Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Aileen Shinaman"'
Autor:
Mark Guttman, David Eidelberg, D. J. Marcinek, S. Lessig, M. Delatycki, V. Collins, Lewis Maltby, B. Bartlett, Terrence Sills, R. C. Block, Anthony L. Vaccarino, D.R. Langbehn, J. H. Cha, Aileen Shinaman, A. Churchyard, Hans J. Johnson, P. Phan, Christopher A. Ross, O. Yastrubetskaya, Peter Como, E. Chiu, S. K. Kostyk, FuRST-pHD, C. A. Beck, C. Cimino, P. Chua, E. H. Aylward, D. A. Kegelmeyer, Charles Sabine, L. Tippett, K. Trembath, Henry L. Paulson, K. Rowe, Todd L. Richards, Kurt E. Weaver, Kenneth E. Evans, Kimberly A. Quaid, A. Goh, G. M. Peavy, A. D. Kloos, Chris C. Tang, V. Magnotta, O. Liang, William Adams, Richard Roxburgh, Dennis Velakoulis, Jess G. Fiedorowicz, P. Gilbert, Jan Bausch, J. C. Stout, Elizabeth Aylward, B. Stell, M. Pugliese, M. Jacobson, L. Veatch Goodman, Kevin Duff, J. Annis, K. L. Poston, L. J. Beglinger, Beth Borowsky, S. Christensen, Jody Goldstein, J. Sanchez-Ramos, E. Shankland, Guerry M. Peavy, M. McCall, A. Callazo, Elise Kayson, Jane S. Paulsen, E. Oster, F. Judd, D. van Kammen, E. R. Dorsey, A. Leserman, L. Ling, A. Feigin, Karen E. Anderson, London C Butterfield, Yilong Ma, E. Pirogovsky, Jody Corey-Bloom, Sharon A. Jubrias, Kevin E. Conley, Peg Nopoulos, David Oakes, V. Hogg, J. F. O’Rourke, Predict-Hd Investigators, J Giuliano, Ronald Pierson, Vijay Dhawan, A. Juhl, L. Oelke, C. Wang, D. Lovecky, C. Amara, B. Tress, Aileen K Ho, I. Shoulson, Z. Horton, D. R. Langbehn, J. S. Paulsen, J. Lloyd, Leon S. Dure, Christopher Steward, Patricia Desmond, Russell Katz
Publikováno v:
Neurotherapeutics. 6:202-212
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86159a893c8dedf5609d7e33ae86e6aa
https://doi.org/10.1016/j.nurt.2008.09.004
https://doi.org/10.1016/j.nurt.2008.09.004
Autor:
Ira Shoulson, David Oakes, E. Ray Dorsey, Emily Oster, Aileen Shinaman, Jan Bausch, Elise Kayson, Kimberly A. Quaid
Publikováno v:
American Journal of Medical Genetics Part A. :2070-2077
Genetic testing in Huntington disease, an inherited ultimately fatal neurodegenerative disorder, is infrequent despite wide availability. Factors influencing the decision to pursue testing are largely unknown. We conducted a prospective longitudinal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77af7f3aa308c9719bdd51c4299d23c5
https://doi.org/10.1002/ajmg.a.32422
https://doi.org/10.1002/ajmg.a.32422
Autor:
William G. Ondo, Stanley Fahn, David Oakes, Samuel Frank, Shirley Eberly, Vicki Hunt, Christine Hunter, Sandra Plumb, Joseph Jankovic, Francis O. Walker, Aileen Shinaman, Ira Shoulson, Frederick J. Marshall, Stewart A. Factor
Publikováno v:
Clinical Neuropharmacology. 31:127-133
Objective To assess tetrabenazine (TBZ) efficacy by evaluating the change in Huntington disease-associated chorea resulting from TBZ treatment withdrawal. Methods Thirty patients treated in the long term were randomized to 1 of 3 groups assigned to w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e69cc4463115a82e8eab9d11c50c3fd1
https://doi.org/10.1097/wnf.0b013e3180ca77ea
https://doi.org/10.1097/wnf.0b013e3180ca77ea
Autor:
E. Fine, T. Cahill, Elise Kayson, M. W. Jacobson, S. Kathuria, S. Leit, J. Smith, C. Tang, J. H. Cha, C. Higginson, Melinda M. Swenson, A. J. Lechich, L. Wasserman, H. Patzke, A. Clarke, S. Gevorkian, Noelle E. Carlozzi, Steven M. Hersch, Peter Como, C. Beck, A.E. Kane, S. Sandler, Robert Pacifici, M. C. Chirieac, T. Gillis, Thomas D. Bird, S. Peng, E. A. de Blieck, S. A. Johnson, A. Tomusk, H. D. Rosas, E. Kayson, R. Chesworth, Dennis J. Zgaljardic, J. Lee, S. Hastings, Danielle A. Simmons, David Eidelberg, Hans J. Johnson, V. Magnotta, Bernhard Landwehrmeyer, J. Wang, Elizabeth Aylward, J. L. Goldstein, Vicki L. Wheelock, N. Ramza, J. L. Marsh, S. Montas, Nonna Stepanov, Christopher A. Ross, P. Beaulieu, Elizabeth McCusker, M. K. Ahlijanian, E. Chiu, R. Deziel, Richard H. Myers, L. Carr, B. Walker, Jess G. Fiedorowicz, G. Chadwick, C. McCallum, B. Di Toro, Shannon A. Johnson, J. Srinidhi Mysore, Sharon L. Sims, Josef Priller, F. P. Albayya, Ira Shoulson, Ronald Pierson, J. F. Gusella, Jan Bausch, Kimberly A. Quaid, L. Veatch Goodman, B. Westphal, Henry L. Paulson, L. Deuel, K. Illes, Vijay Dhawan, G. Shapiro, A. Goh, G. M. Peavy, P. Young, M. Adams, J. Latourelle, Ryan Y. Kim, Aimee Aubeeluck, K. Whitlock, Douglas R. Langbehn, J.S. Paulsen, K. M. Biglan, Hillary Lipe, Kevin Duff, William Adams, J. Klager, J. Pallos, J. Dawson, F. L. Huet, D. Johnson, S. Queller, M. Casale, C. Zuccato, G. Suter, Emily Oster, P. Kingsley, S. Lifer, E. Fossale, Mark W. Jacobson, Katharine Moser, E. R. Dorsey, F. Raeppel, D. L. McArthur, A. Pae, Joan M. Harrison, Guerry M. Peavy, A. Lownie, K. Sigvardt, E. Cattaneo, Z. Li, D. Ecker, Russell Katz, A. Duckett, Aileen Shinaman, J. Besterman, Laura Mickes, Andrew Feigin, B. L. Apostol, Jana M. Hanson, Leigh J. Beglinger, L. Michels Thompson, M. Fournel, C. Moskowitz, Mark Guttman, Teresa Tempkin, Peg Nopoulos, H. Sainte-Croix, L. Beglinger, K.B. Whitlock, David Oakes, S. J. Nolan, T. Massood, N. Carlozzi, Jody Corey-Bloom, P. Mattis, G. Rahil, O. Yastrubetskaya, Marcy E. MacDonald, D.R. Langbehn, Heather Buchanan, Jody Goldstein, S. Perlman, Julie C. Stout, R. Stewart, J. Preston, Stephanie Lessig, A. Barbier, Kevin M. Biglan, Wayne R. Matson, G. Schwartz, Yilong Ma, Jane S. Paulsen
Publikováno v:
Neurotherapeutics. 5:362-375
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bad4ff0e7de53fe6fe4325be2490e29f
https://doi.org/10.1016/j.nurt.2007.10.053
https://doi.org/10.1016/j.nurt.2007.10.053
Autor:
Margaret Marie Cox, Stephanie Sendek, Margaret F. Turk, Julie H. Carter, Susan C. Fagan, Lorelei Derwent, Oksana Suchowersky, Jay S. Schneider, Linda Paul, Gwyn Vernon, Stephen Gollomp, Karl Kieburtz, Debbie Baker, I. Van Bodis-Wollner, Germaine McInnes, Marian A. Perez, G. Webster Ross, Katharine Pabst, Jorge L. Juncos, Chad W. Christine, Jessie Roth, Joseph M. Savitt, Peter A LeWitt, Hubert H. Fernandez, Matthew Brodsky, Mark F. Lew, Jay M. Gorell, Natividad R. Stover, Paulo Guimaraes, Andrew Feigin, Anita Blenke, Martha Nance, Elizabeth Hayes, Andrew Siderowf, W.R. Wayne Martin, Tammie Kelsey, Susan Bennett, Sharon McCarthy, Charles H. Adler, Beverly Olsen, Pauline LeBlanc, Richard B. Dewey, Rodger J. Elble, Richard S. Burns, Carlos Singer, Amy Parsons, John W. Taylor, Tracy Stewart, Maryan DeAngelis, Barbara C. Tilley, William J. Weiner, Brad A. Racette, Wendy R. Galpern, Michael J. Aminoff, Kapil D. Sethi, Jayaraman Rao, Robert A. Hauser, Debbie Fraser, Connie Kawai, David Coffey, Kelly E. Lyons, Kristine Wernette, Becky Dunlop, Holly Delgado, Marlene Lind, Rajesh Pahwa, Chris Weaver, Ray L. Watts, Patricia Deppen, Ryan J. Uitti, Marwan N. Sabbagh, Lynn Marlor, Joann Belden, Burton L. Scott, Theresa McClain, Roger L. Albin, John Y. Fang, Zoran Obradov, Yuko Y. Palesch, Maureen Cook, Pamela Andrews, Jeana Jaglin, Joanne Wojcieszek, Mary Louise Musante Weeks, Susan Peterson, James H. Bower, Maureen A. Leehey, Joanne Field, Lisa M. Shulman, Caroline M. Tanner, Jacob I. Sage, Jordan J. Elm, Joseph Jankovic, Patrick D. Mauldin, Aileen Shinaman, Peng Huang, G. Frederick Wooten, Alicia Brocht, Gordon H. Brown, Peggy Roberge, Dorothy Shearon, Buff Dill, Margaret F. Keller, Charlene Young, Christine Hunter, Janis M. Miyasaki, Susan Torgrimson, Cornelia Kamp, Brigid Hayward, Christopher G. Goetz, Emily Kosa, Marilyn Flewellen, David Simon, Rebecca McMurray, Sue Reichwein, Jacci Bainbridge, Robert W. Hamill, Stephanie Terashita, Kathleen M. Shannon, Frederick Wooten, Danna Jennings, Shana Krstevska, Bernard Ravina
Publikováno v:
Neurology. 68:20-28
Objective: To determine if future studies of coenzyme Q10 and GPI-1485 in Parkinson disease (PD) may be warranted. Methods: We conducted a randomized, double-blind, calibrated futility clinical trial of coenzyme Q10 and GPI-1485 in early untreated PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36f17ff7b2eee66f71cf67f7561841fe
https://doi.org/10.1212/01.wnl.0000250355.28474.8e
https://doi.org/10.1212/01.wnl.0000250355.28474.8e
Autor:
Alan Percy, Cathy Wood-Siverio, Oksana Suchowersky, Claudia Testa, Yvette Bordelon, Kevin M. Biglan, Francis O. Walker, David P. Richman, Rustom Sethna, Eric Siemers, Shirley Eberly, Marie Saint-Hilaire, Alicia Brocht, Madaline B. Harrison, Richard H. Myers, Carlos Singer, Karen Blindauer, Rajeev Ananda Kumar, Jody Goldstein, Diana Rosas, Anne Young, Charles H. Adler, Kimberly Quaid, James F. Gusella, Carolyn Gray, Penelope Hogarth, James B. Caress, J. B. Penney, Kelvin L. Chou, Teresa Tempkin, Christopher Ross, Jody Corey-Bloom, Brad Racette, Victoria Hunt, William Weiner, Thomas D. Bird, J. Decolongon, Greg Suter, Eric Molho, Megan Romer, Blair Leavitt, Mary Lou Klimek, Hillary Lipe, Peter Como, Dawn Radtke, Constance Nickerson, Roger L. Albin, Karen Marder, Marcy E. MacDonald, Sandra Kostyk, Christine Weaver, David Oakes, William Mallonee, Amy Duffy, Tatiana Foroud, Marguerite Wieler, Clifford W. Shults, Sarah Furtado, Julie C. Stout, William C. Johnson, Timothy Greenamyre, Ira Shoulson, Carol Moskowitz, J.S. Paulsen, Karl Kieburtz, Lauren Seeberger, Douglas Hobson, Scott R. Bundlie, Steven M. Hersch, Leon S. Dure, Arthur Watts, Vicki L. Wheelock, Donald S. Higgins, Lorne A. Clarke, Stanley Fahn, Nestor Galvez-Jimenez, Andrew Feigin, Lynn A. Raymond, Joseph Jankovic, Sylvain Chouinard, Caroline M. Tanner, Melissa Wesson, Barbara Shannon, Marie Cox, Cynthia L. Comella, John N. Caviness, Guerry M. Peavy, Adam Rosenblatt, Robert A. Hauser, Carol Zimmerman, Christine Hunter, Christine O'Neill, Juan Sanchez-Ramos, Corrine Baic, Peter Novak, Sharon Evans, Hongwei Zhao, Stewart A. Factor, W.R. Wayne Martin, Candace Cotto, Richard Dubinsky, David D. Song, M. Aileen Shinaman, Susan B. Perlman, Joel S. Perlmutter, Ali Samii, Elise Kayson, Mark Guttman, Frederick J. Marshall, Kathleen L. Shannon, M. Nance
Publikováno v:
JAMA neurology. 73(1)
Identifying measures that are associated with the cytosine-adenine-guanine (CAG) expansion in individuals before diagnosis of Huntington disease (HD) has implications for designing clinical trials.To identify the earliest features associated with the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fa05623ec4df08194f06e5de9f4bc97
https://pubmed.ncbi.nlm.nih.gov/26569098
https://pubmed.ncbi.nlm.nih.gov/26569098
Autor:
S. Chouinard, A. Kaczmarek, Susan Mendick, Sharon Evans, P. M. Conneally, Roberta Winnick, Andrew Feigin, L. Elmer, Nathan Pankratz, Barbara Shannon, E. Aiken, T. Ajax, C. Horn, Christine Hunter, J. Mannetter, Margaret F. Turk, Donald S. Higgins, Miodrag Velickovic, C. Dingmann, Maryan DeAngelis, Kapil D. Sethi, M. Marotta-Kollarus, L. Woodward, M. Stacy, Cheyl A. Halter, Karen Williams, Carolyn Peterson, Nestor Galvez-Jimenez, Margaret C. Lannon, C. Schell, Kelvin L. Chou, Tatyana Simuni, H. Poiffaut, Stewart A. Factor, H. Shill, Joseph Jankovic, Michel Panisset, Tatiana Foroud, Juliette Harris, Deborah Judd, A. Podichetty, S. Phipps, Kathy Davis, Joann Belden, V. E. Elsaesser, S. Narayan, J. Fraser, Clifford W. Shults, K. Williamson, Aileen Shinaman, S. Wilson, William C. Nichols, L. Marlor, John M. Bertoni, Joanne Wojcieszek, Cheryl Halter, Kenneth Marek, P. Ryan, Alice Rudolph, Christopher F. O'Brien, Karen Blindauer, Karyn Boyar, Jayaraman Rao, Kelly E. Lyons, Becky Dunlop, C. Costan-Toth, Lauren Seeberger, Ryan J. Uitti, Karen Marder, Stephen G. Reich, David Oakes, Lisa Scollins, Jean Hall, Joanna Hamann, Mandar Jog, Eric Siemers, E. Ohmann, E. Licari, Frederick J. Marshall, Mark Forrest Gordon, Maureen Cook, Peter A. LeWitt, Vincent Calabrese, Jeannine Petit, Diane K. Marek, Rachel Saunders-Pullman, Peggy Roberge, C. Joubert, Hubert H. Fernandez, K. Ligon, J. Carpenter, Lewis Sudarsky, J. Danielson, William C. Koller, David Simon, Michael W. Pauciulo, Danna Jennings, Joseph H. Friedman, Cliff Shults
Publikováno v:
Movement Disorders. 21:2257-2260
A total of 956 individuals with Parkinson's disease (PD) from 430 multiplex PD pedigrees were screened for 12 previously reported, pathogenic LRRK2 mutations: R793M, L1114L, I1371V, R1441C, R1441G, R1441H, Y1699C, M1869T, I2012T, I2020T, G2385R, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35a3fcbe58940aa04e1e1d38e05490b3
https://doi.org/10.1002/mds.21162
https://doi.org/10.1002/mds.21162
Publikováno v:
American Journal of Medical Genetics. :589-593
At a symposium in June, 2002, biomedical researchers, clinicians, legal experts, policymakers, and representatives of the insurance industry and the advocacy community gathered to address issues of genetic privacy and discrimination; and to identify
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3851778ad6708a5a6ed76cae5565030
https://doi.org/10.1002/ajmg.a.20092
https://doi.org/10.1002/ajmg.a.20092
Autor:
Karen Williams, Carolyn Peterson, S. Narayan, Margaret F. Turk, Julie H. Carter, C. Schell, Carlos Singer, Chad W. Christine, Paul J. Tuite, Robyn Schacherer, J. Whetteckey, S. Phipps, Diane K. Marek, William C. Nichols, John M. Bertoni, A. H. Rajput, Kenneth Marek, An Tran, P. Ryan, J. Hevezi, Joan Werner, Kelvin L. Chou, S. Chouinard, James Sutton, Margaret C. Lannon, T. Ajax, Joan Young, Deborah Judd, L. Zelaya, David Grimes, Magali Fernandez, Theresa A. Zesiewicz, Mark Stacy, Peggy Gray, Debra Berry, Michael J. Aminoff, C. Horn, C. Costan-Toth, J. Mannetter, Patricia Simpson, Susan Rolandelli, Tatiana Foroud, T. Tra, S. Wilson, Judith Dobson, Nestor Galvez-Jimenez, Donna Schwieterman, Shirley Uy, K. Price, J. Wojcieszek, Anette Nieves, Paul Atchison, Susan Bennett, L. Klassen, A. Podichetty, Vincent Calabrese, Becky Dunlop, D. Kamp, Holly Delgado, Sandra Roque, Maureen A. Leehey, Richard Camicioli, Julie So, Jayaraman Rao, Kelly E. Lyons, Kapil D. Sethi, A. Wang, Lynn Marlor, David Oakes, S. Culver, Juan Sanchez-Ramos, L. Woodward, J. Danielson, Jeannine Petit, Joann Belden, E. Licari, M. Meacham, Deborah Fontaine, Sharon Evans, C. Stone, S. Morehouse, Christopher F. O'Brien, G. Podskalny, J. Fraser, Anthony E. Lang, W.R. Wayne Martin, Carmen Serrano, H. Poiffaut, Stewart A. Factor, Joanne Wojcieszek, S. Belber, L. Davis, C. Allen, J. Hall, Judy Richman, Joseph Jankovic, Carson Reider, Stephen G. Reich, Stephanie Thomas, Kathy Davis, Richard B. Dewey, Karen Marder, T. Demarcaida, A. Kaczmarek, Lauren Seeberger, C. Halter, Mary Lou Klimek, Donald S. Higgins, Miodrag Velickovic, Joanna Hamann, Eric Siemers, E. Ohmann, C. Dingmann, Galit Kleiner-Fisman, Shari Niswonger, Theresa Derian, Maryan DeAngelis, Aileen Shinaman, Tilak Mendis, M. Rundle, Susan Mendick, L. Giffin, Karen Blindauer, Paul Gordon, Andrew Feigin, L. Shulman, Maureen Cook, Brian Wulbrecht, Rajesh Pahwa, T. Foroud, Un Jung Kang, Arthur Watts, Oksana Suchowersky, C. Joubert, J. Vo, Mandar Jog, M. Panisset, Roberta Winnick, Ronald F. Pfeiffer, Barbara Shannon, Jean P. Hubble, Clifford W. Shults, T. Gales, Tanya Simuni, M. Wolff, Hubert H. Fernandez, Pam Andrews, Karyn Boyar, Brad A. Racette, Vicki Hunt, Christine Hunter, Daniel D. Truong, L. Good, Robert L. Rodnitzky, P. Rodriguez, Sandra K. Kostyk, T. Shirley, Cheryl Halter, Peter A LeWitt, W. Weiner, Ryan J. Uitti, Lisa Scollins, Marc L. Gordon, J. Carpenter, Alice Rudolph, Lewis Sudarsky, Robert A. Hauser, Cliff Shults, Bala V. Manyam, Francis O. Walker, Juliette Harris, Marguerite Wieler, K. Dustin, Kelli Williamson, Brenda Pfeiffer, William C. Koller, Frederick J. Marshall, V. Hagen, A. Campbell, B. Hutchinson, L. Elmer, Anja Rudolph, K. Haas, Tori Ross, Rachel Saunders-Pullman, Nathan Pankratz, E. Aiken, Mariann DiMinno, Peggy Roberge, Arif Dalvi, B. Hayward, Mayank Pathak, David Simon, Michael W. Pauciulo, Holly A. Shill, M. Marotta-Kollarus, K. Ligon, Alok Sahay, Joseph H. Friedman, Neal Hermanowicz, E. Julian-Baros, Irenita Gardiner, N. Luong, Danna Jennings, R. Kurlan, P. M. Conneally
Publikováno v:
Movement Disorders. 22:254-256
Mutations in LRRK2 were first reported as causing Parkinson's disease (PD) in late 2004. Since then, approximately a dozen LRRK2 substitutions have been identified that are believed to be pathogenic mutations. The substitution of adenine for guanine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c48f0117672933936e1f3bb8ac731d4
https://doi.org/10.1002/mds.21233
https://doi.org/10.1002/mds.21233
Autor:
Karen Blindauer, Lauren Seeberger, Brian Wulbrecht, Joan Young, Victoria Hunt, Judith Dobson, Lisa Byder, Clifford W. Shults, Deborah Fontaine, William C. Nichols, P. Michael Conneally, Carolyn Peterson, Julie H. Carter, Hubert H. Fernandez, Margaret C. Lannon, William C. Koller, Joanne Wojcieszek, Lawrence Elmer, Jayaraman Rao, Mark Stacy, Jo Belden, Bala V. Manyam, Julie So, Theresa Shirley, Stephen G. Reich, Stephanie Thomas, John M. Bertoni, Peggy Gray, Marguerite Wieler, Anette Nieves, Rachel Saunders Pullman, Mayank Pathak, Kenneth Marek, Debra Berry, Holly Delgado, Christopher F. O'Brien, Anthony E. Lang, Karen Marder, Ali H. Rajput, Eric Siemers, Cheryl Halter, Michel Panisset, Galit Kleimer-Fisman, Kelly E. Lyons, Robyn Schacherer, Richard Camicioli, Tatiana Foroud, Alex Rajput, Carson Reider, Kathy Davis, Robert A. Hauser, Theresa A. Zesiewicz, Deborah Judd, Susan Mendick, Maryan De Angelis, Sandra Roque, Alice Rudolph, Becky Dunlop, An Tran, Maureen Cook, Christine Hunter, Daniel D. Truong, Stewart A. Factor, Michael J. Aminoff, David Oakes, Sharon Evans, Paul J. Tuite, Jean Hall, David Grimes, W.R. Wayne Martin, Magali Fernandez, Joanna Hamman, Francis O. Walker, Pam Andrews, Karyn Boyar, Juliette Harris, Tilak Mendis, Nathan Pankratz, Mariann DiMinno, Robert L. Rodnitzky, Rajesh Pahwa, Peter A. LeWitt, Jeannine Petit, William J. Weiner, Un Jung Kang, Joseph Jankovic, Ronald F. Pfeiffer, Aileen Shinaman, Jean P. Hubble, Mark Forrest Gordon, Danna Jennings, Joseph H. Friedman, Carmen Serrano Ramos, Roger Kurlan, Kelli Williamson, Brenda Pfeiffer, Frederick J. Marshall
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 21(1)
The epsilon4 allele of the apolipoprotein E gene (APOE4) has been consistently associated with a greater risk of Alzheimer's disease (AD) as well as an earlier onset of AD. It is possible that APOE4 may also play a role in the etiology of other neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6dad4eef80e5b861c95a811d7fa272c1
https://pubmed.ncbi.nlm.nih.gov/16116614
https://pubmed.ncbi.nlm.nih.gov/16116614