-
1
-
-
13444269543
-
Haploview: analysis and visualization of LD and haplotype maps
-
Barrett J., Fry B., Maller J., and Daly M. Haploview: analysis and visualization of LD and haplotype maps. Bioinformatics 21 (2005) 263-265
-
(2005)
Bioinformatics
, vol.21
, pp. 263-265
-
-
Barrett, J.1
Fry, B.2
Maller, J.3
Daly, M.4
-
2
-
-
33644822969
-
Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease
-
Berg D., Schweitzer K.J., Leitner P., Zimprich A., Lichtner P., Belcredi P., Brussel T., Schulte C., Maass S., Nagele T., Wszolek Z.K., and Gasser T. Type and frequency of mutations in the LRRK2 gene in familial and sporadic Parkinson's disease. Brain 128 (2005) 3000-3011
-
(2005)
Brain
, vol.128
, pp. 3000-3011
-
-
Berg, D.1
Schweitzer, K.J.2
Leitner, P.3
Zimprich, A.4
Lichtner, P.5
Belcredi, P.6
Brussel, T.7
Schulte, C.8
Maass, S.9
Nagele, T.10
Wszolek, Z.K.11
Gasser, T.12
-
3
-
-
28544446980
-
G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort
-
Bras J.M., Guerreiro R.J., Ribeiro M.H., Januario C., Morgadinho A., Oliveira C.R., Cunha L., Hardy J., and Singleton A. G2019S dardarin substitution is a common cause of Parkinson's disease in a Portuguese cohort. Mov. Disord. 20 (2005) 1653-1655
-
(2005)
Mov. Disord.
, vol.20
, pp. 1653-1655
-
-
Bras, J.M.1
Guerreiro, R.J.2
Ribeiro, M.H.3
Januario, C.4
Morgadinho, A.5
Oliveira, C.R.6
Cunha, L.7
Hardy, J.8
Singleton, A.9
-
4
-
-
34548189984
-
CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes
-
Chitsazian F., Tusi B., Elahi E., Saroei H., Sanati M., Yazdani S., Pakravan M., Nilforooshan N., Eslami Y., Mehrjerdi M., Zareei R., Jabbarvand M., Abdolahi A., Lasheyee A., Etemadi A., Bayat B., Sadeghi M., Banoei M., Ghafarzadeh B., Rohani M., Rismanchian A., Thorstenson Y., and Sarfarazi M. CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes. J. Mol. Diagn. 9 (2007) 382-393
-
(2007)
J. Mol. Diagn.
, vol.9
, pp. 382-393
-
-
Chitsazian, F.1
Tusi, B.2
Elahi, E.3
Saroei, H.4
Sanati, M.5
Yazdani, S.6
Pakravan, M.7
Nilforooshan, N.8
Eslami, Y.9
Mehrjerdi, M.10
Zareei, R.11
Jabbarvand, M.12
Abdolahi, A.13
Lasheyee, A.14
Etemadi, A.15
Bayat, B.16
Sadeghi, M.17
Banoei, M.18
Ghafarzadeh, B.19
Rohani, M.20
Rismanchian, A.21
Thorstenson, Y.22
Sarfarazi, M.23
more..
-
5
-
-
32944478901
-
A haplotype framework for cystic fibrosis mutations in Iran
-
Elahi E., Khodadad A., Kupershmidt I., Ghasemi F., Alinasab B., Naghizadeh R., Eason R., Amini M., Esmaili M., Dooki M.E., Sanati M., Davis R., Ronaghi M., and Thorstenson Y. A haplotype framework for cystic fibrosis mutations in Iran. J. Mol. Diagn. 8 (2006) 119-127
-
(2006)
J. Mol. Diagn.
, vol.8
, pp. 119-127
-
-
Elahi, E.1
Khodadad, A.2
Kupershmidt, I.3
Ghasemi, F.4
Alinasab, B.5
Naghizadeh, R.6
Eason, R.7
Amini, M.8
Esmaili, M.9
Dooki, M.E.10
Sanati, M.11
Davis, R.12
Ronaghi, M.13
Thorstenson, Y.14
-
6
-
-
50249165832
-
LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease
-
Elbaz N.A. LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease. Lancet Neurol. 7 (2008) 562-564
-
(2008)
Lancet Neurol.
, vol.7
, pp. 562-564
-
-
Elbaz, N.A.1
-
7
-
-
33847267765
-
Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia
-
Farrer M.J., Stone J.T., Lin C.-H., Dachsel J.C., Hulihan M.M., Haugarvoll K., Ross O.A., and Wu R.-M. Lrrk2 G2385R is an ancestral risk factor for Parkinson's disease in Asia. Parkinsonism Relat. Disord. 13 (2007) 89-92
-
(2007)
Parkinsonism Relat. Disord.
, vol.13
, pp. 89-92
-
-
Farrer, M.J.1
Stone, J.T.2
Lin, C.-H.3
Dachsel, J.C.4
Hulihan, M.M.5
Haugarvoll, K.6
Ross, O.A.7
Wu, R.-M.8
-
8
-
-
33746079596
-
A common missense variant in the LRRK2gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan
-
Fonzo A.D., Wu-Chou Y.-H., Lu C.-S., Doeselaar M.v., Simons E.J., Rohé C.F., Chang H.-C., Chen R.-S., Weng Y.-H., Vanacore N., Breedveld G.J., Oostra B.A., and Bonifati V. A common missense variant in the LRRK2gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan. Neurogenetics 7 (2006) 133-138
-
(2006)
Neurogenetics
, vol.7
, pp. 133-138
-
-
Fonzo, A.D.1
Wu-Chou, Y.-H.2
Lu, C.-S.3
Doeselaar, M.v.4
Simons, E.J.5
Rohé, C.F.6
Chang, H.-C.7
Chen, R.-S.8
Weng, Y.-H.9
Vanacore, N.10
Breedveld, G.J.11
Oostra, B.A.12
Bonifati, V.13
-
9
-
-
33644929033
-
LRRK2 mutations in Spanish patients with Parkinson disease
-
Gaig C., Ezquerra M., Marti M.J., Munoz E., Valldeoriola F., and Tolosa E. LRRK2 mutations in Spanish patients with Parkinson disease. Arch. Neurol. 63 (2006) 377-382
-
(2006)
Arch. Neurol.
, vol.63
, pp. 377-382
-
-
Gaig, C.1
Ezquerra, M.2
Marti, M.J.3
Munoz, E.4
Valldeoriola, F.5
Tolosa, E.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., Tan E.-K., Gaig C., Tolosa E., Goldwurm S., Guidi M., Riboldazzi G., Brown L., Walter U., Benecke R., Berg D., Gasser T., Theuns J., Pals P., Cras P., Deyn P.P.D., Engelborghs S., Pickut B., Uitti R.J., Foroud T., Nichols W.C., Hagenah J., Klein C., Samii A., Zabetian C.P., Bonifati V., Broeckhoven C.V., Farrer M.J., and Wszolek Z.K. Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease. Neurology 70 (2008) 1456-1460
-
(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
Tan, E.-K.7
Gaig, C.8
Tolosa, E.9
Goldwurm, S.10
Guidi, M.11
Riboldazzi, G.12
Brown, L.13
Walter, U.14
Benecke, R.15
Berg, D.16
Gasser, T.17
Theuns, J.18
Pals, P.19
Cras, P.20
Deyn, P.P.D.21
Engelborghs, S.22
Pickut, B.23
Uitti, R.J.24
Foroud, T.25
Nichols, W.C.26
Hagenah, J.27
Klein, C.28
Samii, A.29
Zabetian, C.P.30
Bonifati, V.31
Broeckhoven, C.V.32
Farrer, M.J.33
Wszolek, Z.K.34
more..
-
11
-
-
10744226640
-
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
-
Hedrich K., Djarmati A., Schäfer N., Hering R., Wellenbrock C., Weiss P.H., Hilker R., Vieregge P., Heutink L.J.O.P., Bonifati V., Schwinger E., Lang A.E., Noth J., Bressman S.B., Pramstaller P.P., Riess O., and Klein C. DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease. Neurology 62 (2004) 389-394
-
(2004)
Neurology
, vol.62
, pp. 389-394
-
-
Hedrich, K.1
Djarmati, A.2
Schäfer, N.3
Hering, R.4
Wellenbrock, C.5
Weiss, P.H.6
Hilker, R.7
Vieregge, P.8
Heutink, L.J.O.P.9
Bonifati, V.10
Schwinger, E.11
Lang, A.E.12
Noth, J.13
Bressman, S.B.14
Pramstaller, P.P.15
Riess, O.16
Klein, C.17
-
12
-
-
33750305328
-
Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease
-
Hedrich K., Winkler S., Hagenah J., Kabakci K., Kasten M., Schwinger E., Volkmann J., Pramstaller P.P., Kostic V., Vieregge P., and Klein C. Recurrent LRRK2 (Park8) mutations in early-onset Parkinson's disease. Mov. Disord. 21 (2006) 1506-1510
-
(2006)
Mov. Disord.
, vol.21
, pp. 1506-1510
-
-
Hedrich, K.1
Winkler, S.2
Hagenah, J.3
Kabakci, K.4
Kasten, M.5
Schwinger, E.6
Volkmann, J.7
Pramstaller, P.P.8
Kostic, V.9
Vieregge, P.10
Klein, C.11
-
13
-
-
20044394901
-
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2
-
Hernandez D.G., Paisán-Ruíz C., McInerney-Leo A., Jain S., Meyer-Lindenberg A., Evans E.W., Berman K.F., Johnson J., Auburger G., Schäffer A.A., Lopez G.J., Nussbaum R.L., and Singleton A.B. Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. Ann. Neurol. 57 (2005) 453-456
-
(2005)
Ann. Neurol.
, vol.57
, pp. 453-456
-
-
Hernandez, D.G.1
Paisán-Ruíz, C.2
McInerney-Leo, A.3
Jain, S.4
Meyer-Lindenberg, A.5
Evans, E.W.6
Berman, K.F.7
Johnson, J.8
Auburger, G.9
Schäffer, A.A.10
Lopez, G.J.11
Nussbaum, R.L.12
Singleton, A.B.13
-
14
-
-
20144387207
-
Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations
-
Kachergus J., Mata I.F., Hulihan M., Taylor J.P., Lincoln S., Aasly J., Gibson J.M., Ross O.A., Lynch T., Wiley J., Payami H., Nutt J., Maraganore D.M., Czyzewski K., Styczynska M., Wszolek Z.K., Farrer M.J., and Toft M. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. Am. J. Hum. Genet. 76 (2005) 672-680
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 672-680
-
-
Kachergus, J.1
Mata, I.F.2
Hulihan, M.3
Taylor, J.P.4
Lincoln, S.5
Aasly, J.6
Gibson, J.M.7
Ross, O.A.8
Lynch, T.9
Wiley, J.10
Payami, H.11
Nutt, J.12
Maraganore, D.M.13
Czyzewski, K.14
Styczynska, M.15
Wszolek, Z.K.16
Farrer, M.J.17
Toft, M.18
-
15
-
-
57649188649
-
The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study
-
Latourelle J., Sun M., Lew M., Suchowersky O., Klein C., Golbe L., Mark M., Growdon J., Wooten G., Watts R., Guttman M., Perlmutter B.R.J., Ahmed A., Shill H., Singer C., Goldwurm S., Pezzoli G., Zini M., Hendricks M.S.-H.A., Williamson S., Nagle M., Wilk J., Massood T., Huskey K., Laramie J., DeStefano A., Baker K., Itin I., Litvan I., Nicholson G., Corbett A., Nance M., Drasby E., Isaacson S., Burn D., Chinnery P., Pramstaller P., Al-hinti J., Moller A., Ostergaard K., Sherman S., Snow R.R.B., Slevin J., Cambi F., Gusella J., and Myers R. The Gly2019Ser mutation in LRRK2 is not fully penetrant in familial Parkinson's disease: the GenePD study. BMC Med. 6 (2008) 32
-
(2008)
BMC Med.
, vol.6
, pp. 32
-
-
Latourelle, J.1
Sun, M.2
Lew, M.3
Suchowersky, O.4
Klein, C.5
Golbe, L.6
Mark, M.7
Growdon, J.8
Wooten, G.9
Watts, R.10
Guttman, M.11
Perlmutter, B.R.J.12
Ahmed, A.13
Shill, H.14
Singer, C.15
Goldwurm, S.16
Pezzoli, G.17
Zini, M.18
Hendricks, M.S.-H.A.19
Williamson, S.20
Nagle, M.21
Wilk, J.22
Massood, T.23
Huskey, K.24
Laramie, J.25
DeStefano, A.26
Baker, K.27
Itin, I.28
Litvan, I.29
Nicholson, G.30
Corbett, A.31
Nance, M.32
Drasby, E.33
Isaacson, S.34
Burn, D.35
Chinnery, P.36
Pramstaller, P.37
Al-hinti, J.38
Moller, A.39
Ostergaard, K.40
Sherman, S.41
Snow, R.R.B.42
Slevin, J.43
Cambi, F.44
Gusella, J.45
Myers, R.46
more..
-
16
-
-
27644455523
-
G2019S LRRK2 mutation in French and North African families with Parkinson's disease
-
Lesage S., Ibanez P., Lohmann E., Pollak P., Tison F.o., Tazir M., Leutenegger A.-L., Guimaraes J., Bonnet A.-M., Agid Y., Dürr A., and Brice A. G2019S LRRK2 mutation in French and North African families with Parkinson's disease. Ann. Neurol. 58 (2005) 784-787
-
(2005)
Ann. Neurol.
, vol.58
, pp. 784-787
-
-
Lesage, S.1
Ibanez, P.2
Lohmann, E.3
Pollak, P.4
Tison, F.o.5
Tazir, M.6
Leutenegger, A.-L.7
Guimaraes, J.8
Bonnet, A.-M.9
Agid, Y.10
Dürr, A.11
Brice, A.12
-
17
-
-
38549097049
-
The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease
-
Li C., Ting Z., Qin X., Ying W., Li B., Qiang L.G., Fang M.J., Jing Z., Qing D.J., and Di C.S. The prevalence of LRRK2 Gly2385Arg variant in Chinese Han population with Parkinson's disease. Mov. Disord. 22 (2007) 2439-2443
-
(2007)
Mov. Disord.
, vol.22
, pp. 2439-2443
-
-
Li, C.1
Ting, Z.2
Qin, X.3
Ying, W.4
Li, B.5
Qiang, L.G.6
Fang, M.J.7
Jing, Z.8
Qing, D.J.9
Di, C.S.10
-
18
-
-
27744446035
-
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease
-
Lu C.-S., Simons E.J., Wu-Chou Y.-H., Fonzo A.D., Chang H.-C., Chen R.-S., Weng Y.-H., Rohe C.F., Breedveld G.J., Hattori N., ThomasGasser, Oostra B.A., and Bonifati V. The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's disease. Parkinsonism Relat. Disord. 11 (2005) 521-522
-
(2005)
Parkinsonism Relat. Disord.
, vol.11
, pp. 521-522
-
-
Lu, C.-S.1
Simons, E.J.2
Wu-Chou, Y.-H.3
Fonzo, A.D.4
Chang, H.-C.5
Chen, R.-S.6
Weng, Y.-H.7
Rohe, C.F.8
Breedveld, G.J.9
Hattori, N.10
ThomasGasser11
Oostra, B.A.12
Bonifati, V.13
-
19
-
-
21144451648
-
LRRK2 R1441G in Spanish patients with Parkinson's disease
-
Mata I.F., Taylor J.P., Kachergus J., Hulihan M., Huerta C., Lahoz C., Blazquez M., Guisasola L.M., Salvador C., Ribacoba R., Martinez C., Farrer M., and Alvarez V. LRRK2 R1441G in Spanish patients with Parkinson's disease. Neurosci. Lett. 382 (2005) 309-311
-
(2005)
Neurosci. Lett.
, vol.382
, pp. 309-311
-
-
Mata, I.F.1
Taylor, J.P.2
Kachergus, J.3
Hulihan, M.4
Huerta, C.5
Lahoz, C.6
Blazquez, M.7
Guisasola, L.M.8
Salvador, C.9
Ribacoba, R.10
Martinez, C.11
Farrer, M.12
Alvarez, V.13
-
20
-
-
0034895295
-
Parkin and Parkinson's disease
-
Mizuno Y., Hattori N., Mori H., Suzuki T., and Tanaka K. Parkin and Parkinson's disease. Curr. Opin. Neurol. 14 4 (2001) 477-482
-
(2001)
Curr. Opin. Neurol.
, vol.14
, Issue.4
, pp. 477-482
-
-
Mizuno, Y.1
Hattori, N.2
Mori, H.3
Suzuki, T.4
Tanaka, K.5
-
21
-
-
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., Pooter T.d., Peeters K., Mattheijssens M., Broeck M.V.d., Cras P., Deyn P.P.D., and Broeckhoven C.v. Founder mutation p.R1441C in the leucine-rich repeat kinase 2 gene in Belgian Parkinson's disease patients. Eur. J. Hum. Genet. 16 (2008) 1-9
-
(2008)
Eur. J. Hum. Genet.
, vol.16
, pp. 1-9
-
-
Nuytemans, K.1
Rademakers, R.2
Theuns, J.3
Pals, P.4
Engelborghs, S.5
Pickut, B.6
Pooter, T.d.7
Peeters, K.8
Mattheijssens, M.9
Broeck, M.V.d.10
Cras, P.11
Deyn, P.P.D.12
Broeckhoven, C.v.13
-
22
-
-
31344439221
-
LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews
-
Ozelius L.J., Geetha Senthil P.D., Saunders-Pullma R., Ohmann E., Deligtisch A., Tagliati M., Hunt A.L., Klein C., Henick B., Hailpern S.M., Lipton R.B., Soto-Valencia J., Risch N., and Bressman S.B. LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews. N. Engl. J. Med. 354 (2006) 424-425
-
(2006)
N. Engl. J. Med.
, vol.354
, pp. 424-425
-
-
Ozelius, L.J.1
Geetha Senthil, P.D.2
Saunders-Pullma, R.3
Ohmann, E.4
Deligtisch, A.5
Tagliati, M.6
Hunt, A.L.7
Klein, C.8
Henick, B.9
Hailpern, S.M.10
Lipton, R.B.11
Soto-Valencia, J.12
Risch, N.13
Bressman, S.B.14
-
23
-
-
8844266996
-
Cloning of the gene containing mutations that Cause PARK8-linked Parkinson's disease
-
Paisan-Rui{dotless}z C., Jain S., Evans E.W., Gilks W.P., Simon J., Brug M.v.d., Munain A.L.d., Aparicio S., Gil A.M., Khan N., Johnson J., Martinez J.R., Nicholl D., Carrera I.M., Pena A.S., Silva R.d., Lees A., Marti{dotless}-Masso J., Perez-Tur J., Wood N.W., and Singleton A.B. Cloning of the gene containing mutations that Cause PARK8-linked Parkinson's disease. Neuron 44 (2004) 595-600
-
(2004)
Neuron
, vol.44
, pp. 595-600
-
-
Paisan-Ruiz, C.1
Jain, S.2
Evans, E.W.3
Gilks, W.P.4
Simon, J.5
Brug, M.v.d.6
Munain, A.L.d.7
Aparicio, S.8
Gil, A.M.9
Khan, N.10
Johnson, J.11
Martinez, J.R.12
Nicholl, D.13
Carrera, I.M.14
Pena, A.S.15
Silva, R.d.16
Lees, A.17
Marti-Masso, J.18
Perez-Tur, J.19
Wood, N.W.20
Singleton, A.B.21
more..
-
24
-
-
42049122637
-
Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls
-
Paisan-Rui{dotless}z C., Nath P., Washecka N., Gibbs J.R., and Singleton A.B. Comprehensive analysis of LRRK2 in publicly available Parkinson's disease cases and neurologically normal controls. Hum. Mutat. 29 (2008) 485-490
-
(2008)
Hum. Mutat.
, vol.29
, pp. 485-490
-
-
Paisan-Ruiz, C.1
Nath, P.2
Washecka, N.3
Gibbs, J.R.4
Singleton, A.B.5
-
25
-
-
0029435462
-
Prevalence of Parkinson's disease in the elderly: the Rotterdam study
-
Rijk M.d., Breteler M., Graveland G., Ott A., Grobbee D., Meché F.v.d., and Hofman A. Prevalence of Parkinson's disease in the elderly: the Rotterdam study. Neurology 45 (1995) 2143-2146
-
(1995)
Neurology
, vol.45
, pp. 2143-2146
-
-
Rijk, M.d.1
Breteler, M.2
Graveland, G.3
Ott, A.4
Grobbee, D.5
Meché, F.v.d.6
Hofman, A.7
-
26
-
-
48949092066
-
Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease
-
Ross O.A., Wu Y.-R., Lee M.-C., Funayama M., Chen M.-L., Soto A.I., Mata I.F., Lee-Chen G.-J., Chen C.M., Tang M., Zhao Y., Hattori N., Farrer M.J., Tan E.-K., and Wu R.-M. Analysis of Lrrk2 R1628P as a risk factor for Parkinson's disease. Ann. Neurol. 64 (2008) 88-92
-
(2008)
Ann. Neurol.
, vol.64
, pp. 88-92
-
-
Ross, O.A.1
Wu, Y.-R.2
Lee, M.-C.3
Funayama, M.4
Chen, M.-L.5
Soto, A.I.6
Mata, I.F.7
Lee-Chen, G.-J.8
Chen, C.M.9
Tang, M.10
Zhao, Y.11
Hattori, N.12
Farrer, M.J.13
Tan, E.-K.14
Wu, R.-M.15
-
27
-
-
33646887782
-
Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia
-
Saunders-Pullman R., Lipton R.B., Senthil G., Katz M., Costan-Toth C., Derby C., Bressman S., Verghese J., and Ozelius L.J. Increased frequency of the LRRK2 G2019S mutation in an elderly Ashkenazi Jewish population is not associated with dementia. Neurosci. Lett. 402 (2006) 92-96
-
(2006)
Neurosci. Lett.
, vol.402
, pp. 92-96
-
-
Saunders-Pullman, R.1
Lipton, R.B.2
Senthil, G.3
Katz, M.4
Costan-Toth, C.5
Derby, C.6
Bressman, S.7
Verghese, J.8
Ozelius, L.J.9
-
28
-
-
67651166905
-
A clinic-based screening of mutations in exons 31, 34, 35, 41 and 48 of LRRK2 in Iranian Parkinson's disease patients
-
Shojaee S., Sina F., Farboodi N., Fazlali Z., Ghazavi F., Ghorashi S.A., Parsa K., Sadeghi H., Shahidi G.-A., Ronaghi M., and Elahi E. A clinic-based screening of mutations in exons 31, 34, 35, 41 and 48 of LRRK2 in Iranian Parkinson's disease patients. Mov. Disord. 24 7 (2009) 1023-1027
-
(2009)
Mov. Disord.
, vol.24
, Issue.7
, pp. 1023-1027
-
-
Shojaee, S.1
Sina, F.2
Farboodi, N.3
Fazlali, Z.4
Ghazavi, F.5
Ghorashi, S.A.6
Parsa, K.7
Sadeghi, H.8
Shahidi, G.-A.9
Ronaghi, M.10
Elahi, E.11
-
29
-
-
0036136951
-
E.C.o.G.S.i.P.s. disease, PARK6-linked parkinsonism occurs in several European families
-
Valente E., Brancati F., Ferraris A., Graham E., Davis M., Breteler M., Gasser T., Bonifati V., Bentivoglio A., Michele G.D., Dürr A., Ortelli P., Wassilowsky D., Harhangi B., Rawal N., Caputo V., Filla A., Meco G., Oostra B., Brice A., Albanese A., Dallapiccola B., and Wood N. E.C.o.G.S.i.P.s. disease, PARK6-linked parkinsonism occurs in several European families. Ann. Neurol. 51 1 (2002) 14-18
-
(2002)
Ann. Neurol.
, vol.51
, Issue.1
, pp. 14-18
-
-
Valente, E.1
Brancati, F.2
Ferraris, A.3
Graham, E.4
Davis, M.5
Breteler, M.6
Gasser, T.7
Bonifati, V.8
Bentivoglio, A.9
Michele, G.D.10
Dürr, A.11
Ortelli, P.12
Wassilowsky, D.13
Harhangi, B.14
Rawal, N.15
Caputo, V.16
Filla, A.17
Meco, G.18
Oostra, B.19
Brice, A.20
Albanese, A.21
Dallapiccola, B.22
Wood, N.23
more..
-
30
-
-
33750370804
-
Understanding the molecular causes of Parkinson's disease
-
Wood-Kaczmar A., Gandhi S., and Wood N. Understanding the molecular causes of Parkinson's disease. Trends Mol. Med. 12 (2006) 521-528
-
(2006)
Trends Mol. Med.
, vol.12
, pp. 521-528
-
-
Wood-Kaczmar, A.1
Gandhi, S.2
Wood, N.3
-
31
-
-
24644486896
-
A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations
-
Zabetian C.P., Samii A., Mosley A.D., Roberts J.W., Leis B.C., Yearout D., Raskind W.H., and Griffith M.A. A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations. Neurology 65 (2005) 741-744
-
(2005)
Neurology
, vol.65
, pp. 741-744
-
-
Zabetian, C.P.1
Samii, A.2
Mosley, A.D.3
Roberts, J.W.4
Leis, B.C.5
Yearout, D.6
Raskind, W.H.7
Griffith, M.A.8
-
32
-
-
8844233579
-
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
-
Zimprich A., Biskup S., Leitner P., Lichtner P., Farrer M., Lincoln S., Kachergus J., Hulihan M., Uitti R.J., Calne D.B., Stoessl A.J., Pfeiffer R.F., Patenge N., Carbajal I.C., Vieregge P., Asmus F., Muller-Myhsok B., Dickson D.W., Meitinger T., Strom T.M., Wszolek Z.K., and Gasser T. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Neuron 44 (2004) 601-607
-
(2004)
Neuron
, vol.44
, pp. 601-607
-
-
Zimprich, A.1
Biskup, S.2
Leitner, P.3
Lichtner, P.4
Farrer, M.5
Lincoln, S.6
Kachergus, J.7
Hulihan, M.8
Uitti, R.J.9
Calne, D.B.10
Stoessl, A.J.11
Pfeiffer, R.F.12
Patenge, N.13
Carbajal, I.C.14
Vieregge, P.15
Asmus, F.16
Muller-Myhsok, B.17
Dickson, D.W.18
Meitinger, T.19
Strom, T.M.20
Wszolek, Z.K.21
Gasser, T.22
more..
|