부산대학교 도서관

Gallagher, MD; Suh, E; Grossman, M; Elman, L; McCluskey, L; Van, Swieten JC; Al-Sarraj, S; Neumann, M; Gelpi, E; Ghetti, B

ACTA NEUROPATHOLOGICA. 127(3):407-418

Zhang, JV; Irwin, DJ; Blennow, K; Zetterberg, H; Lee, EB; Shaw, LM; Rascovsky, K; Massimo, L; McMillan, CT; Chen-Plotkin, A; Elman, L; Lee, VM-Y; McCluskey, L; Toledo, JB; Weintraub, D; Wolk, D; Trojanowski, JQ; Grossman, M

Neurology Clinical Practice. 11:105-116

Lin, K; Pulit, SL; Van Rheenen, W; Shatunov, A; Dekker, AM; McLaughlin, RL; Diekstra, FP; Van Der Spek, RAA; Võsa, U; De Jong, S; Robinson, MR; Yang, J; Fogh, I; Van Doormaal, PT; Tazelaar, GHP; Koppers, M; Blokhuis, AM; Sproviero, W; Jones, AR; Kenna, KP; Van Eijk, KR; Harschnitz, O; Schellevis, RD; Brands, WJ; Medic, J; Menelaou, A; Vajda, A; Ticozzi, N; Rogelj, B; Vrabec, K; Ravnik-Glavač, M; Koritnik, B; Zidar, J; Leonardis, L; Grošelj, LD; Millecamps, S; Salachas, F; Meininger, V; De Carvalho, M; Pinto, S; Mora, JS; Rojas-García, R; Polak, M; Chandran, S; Colville, S; Swingler, R; Morrison, KE; Shaw, PJ; Hardy, J; Orrell, RW; Pittman, A; Sidle, K; Fratta, P; Malaspina, A; Topp, S; Petri, S; Abdulla, S; Drepper, C; Sendtner, M; Meyer, T; Ophoff, RA; Staats, KA; Wiedau-Pazos, M; Lomen-Hoerth, C; Van Deerlin, VM; Trojanowski, JQ; Elman, L; McCluskey, L; Basak, AN; Tunca, C; Hamzeiy, H; Parman, Y; Meitinger, T; Lichtner, P; Radivojkov-Blagojevic, M; Andres, CR; Maurel, C; Bensimon, G; Landwehrmeyer, B; Brice, A; Payan, CAM; Saker-Delye, S; Dürr, A; Wood, NW; Tittmann, L; Lieb, W; Franke, A; Rietschel, M; Cichon, S; Nöthen, MM; Amouyel, P; Tzourio, C; Dartigues, J-F; Uitterlinden, AG; Rivadeneira, F; Estrada, K; Hofman, A; Curtis, C; Blauw, HM; Van Der Kooi, AJ; De Visser, M; Goris, A; Weber, M; Shaw, CE; Smith, BN; Pansarasa, O; Cereda, C; Del Bo, R; Comi, GP; D'Alfonso, S; Bertolin, C; Sorarù, G; Mazzini, L; Pensato, V; Gellera, C; Tiloca, C; Ratti, A; Calvo, A; Moglia, C; Brunetti, M; Arcuti, S; Capozzo, R; Zecca, C; Lunetta, C; Penco, S; Riva, N; Padovani, A; Filosto, M; Muller, B; Stuit, RJ; Registry, P; Group, Slalom; Registry, S; Consortium, Fals Sequencing; Consortium, Slagen; Group, Nnipps Study; Blair, I; Zhang, K; McCann, EP; Fifita, JA; Nicholson, GA; Rowe, DB; Pamphlett, R; Kiernan, MC; Grosskreutz, J; Witte, OW; Ringer, T; Prell, T; Stubendorff, B; Kurth, I; Hübner, CA; Leigh, PN; Casale, F; Chio, A; Beghi, E; Pupillo, E; Tortelli, R; Logroscino, G; Powell, J; Ludolph, AC; Weishaupt, JH; Robberecht, W; Van Damme, P; Franke, L; Pers, TH; Brown, RH; Glass, JD; Landers, JE; Hardiman, O; Andersen, PM; Corcia, P; Vourc'H, P; Silani, V; Wray, NR; Visscher, PM; De Bakker, PIW; Van Es, MA; Pasterkamp, RJ; Lewis, CM; Breen, G; Al-Chalabi, A; Van Den Berg, LH; Veldink, JH

NATURE GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Institut d’Investigació Biomèdica Sant Pau (IIB Sant Pau)
instname
van Rheenen, W, Shatunov, A, Dekker, A M, McLaughlin, R L, Diekstra, F P, Pulit, S L, van der Spek, R A A, Võsa, U, de Jong, S, Robinson, M R, Yang, J, Fogh, I, van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-Glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, de Carvalho, M, Pinto, S, Fratta, P, Topp, S, Curtis, C, Shaw, C E, Smith, B N, Leigh, P N, Powell, J, Lewis, C M, Breen, G, Al-Chalabi, A 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics, vol. 48, pp. 1043–1048 . https://doi.org/10.1038/ng.3622
Van Rheenen, W, Shatunov, A, Dekker, A M, Mclaughlin, R L, Diekstra, F P, Pulit, S L, Van Der Spek, R A A, Võsa, U, De Jong, S, Robinson, M R, Yang, J, Fogh, I, Van Doormaal, P T, Tazelaar, G H P, Koppers, M, Blokhuis, A M, Sproviero, W, Jones, A R, Kenna, K P, Van Eijk, K R, Harschnitz, O, Schellevis, R D, Brands, W J, Medic, J, Menelaou, A, Vajda, A, Ticozzi, N, Lin, K, Rogelj, B, Vrabec, K, Ravnik-glavač, M, Koritnik, B, Zidar, J, Leonardis, L, Grošelj, L D, Millecamps, S, Salachas, F, Meininger, V, De Carvalho, M, Pinto, S, Mora, J S, Rojas-garcía, R, Polak, M, Chandran, S, Colville, S, Swingler, R, Morrison, K E, Shaw, P J, Hardy, J, Orrell, R W, Pittman, A, Sidle, K, Fratta, P, Malaspina, A, Topp, S, Petri, S, Abdulla, S, Drepper, C, Sendtner, M, Meyer, T, Ophoff, R A, Staats, K A, Wiedau-pazos, M, Lomen-hoerth, C, Van Deerlin, V M, Trojanowski, J Q, Elman, L, Mccluskey, L, Basak, A N, Tunca, C, Hamzeiy, H, Parman, Y, Meitinger, T, Lichtner, P, Radivojkov-blagojevic, M, Andres, C R, Maurel, C, Bensimon, G, Landwehrmeyer, B, Brice, A, Payan, C A M, Saker-delye, S, Dürr, A, Wood, N W, Tittmann, L, Lieb, W, Franke, A, Rietschel, M, Cichon, S, Nöthen, M M, Amouyel, P, Tzourio, C, Dartigues, J, Uitterlinden, A G, Rivadeneira, F, Estrada, K, Hofman, A, Curtis, C, Blauw, H M, Van Der Kooi, A J, De Visser, M, Goris, A, Weber, M, Shaw, C E, Smith, B N, Pansarasa, O, Cereda, C, Del Bo, R, Comi, G P, D'alfonso, S, Bertolin, C, Sorarù, G, Mazzini, L, Pensato, V, Gellera, C, Tiloca, C, Ratti, A, Calvo, A, Moglia, C, Brunetti, M, Arcuti, S, Capozzo, R, Zecca, C, Lunetta, C, Penco, S, Riva, N, Padovani, A, Filosto, M, Muller, B, Stuit, R J, Blair, I, Zhang, K, Mccann, E P, Fifita, J A, Nicholson, G A, Rowe, D B, Pamphlett, R, Kiernan, M C, Grosskreutz, J, Witte, O W, Ringer, T, Prell, T, Stubendorff, B, Kurth, I, Hübner, C A, Leigh, P N, Casale, F, Chio, A, Beghi, E, Pupillo, E, Tortelli, R, Logroscino, G, Powell, J, Ludolph, A C, Weishaupt, J H, Robberecht, W, Van Damme, P, Franke, L, Pers, T H, Brown, R H, Glass, J D, Landers, J E, Hardiman, O, Andersen, P M, Corcia, P, Vourc'h, P, Silani, V, Wray, N R, Visscher, P M, De Bakker, P I W, Van Es, M A, Pasterkamp, R J, Lewis, C M, Breen, G, Al-chalabi, A, Van Den Berg, L H & Veldink, J H 2016, ' Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis ', Nature Genetics . https://doi.org/10.1038/ng.3622
Nat. Genet. 48, 1043-1048 (2016)
Nature Genetics

Hu WT; Chen-Plotkin A; Grossman M; Arnold SE; Clark CM; Shaw LM; McCluskey L; Elman L; Hurtig HI; Siderowf A; Lee VM; Soares H; Trojanowski JQ; Hu, W T; Chen-Plotkin, A; Grossman, M; Arnold, S E; Clark, C M; Shaw, L M; McCluskey, L

Neurology. 12/7/2010, Vol. 75 Issue 23, p2079-2086. 8p.

Cirulli, Elizabeth T; Lasseigne, Brittany N; Petrovski, Slavé; Sapp, Peter C; Dion, Patrick A; Leblond, Claire S; Couthouis, Julien; Lu, Yi Fan; Wang, Quanli; Krueger, Brian J; Ren, Zhong; Keebler, Jonathan; Han, Yujun; Levy, Shawn E; Boone, Braden E; Wimbish, Jack R; Waite, Lindsay L; Jones, Angela L; Carulli, John P; Day Williams, Aaron G; Staropoli, John F; Xin, Winnie W; Chesi, Alessandra; Raphael, Alya R; McKenna Yasek, Diane; Cady, Janet; Vianney de Jong, J. M. B; Kenna, Kevin P; Smith, Bradley N; Topp, Simon; Miller, Jack; Gkazi, Athina; Al Chalabi, Ammar; van den Berg, Leonard H; Veldink, Jan; Silani, Vincenzo; Ticozzi, Nicola; Shaw, Christopher E; Baloh, Robert H; Appel, Stanley; Simpson, Ericka; Lagier Tourenne, Clotilde; Pulst, Stefan M; Gibson, Summer; Trojanowski, John Q; Elman, Lauren; Mccluskey, Leo; Grossman, Murray; Shneider, Neil A; Chung, Wendy K; Ravits, John M; Glass, Jonathan D; Sims, Katherine B; Van Deerlin, Vivianna M; Maniatis, Tom; Hayes, Sebastian D; Ordureau, Alban; Swarup, Sharan; Landers, John; Baas, Frank; Allen, Andrew S; Bedlack, Richard S; Harper, J. Wade; Gitler, Aaron D; Rouleau, Guy A; Brown, Robert; Harms, Matthew B; Cooper, Gregory M; Harris, Tim; Myers, Richard M; Goldstein, David B; Sapp, PC; Leblond, CS; McKenna Yasek, D; Kenna, KP; Smith, BN; Topp, S; Miller, J; Gkazi, A; Al Chalabi, A; van den Berg, LH; Veldink, J; Silani, V; Ticozzi, N; Landers, J; Baas, F; Shaw, CE; Glass, JD; Rouleau, GA; Brown, R; Hardiman, O; McLaughlin, RL; Mazzini, L; Blair, IP; Williams, KL; Nicholson, GA; Al Sarraj, S; King, A; Scotter, EL; Troakes, C; Vance, C; D'ALFONSO, Sandra; Duga, S; CORRADO, Lucia; ten Asbroek, AL; Calini, D; Colombrita, C; Ratti, A; Tiloca, C; Wu, Z; Asress, S; Polak, M; Diekstra, F; van Rheenen, W; Danielson, EW; Fallini, C; Keagle, P; Lewis, EA; Kost, J; Sorarù, G; Bertolin, C; Querin, G; Castellotti, B; Gellera, C; Pensato, V; Taroni, F; Cereda, C; Gagliardi, S; Ceroni, M; Lauria, G; de Belleroche, J; Comi, GP; Corti, S; Del, Bo; R; Turner, MR; Talbot, K; Pall, H; Morrison, KE; Shaw, PJ; Esteban Pérez, J; García Redondo, A; Muñoz Blanco, JL

The Scientific monthly, vol 347, iss 6229
Science

Liang, T-W; Forman, M S; Duda, J E; McCluskey, L; Trojanowski, J Q; Siderowf, A

JOURNAL OF NEUROLOGY, NEUROSURGERY, & PSYCHIATRY. Feb 01, 2005 76(2):252-255

McCluskey, Leo; Feinberg, Daniel; Cantor, Charles; Bird, Shawn; McCluskey, L; Feinberg, D; Cantor, C; Bird, S

Muscle & Nerve; 1999, Vol. 22 Issue 10, p1361-1366, 6p

McCluskey, Leo; Feinberg, Daniel; Dolinskas, Carol; McCluskey, L; Feinberg, D; Dolinskas, C

Muscle & Nerve; 1999, Vol. 22 Issue 6, p772-777, 6p

Majounie E; Renton AE; Mok K; Dopper EG; Waite A; Rollinson S; Chiò A; Restagno G; Nicolaou N; Simon Sanchez J; van Swieten JC; Abramzon Y; Johnson JO; Sendtner M; Pamphlett R; Orrell RW; Mead S; Sidle KC; Houlden H; Rohrer JD; Morrison KE; Pall H; Talbot K; Ansorge O; Chromosome 9 ALS/FTD Consortium; French research network on FTLD/FTLD/ALS; ITALSGEN Consortium; Hernandez DG; Arepalli S; Sabatelli M; Mora G; Corbo M; Giannini F; Calvo A; Englund E; Borghero G; Floris GL; Remes AM; Laaksovirta H; McCluskey L; Trojanowski JQ; Van Deerlin VM; Schellenberg GD; Nalls MA; Drory VE; Lu CS; Yeh TH; Ishiura H; Takahashi Y; Tsuji S; Le Ber I; Brice A; Drepper C; Williams N; Kirby J; Shaw P; Hardy J; Tienari PJ; Heutink P; Morris HR; Pickering Brown S; Traynor BJ; Adamson G; Bayer AJ; Beck J; Callister JB; Blake DJ; Blumen SC; Collinge J; Dunckley T; Ealing J; East S; Elman L; Gerhard A; Guerreiro RJ; Gwinn K; Halliwell N; Hamdalla HH; Hewitt C; Ince P; Jablonka S; James C; Kent L; Knock JC; Lynch T; Mahoney C; Mann D; Neal J; Norris D; O'Dowd S; Richardson A; Rossor M; Rothstein J; Scholz SW; Snowden J; Stephan DA; Toulson G; Turner MR; Warren JD; Young K; Weng YH; Kuo HC; Lai SC; Huang CL; Camuzat A; Entraingues L; Guillot Noël; Verpillat P; Blanc F; Camu W; Clerget Darpoux F; Corcia P; Couratier P; Didic M; Dubois B; Duyckaerts C; Guedj E; Golfier V; Habert MO; Hannequin D; Lacomblez L; Meininger V; Salachas F; Levy R; Michel BF; Pasquier F; Puel M; Thomas Anterion C; Sellal F; Vercelletto M; Moglia C; Cammarosano S; Canosa A; Gallo S; Brunetti M; Ossola I; Marinou K; Papetti L; Pisano F; Pinter GL; Conte A; Luigetti M; Zollino M; Lattante S; Marangi G; la Bella V; Spataro R; Colletti T; Battistini S; RICCI, PIER CARLO; Caponnetto C; Mancardi G; Mandich P; Salvi F; Bartolomei I; Mandrioli J; Sola P; Lunetta C; Penco S; Monsurrò MR; Tedeschi G; Conforti FL; Gambardella A; Quattrone A; Volanti P; Floris G; Cannas A; Piras V; MARROSU, FRANCESCO; MARROSU, MARIA GIOVANNA; Murru MR; Pugliatti M; Parish LD; Sotgiu A; Solinas G; Ulgheri L; Ticca A; Simone I; Logroscino G.

Lancet Neurol
The Lancet Neurology; Vol 11
Majounie, E, Renton, A E, Mok, K, Dopper, E G P, Waite, A, Rollinson, S, Chio, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J C, Abramzon, Y, Johnson, J O, Sendtner, M, Pamphlett, R, Orrell, R W, Mead, S, Sidle, K C, Houlden, H, Rohrer, J D, Morrison, K E, Pall, H, Talbot, K, Ansorge, O, Hernandez, D G, Arepalli, S, Sabatelli, M, Mora, G, Corbo, M, Giannini, F, Calvo, A, Englund, E, Borghero, G, Foris, G L, Remes, A M, Laaksovirta, H, McCluskey, L, Trojanowski, J Q, Van Deerlin, V M, Schellenberg, G D, Nalls, M A, Drory, V E, Lu, C S, Yeh, T H, Ishiura, H, Takahashi, Y, Tsuji, S, Le Ber, I, Brice, A, Drepper, C, Williams, N, Kirby, J, Shaw, P, Hardy, J, Tienari, P J, Heutink, P, Morris, H R, Pickering-Brown, S & Traynor, B J 2012, 'Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study', Lancet Neurology, vol. 11, no. 4, pp. 323-330. https://doi.org/10.1016/S1474-4422(12)70043-1
Lancet Neurology; 11(4), pp 323-330 (2012)
Majounie, E, Renton, A E, Mok, K, Dopper, E G P, Waite, A, Rollinson, S, Chiò, A, Restagno, G, Nicolaou, N, Simon-Sanchez, J, van Swieten, J C, Abramzon, Y, Johnson, J O, Sendtner, M, Pamphlett, R, Orrell, R W, Mead, S, Sidle, K C, Houlden, H, Rohrer, J D, Morrison, K E, Pall, H, Talbot, K, Ansorge, O, Hernandez, D G, Arepalli, S, Sabatelli, M, Mora, G, Corbo, M, Giannini, F, Calvo, A, Englund, E, Borghero, G, Floris, G L, Remes, A M, Laaksovirta, H, McCluskey, L, Trojanowski, J Q, Van Deerlin, V M, Schellenberg, G D, Nalls, M A, Drory, V E, Lu, C S, Yeh, T H, Ishiura, H, Takahashi, Y, Tsuji, S, Le Ber, I, Brice, A, Drepper, C, Williams, N, Kirby, J, Shaw, P, Hardy, J, Tienari, P J, Heutink, P, Morris, H R, Pickering-Brown, S, Traynor, B J & Snowden, J 2012, 'Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: A cross-sectional study', The Lancet Neurology, vol. 11, no. 4, pp. 323-330. https://doi.org/10.1016/S1474-4422(12)70043-1
Lancet Neurology, The

McLaughlin, RL; Schijven, D; Van Rheenen, W; Van Eijk, KR; O'Brien, M; Kahn, RS; Ophoff, RA; Goris, A; Bradley, DG; Al-Chalabi, A; Van Den Berg, LH; Luykx, JJ; Hardiman, O; Veldink, JH; Shatunov, A; Dekker, AM; Diekstra, FP; Pulit, SL; Van Der Spek, RAA; Van Doormaal, PTC; Sproviero, W; Jones, AR; Nicholson, GA; Rowe, DB; Pamphlett, R; Kiernan, MC; Bauer, D; Kahlke, T; Williams, K; Eftimov, F; Fogh, I; Ticozzi, N; Lin, K; Millecamps, S; Salachas, F; Meininger, V; Carvalho, MD; Pinto, S; Mora, JS; Rojas-Garcyá, R; Polak, M; Chandran, S; Colville, S; Swingler, R; Morrison, KE; Shaw, PJ; Hardy, J; Orrell, RW; Pittman, A; Sidle, K; Fratta, P; Malaspina, A; Petri, S; Abdulla, S; Drepper, C; Sendtner, M; Meyer, T; Wiedau-Pazos, M; Lomen-Hoerth, C; Deerlin, VMV; Trojanowski, JQ; Elman, L; McCluskey, L; Basak, N; Meitinger, T; Lichtner, P; Blagojevic-Radivojkov, M; Andres, CR; Maurel, C; Bensimon, G; Landwehrmeyer, B; Brice, A; Payan, CAM; Saker-Delye, S; Durr, A; Wood, N; Tittmann, L; Lieb, W; Franke, A; Rietschel, M; Cichon, S

Nat. Commun. 8:14774 (2017)

Olsson, B; Portelius, E; Cullen, NC; Sandelius, Å; Zetterberg, H; Andreasson, U; Höglund, K; Irwin, DJ; Grossman, M; Weintraub, D; Chen-Plotkin, A; Wolk, D; McCluskey, L; Elman, L; Shaw, LM; Toledo, JB; McBride, J; Hernandez-Con, P; Lee, VM-Y; Trojanowski, JQ; Blennow, K

JAMA Neurology. 76:318

Grossman, M; Anderson, C; Khan, A; Avants, B; Elman, L; McCluskey, L

Neurology (NEUROLOGY), 10/28/2008; 71(18): 1396-1401. (6p)

Majounie, E; Renton, AE; Mok, K; Dopper, EG; Waite, A; Rollinson, S; Chiò, A; Restagno, G; Nicolaou, N; Simon-Sanchez, J; van Swieten, JC; Abramzon, Y; Johnson, JO; Sendtner, M; Pamphlett, R; Orrell, RW; Mead, S; Sidle, KC; Houlden, H; Rohrer, JD; Morrison, KE; Pall, H; Talbot, K; Ansorge, O; Chromosome 9-ALS/FTD Consortium, The; French research network on FTLD/FTLD/ALS, The; ITALSGEN Consortium, The; Hernandez, DG; Arepalli, S; Sabatelli, M; Mora, G; Corbo, M; Giannini, F; Calvo, A; Englund, E; Borghero, G; Floris, GL; Remes, AM; Laaksovirta, H; McCluskey, L; Trojanowski, JQ; Van Deerlin, VM; Schellenberg, GD; Nalls, MA; Drory, VE; Lu, CS; Yeh, TH; Ishiura, H; Takahashi, Y; Tsuji, S; Le Ber, I; Brice, A; Drepper, C; Williams, N; Kirby, J; Shaw, P; Hardy, J; Tienari, PJ; Heutink, P; Morris, HR; Pickering-Brown, S; Traynor, BJ

Lancet neurology
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info:cnr-pdr/source/autori:Majounie E, Renton AE, Mok K, Dopper EG, Waite A, Rollinson S, Chiò A, Restagno G, Nicolaou N, Simon-Sanchez J, van Swieten JC, Abramzon Y, Johnson JO, Sendtner M, Pamphlett R, Orrell RW, Mead S, Sidle KC, Houlden H, Rohrer JD, Morrison KE, Pall H, Talbot K, Ansorge O, The Chromosome 9-ALS%2FFTD Consortium, The French research network on FTLD%2FFTLD%2FALS, The ITALSGEN Consortium, Hernandez DG, Arepalli S, Sabatelli M, Mora G, Corbo M, Giannini F, Calvo A, Englund E, Borghero G, Floris GL, Remes AM, Laaksovirta H, McCluskey L, Trojanowski JQ, Van Deerlin VM, Schellenberg GD, Nalls MA, Drory VE, Lu CS, Yeh TH, Ishiura H, Takahashi Y, Tsuji S, Le Ber I, Brice A, Drepper C, Williams N, Kirby J, Shaw P, Hardy J, Tienari PJ, Heutink P, Morris HR, Pickering-Brown S, Traynor BJ./titolo:Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study./doi:/rivista:Lancet neurology (Print)/anno:2012/pagina_da:/pagina_a:/intervallo_pagine:/volume

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