-
1
-
-
77952012782
-
More is less: Inactivation and deletion events and the search for tumor suppressor genes
-
Bradley WE, Di Paola D, Rampakakis E, Zannis-Hadjopoulos M. 2010a. More is less: Inactivation and deletion events and the search for tumor suppressor genes. J Cell Biochem 110: 281-287.
-
(2010)
J Cell Biochem
, vol.110
, pp. 281-287
-
-
Bradley, W.E.1
Di Paola, D.2
Rampakakis, E.3
Zannis-Hadjopoulos, M.4
-
2
-
-
77949676046
-
Hotspots of large rare deletions in the human genome
-
Bradley WE, Raelson JV, Dubois DY, Godin E, Fournier H, Privé C, Allard R, Pinchuk V, Lapalme M, Paulussen RJ, Belouchi A. 2010b. Hotspots of large rare deletions in the human genome. PLoS One 5: e9401.
-
(2010)
PLoS One
, vol.5
-
-
Bradley, W.E.1
Raelson, J.V.2
Dubois, D.Y.3
Godin, E.4
Fournier, H.5
Privé, C.6
Allard, R.7
Pinchuk, V.8
Lapalme, M.9
Paulussen, R.J.10
Belouchi, A.11
-
3
-
-
67549146854
-
Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers
-
Brüggemann N, Mitterer M, Lanthaler AJ, Djarmati A, Hagenah J, Wiegers K, Winkler S, Pawlack H, Lohnau T, Pramstaller PP, Klein C, Lohmann K. 2009. Frequency of heterozygous Parkin mutations in healthy subjects: Need for careful prospective follow-up examination of mutation carriers. Parkinson Relat Disord 15: 425-429.
-
(2009)
Parkinson Relat Disord
, vol.15
, pp. 425-429
-
-
Brüggemann, N.1
Mitterer, M.2
Lanthaler, A.J.3
Djarmati, A.4
Hagenah, J.5
Wiegers, K.6
Winkler, S.7
Pawlack, H.8
Lohnau, T.9
Pramstaller, P.P.10
Klein, C.11
Lohmann, K.12
-
4
-
-
0038732456
-
Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27
-
Cesari R, Martin ES, Calin GA, Pentimalli F, Bichi R, McAdams H, Trapasso F, Drusco A, Shimizu M, Masciullo V, D'Andrilli G, Scambia G, Picchio MC, Alder H, Godwin AK, Croce CM. 2003. Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27. Proc Natl Acad Sci USA 100: 5956-5961.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, pp. 5956-5961
-
-
Cesari, R.1
Martin, E.S.2
Calin, G.A.3
Pentimalli, F.4
Bichi, R.5
McAdams, H.6
Trapasso, F.7
Drusco, A.8
Shimizu, M.9
Masciullo, V.10
D'Andrilli, G.11
Scambia, G.12
Picchio, M.C.13
Alder, H.14
Godwin, A.K.15
Croce, C.M.16
-
5
-
-
0017412603
-
One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice
-
Fogh J, Fogh JM, Orfeo T. 1977. One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice. J Natl Cancer Inst 59: 221-226.
-
(1977)
J Natl Cancer Inst
, vol.59
, pp. 221-226
-
-
Fogh, J.1
Fogh, J.M.2
Orfeo, T.3
-
6
-
-
77954854724
-
Prevalence of human papillomavirus 16/18/33 infection and p53 mutation in lung adenocarcinoma
-
Iwakawa R, Kohno T, Enari M, Kiyono T, Yokota J. 2010. Prevalence of human papillomavirus 16/18/33 infection and p53 mutation in lung adenocarcinoma. Cancer Sci 101: 1891-1896.
-
(2010)
Cancer Sci
, vol.101
, pp. 1891-1896
-
-
Iwakawa, R.1
Kohno, T.2
Enari, M.3
Kiyono, T.4
Yokota, J.5
-
7
-
-
79952732654
-
MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis
-
Iwakawa R, Kohno T, Kato M, Shiraishi K, Tsuta K, Noguchi M, Ogawa S, Yokota J. 2011. MYC amplification as a prognostic marker of early-stage lung adenocarcinoma identified by whole genome copy number analysis. Clin Cancer Res 17: 1481-1489.
-
(2011)
Clin Cancer Res
, vol.17
, pp. 1481-1489
-
-
Iwakawa, R.1
Kohno, T.2
Kato, M.3
Shiraishi, K.4
Tsuta, K.5
Noguchi, M.6
Ogawa, S.7
Yokota, J.8
-
8
-
-
77957968209
-
A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2
-
Kay DM, Stevens CF, Hamza TH, Montimurro JS, Zabetian CP, Factor SA, Samii A, Griffith A, Roberts JW, Molho ES, Higgins DS, Gancher S, Moses L, Zareparsi S, Poorkaj P, Bird T, Nutt J, Schellenberg GD, Payami H. 2010. A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2. Neurology 75: 1189-1194.
-
(2010)
Neurology
, vol.75
, pp. 1189-1194
-
-
Kay, D.M.1
Stevens, C.F.2
Hamza, T.H.3
Montimurro, J.S.4
Zabetian, C.P.5
Factor, S.A.6
Samii, A.7
Griffith, A.8
Roberts, J.W.9
Molho, E.S.10
Higgins, D.S.11
Gancher, S.12
Moses, L.13
Zareparsi, S.14
Poorkaj, P.15
Bird, T.16
Nutt, J.17
Schellenberg, G.D.18
Payami, H.19
-
9
-
-
33846200292
-
Correlated break at PARK2/FRA6E and loss of AF-6/Afadin protein expression are associated with poor outcome in breast cancer
-
Letessier A, Garrido-Urbani S, Ginestier C, Fournier G, Esterni B, Monville F, Adélaïde J, Geneix J, Xerri L, Dubreuil P, Viens P, Charafe-Jauffret E, Jacquemier J, Birnbaum D, Lopez M, Chaffanet M. 2007. Correlated break at PARK2/FRA6E and loss of AF-6/Afadin protein expression are associated with poor outcome in breast cancer. Oncogene 26: 298-307.
-
(2007)
Oncogene
, vol.26
, pp. 298-307
-
-
Letessier, A.1
Garrido-Urbani, S.2
Ginestier, C.3
Fournier, G.4
Esterni, B.5
Monville, F.6
Adélaïde, J.7
Geneix, J.8
Xerri, L.9
Dubreuil, P.10
Viens, P.11
Charafe-Jauffret, E.12
Jacquemier, J.13
Birnbaum, D.14
Lopez, M.15
Chaffanet, M.16
-
10
-
-
27744552014
-
Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease
-
Li X, Kitami T, Wang M, Mizuno Y, Hattori N. 2005. Geographic and ethnic differences in frequencies of two polymorphisms (D/N394 and L/I272) of the parkin gene in sporadic Parkinson's disease. Parkinson Relat Disord 11: 485-491.
-
(2005)
Parkinson Relat Disord
, vol.11
, pp. 485-491
-
-
Li, X.1
Kitami, T.2
Wang, M.3
Mizuno, Y.4
Hattori, N.5
-
11
-
-
1342347411
-
Parkin variants in North American Parkinson's disease: Cases and controls
-
Lincoln SJ, Maraganore DM, Lesnick TG, Bounds R, de Andrade M, Bower JH, Hardy JA, Farrer MJ. 2003. Parkin variants in North American Parkinson's disease: Cases and controls. Mov Disord 18: 1306-1311.
-
(2003)
Mov Disord
, vol.18
, pp. 1306-1311
-
-
Lincoln, S.J.1
Maraganore, D.M.2
Lesnick, T.G.3
Bounds, R.4
de Andrade, M.5
Bower, J.H.6
Hardy, J.A.7
Farrer, M.J.8
-
12
-
-
0026315149
-
Establishment and characterization of 20 human non-small cell lung cancer cell lines in a serum-free defined medium (ACL-4)
-
Masuda N, Fukuoka M, Takada M, Kudoh S, Kusunoki Y. 1991. Establishment and characterization of 20 human non-small cell lung cancer cell lines in a serum-free defined medium (ACL-4). Chest 100: 429-438.
-
(1991)
Chest
, vol.100
, pp. 429-438
-
-
Masuda, N.1
Fukuoka, M.2
Takada, M.3
Kudoh, S.4
Kusunoki, Y.5
-
13
-
-
52949141845
-
Integrated detection and population-genetic analysis of SNPs and copy number variation
-
McCarroll SA, Kuruvilla FG, Korn JM, Cawley S, Nemesh J, Wysoker A, Shapero MH, de Bakker PI, Maller JB, Kirby A, Elliott AL, Parkin M, Hubbell E, Webster T, Mei R, Veitch J, Collins PJ, Handsaker R, Lincoln S, Nizzari M, Blume J, Jones KW, Rava R, Daly MJ, Gabriel SB, Altshuler D. 2008. Integrated detection and population-genetic analysis of SNPs and copy number variation. Nat Genet 40: 1166-1174.
-
(2008)
Nat Genet
, vol.40
, pp. 1166-1174
-
-
McCarroll, S.A.1
Kuruvilla, F.G.2
Korn, J.M.3
Cawley, S.4
Nemesh, J.5
Wysoker, A.6
Shapero, M.H.7
de Bakker, P.I.8
Maller, J.B.9
Kirby, A.10
Elliott, A.L.11
Parkin, M.12
Hubbell, E.13
Webster, T.14
Mei, R.15
Veitch, J.16
Collins, P.J.17
Handsaker, R.18
Lincoln, S.19
Nizzari, M.20
Blume, J.21
Jones, K.W.22
Rava, R.23
Daly, M.J.24
Gabriel, S.B.25
Altshuler, D.26
more..
-
14
-
-
77955084425
-
Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines
-
Mitsui J, Takahashi Y, Goto J, Tomiyama H, Ishikawa S, Yoshino H, Minami N, Smith DI, Lesage S, Aburatani H, Nishino I, Brice A, Hattori N, Tsuji S. 2010. Mechanisms of genomic instabilities underlying two common fragile-site-associated loci, PARK2 and DMD, in germ cell and cancer cell lines. Am J Hum Genet 87: 75-89.
-
(2010)
Am J Hum Genet
, vol.87
, pp. 75-89
-
-
Mitsui, J.1
Takahashi, Y.2
Goto, J.3
Tomiyama, H.4
Ishikawa, S.5
Yoshino, H.6
Minami, N.7
Smith, D.I.8
Lesage, S.9
Aburatani, H.10
Nishino, I.11
Brice, A.12
Hattori, N.13
Tsuji, S.14
-
15
-
-
43749094765
-
Progress in the pathogenesis and genetics of Parkinson's disease
-
Mizuno Y, Hattori N, Kubo S, Sato S, Nishioka K, Hatano T, Tomiyama H, Funayama M, Machida Y, Mochizuki H. 2008. Progress in the pathogenesis and genetics of Parkinson's disease. Philos Trans R Soc Lond B Biol Sci 363: 2215-2227.
-
(2008)
Philos Trans R Soc Lond B Biol Sci
, vol.363
, pp. 2215-2227
-
-
Mizuno, Y.1
Hattori, N.2
Kubo, S.3
Sato, S.4
Nishioka, K.5
Hatano, T.6
Tomiyama, H.7
Funayama, M.8
Machida, Y.9
Mochizuki, H.10
-
16
-
-
77953801296
-
Genetic determinants at the interface of cancer and neurodegenerative disease
-
Morris LG, Veeriah S, Chan TA. 2010. Genetic determinants at the interface of cancer and neurodegenerative disease. Oncogene 29: 3453-3464.
-
(2010)
Oncogene
, vol.29
, pp. 3453-3464
-
-
Morris, L.G.1
Veeriah, S.2
Chan, T.A.3
-
17
-
-
22244453416
-
A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays
-
Nannya Y, Sanada M, Nakazaki K, Hosoya N, Wang L, Hangaishi A, Kurokawa M, Chiba S, Bailey DK, Kennedy GC, Ogawa S. 2005. A robust algorithm for copy number detection using high-density oligonucleotide single nucleotide polymorphism genotyping arrays. Cancer Res 65: 6071-6079.
-
(2005)
Cancer Res
, vol.65
, pp. 6071-6079
-
-
Nannya, Y.1
Sanada, M.2
Nakazaki, K.3
Hosoya, N.4
Wang, L.5
Hangaishi, A.6
Kurokawa, M.7
Chiba, S.8
Bailey, D.K.9
Kennedy, G.C.10
Ogawa, S.11
-
18
-
-
77954104112
-
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: A mutation update
-
Nuytemans K, Theuns J, Cruts M, Van Broeckhoven C. 2010. Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: A mutation update. Hum Mutat 31: 763-780.
-
(2010)
Hum Mutat
, vol.31
, pp. 763-780
-
-
Nuytemans, K.1
Theuns, J.2
Cruts, M.3
Van Broeckhoven, C.4
-
19
-
-
77951719393
-
Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing
-
Park H, Kim JI, Ju YS, Gokcumen O, Mills RE, Kim S, Lee S, Suh D, Hong D, Kang HP, Yoo YJ, Shin JY, Kim HJ, Yavartanoo M, Chang YW, Ha JS, Chong W, Hwang GR, Darvishi K, Kim H, Yang SJ, Yang KS, Kim H, Hurles ME, Scherer SW, Carter NP, Tyler-Smith C, Lee C, Seo JS. 2010. Discovery of common Asian copy number variants using integrated high-resolution array CGH and massively parallel DNA sequencing. Nat Genet 42: 400-405.
-
(2010)
Nat Genet
, vol.42
, pp. 400-405
-
-
Park, H.1
Kim, J.I.2
Ju, Y.S.3
Gokcumen, O.4
Mills, R.E.5
Kim, S.6
Lee, S.7
Suh, D.8
Hong, D.9
Kang, H.P.10
Yoo, Y.J.11
Shin, J.Y.12
Kim, H.J.13
Yavartanoo, M.14
Chang, Y.W.15
Ha, J.S.16
Chong, W.17
Hwang, G.R.18
Darvishi, K.19
Kim, H.20
Yang, S.J.21
Yang, K.S.22
Kim, H.23
Hurles, M.E.24
Scherer, S.W.25
Carter, N.P.26
Tyler-Smith, C.27
Lee, C.28
Seo, J.S.29
more..
-
20
-
-
33646953271
-
NCI-Navy Medical Oncology Branch cell line data base
-
Phelps RM, Johnson BE, Ihde DC, Gazdar AF, Carbone DP, McClintock PR, Linnoila RI, Matthews MJ, Bunn PA Jr, Carney D, Minna JD, Mulshine JL. 1996. NCI-Navy Medical Oncology Branch cell line data base. J Cell Biochem Suppl 24: 32-91.
-
(1996)
J Cell Biochem Suppl
, vol.24
, pp. 32-91
-
-
Phelps, R.M.1
Johnson, B.E.2
Ihde, D.C.3
Gazdar, A.F.4
Carbone, D.P.5
McClintock, P.R.6
Linnoila, R.I.7
Matthews, M.J.8
Bunn Jr, P.A.9
Carney, D.10
Minna, J.D.11
Mulshine, J.L.12
-
21
-
-
11144355981
-
Alterations of the tumor suppressor gene Parkin in non-small cell lung cancer
-
Picchio MC, Martin ES, Cesari R, Calin GA, Yendamuri S, Kuroki T, Pentimalli F, Sarti M, Yoder K, Kaiser LR, Fishel R, Croce CM. 2004. Alterations of the tumor suppressor gene Parkin in non-small cell lung cancer. Clin Cancer Res 10: 2720-2724.
-
(2004)
Clin Cancer Res
, vol.10
, pp. 2720-2724
-
-
Picchio, M.C.1
Martin, E.S.2
Cesari, R.3
Calin, G.A.4
Yendamuri, S.5
Kuroki, T.6
Pentimalli, F.7
Sarti, M.8
Yoder, K.9
Kaiser, L.R.10
Fishel, R.11
Croce, C.M.12
-
22
-
-
77956990244
-
PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice
-
Poulogiannis G, McIntyre RE, Dimitriadi M, Apps JR, Wilson CH, Ichimura K, Luo F, Cantley LC, Wyllie AH, Adams DJ, Arends MJ. 2010. PARK2 deletions occur frequently in sporadic colorectal cancer and accelerate adenoma development in Apc mutant mice. Proc Natl Acad Sci USA 107: 15145-15150.
-
(2010)
Proc Natl Acad Sci USA
, vol.107
, pp. 15145-15150
-
-
Poulogiannis, G.1
McIntyre, R.E.2
Dimitriadi, M.3
Apps, J.R.4
Wilson, C.H.5
Ichimura, K.6
Luo, F.7
Cantley, L.C.8
Wyllie, A.H.9
Adams, D.J.10
Arends, M.J.11
-
23
-
-
77956502467
-
Discovering tumor suppressor genes through genome-wide copy number analysis
-
Rothenberg SM, Settleman J. 2010. Discovering tumor suppressor genes through genome-wide copy number analysis. Curr Genom 11: 297-310.
-
(2010)
Curr Genom
, vol.11
, pp. 297-310
-
-
Rothenberg, S.M.1
Settleman, J.2
-
24
-
-
77950280030
-
A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers
-
Rothenberg SM, Mohapatra G, Rivera MN, Winokur D, Greninger P, Nitta M, Sadow PM, Sooriyakumar G, Brannigan BW, Ulman MJ, Perera RM, Wang R, Tam A, Ma XJ, Erlander M, Sgroi DC, Rocco JW, Lingen MW, Cohen EE, Louis DN, Settleman J, Haber DA. 2010. A genome-wide screen for microdeletions reveals disruption of polarity complex genes in diverse human cancers. Cancer Res 70: 2158-2164.
-
(2010)
Cancer Res
, vol.70
, pp. 2158-2164
-
-
Rothenberg, S.M.1
Mohapatra, G.2
Rivera, M.N.3
Winokur, D.4
Greninger, P.5
Nitta, M.6
Sadow, P.M.7
Sooriyakumar, G.8
Brannigan, B.W.9
Ulman, M.J.10
Perera, R.M.11
Wang, R.12
Tam, A.13
Ma, X.J.14
Erlander, M.15
Sgroi, D.C.16
Rocco, J.W.17
Lingen, M.W.18
Cohen, E.E.19
Louis, D.N.20
Settleman, J.21
Haber, D.A.22
more..
-
25
-
-
0009426179
-
Transforming gene from human stomach cancers and a noncancerous portion of stomach mucosa
-
Sakamoto H, Mori M, Taira M, Yoshida T, Matsukawa S, Shimizu K, Sekiguchi M, Terada M, Sugimura T. 1986. Transforming gene from human stomach cancers and a noncancerous portion of stomach mucosa. Proc Natl Acad Sci USA 83: 3997-4001.
-
(1986)
Proc Natl Acad Sci USA
, vol.83
, pp. 3997-4001
-
-
Sakamoto, H.1
Mori, M.2
Taira, M.3
Yoshida, T.4
Matsukawa, S.5
Shimizu, K.6
Sekiguchi, M.7
Terada, M.8
Sugimura, T.9
-
26
-
-
0033933048
-
Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase
-
Shimura H, Hattori N, Kubo S, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T. 2000. Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase. Nat Genet 25: 302-305.
-
(2000)
Nat Genet
, vol.25
, pp. 302-305
-
-
Shimura, H.1
Hattori, N.2
Kubo, S.3
Mizuno, Y.4
Asakawa, S.5
Minoshima, S.6
Shimizu, N.7
Iwai, K.8
Chiba, T.9
Tanaka, K.10
Suzuki, T.11
-
27
-
-
15944393532
-
-
Sobin LH, Wittekind CH, eds. 6th ed. New York: Wiley-Liss
-
Sobin LH, Wittekind CH, eds. 2002. TNM Classification of Malignant Tumors, 6th ed. New York: Wiley-Liss, pp. 99-103.
-
(2002)
TNM Classification of Malignant Tumors
, pp. 99-103
-
-
-
28
-
-
73349125417
-
Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies
-
Veeriah S, Taylor BS, Meng S, Fang F, Yilmaz E, Vivanco I, Janakiraman M, Schultz N, Hanrahan AJ, Pao W, Ladanyi M, Sander C, Heguy A, Holland EC, Paty PB, Mischel PS, Liau L, Cloughesy TF, Mellinghoff IK, Solit DB, Chan TA. 2010. Somatic mutations of the Parkinson's disease-associated gene PARK2 in glioblastoma and other human malignancies. Nat Genet 42: 77-82.
-
(2010)
Nat Genet
, vol.42
, pp. 77-82
-
-
Veeriah, S.1
Taylor, B.S.2
Meng, S.3
Fang, F.4
Yilmaz, E.5
Vivanco, I.6
Janakiraman, M.7
Schultz, N.8
Hanrahan, A.J.9
Pao, W.10
Ladanyi, M.11
Sander, C.12
Heguy, A.13
Holland, E.C.14
Paty, P.B.15
Mischel, P.S.16
Liau, L.17
Cloughesy, T.F.18
Mellinghoff, I.K.19
Solit, D.B.20
Chan, T.A.21
more..
-
29
-
-
0031971078
-
Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types
-
Virmani AK, Fong KM, Kodagoda D, McIntire D, Hung J, Tonk V, Minna JD, Gazdar AF. Allelotyping demonstrates common and distinct patterns of chromosomal loss in human lung cancer types. 1998. Genes Chromosomes Cancer 21: 308-319.
-
(1998)
Genes Chromosomes Cancer
, vol.21
, pp. 308-319
-
-
Virmani, A.K.1
Fong, K.M.2
Kodagoda, D.3
McIntire, D.4
Hung, J.5
Tonk, V.6
Minna, J.D.7
Gazdar, A.F.8
-
30
-
-
34347229790
-
Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays
-
Yamamoto G, Nannya Y, Kato M, Sanada M, Levine RL, Kawamata N, Hangaishi A, Kurokawa M, Chiba S, Gilliland DG, Koeffler HP, Ogawa S. 2007. Highly sensitive method for genomewide detection of allelic composition in nonpaired, primary tumor specimens by use of affymetrix single-nucleotide-polymorphism genotyping microarrays. Am J Hum Genet 81: 114-126.
-
(2007)
Am J Hum Genet
, vol.81
, pp. 114-126
-
-
Yamamoto, G.1
Nannya, Y.2
Kato, M.3
Sanada, M.4
Levine, R.L.5
Kawamata, N.6
Hangaishi, A.7
Kurokawa, M.8
Chiba, S.9
Gilliland, D.G.10
Koeffler, H.P.11
Ogawa, S.12
-
31
-
-
79960766955
-
Genetics of Parkinson's disease and essential tremor
-
Zimprich A. 2011. Genetics of Parkinson's disease and essential tremor. Curr Opin Neurol 24: 318-323.
-
(2011)
Curr Opin Neurol
, vol.24
, pp. 318-323
-
-
Zimprich, A.1
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