Clinical and genetic study of familial Parkinson's disease in Tunisia

Neurology

Volumn 54, Issue 8, 2000, Pages 1603-1609

  Gouider Khouja, Neziha ^a   Belal, S ^a   Hamida, M Ben ^a   Hentati, F ^a  

^a Institut National de Neurologie Tunisia   (Tunisia)

Author keywords

Autosomal dominant inheritance; Autosomal recessive inheritance; Genetics; PD

Indexed keywords

LEVODOPA;

ADULT; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CLINICAL ARTICLE; FAMILIAL DISEASE; FEMALE; GENETIC RISK; HUMAN; HUMAN CELL; HUMAN TISSUE; MALE; PARKINSON DISEASE; PEDIGREE; PRIORITY JOURNAL; RATING SCALE; TUNISIA;

EID: 0034053093     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.54.8.1603     Document Type: Article

References (17)

1. Polymeropoulos MH, Higgins JJ, Golbe LI, et al. Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science 1996;274:1197-1199.
2. Polymeropoulos MH, Lavedan C, Leroy E, et al. Mutation of the Alpha-Synuclein gene identified in families with Parkinson's disease. Science 1997;276:2045-2047.
3. Matsumine H, Saito M, Shimoda-Matsubayashi S, et al. Localisation of a gene for an autosomal recessive form of juvenile Parkinsonism to chromosome 6q25.2-27. Am J Hum Genet 1997;60:588-596.
4. Vaughan JR, Farrer MJ, Wszolek ZK, et al. Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. Hum Mol Genet 1998;7:751-753.
5. Ward CD, Gibb WR. Research diagnostic criteria for Parkinson's disease. In: Streifer MB, Korczyn AD, Melamed E, Youdim MBH, eds. Parkinson's disease: anatomy, pathology and therapy. Advances in Neurology. New York: Raven Press, 1990:553-558.
6. Fahn S, Elton RL. Unified Parkinson's Disease Rating Scale. In: Fahn S, Marsden CD, Goldstein M, Calne DB, eds. Recent developments in Parkinson's disease. New York: MacMillan, 1987:153-163.
7. Hoehn MM, Yahr MD. Parkinsonism: onset, progression and mortality. Neurology 1967;17:427-442.
8. Maraganore DM, Harding AE, Marsden CD. A clinical and genetic study of familial Parkinson's disease. Mov Disord 1991;6:205-211.
9. 9. Planté-Bordeneuve V, Taussig D, Thomas F, Ziégler M, Said G. A clinical and genetic study of familial cases of Parkinson's disease. J Neurol Sci 1995;133:164-172.
10. Payami H, Larsen K, Bernard S, Nutt J. Increased risk ofParkinson's disease in parents and siblings of patients. Ann Neurol 1994;36:659-661.
11. Lazzarini AM, Myers RH, Zimmerman TR. A clinical genetic study of Parkinson's disease: evidence for dominant transmission. Neurology 1994;44:499-506.
12. Golbe LI, Di Iorio G, Bonavita V, Miller DC, Duvoisin RC. A large kindred with autosomal dominant Parkinson's disease. Ann Neurol 1990;27:276-282.
13. Gouider-Khouja N. La maladie de Parkinson en Tunisie. Aspects épidémiologiques, cliniques, évolutifs et thérapeutiques. Faculté de Médecine de Tunis: Thèse en Médecine, 1991.
14. 18F-DOPA PET study. Neurology 1992;42:1554-1560.
15. Dobyns WB, Ozelis LJ, Kramer PL, et al. Rapid onset dystonia-parkinsonism. Neurology 1993;43:2596-2602.
16. Yamamura Y, Sobue I, Ando K, Iida M, Yanagi T, Kono C. Paralysis agitans of early onset with marked diurnal fluctuation of symptoms. Neurology 1973;23:239-244.
17. Yamamura Y, Kohriyama T, Kaseda Y, et al. Clinical manifestations of autosomal recessive early-onset parkinsonism with diurnal fluctuation in the basal ganglia. In: Ohye V, et al, eds. New York: Plenum Press, 1996:485-489.