Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Madeline Harrison"'
Autor:
Maleesa M. Pathirana, Prabha H. Andraweera, Emily Aldridge, Madeline Harrison, Jade Harrison, Shalem Leemaqz, Margaret A. Arstall, Gustaaf A. Dekker, Claire T. Roberts
Publikováno v:
International Breastfeeding Journal, Vol 18, Iss 1, Pp 1-12 (2023)
Abstract Background Breastfeeding is important for both mother and child in reducing risk of future cardiovascular disease. Therefore, it may be an effective method to improve cardio-metabolic health, particularly those who are exposed to pregnancy c
Externí odkaz:
https://doaj.org/article/a789def7588f4dd3816516f764c70760
Publikováno v:
Biomedicines, Vol 12, Iss 3, p 511 (2024)
Endothelin-1 (ET-1) plays a physiological role as a potent vasoconstrictor. It is implicated in an array of diseases, and its signalling is often found to be overactivated within cancers. ET-1 has been found to potentiate hallmarks of cancer progress
Externí odkaz:
https://doaj.org/article/c463d2f880ca4584a642dc4610031b8f
Autor:
Maleesa M. Pathirana, Prabha H. Andraweera, Emily Aldridge, Shalem Y. Leemaqz, Madeline Harrison, Jade Harrison, Petra E. Verburg, Margaret A. Arstall, Gustaaf A. Dekker, Claire T. Roberts
Publikováno v:
Acta diabetologica. 59(9)
IntroductionGestational diabetes mellitus (GDM) is thought to be associated with cardio-metabolic risk factor development in women and their children during the early postpartum period and early childhood. We hypothesized that these women and their c
Autor:
Caviness, Madeline Harrison
Publikováno v:
The Art Bulletin, 1979 Mar 01. 61(1), 38-58.
Externí odkaz:
https://www.jstor.org/stable/3049863
Autor:
Ira Shoulson, Donald S. Higgins, Mark Guttman, Marie Saint-Hilaire, Gina Rohs, Rose Schwarz, M. Sherr, Jackie Thomson, Vicki L. Wheelock, Charlyne Hickey, Kathleen M. Shannon, Kathleen Francis, Eric Siemers, Andrew Feigin, Elan D. Louis, Phillipa Hedges, Jang Ho John Cha, Greg Rudolf, Stuart Taylor, Joseph H. Friedman, Francis O. Walker, Cindy Lied, Frederick J. Marshall, Joseph Jankovic, J. Timothy Greenamyre, Peter Como, Alexander P. Auchus, Karen Caplan, Carmen Polanco, Kathy Claude, Irenita Gardiner, Lynn A. Raymond, M. Nance, Ronald Trent, Michael R. Hayden, Robert L. Rodnitzky, Nanette Mercado, Neal R. Swerdlow, Jennifer Mazurkiewicz, Adam Rosenblatt, Vicki Hunt, Charles H. Adler, Kristine Wernette, Joanne Wojcieszek, Richard Dubinsky, Carol Zimmerman, Stephanie Newman, Diane Brown, Henry L. Paulson, Samantha Pearce, Carol A. Manning, Janet S. Cellar, Elise Kayson, Michael R. Swenson, Michael P. McDermott, Margaret C. Lannon, Ruth Cummings, Walter J. Koroshetz, Roger L. Albin, Kenneth Marek, Sandra Russell, Tetsuo Ashizawa, Douglas R. Langbehn, Ann Catherine Bachoud-Levi, Ted M. Dawson, Paula Sexton, Jonelle Adams, Susan Cleary, Carolyn Gray, Dwight J. Stewart, John N. Caviness, Jane B. Lane, Elizabeth McCusker, Leon S. Dure, Juan Sanchez-Ramos, David A. Abwender, Naomi Zubin, W.R. Wayne Martin, Karen Marder, Audrey Walker, Nancy Pearson, Allen Rubin, Kerry Duncan, Jackie Gray, Randi Jones, Lynn Vining, Robert A. Hauser, Carol Moskowitz, Carson Reider, Stewart A. Factor, Elke Rost-Ruffner, Lauren Seeberger, Hartmut Meierkord, Alicia Facca, J. Beach, Oksana Suchowersky, Elizabeth Leritz, Marguerite Wieler, Catherine Brown, Merit Cudkowicz, Jane S. Paulsen, Cindy Hunter, Kim Lane, Karl Kieburtz, Joan Lawrence, Eric Molho, Alicia Brocht, Steven M. Hersch, Jill Burke-Holder, Madeline Harrison, Joshua L. Goldstein, Anders Lundin, Gustavo Rey, Anne B. Young, Jeana Jaglin, David Olson, Daniel S. Sax, William J. Weiner, Candace Young, David Oakes, Jody Corey-Bloom
Publikováno v:
Neurology. 68:1710-1717
Objective: Subtle signs and symptoms of Huntington disease (HD) are often present before impairments reach a point where the neurologic disease is manifest and a diagnosis must be considered. The objective is to examine the prognostic significance of
Autor:
Colin J. D. Ross, Estrella Gómez-Tortosa, L. A. Cupples, Qiong Yang, Catherine Dodé, Martha Nance, Ronald J. Trent, Ruth K. Abramson, Elizabeth McCusker, Luc Djoussé, D. Mayo, Marina Frontali, Patrick J. Morrison, Jane S. Paulsen, Randi Jones, Russell L. Margolis, Ryan R. Brinkman, Madeline Harrison, J. F. Gusella, Andrea Zanko, Oksana Suchowersky, Adam Rosenblatt, Alexandra Durr, Richard H. Myers, Andrea Novelletto, E. Almqvist, Beth Knowlton, Marcy E. MacDonald, Michael R. Hayden
Publikováno v:
American Journal of Medical Genetics Part A. :279-282
Huntington disease (HD) is a neurodegenerative disorder caused by the abnormal expansion of CAG repeats in the HD gene on chromosome 4p16.3. Past studies have shown that the size of expanded CAG repeat is inversely associated with age at onset (AO) o
Autor:
Madeline Harrison, Richard Peppard, Richard G. Bittar, Melina Ortigas, Edmund Cornman, i J Hagerman, Robert Frysinger, Lin Zhang, John M Olichney, Jamie S Pak, Danuta Z. Loesch, Kiarash Shahlaie
Publikováno v:
Brain Disorders & Therapy.
Objective: We describe 3 carriers of the FMR1 premutation with the Fragile X-associated Tremor Ataxia Syndrome (FXTAS) whose tremor was significantly improved by bilateral Deep Brain Stimulation (DBS) to Ventral Intermediate nucleus (Vim) of the thal
Autor:
Caviness, Madeline Harrison
Publikováno v:
Speculum, 1966 Apr 01. 41(2), 338-341.
Externí odkaz:
https://www.jstor.org/stable/2851280
Autor:
L. Adrienne Cupples, Marie Saint-Hilaire, Richard H. Myers, Estrella Gómez-Tortosa, Larry D. Atwood, Andrea Novelletto, Steven M. Hersch, Marina Frontali, Suzanne Tariot, Catherine Dodé, Jane S. Paulsen, E. Almqvist, Luc Djoussé, Ronald J. Trent, Vanessa C. Wheeler, Beth Knowlton, Marcy E. MacDonald, Martha Nance, Alexandra Durr, Ryan R. Brinkman, James F. Gusella, Jayalakshmi S. Mysore, Walter J. Koroshetz, Oksana Suchowersky, Andrea Zanko, Patrick J. Morrison, Ruth K. Abramson, Ana L. Russ, Madeline Harrison, Christopher A. Ross, Michael R. Hayden, Jang Ho J. Cha, David Mayo Cabrero, Michael F. Gusella, Adam Rosenblatt, Elizabeth McCusker, Randi Jones, Russell L. Margolis, Jian-Liang Li
Publikováno v:
American journal of human genetics. 73(3)
Huntington disease (HD) is caused by the expansion of a CAG repeat within the coding region of a novel gene on 4p16.3. Although the variation in age at onset is partly explained by the size of the expanded repeat, the unexplained variation in age at
Autor:
Clifford W. Shults, Richard Haas, David Oakes, Karl Kieburtz, Sandra Plumb, Ira Shoulson, Roger Kurlan, M. Flint Beal, Jorge Juncos, Ray Watts, John Nutt, Julie Carter, Katie Kompoliti, Joel Perlmutter, Stephen Reich, Matt Stern, Eric Molho, Madeline Harrison, Mark Lew
Publikováno v:
Archives of Neurology. 60:1172