-
1
-
-
10544234193
-
Mapping of a gene for Parkinson's disease to chromosome 4q21-q23
-
Polymeropoulos M. H., Higgins J. J., Golbe L. I. Mapping of a gene for Parkinson's disease to chromosome 4q21-q23. Science 1996; 274: 1197-1199.
-
(1996)
Science
, vol.274
, pp. 1197-1199
-
-
Polymeropoulos, M.H.1
Higgins, J.J.2
Golbe, L.I.3
-
2
-
-
0032499264
-
Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism
-
Kitada T., Asakawa S., Matsumine H. Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism. Nature 1998; 392: 605-608.
-
(1998)
Nature
, vol.392
, pp. 605-608
-
-
Kitada, T.1
Asakawa, S.2
Matsumine, H.3
-
3
-
-
33746655119
-
Genetic heterogeneity in familial parkinsonism: No linkage to the PD-1 locus on chromosome 4q in 11 of 13 families
-
Gasser T., Muller-Myhsok B., Wszolek Z. K. Genetic heterogeneity in familial parkinsonism: no linkage to the PD-1 locus on chromosome 4q in 11 of 13 families. Science 1997; 276: 2045-2047.
-
(1997)
Science
, vol.276
, pp. 2045-2047
-
-
Gasser, T.1
Muller-Myhsok, B.2
Wszolek, Z.K.3
-
4
-
-
0030744876
-
Mutation in the alpha-synuclein gene identified in families with Parkinson's disease
-
Polymeropoulos M. H., Lavedan C., Leroy E. et al. Mutation in the alpha-synuclein gene identified in families with Parkinson's disease. Science 1997; 276(5321): 2045-2047.
-
(1997)
Science
, vol.276
, Issue.5321
, pp. 2045-2047
-
-
Polymeropoulos, M.H.1
Lavedan, C.2
Leroy, E.3
-
5
-
-
0030056696
-
Risk of Parkinson's disease among first-degree relatives: A community-based study
-
Marder K., Tang M-X., Mejia H. et al. Risk of Parkinson's disease among first-degree relatives: A community-based study. Neurology 1996; 47: 155-160.
-
(1996)
Neurology
, vol.47
, pp. 155-160
-
-
Marder, K.1
Tang, M.-X.2
Mejia, H.3
-
6
-
-
0033016210
-
Familial aggregation of Parkinson's disease: A population based case-control study in Europe
-
EUROPARKINSON study Group
-
Elbaz F., Grigoletto F., Baldereschi M. et al. Familial aggregation of Parkinson's disease: a population based case-control study in Europe. EUROPARKINSON study Group. Neurology 1999; 52: 1876-1882.
-
(1999)
Neurology
, vol.52
, pp. 1876-1882
-
-
Elbaz, F.1
Grigoletto, F.2
Baldereschi, M.3
-
7
-
-
0032937416
-
Polymorphisms in the parkin gene in sporadic Parkinson's disease
-
Wang M., Hattori N., Kobayashi T. Polymorphisms in the parkin gene in sporadic Parkinson's disease. Ann Neurol 1999; 45: 655-658.
-
(1999)
Ann Neurol
, vol.45
, pp. 655-658
-
-
Wang, M.1
Hattori, N.2
Kobayashi, T.3
-
8
-
-
0001077573
-
-
Oxford: Butterworth-Heinemann Ltd; 1994; Epidemiological clues to the cause of Parkinson's disease
-
Tanner C. M., Marsden C. D., Fahn S., eds. Movement Disorders Vol. 3. Oxford: Butterworth-Heinemann Ltd; 1994; Epidemiological clues to the cause of Parkinson's disease, p. 124-146.
-
Movement Disorders
, vol.3
, pp. 124-146
-
-
Tanner, C.M.1
Marsden, C.D.2
Fahn, S.3
-
9
-
-
0027358350
-
Worldwide occurrence of Parkinson's disease: An updated review
-
Zhang Z., Roman G. C. Worldwide occurrence of Parkinson's disease: An updated review. Neuroepidemiology 1993; 12: 195-208.
-
(1993)
Neuroepidemiology
, vol.12
, pp. 195-208
-
-
Zhang, Z.1
Roman, G.C.2
-
10
-
-
0030054732
-
How far are we in understanding the cause of Parkinson's disease?
-
Ben-Shlomo Y. How far are we in understanding the cause of Parkinson's disease? J Neurol Neurosurg Psychiatry 1996; 61: 4-16.
-
(1996)
J Neurol Neurosurg Psychiatry
, vol.61
, pp. 4-16
-
-
Ben-Shlomo, Y.1
-
11
-
-
0031914408
-
Low numbers and no loss of melanized nigral neurons with increasing age in normal human brains from India
-
Muthane U., Yasha T. C., Shankar S. K. Low Numbers and No Loss of Melanized Nigral Neurons with Increasing Age in Normal Human Brains from India. Ann Neurol 1998; 43: 283-287.
-
(1998)
Ann Neurol
, vol.43
, pp. 283-287
-
-
Muthane, U.1
Yasha, T.C.2
Shankar, S.K.3
-
12
-
-
0025079501
-
Multiple Sclerosis is prevalent in the Zoroastrians (Parsis) of India
-
Wadia N. H., Bhatia K. Multiple Sclerosis is prevalent in the Zoroastrians (Parsis) of India. Ann Neurol 1990; 28: 177-179.
-
(1990)
Ann Neurol
, vol.28
, pp. 177-179
-
-
Wadia, N.H.1
Bhatia, K.2
-
13
-
-
0023879135
-
Comparison of the prevalence of Parkinson's disease in black populations in the rural United States and in rural Nigeria: Door-to-door community studies
-
Schoenberg B. S., Osuntokun B. O., Adeuja A. O. G., Bademosi O., Nottidge V., Anderson D. W. Comparison of the prevalence of Parkinson's disease in black populations in the rural United States and in rural Nigeria: Door-to-door community studies. Neurology 1988; 38: 645-646.
-
(1988)
Neurology
, vol.38
, pp. 645-646
-
-
Schoenberg, B.S.1
Osuntokun, B.O.2
Adeuja, A.O.G.3
Bademosi, O.4
Nottidge, V.5
Anderson, D.W.6
-
14
-
-
0032990407
-
Patterns of singlenucleotide polymorphisms in candidate genes for blood-pressure homeostasis
-
Halushka M. K., Fan J. B., Bentley K. et al. Patterns of singlenucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nat Genet 1999; 22: 239-247.
-
(1999)
Nat Genet
, vol.22
, pp. 239-247
-
-
Halushka, M.K.1
Fan, J.B.2
Bentley, K.3
-
15
-
-
0032005372
-
The DNA revolution in population genetics
-
Cavalli-Sforza L. L. The DNA revolution in population genetics. TIG 1998; 14 (2): 60-65.
-
(1998)
TIG
, vol.14
, Issue.2
, pp. 60-65
-
-
Cavalli-Sforza, L.L.1
-
16
-
-
0032531204
-
Population studies of polymorphisms at loci of neuropsychiatric interest Tryptophan hydroxylase (TPH), Dopamine transporter protein (SLC6A3), D3 dopamine receptor (DRD3), Apolipoprotrin E (APOE), μ opiod receptor (OPRM1), and Ciliary neurotrophic factor (CNTF)
-
Gelernter J., Kranzler H., Lacobelle J. Population studies of polymorphisms at loci of neuropsychiatric interest Tryptophan hydroxylase (TPH), Dopamine transporter protein (SLC6A3), D3 dopamine receptor (DRD3), Apolipoprotrin E (APOE), μ opiod receptor (OPRM1), and Ciliary neurotrophic factor (CNTF). Genomics 1999; 52: 289-297.
-
(1999)
Genomics
, vol.52
, pp. 289-297
-
-
Gelernter, J.1
Kranzler, H.2
Lacobelle, J.3
-
17
-
-
0029865576
-
Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder
-
Jain S., Leggo J., DeLisi L. E. et al. Analysis of thirteen trinucleotide repeat loci as candidate genes for schizophrenia and bipolar affective disorder. Am J Med Genet 1996; 67 (2): 139-146.
-
(1996)
Am J Med Genet
, vol.67
, Issue.2
, pp. 139-146
-
-
Jain, S.1
Leggo, J.2
DeLisi, L.E.3
-
18
-
-
0031664779
-
Variation at the MJD locus in the major psychoses
-
Saleem Q., Vijaykumar M., Mutsuddi M., Chowdhary N. Jain S. Variation at the MJD locus in the major psychoses. Am J Med Genet (Neuropsychiatric Genetics) 1998; 67: 139-146.
-
(1998)
Am J Med Genet (Neuropsychiatric Genetics)
, vol.67
, pp. 139-146
-
-
Saleem, Q.1
Vijaykumar, M.2
Mutsuddi, M.3
Chowdhary, N.4
Jain, S.5
-
19
-
-
0342950666
-
Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype
-
Kruger R., Vieira-Saecker A. M., Kuhn W., Berg D., Muller T., Kuhnl N., Fuchs G. A., Hungs M., Woitalla D., Przuntek H. et al. Increased susceptibility to sporadic Parkinson's disease by a certain combined alpha-synuclein/apolipoprotein E genotype. Ann Neurol 1999; 45: 611-617.
-
(1999)
Ann Neurol
, vol.45
, pp. 611-617
-
-
Kruger, R.1
Vieira-Saecker, A.M.2
Kuhn, W.3
Berg, D.4
Muller, T.5
Kuhnl, N.6
Fuchs, G.A.7
Hungs, M.8
Woitalla, D.9
Przuntek, H.10
|