-
1
-
-
84887956934
-
Genetics of Parkinson's disease-state of the art, 2013
-
Bonifati V. Genetics of Parkinson's disease-state of the art, 2013. Park Relat Disord 2014, 20(Suppl.1):S23-S28. 10.1016/S1353-8020(13)70009-9.
-
(2014)
Park Relat Disord
, vol.20
, pp. S23-S28
-
-
Bonifati, V.1
-
2
-
-
33845204840
-
Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques
-
Simon-Sanchez J., Marti-Masso J.F., Sanchez-Mut J.V., Paisan-Ruiz C., Martinez-Gil A., Ruiz-Martinez J., et al. Parkinson's disease due to the R1441G mutation in Dardarin: a founder effect in the Basques. Mov Disord 2006, 21:1954-1959. 10.1002/mds.21114.
-
(2006)
Mov Disord
, vol.21
, pp. 1954-1959
-
-
Simon-Sanchez, J.1
Marti-Masso, J.F.2
Sanchez-Mut, J.V.3
Paisan-Ruiz, C.4
Martinez-Gil, A.5
Ruiz-Martinez, J.6
-
3
-
-
50049104725
-
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study
-
Healy D.G., Falchi M., O'Sullivan S.S., Bonifati V., Durr A., Bressman S., et al. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol 2008, 7:583-590. 10.1016/S1474-4422(08)70117-0.
-
(2008)
Lancet Neurol
, vol.7
, pp. 583-590
-
-
Healy, D.G.1
Falchi, M.2
O'Sullivan, S.S.3
Bonifati, V.4
Durr, A.5
Bressman, S.6
-
4
-
-
84857440387
-
Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease
-
Ben Sassi S., Nabli F., Hentati E., Nahdi H., Trabelsi M., Ben Ayed H., et al. Cognitive dysfunction in Tunisian LRRK2 associated Parkinson's disease. Park Relat Disord 2012, 18:243-246. 10.1016/j.parkreldis.2011.10.009.
-
(2012)
Park Relat Disord
, vol.18
, pp. 243-246
-
-
Ben Sassi, S.1
Nabli, F.2
Hentati, E.3
Nahdi, H.4
Trabelsi, M.5
Ben Ayed, H.6
-
5
-
-
78649788364
-
LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort
-
Belarbi S., Hecham N., Lesage S., Kediha M.I., Smail N., Benhassine T., et al. LRRK2 G2019S mutation in Parkinson's disease: a neuropsychological and neuropsychiatric study in a large Algerian cohort. Park Relat Disord 2010, 16:676-679. 10.1016/j.parkreldis.2010.09.003.
-
(2010)
Park Relat Disord
, vol.16
, pp. 676-679
-
-
Belarbi, S.1
Hecham, N.2
Lesage, S.3
Kediha, M.I.4
Smail, N.5
Benhassine, T.6
-
6
-
-
33748946787
-
LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample
-
Goldwurm S., Zini M., Di Fonzo A., De Gaspari D., Siri C., Simons E.J., et al. LRRK2 G2019S mutation and Parkinson's disease: a clinical, neuropsychological and neuropsychiatric study in a large Italian sample. Park Relat Disord 2006, 12:410-419. 10.1016/j.parkreldis.2006.04.001.
-
(2006)
Park Relat Disord
, vol.12
, pp. 410-419
-
-
Goldwurm, S.1
Zini, M.2
Di Fonzo, A.3
De Gaspari, D.4
Siri, C.5
Simons, E.J.6
-
7
-
-
80051505298
-
Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers
-
Marras C., Schule B., Munhoz R.P., Rogaeva E., Langston J.W., Kasten M., et al. Phenotype in parkinsonian and nonparkinsonian LRRK2 G2019S mutation carriers. Neurology 2011, 77:325-333. 10.1212/WNL.0b013e318227042d.
-
(2011)
Neurology
, vol.77
, pp. 325-333
-
-
Marras, C.1
Schule, B.2
Munhoz, R.P.3
Rogaeva, E.4
Langston, J.W.5
Kasten, M.6
-
8
-
-
0029049738
-
Western Nebraska family (family D) with autosomal dominant parkinsonism
-
Wszolek Z.K., Pfeiffer B., Fulgham J.R., Parisi J.E., Thompson B.M., Uitti R.J., et al. Western Nebraska family (family D) with autosomal dominant parkinsonism. Neurology 1995, 45:502-505.
-
(1995)
Neurology
, vol.45
, pp. 502-505
-
-
Wszolek, Z.K.1
Pfeiffer, B.2
Fulgham, J.R.3
Parisi, J.E.4
Thompson, B.M.5
Uitti, R.J.6
-
9
-
-
41049086705
-
Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients
-
Nuytemans K., Rademakers R., Theuns J., Pals P., Engelborghs S., Pickut B., et al. Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients. Eur J Hum Genet 2008, 16:471-479. 10.1038/sj.ejhg.5201986.
-
(2008)
Eur J Hum Genet
, vol.16
, pp. 471-479
-
-
Nuytemans, K.1
Rademakers, R.2
Theuns, J.3
Pals, P.4
Engelborghs, S.5
Pickut, B.6
-
10
-
-
42049094200
-
Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
-
Haugarvoll K., Rademakers R., Kachergus J.M., Nuytemans K., Ross O.A., Gibson J.M., et al. Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology 2008, 70:1456-1460. 10.1212/01.wnl.0000304044.22253.03.
-
(2008)
Neurology
, vol.70
, pp. 1456-1460
-
-
Haugarvoll, K.1
Rademakers, R.2
Kachergus, J.M.3
Nuytemans, K.4
Ross, O.A.5
Gibson, J.M.6
-
11
-
-
84908145945
-
Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2
-
Estanga A., Rodriguez-Oroz M.C., Ruiz-Martinez J., Barandiaran M., Gorostidi A., Bergareche A., et al. Cognitive dysfunction in Parkinson's disease related to the R1441G mutation in LRRK2. Park Relat Disord 2014, 20:1097-1100. 10.1016/j.parkreldis.2014.07.005.
-
(2014)
Park Relat Disord
, vol.20
, pp. 1097-1100
-
-
Estanga, A.1
Rodriguez-Oroz, M.C.2
Ruiz-Martinez, J.3
Barandiaran, M.4
Gorostidi, A.5
Bergareche, A.6
-
12
-
-
14844325314
-
Familial Parkinson's disease: clinical and genetic analysis of four Basque families
-
Paisan-Ruiz C., Saenz A., Lopez de Munain A., Marti I., Martinez Gil A., Marti-Masso J.F., et al. Familial Parkinson's disease: clinical and genetic analysis of four Basque families. Ann Neurol 2005, 57:365-372. 10.1002/ana.20391.
-
(2005)
Ann Neurol
, vol.57
, pp. 365-372
-
-
Paisan-Ruiz, C.1
Saenz, A.2
Lopez de Munain, A.3
Marti, I.4
Martinez Gil, A.5
Marti-Masso, J.F.6
-
13
-
-
84859718086
-
Clinical and pathological characteristics of LRRK2 G2019S patients with PD
-
Poulopoulos M., Cortes E., Vonsattel J.P., Fahn S., Waters C., Cote L.J., et al. Clinical and pathological characteristics of LRRK2 G2019S patients with PD. JMol Neurosci 2012, 47:139-143. 10.1007/s12031-011-9696-y.
-
(2012)
JMol Neurosci
, vol.47
, pp. 139-143
-
-
Poulopoulos, M.1
Cortes, E.2
Vonsattel, J.P.3
Fahn, S.4
Waters, C.5
Cote, L.J.6
-
14
-
-
77957276285
-
Involvement of the cerebral cortex in Parkinson disease linked with G2019S LRRK2 mutation without cognitive impairment
-
Gomez A., Ferrer I. Involvement of the cerebral cortex in Parkinson disease linked with G2019S LRRK2 mutation without cognitive impairment. Acta Neuropathol 2010, 120:155-167. 10.1007/s00401-010-0669-y.
-
(2010)
Acta Neuropathol
, vol.120
, pp. 155-167
-
-
Gomez, A.1
Ferrer, I.2
-
15
-
-
70450177430
-
Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2
-
Marti-Masso J.F., Ruiz-Martinez J., Bolano M.J., Ruiz I., Gorostidi A., Moreno F., et al. Neuropathology of Parkinson's disease with the R1441G mutation in LRRK2. Mov Disord 2009, 24:1998-2001. 10.1002/mds.22677.
-
(2009)
Mov Disord
, vol.24
, pp. 1998-2001
-
-
Marti-Masso, J.F.1
Ruiz-Martinez, J.2
Bolano, M.J.3
Ruiz, I.4
Gorostidi, A.5
Moreno, F.6
-
16
-
-
0026514953
-
Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases
-
Hughes A.J., Daniel S.E., Kilford L., Lees A.J. Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases. JNeurol Neurosurg Psychiatr 1992, 55:181-184.
-
(1992)
JNeurol Neurosurg Psychiatr
, vol.55
, pp. 181-184
-
-
Hughes, A.J.1
Daniel, S.E.2
Kilford, L.3
Lees, A.J.4
-
17
-
-
78349261173
-
Systematic review of levodopa dose equivalency reporting in Parkinson's disease
-
Tomlinson C.L., Stowe R., Patel S., Rick C., Gray R., Clarke C.E. Systematic review of levodopa dose equivalency reporting in Parkinson's disease. Mov Disord 2010, 25:2649-2653. 10.1002/mds.23429.
-
(2010)
Mov Disord
, vol.25
, pp. 2649-2653
-
-
Tomlinson, C.L.1
Stowe, R.2
Patel, S.3
Rick, C.4
Gray, R.5
Clarke, C.E.6
-
18
-
-
0019815552
-
Mattis dementia rating scale: internal reliability study using a diffusely impaired population
-
Gardner R., Oliver-Munoz S., Fisher L., Empting L. Mattis dementia rating scale: internal reliability study using a diffusely impaired population. JClin Neuropsychol 1981, 3:271-275.
-
(1981)
JClin Neuropsychol
, vol.3
, pp. 271-275
-
-
Gardner, R.1
Oliver-Munoz, S.2
Fisher, L.3
Empting, L.4
-
19
-
-
0001001317
-
L'examen psychologique dans les cas d'encephalopathic traumatique
-
Rey A. L'examen psychologique dans les cas d'encephalopathic traumatique. Arch Psychol 1941, 28:21.
-
(1941)
Arch Psychol
, vol.28
, pp. 21
-
-
Rey, A.1
-
20
-
-
0000399490
-
Avisual retention test for clinical use
-
Benton A.L. Avisual retention test for clinical use. Arch Neurol Psychiatry 1945, 54:212-216.
-
(1945)
Arch Neurol Psychiatry
, vol.54
, pp. 212-216
-
-
Benton, A.L.1
-
21
-
-
0016717781
-
Visual perception of line direction in patients with unilateral brain disease
-
Benton A., Hannay H.J., Varney N.R. Visual perception of line direction in patients with unilateral brain disease. Neurology 1975, 25:907-910.
-
(1975)
Neurology
, vol.25
, pp. 907-910
-
-
Benton, A.1
Hannay, H.J.2
Varney, N.R.3
-
22
-
-
0030341203
-
The 'clock drawing test' in healthy elderly people
-
Cacho J., Garcia-Garcia R., Arcaya J., Gay J., Guerrero-Peral A.L., Gomez-Sanchez J.C., et al. The 'clock drawing test' in healthy elderly people. Rev Neurol 1996, 24:1525-1528.
-
(1996)
Rev Neurol
, vol.24
, pp. 1525-1528
-
-
Cacho, J.1
Garcia-Garcia, R.2
Arcaya, J.3
Gay, J.4
Guerrero-Peral, A.L.5
Gomez-Sanchez, J.C.6
-
23
-
-
33947195230
-
Role of frontal versus temporal cortex in verbal fluency as revealed by voxel-based lesion symptom mapping
-
Baldo J.V., Schwartz S., Wilkins D., Dronkers N.F. Role of frontal versus temporal cortex in verbal fluency as revealed by voxel-based lesion symptom mapping. JInt Neuropsychol Soc 2006, 12:896-900. 10.1017/S1355617706061078.
-
(2006)
JInt Neuropsychol Soc
, vol.12
, pp. 896-900
-
-
Baldo, J.V.1
Schwartz, S.2
Wilkins, D.3
Dronkers, N.F.4
-
24
-
-
35348939603
-
Clinical diagnostic criteria for dementia associated with Parkinson's disease
-
quiz 837
-
Emre M., Aarsland D., Brown R., Burn D.J., Duyckaerts C., Mizuno Y., et al. Clinical diagnostic criteria for dementia associated with Parkinson's disease. Mov Disord 2007, 22:1689-1707. quiz 837. 10.1002/mds.21507.
-
(2007)
Mov Disord
, vol.22
, pp. 1689-1707
-
-
Emre, M.1
Aarsland, D.2
Brown, R.3
Burn, D.J.4
Duyckaerts, C.5
Mizuno, Y.6
-
25
-
-
84858298114
-
Diagnostic criteria for mild cognitive impairment in Parkinson's disease: movement disorder society task force guidelines
-
Litvan I., Goldman J.G., Troster A.I., Schmand B.A., Weintraub D., Petersen R.C., et al. Diagnostic criteria for mild cognitive impairment in Parkinson's disease: movement disorder society task force guidelines. Mov Disord 2012, 27:349-356. 10.1002/mds.24893.
-
(2012)
Mov Disord
, vol.27
, pp. 349-356
-
-
Litvan, I.1
Goldman, J.G.2
Troster, A.I.3
Schmand, B.A.4
Weintraub, D.5
Petersen, R.C.6
-
26
-
-
0030958347
-
The Neuropsychiatric Inventory: assessing psychopathology in dementia patients
-
Cummings J.L. The Neuropsychiatric Inventory: assessing psychopathology in dementia patients. Neurology 1997, 48:S10-S16.
-
(1997)
Neurology
, vol.48
, pp. S10-S16
-
-
Cummings, J.L.1
-
27
-
-
0032542897
-
What's wrong with Bonferroni adjustments
-
Perneger T.V. What's wrong with Bonferroni adjustments. BMJ 1998, 316:1236-1238.
-
(1998)
BMJ
, vol.316
, pp. 1236-1238
-
-
Perneger, T.V.1
-
28
-
-
77955071135
-
Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease
-
Alcalay R.N., Mejia-Santana H., Tang M.X., Rakitin B., Rosado L., Ross B., et al. Self-report of cognitive impairment and mini-mental state examination performance in PRKN, LRRK2, and GBA carriers with early onset Parkinson's disease. JClin Exp Neuropsychol 2010, 32:775-779. 10.1080/13803390903521018.
-
(2010)
JClin Exp Neuropsychol
, vol.32
, pp. 775-779
-
-
Alcalay, R.N.1
Mejia-Santana, H.2
Tang, M.X.3
Rakitin, B.4
Rosado, L.5
Ross, B.6
-
29
-
-
84889675482
-
Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations
-
Alcalay R.N., Mirelman A., Saunders-Pullman R., Tang M.X., Mejia Santana H., Raymond D., et al. Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations. Mov Disord 2013, 28:1966-1971. 10.1002/mds.25647.
-
(2013)
Mov Disord
, vol.28
, pp. 1966-1971
-
-
Alcalay, R.N.1
Mirelman, A.2
Saunders-Pullman, R.3
Tang, M.X.4
Mejia Santana, H.5
Raymond, D.6
-
30
-
-
27644455523
-
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
-
Lesage S., Ibanez P., Lohmann E., Pollak P., Tison F., Tazir M., et al. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann Neurol 2005, 58:784-787. 10.1002/ana.20636.
-
(2005)
Ann Neurol
, vol.58
, pp. 784-787
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
Pollak, P.4
Tison, F.5
Tazir, M.6
-
31
-
-
81955164797
-
Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers
-
Brockmann K., Groger A., Di Santo A., Liepelt I., Schulte C., Klose U., et al. Clinical and brain imaging characteristics in leucine-rich repeat kinase 2-associated PD and asymptomatic mutation carriers. Mov Disord 2011, 26:2335-2342. 10.1002/mds.23991.
-
(2011)
Mov Disord
, vol.26
, pp. 2335-2342
-
-
Brockmann, K.1
Groger, A.2
Di Santo, A.3
Liepelt, I.4
Schulte, C.5
Klose, U.6
|