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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
Journal Article
Neurology, ISSN 0028-3878, 01/2017, Volume 88, Issue 2, pp. 152 - 159
Journal Article
Movement Disorders, ISSN 0885-3185, 12/2015, Volume 30, Issue 14, pp. 1961 - 1964
Journal Article
1975, Bibliotheca phycologica, ISBN 3768209547, Volume 18., 177
Utah Power and Light Company is currently constructing an electrical generating station in lower Huntington Canyon, Emery County, Utah. This plant is located... 
identification keys | USA | Huntington Canyon, algae | sampling | flora | Huntington Creek | freshwater | algology | Utah
Book
Movement Disorders, ISSN 0885-3185, 12/2019, Volume 34, Issue 12, pp. 1910 - 1914
Purpose This study examined the relationships between different aspects of motor dysfunction (chorea, dystonia, rigidity, incoordination, oculomotor... 
chorea | HDQLIFE | motor function | Huntington's disease | Health‐related quality of life | dystonia | Huntingtons disease | Discriminant analysis | Factor analysis | Gait | Chorea | Dystonia
Journal Article
Human Genetics, ISSN 0340-6717, 12/2012, Volume 131, Issue 12, pp. 1833 - 1840
Journal Article
Neurobiology of Disease, ISSN 0969-9961, 10/2001, Volume 8, Issue 5, pp. 807 - 821
Huntington's disease (HD) is a late-onset neurodegenerative disease for which the mutation is CAG/polyglutamine repeat expansion. The R6 mouse lines expressing... 
NEURONAL INTRANUCLEAR INCLUSIONS | MESSENGER-RNA EXPRESSION | RAT CEREBRAL-CORTEX | MUTANT HUNTINGTIN | IN-SITU HYBRIDIZATION | HIGH-AFFINITY | TRANSPORTER GLT-1 | STRIATAL NEURONS | NEUROSCIENCES | MOUSE MODELS | COMPARATIVE IMMUNOCYTOCHEMISTRY | Nuclear Proteins - analysis | Humans | Nerve Tissue Proteins - deficiency | Nerve Tissue Proteins - analysis | Glutamate Plasma Membrane Transport Proteins | Corpus Striatum - metabolism | Cerebral Cortex - metabolism | RNA, Messenger - biosynthesis | Excitatory Amino Acid Transporter 1 | Biological Transport | Symporters | Mice, Inbred CBA | Amino Acid Transport System X-AG - biosynthesis | Disease Models, Animal | Carrier Proteins - biosynthesis | Excitatory Amino Acid Transporter 2 - deficiency | Glial Fibrillary Acidic Protein - analysis | Glutamate-Ammonia Ligase - deficiency | Mice, Inbred C57BL | RNA, Messenger - genetics | Amino Acid Transport System X-AG - genetics | Mice, Transgenic | Excitatory Amino Acid Transporter 3 | Huntington Disease - metabolism | Nerve Tissue Proteins - genetics | Nerve Tissue Proteins - metabolism | Carrier Proteins - genetics | Huntingtin Protein | Phenotype | Animals | Glutamate-Ammonia Ligase - genetics | Huntington Disease - genetics | Aspartic Acid - metabolism | Glutamic Acid - pharmacokinetics | Glutamate-Ammonia Ligase - biosynthesis | Mice | Models, Neurological | Peptides - analysis | Astrocytes - metabolism | Crosses, Genetic | Genetic engineering | RNA | Glutamate | Glutamine
Journal Article
Psychological assessment, ISSN 1040-3590, 4/2018, Volume 30, Issue 4, pp. 450 - 458
Social functioning is an essential but poorly understood component of health-related quality of life for people with Huntington disease. We report on the... 
HDQLIFE | social participation | community integration | Huntington disease | health-related quality of life | prodromal | Neuro-QoL | patient reported outcome (PRO)
Journal Article
Journal Article