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2002, 3rd ed., Oxford monographs on medical genetics, ISBN 0198510608, Volume no. 45., xvi, 558
Book
1981, ISBN 0387105883, xvii, 192
Book
by Frank, Samuel and Testa, Claudia M and Stamler, David and Kayson, Elise and Davis, Charles and Edmondson, Mary C and Kinel, Shari and Leavitt, Blair and Oakes, David and O’Neill, Christine and Vaughan, Christina and Goldstein, Jody and Herzog, Margaret and Snively, Victoria and Whaley, Jacquelyn and Wong, Cynthia and Suter, Greg and Jankovic, Joseph and Jimenez-Shahed, Joohi and Hunter, Christine and Claassen, Daniel O and Roman, Olivia C and Sung, Victor and Smith, Jenna and Janicki, Sarah and Clouse, Ronda and Saint-Hilaire, Marie and Hohler, Anna and Turpin, Denyse and James, Raymond C and Rodriguez, Ramon and Rizer, Kyle and Anderson, Karen E and Heller, Hope and Carlson, Alexis and Criswell, Susan and Racette, Brad A and Revilla, Fredy J and Nucifora, Frederick and Margolis, Russell L and Ong, MaryJane and Mendis, Tilak and Mendis, Neila and Singer, Carlos and Quesada, Monica and Paulsen, Jane S and Brashers-Krug, Thomas and Miller, Amanda and Kerr, Jane and Dubinsky, Richard M and Gray, Carolyn and Factor, Stewart A and Sperin, Elaine and Molho, Eric and Eglow, Mary and Evans, Sharon and Kumar, Rajeev and Reeves, Christina and Samii, Ali and Chouinard, Sylvain and Beland, Monica and Scott, Burton L and Hickey, Patrick T and Esmail, Sherali and Fung, Wai Lun Alan and Gibbons, Clare and Qi, Lina and Colcher, Amy and Hackmyer, Cory and McGarry, Andrew and Klos, Kevin and Gudesblatt, Mark and Fafard, Lori and Graffitti, Laura and Schneider, Daniel P and Dhall, Rohit and Wojcieszek, Joanne M and LaFaver, Kathrin and Duker, Andrew and Neefus, Erin and Wilson-Perez, Hilary and Shprecher, David and Wall, Paola and Blindauer, Karen A and Wheeler, Lynn and Boyd, James T and Houston, Emily and Farbman, Eric S and Agarwal, Pinky and Eberly, Shirley W and Watts, Arthur and Tariot, Pierre N and Feigin, Andrew and Evans, Scott and Beck, Chris and Orme, Constance and Edicola, Jon and Christopher, Emily and Huntington Study Grp and Huntington Study Group
JAMA, ISSN 0098-7484, 07/2016, Volume 316, Issue 1, pp. 40 - 50
Journal Article
1993, ISBN 0521459834, Volume 23., 46
This report presents the findings of a study of people affected by Huntington's chorea and their unaffected relatives, and in particular, of the incidence of... 
Book
2011, Frontiers in neuroscience, ISBN 0849390001, xx, 312
In 1993, the genetic mutation responsible for Huntington’s disease (HD) was identified. Considered a milestone in human genomics, this discovery has led to... 
Huntington Disease | physiopathology | drug therapy | Molelcular aspects | Pathophysiology | methods | Neuropharmacology | Huntington's disease | Drug Discovery | Biotechnology | Neuroscience
Book
1989, Johns Hopkins series in contemporary medicine and public health., ISBN 0801838606, x, 251
Book
BMJ, ISSN 1756-1833, 01/2010, p. b5353
Journal Article
04/2018, ISBN 9781536138542
Book
Drugs, ISSN 0012-6667, 1/2017, Volume 77, Issue 1, pp. 29 - 46
Journal Article
Anadolu Psikiyatri Dergisi, ISSN 1302-6631, 01/2018, Volume 19, Issue 1, pp. 110 - 110
Huntington's chorea (HC) is a dominantly inherited, fatal neurodegenerative disease characterized by movement disorders, cognitive decline and psychiatric... 
Felsefe & Psikoloji & Sosyoloji | Huntingtons disease | Delirium | Family medical history | Quantitative psychology | Dementia
Journal Article
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