Results 151 to 160 of about 93,886 (309)

PIAS1 Regulates Mutant Huntingtin Accumulation and Huntington’s Disease-Associated Phenotypes In Vivo [PDF]

, 2016
Joseph Ochaba, Alex Mas Monteys, Jacqueline G. O’Rourke, Jack C. Reidling, Joan S. Steffan, Beverly L. Davidson, Leslie M. Thompson   +6 more
openalex   +1 more source

Huntington's Disease and Huntington's Disease‐like 2 (HDL2) in Martinique

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Huntington's Disease‐like 2 (HDL2), caused by a CAG repeat expansion in JPH3, closely resembles HD. All reported HDL2 patients to date have some African ancestry. While both disorders exist in the Caribbean, their relative frequency and clinical characteristics remain largely unknown.
Ignacio Antolin‐Sanfeliz, Anna‐Gaelle Giguet‐Valard, Sophie Duclos, Cécile Cazeneuve, Chloé Angelini, Aïssatou Signaté, Russell L. Margolis, Cyril Goizet, Rémi Bellance   +8 more
wiley   +1 more source

Correlation Between CCG Polymorphisms and CAG Repeats During Germline Transmission in Chinese Patients with Huntington’s Disease

, 2020
Hong-Rong Cheng, Xiaoyan Li, YU Hui-li, Miao Xu, Yanbin Zhang, Shi‐Rui Gan, Honglei Li, Zhi‐Ying Wu   +7 more
openalex   +2 more sources

Development and Validation of a Brief Fall Questionnaire (FALL‐HD) for Patients with Huntington's Disease

Movement Disorders Clinical Practice, EarlyView.
ABSTRACT Background Huntington's disease (HD) is an autosomal dominant neurodegenerative disorder caused by a mutation in the huntingtin gene on chromosome 4, leading to progressive cognitive decline, motor impairment, and functional disability. Falls represent the leading cause of nursing home placement in HD.
Japleen Kaur, Deng‐Yuan Liou, Krisha Bagga, Nadeen Youhanan, Andrew Hall, Paul E. Gilbert, Daniel J. Goble, Jody Corey‐Bloom   +7 more
wiley   +1 more source

Review for "Hippocampal and striatal volumes correlate with spatial memory impairment in Huntington’s disease"

, 2021
Jee Bang
openalex   +1 more source

Economic Cost of Current and Alternative Models of Multidisciplinary Care of Juvenile‐Onset Huntington's Disease

Movement Disorders Clinical Practice, EarlyView.
Abstract Background Multidisciplinary care has been advocated for Juvenile‐onset Huntington's Disease but there has been no detailed analysis of this. Objectives To evaluate the current economic costs of providing health care for patients with Juvenile‐onset Huntington's disease (JoHD) and to model the effects and economic costs of providing a ...
Tracey A. Young, Penny A. Curtis, Jill Thompson, Aileen K. Ho, Helen Santini, Oliver W. Quarrell   +5 more
wiley   +1 more source

Genetic Information and the Workplace - Full Report [PDF]

, 1998
Joint Agency ReportGeneticInfoWorkplace1998.pdf: 800 downloads, before Oct.
Department of Health and Human Services, U.S., Department of Labor, U.S., Equal Employment Opportunity Commission, U.S.   +2 more
core   +1 more source

Mutant huntingtin and neurofilament light have distinct longitudinal dynamics in Huntington’s disease

, 2020
Filipe B. Rodrigues, Lauren M. Byrne, Rosanna Tortelli, Eileanoir B. Johnson, P. A. Wijeratne, Marzena Arridge, Enrico De Vita, Naghmeh Ghazaleh, Richard Houghton, Hannah Furby, Daniel C. Alexander, Sarah J. Tabrizi, Scott Schobel, Rachael I. Scahill, Amanda Heslegrave, Henrik Zetterberg, Edward J. Wild   +16 more
openalex   +2 more sources

E05 Mutation-related apparent myelin, not axon density, drives white matter pathology in premanifest huntington’s disease: evidence from in vivo ultra-strong gradient MRI [PDF]

, 2021
Chiara Casella, Maxime Chamberland, Pedro Luque Laguna, Greg D. Parker, Anne Rosser, Elizabeth Coulthard, Hugh Rickards, Derek K. Jones, Claudia Metzler‐Baddeley   +8 more
openalex   +1 more source

Experience of using MRI morphometry in Huntington’s disease

, 2013
E. N. Yudina, Р. Н. Коновалов, N. Yu. Abramycheva, Abramycheva N. Yu., S. A. Klyushnikov, С. Н. Иллариошкин   +5 more
openalex   +2 more sources