Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Cliff Shults"'
Autor:
Nathan Pankratz, Alice Rudolph, Cliff Shults, Tatiana Foroud, Cheryl A. Halter, Karen Marder, William C. Nichols
Publikováno v:
Movement Disorders. 23:2216-2223
Depression is one of the most common nonmotor complications of Parkinson's disease (PD) and has a major impact on quality of life. Although several clinical factors have been associated with depression in PD, the relationship between depression and s
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
Autor:
Francis O. Walker, Juliette Harris, Holly Delgado, David Simon, Paul J. Tuite, Jayaraman Rao, Kelly E. Lyons, Tilak Mendis, Bala V. Manyam, Joanna Hamman, Deborah Fontaine, Terry Reed, William C. Nichols, Sharon Evans, Joanne Wojcieszek, Peggy Gray, Anette Nieves, Carson Reider, P. Michael Conneally, W.R. Wayne Martin, Kathy Davis, Christine Hunter, Daniel D. Truong, John M. Bertoni, Hubert H. Fernandez, Joseph H. Friedman, Nathan Pankratz, Margaret C. Lannon, Kenneth Marek, Maryan DeAngelis, Mark Stacy, Debra Berry, Mariann DiMinno, Robyn Schacherer, Becky Dunlop, Michel Panisset, Carmen Serrano Ramos, Alice Rudolph, Tatiana Foroud, Theresa A. Zesiewicz, David Grimes, An Tran, Joan Werner, Jean Hall, Sandra Roque, Magali Fernandez, Joseph Jankovic, Michael J. Aminoff, Rachel Saunders Pullman, Maureen A. Leehey, Cliff Shults, Deborah Judd, William C. Koller, Mark Forrest Gordon, Cheryl Halter, Ali H. Rajput, Pam Andrews, Stephen G. Reich, Theresa Derian, Alex Rajput, Stephanie Thomas, Galit Kleimer-Fisman, Susan Mendick, Robert A. Hauser, Danna Jennings, Paul Gordon, Stewart A. Factor, Peter A. LeWitt, Un Jung Kang, Karyn Boyar, Ronald F. Pfeiffer, Robert L. Rodnitzky, Jean P. Hubble, Jeannine Petit, Mayank Pathak, Julie H. Carter, Maureen Cook, William J. Weiner, Rajesh Pahwa, Christopher F. O'Brien, Karen Marder, Joan Young, Judith Dobson, Richard Camicioli, Lawrence Elmer, Jo Belden, Julie So, Theresa Shirley, Anthony E. Lang, Roger Kurlan, Kelli Williamson, Brenda Pfeiffer, Victoria Hunt, Sean K. Uniacke, Clifford W. Shults, Karen Blindauer, Lauren Seeberger, Brian Wulbrecht, Carolyn Peterson
Publikováno v:
Movement Disorders. 19:649-655
Parkinson's disease (PD) is a common neurodegenerative disorder in humans with wide variability in the age of disease onset. Although the disease has been thought previously to occur sporadically in most patients, there is increasing evidence of a ge
Autor:
Kapil D. Sethi, Irene Litvan, Kailash P. Bhatia, Cliff Shults, David J. Burn, Gregor K. Wenning, Christopher G. Goetz, Anthony E. Lang, Ian G. McKeith, Niall Quinn
Publikováno v:
Movement Disorders. 18:467-486
As there are no biological markers for the antemortem diagnosis of degenerative parkinsonian disorders, diagnosis currently relies upon the presence and progression of clinical features and confirmation depends on neuropathology. Clinicopathologic st
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
Autor:
Susan L. Hickenbottom, Kathleen M. Shannon, Frederick Wooten, Danna Jennings, Lynn A. Raymond, Brad A. Racette, Elise Kayson, Joel S. Perlmutter, Mark Guttman, Robert L. Rodnitzky, James Duffy, Steven M. Hersch, Anne B. Young, Joseph Jankovic, Karen Blindauer, Tetsuo Ashizawa, Marc J. Mentis, Nancy S. Wexler, Donald S. Higgins, Neil Schimke, Robert Snodgrass, Alan K. Percy, Paul Shelton, Aileen Shinaman, Stewart A. Factor, Cynthia L. Comella, Ted E. Roberts, Christopher A. Ross, Joanne Wojcieszek, Amerigo Negrette, Thomas D. Bird, Elan D. Louis, Diana Rosas, Martha Nance, Penelope Hogarth, John N. Caviness, Charles H. Adler, Andrew Feigin, George W. Paulson, Francis O. Walker, Hubert H. Fernandez, B. Hersh, Allen Rubin, James B. Caress, Susan Perlman, John B. Penney, Carl Leventhal, Robert A. Hauser, Roger L. Albin, Leslie M. Thompson, William Weiner, Gerald Podskalny, W.R. Wayne Martin, Christopher F. O'Brien, Hongwei Zhao, Sylvain Chouinard, Jody Corey-Bloom, Ira Shoulson, Eric Siemers, Wallace Deckel, Jang Ho Cha, Timothy Greenamyre, Eric Molho, Cliff Shults, William C. Koller, Daniel S. Sax, Karen Marder, Scott R. Bundlie, David Palmer, Leon S. Dure, George R. Jackson, Peter Como, Oksana Suchowersky, Karl Kieburtz, Joseph Friedman, Margot Mejia de Young, Anne Louis Lafontaine, Kenneth Marek, Jane S. Paulsen, Timothy J Counihan, David Oakes, Richard Dubinsky, Ernesto Bonilla, Guy A. Rouleau, Kenneth H. Fischbeck, Kimberly Quiad, David P. Richman, Juan Rachez-Ramos, Constance Orme, Douglas E. Hobson, Leslie A. Shinobu, William Mallonee, William C. Johnson, Vicki L. Wheelock, Maria Ramos
Publikováno v:
Movement disorders : official journal of the Movement Disorder Society. 20(3)
With prospects improving for experimental therapeutics aimed at postponing the onset of illness in preclinical carriers of the Huntington's disease (HD) gene, we assessed agreement among experienced clinicians with respect to the motor manifestations
Autor:
Arthur Watts, Blair Ford, Marsha Tennis, Ronald F. Pfeiffer, Jean P. Hubble, Cliff Shults, Mickie Welsh, John Seibyl, Carolyn Weeks, Sandra Dillon, John P. Hammerstad, Amy Montgomery, Stewart A. Factor, Farah Atassi, William J. Weiner, Barbara Alexander-Brown, Karl Kieburtz, Roger Kurlan, David S. Russell, Stanley Fahn, Ali H. Rajput, Jean Hall, Ira Shoulson, Brenda Pfeiffer, Bruno Musch, Karen Richard, Deborah Fontaine, David G. Standaert, Kevin M. Biglan, Mark Stacy, Debra Berry, Frederick Wooten, Diane Brown, Michael P. McDermott, Tori Ross, Giselle Petsinger, Theresa Shirley, Susan E. Bennett, Leona Borchert, Kenneth Marek, Laura Sutherland, Rajesh Pahwa, Janis M. Miyasaki, Susan Wood, Robert G. Holloway, Cornelia Kamp, Sharon Evans, Pamela Rainey, Anthony E. Lang, Michel Panisset, Elspeth Sime, Carol Pantella, Susan Daigneault, Barbara Fussell, Carolynn O'Connell, Joseph Jankovic, Aileen Shinaman, Elke Rost-Ruffner, Peter A. LeWitt, Alicia Brocht, Karen Hodgeman, Cheryl Waters, Mary Harrigan, Robert L. Rodnitzky, Judith Dobson, David E. Riley, Oksana Suchowersky, Maryan DeAngelis, Lynn Barclay
Publikováno v:
Archives of Neurology. 61
BACKGROUND The best way to initiate dopaminergic therapy for early Parkinson disease remains unclear. OBJECTIVE To compare initial treatment with pramipexole vs levodopa in early Parkinson disease, followed by levodopa supplementation, with respect t
Autor:
Cliff Shults, Sid Gilman
Publisher Summary A progressive neurodegenerative disorder, multiple system atrophy (MSA) presents clinically with varying degrees of Parkinsonism, autonomic dysfunction, and impaired cerebellar function. The current nomenclature utilizes the abbrevi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::54edce0852feed4b8d28cf1efd7e34f1
https://doi.org/10.1016/b978-012566652-7/50025-3
https://doi.org/10.1016/b978-012566652-7/50025-3
Publikováno v:
International Journal of Developmental Neuroscience. 5:11-15
Events which alter the chemical environment of the developing nervous system have long-term consequences for neural function and behavior. Neonatal exposure to a peptide neurotransmitter, substance P (SP), increased the number of SP binding sites in
Autor:
William C. Nichols, P. Michael Conneally, Tatiana Foroud, Alice Rudolph, Cheryl Halter, Cliff Shults, Sean K. Uniacke, Nathan Pankratz
Publikováno v:
The American Journal of Human Genetics. (1):124-135
Parkinson disease (PD) is a common neurodegenerative disorder characterized by bradykinesia, resting tremor, muscular rigidity, and postural instability, as well as by a clinically significant response to treatment with levodopa. Mutations in the alp