F; Bertini E; Capuano A Acta Neurol Belg; 2019 Dec; 119(4):619-620. PubMed ID: 30729410 [No Abstract] [Full Text] [Related]
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12. Adult-onset Krabbe disease with homozygous T1853C mutation in the galactocerebrosidase gene. Unusual MRI findings of corticospinal tract demyelination. Satoh JI; Tokumoto H; Kurohara K; Yukitake M; Matsui M; Kuroda Y; Yamamoto T; Furuya H; Shinnoh N; Kobayashi T; Kukita Y; Hayashi K Neurology; 1997 Nov; 49(5):1392-9. PubMed ID: 9371928 [TBL] [Abstract][Full Text] [Related]
13. Late onset Krabbe's leukodystrophy: a report of four cases. Phelps M; Aicardi J; Vanier MT J Neurol Neurosurg Psychiatry; 1991 Apr; 54(4):293-6. PubMed ID: 2056315 [TBL] [Abstract][Full Text] [Related]
14. Deletion of exons 11-17 and novel mutations of the galactocerebrosidase gene in adult- and early-onset patients with Krabbe disease. Selleri S; Torchiana E; Pareyson D; Lulli L; Bertagnolio B; Savoiardo M; Farina L; Carrara F; Filocamo M; Gatti R; Sghirlanzoni A; Uziel G; Finocchiaro G J Neurol; 2000 Nov; 247(11):875-7. PubMed ID: 11151421 [No Abstract] [Full Text] [Related]