Results 131 to 140 of about 52,129 (204)

Physiotherapy in Huntington’s disease

Fysioterapeuten, 2013
Introduction:Huntington’s disease is hereditary and causes motor, cognitive and behavioural symptoms that progress over time. The aim of this article is to describe the disease and to highlight why physiotherapy is important and to point out potential ...
Hanne Ludt Fossmo, Anu Piira, Jeanette Ullmann Miller, Jan C. Frich   +3 more
doaj  

Immune markers for Huntington’s disease? [PDF]

, 2008
Edward J. Wild, Maria Björkqvist, Sarah J. Tabrizi   +2 more
openalex   +1 more source

Lumbar Puncture Alleviates Chorea in a Patient with Huntington’s Disease and Normal Pressure Hydrocephalus [PDF]

, 2009
Peyman Shirani, Alicia R. Salamone, Elham Lahijani, Michele K. York, Paul E. Schulz   +4 more
openalex   +1 more source

Quetiapine in the Treatment of Behavioral Disturbances in Patients With Huntington’s Disease

, 2005
Menekse Alpay, Walter J. Koroshetz
openalex   +1 more source

Analysis of the Striato-Thalamo-Cortical Connectivity on the Cortical Surface to Infer Biomarkers of Huntington’s Disease [PDF]

, 2010
Linda Marrakchi‐Kacem, Christine Delmaire, Alan Tucholka, Pauline Roca, Pamela Guevara, Fabrice Poupon, Jérôme Yelnik, Alexandra Dürr, Jean‐François Mangin, Stéphane Lehéricy, Cyril Poupon   +10 more
openalex   +1 more source

Striato-cortical connectivity patterns predict clinical profiles in Huntington’s disease

NeuroImage: Clinical
Background: Huntington’s disease is an inherited neurodegenerative disorder affecting striato-cortical circuits, with significant heterogeneity in the severity and progression of symptoms and neurodegenerative patterns.
Audrey E. De Paepe, Vasiliki Bikou, Eylül Turan, Alexis Pérez-Bellido, Clara Garcia-Gorro, Nadia Rodriguez-Dechicha, Irene Vaquer, Matilde Calopa, Ruth de Diego-Balaguer, Estela Camara   +9 more
doaj  

Early defect of transforming growth factor β1 formation in Huntington’s disease [PDF]

, 2010
Giuseppe Battaglia, Milena Cannella, Barbara Riozzi, S. Orobello, Marion L. C. Maat–Schieman, Eleonora Aronica, Carla L. Busceti, Andrea Ciarmiello, Silvia Alberti, Enrico Amico, Jenny Sassone, Simonetta Sipione, Valeria Bruno, Luigi Frati, Ferdinando Nicoletti, Ferdinando Squitieri   +15 more
openalex   +1 more source

Huntingtin Aggregation Impairs Autophagy, Leading to Argonaute-2 Accumulation and Global MicroRNA Dysregulation

Cell Reports, 2018
Summary: Many neurodegenerative diseases are characterized by the presence of intracellular protein aggregates, resulting in alterations in autophagy. However, the consequences of impaired autophagy for neuronal function remain poorly understood. In this
Karolina Pircs, Rebecca Petri, Sofia Madsen, Per Ludvik Brattås, Romina Vuono, Daniella R. Ottosson, Isabelle St-Amour, Bob A. Hersbach, Monika Matusiak-Brückner, Sofia Hult Lundh, Åsa Petersén, Nicole Déglon, Sébastien S. Hébert, Malin Parmar, Roger A. Barker, Johan Jakobsson   +15 more
doaj  

Rescue of gene expression by modified REST decoy oligonucleotides in a cellular model of Huntington’s disease [PDF]

, 2010
Chiara Soldati, Angela Bithell, Paola Conforti, Elena Cattaneo, Noel J. Buckley   +4 more
openalex   +1 more source

Composite Primary Neuronal High-Content Screening Assay for Huntington’s Disease Incorporating Non-Cell-Autonomous Interactions [PDF]

, 2010
Linda S. Kaltenbach, M. McLean Bolton, Bijal Shah, Patrick Kanju, Gwendolyn M. Lewis, Gregory J. Turmel, Jennifer C. Whaley, O. Joseph Trask, Donald C. Lo   +8 more
openalex   +1 more source