-
1
-
-
0001788756
-
Parkinson's disease: The clinical picture
-
Clark CM, Trojanoswki JQ, eds. New York: McGraw-Hill
-
Simuni T, Hurtig HI. Parkinson's disease: the clinical picture. In: Clark CM, Trojanoswki JQ, eds. Neurodegenerative dementias. New York: McGraw-Hill, 2000:193-203.
-
(2000)
Neurodegenerative Dementias
, pp. 193-203
-
-
Simuni, T.1
Hurtig, H.I.2
-
2
-
-
0032937059
-
Diagnostic criteria for Parkinson disease
-
Gelb DJ, Oliver E, Gilman S. Diagnostic criteria for Parkinson disease. Arch Neurol 1999;56:33-39.
-
(1999)
Arch Neurol
, vol.56
, pp. 33-39
-
-
Gelb, D.J.1
Oliver, E.2
Gilman, S.3
-
3
-
-
0029348609
-
The neuropathology of parkinsonism: An overview
-
Cronford ME, Chang L, Miller, BL. The neuropathology of parkinsonism: an overview. Brain Cogn 1995;28:321-341.
-
(1995)
Brain Cogn
, vol.28
, pp. 321-341
-
-
Cronford, M.E.1
Chang, L.2
Miller, B.L.3
-
4
-
-
0029981526
-
Neuropathology of Parkinson's disease
-
Forno LS. Neuropathology of Parkinson's disease. J Neuropathol Exp Neurol 1996;55:259-272.
-
(1996)
J Neuropathol Exp Neurol
, vol.55
, pp. 259-272
-
-
Forno, L.S.1
-
5
-
-
23744443327
-
Nosology of Parkinson's disease: Looking for the way out of a quackmire
-
Forman MS, Lee VM-Y, Trojanowski JQ. Nosology of Parkinson's disease: looking for the way out of a quackmire. Neuron. 2005;47:479-482.
-
(2005)
Neuron
, vol.47
, pp. 479-482
-
-
Forman, M.S.1
Lee, V.M.-Y.2
Trojanowski, J.Q.3
-
6
-
-
0035409575
-
Alpha-synuclein and neurodegenerative diseases
-
Goedert M. Alpha-synuclein and neurodegenerative diseases. Nat Rev Neurosci 2001;2:492-501.
-
(2001)
Nat Rev Neurosci
, vol.2
, pp. 492-501
-
-
Goedert, M.1
-
7
-
-
0037333666
-
Staging of brain pathology related to sporadic Parkinson's disease
-
Braak H, Del Tredici K, Rub U, et al. Staging of brain pathology related to sporadic Parkinson's disease. Neurobiol Aging 2003;24:197-211.
-
(2003)
Neurobiol Aging
, vol.24
, pp. 197-211
-
-
Braak, H.1
Del Tredici, K.2
Rub, U.3
-
8
-
-
23844546218
-
Pathophysiology, pleotrophy and paradigm shifts: Genetic lessons from Parkinson's disease
-
Ross OA, Farrer MJ. Pathophysiology, pleotrophy and paradigm shifts: genetic lessons from Parkinson's disease. Biochem Soc Trans 2005;33:586-590.
-
(2005)
Biochem Soc Trans
, vol.33
, pp. 586-590
-
-
Ross, O.A.1
Farrer, M.J.2
-
9
-
-
0342368772
-
Association between early-onset Parkinson's disease and mutations in the parkin gene
-
French Parkinson's Disease Genetics Study Group
-
Lucking CB, Durr A, Bonifati V, et al. Association between early-onset Parkinson's disease and mutations in the parkin gene. French Parkinson's Disease Genetics Study Group. N Engl J Med 2000;342:1560-1567
-
(2000)
N Engl J Med
, vol.342
, pp. 1560-1567
-
-
Lucking, C.B.1
Durr, A.2
Bonifati, V.3
-
10
-
-
0035959931
-
Parkin and the molecular pathways of Parkinson's disease
-
Giasson BI, Lee VM-Y. Parkin and the molecular pathways of Parkinson's disease. Neuron 2001;31:885-888.
-
(2001)
Neuron
, vol.31
, pp. 885-888
-
-
Giasson, B.I.1
Lee, V.M.-Y.2
-
11
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich A, Biskup S, Leitner P, et al. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 2004;44:601-607.
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
-
12
-
-
8844266996
-
Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease
-
Paisan-Ruiz C, Jain S, Evans EW, et al. Cloning of the gene containing mutations that cause PARK8-linked Parkinson's disease. Neuron 2004;44:595-600.
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
-
13
-
-
24644497562
-
LRRK2 mutations in Parkinson disease
-
Farrer M, Stone J, Mata IF, et al. LRRK2 mutations in Parkinson disease. Neurology 2005;65:738-740.
-
(2005)
Neurology
, vol.65
, pp. 738-740
-
-
Farrer, M.1
Stone, J.2
Mata, I.F.3
-
14
-
-
24644486896
-
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
-
Zabetian CP, Samii A, Mosley AD, et al. A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations. Neurology 2005;65:741-744.
-
(2005)
Neurology
, vol.65
, pp. 741-744
-
-
Zabetian, C.P.1
Samii, A.2
Mosley, A.D.3
-
16
-
-
20444414834
-
Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation
-
Deng H, Le W, Guo Y, et al. Genetic and clinical identification of Parkinson's disease patients with LRRK2 G2019S mutation. Ann Neurol 2005;57:933-934.
-
(2005)
Ann Neurol
, vol.57
, pp. 933-934
-
-
Deng, H.1
Le, W.2
Guo, Y.3
-
17
-
-
19944432921
-
A common LRRK2 mutation in idiopathic Parkinson's disease
-
Gilks WP, Abou-Sleiman PM, Gandhi S, et al. A common LRRK2 mutation in idiopathic Parkinson's disease. Lancet 2005;365:415-416.
-
(2005)
Lancet
, vol.365
, pp. 415-416
-
-
Gilks, W.P.1
Abou-Sleiman, P.M.2
Gandhi, S.3
-
18
-
-
19944431081
-
A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease
-
Di Fonzo A, Rohe CF, Ferreira J, et al. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease. Lancet 2005;365:412-415.
-
(2005)
Lancet
, vol.365
, pp. 412-415
-
-
Di Fonzo, A.1
Rohe, C.F.2
Ferreira, J.3
-
19
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: Evidence of a common founder across European populations
-
Kachergus J, Mata IF, Hulihan M, et al. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am J Hum Genet 2005;76:672-680.
-
(2005)
Am J Hum Genet
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
-
20
-
-
24644474856
-
The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases
-
Hernandez D, Paisan RC, Crawley A, et al. The dardarin G2019S mutation is a common cause of Parkinson's disease but not other neurodegenerative diseases. Neurosci Lett 2005;389:137-139.
-
(2005)
Neurosci Lett
, vol.389
, pp. 137-139
-
-
Hernandez, D.1
Paisan, R.C.2
Crawley, A.3
-
21
-
-
19944432606
-
Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease
-
Nichols WC, Pankratz N, Hernandez D, et al. Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease. Lancet 2005;365:410-412.
-
(2005)
Lancet
, vol.365
, pp. 410-412
-
-
Nichols, W.C.1
Pankratz, N.2
Hernandez, D.3
-
22
-
-
2342605968
-
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
-
Wszolek ZK, Pfeiffer RF, Tsuboi Y, et al. Autosomal dominant parkinsonism associated with variable synuclein and tau pathology. Neurology 2004;62:1619-1622.
-
(2004)
Neurology
, vol.62
, pp. 1619-1622
-
-
Wszolek, Z.K.1
Pfeiffer, R.F.2
Tsuboi, Y.3
-
23
-
-
20444420103
-
An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family
-
Funayama M, Hasegawa K, Ohta E, et al. An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family. Ann Neurol 2005;57:918-921.
-
(2005)
Ann Neurol
, vol.57
, pp. 918-921
-
-
Funayama, M.1
Hasegawa, K.2
Ohta, E.3
-
24
-
-
0030875612
-
Autosomal dominant familial Parkinson disease: Older onset of age, and good response to levodopa therapy
-
Hasegawa K, Kowa H. Autosomal dominant familial Parkinson disease: older onset of age, and good response to levodopa therapy. Eur Neurol 1997;38(suppl 1):39-43.
-
(1997)
Eur Neurol
, vol.38
, Issue.SUPPL. 1
, pp. 39-43
-
-
Hasegawa, K.1
Kowa, H.2
-
25
-
-
0031941058
-
Aggregation of alpha-synuclein in Lewy bodies of sporadic Parkinson's disease and dementia with Lewy bodies
-
Baba M, Nakajo S, Tu PH, et al. Aggregation of alpha-synuclein in Lewy bodies of sporadic Parkinson's disease and dementia with Lewy bodies. Am J Pathol 1998;152:879-884.
-
(1998)
Am J Pathol
, vol.152
, pp. 879-884
-
-
Baba, M.1
Nakajo, S.2
Tu, P.H.3
-
26
-
-
0036322266
-
Novel antibodies to oxidized α-synuclein reveal abundant neuritic pathology in Lewy body disease
-
Duda JE, Giasson BI, Mabon ME, et al. Novel antibodies to oxidized α-synuclein reveal abundant neuritic pathology in Lewy body disease. Ann Neurol 2002;52:205-210.
-
(2002)
Ann Neurol
, vol.52
, pp. 205-210
-
-
Duda, J.E.1
Giasson, B.I.2
Mabon, M.E.3
-
27
-
-
0033800039
-
Immunohistochemical and biochemical studies demonstrate a distinct profile of alpha-synuclein permutations in multiple system atrophy
-
Duda JE, Giasson BI, Gur TL, et al. Immunohistochemical and biochemical studies demonstrate a distinct profile of alpha-synuclein permutations in multiple system atrophy. J Neuropathol Exp Neurol 2000;59:830-841.
-
(2000)
J Neuropathol Exp Neurol
, vol.59
, pp. 830-841
-
-
Duda, J.E.1
Giasson, B.I.2
Gur, T.L.3
-
28
-
-
25144468286
-
LRRK2 mutations are not common in Alzheimer's disease
-
Toft M, Sando SB, Melquist S, et al. LRRK2 mutations are not common in Alzheimer's disease. Mech Ageing Dev 2005;126:1201-1205.
-
(2005)
Mech Ageing Dev
, vol.126
, pp. 1201-1205
-
-
Toft, M.1
Sando, S.B.2
Melquist, S.3
-
29
-
-
20044394901
-
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2
-
Hernandez DG, Paisan-Ruiz C, McInerney-Leo A, et al. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Ann Neurol 2005;57:453-456.
-
(2005)
Ann Neurol
, vol.57
, pp. 453-456
-
-
Hernandez, D.G.1
Paisan-Ruiz, C.2
McInerney-Leo, A.3
-
30
-
-
18244394793
-
Clinical features of LRRK2-associated Parkinson's disease in central Norway
-
Aasly JO, Toft M, Fernandez-Mata I, et al. Clinical features of LRRK2-associated Parkinson's disease in central Norway. Ann Neurol 2005;57:762-765.
-
(2005)
Ann Neurol
, vol.57
, pp. 762-765
-
-
Aasly, J.O.1
Toft, M.2
Fernandez-Mata, I.3
|