Highly disabling cerebellar presentation in Huntington disease

European Journal of Neurology

Volumn 10, Issue 4, 2003, Pages 443-444

  Squitieri, Ferdinando ^a   Pustorino, G ^b   Cannella, M ^a   Toscano, A ^b   Maglione, V ^a   Morgante, L ^b   Tortorella, G ^b  

^a IRCCS NEUROMED   (Italy)

^b UNIVERSITY OF MESSINA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ANAMNESIS; ARTICLE; CASE REPORT; CEREBELLUM ATROPHY; CLINICAL FEATURE; DISEASE CLASSIFICATION; DISEASE DURATION; ELECTROENCEPHALOGRAM; HOSPITAL ADMISSION; HUMAN; HUNTINGTON CHOREA; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; PRIORITY JOURNAL; SCHOOL CHILD; CHILD; EPILEPSY; GENETICS; MEMORY DISORDER; PATHOLOGY; SPINOCEREBELLAR DEGENERATION; TRINUCLEOTIDE REPEAT;

CHILD; EPILEPSY; HUMANS; HUNTINGTON DISEASE; MAGNETIC RESONANCE IMAGING; MALE; MEMORY DISORDERS; SPINOCEREBELLAR ATAXIAS; TRINUCLEOTIDE REPEATS;

EID: 0042786882     PISSN: 13515101     EISSN: 14681331     Source Type: Journal    
DOI: 10.1046/j.1468-1331.2003.00601.x     Document Type: Article

References (11)

1. Bachoud-Lèvi AC, Remy P, Nguyen JP et al. (2000). Motor and cognitive improvements in patients with Huntington's disease after neural transplantation. Lancet 356:1975-1979.
2. Brunet-Lezine Scale Brunèt O, Lezine I (1962). Lo Sviluppo Psicologico Della Prima Infanzia. Boringhieri, Torino.
3. Deckel AW (1995). Is Huntington's disease of cerebellar/brainstem origin? Lancet 345:263-264.
4. Griffiths R (1970). The abilities of young children: A comprehensive system of measurement for the first eight years of life. London. Child Development Research Centre.
5. Harper PS (1991). Huntington's Disease. W B Saunders, London.
6. Ho VB, Chuang S, Rovira M, Koo B (1995). Juvenile Huntington disease: CT and MR features. Am J Neuroradiol 16:1405-1412.
7. Huntington Study Group (1996). Unified Huntington's Disease Rating Scale: reliability and consistency. Mov Disord 11:136-142.
8. Myers RH, Sax DS, Koroshetz WJ et al. (1991). Factors associated with slow progression in Huntington's disease. Arch Neurol 48:800-804.
9. Rodda RA (1981). Cerebellar atrophy in Huntington's disease. J Neurol Sci 50:147-157.
10. Squitieri F, Berardelli A, Nargi E et al. (2000). Atypical movement disorders in the early stages of Huntington's disease: clinical and genetic analysis. Clin Genet 58:50-56.
11. White SM, Gobbay SS, Nabury CG et al. (2000). Diagnostic re-evaluation of a case of cerebellar atrophy with Huntington's disease. J Neurol Sci 174:47-48.