Results 161 to 170 of about 55,726 (206)

J11 Can Music Therapy Improve The Quality Of Life In Huntington's Disease?

Journal of Neurology, Neurosurgery & Psychiatry, 2014
Background Since there is no cure for Huntington’s disease (HD) yet the intention of all forms of treatment is to improve quality of life. All treatment must be individually tailored, as the symptoms and signs are different for each person and change over time. Music therapy (MT) recognises individual needs and can be adapted to meet them.
M. van Bruggen-Rufi, R. Roos, W. Achterberg, A. Vink   +3 more
openaire   +1 more source

J11 A pilot study on respiratory function in people with huntington's disease

Journal of Neurology, Neurosurgery & Psychiatry, 2010
Background Huntington9s disease (HD) is a neurodegenerative condition resulting in motor, cognitive and behavioural dysfunction. Physiotherapists are involved in the management of respiratory problems during the later stages of the disease1 yet little is known about the respiratory system during the progression through the stages of the disease. Aim
U Jones, S Enright, M Busse, A Rosser
openaire   +1 more source

Purification and characterization of a cellulolytic multienzyme complex produced by Neocallimastix patriciarum J11

Biochemical and Biophysical Research Communications, 2014
Understanding the roles of the components of the multienzyme complex of the anaerobial cellulase system, acting on complex substrates, is crucial to the development of efficient cellulase systems for industrial applications such as converting lignocellulose to sugars for bioethanol production.
Hui-Chang, Wang, Yo-Chia, Chen, Ruey-Shyang, Hseu   +2 more
openaire   +2 more sources

Éclampsie retardée : leçons à tirer d’un cas survenu à j11 post-partum

Gynécologie Obstétrique & Fertilité, 2008
We report a case of late postpartum eclampsia at Day 11 in a 40-year-old woman after normal pregnancy and delivery. The delayed eclamptic episode is defined by seizures between two days and four weeks after delivery. About 40% of late eclampsia has no premonitory symptoms.
M. Valentin, G. Ducarme, A. Wernet, J. Mantz, D. Luton   +4 more
openaire   +1 more source

J11 Contemporary dance improves motor function and body perception in huntington disease

Clinical therapeutics, 2018
Background Physical exercise improves neurological conditions, but adherence is hard to establish. Dance might be a promising alternative. However, for patients with Huntington Disease (HD), who suffer from rhythmic movement execution deficits, metric dance practice might be unsuitable and alternatives must be explored.
Iris Trinkler, Philippe Chéhère, Julie Salgues, Marie-Lorraine Monin, Sophie Tezenas du Montcel, Sonia Khani, Marcela Gargiulo, Alexandra Durr   +7 more
openaire   +1 more source

MPEC 2025-J11 : 2025 HX22

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
openaire   +1 more source

MPEC 2024-J11 : 2011 HO5

The Minor Planet Electronic Circulars contain information on unusual minor planets, routine data on comets and natural satellites, and occasional editorial announcements. They are published on behalf of Division F of the International Astronomical Union by the Minor Planet Center, Smithsonian Astrophysical Observatory, Cambridge, MA 02138, U.S.A.
openaire   +1 more source

J11 Investigating phenocopies in a cohort of south african patients with a huntington’s disease-like phenotype

Journal of Neurology, Neurosurgery & Psychiatry, 2016
Background Huntington’s disease (HD) is caused by an unstable expanded trinucleotide (CAG) repeat in the huntingtin (HTT) gene. Presentation involves a clinical triad of symptoms: behavioural problems, movement disorder and cognitive decline. Elsewhere, between 1 and 7% of individuals diagnosed do not carry the mutation and are said to have an HD ...
Fiona K Baine, Amanda Krause
openaire   +1 more source

J11 Altered reward processing in pre-symptomatic carriers of the Huntington gene—hypercompensation as a potential mechanism

Journal of Neurology, Neurosurgery & Psychiatry, 2012
Background and Aims The characteristic symptoms of chorea in Huntington9s disease, have been related to a dysfunction of dopamine transmission. Furthermore, psychological symptoms like anhedonia and altered motivation and drive as functions of the dopaminergic reward system are common and often manifest already early in the course of the disease ...
K Malejko, SD Süssmuth, M Orth, B Abler, P Weydt   +4 more
openaire   +1 more source

Two new ketene derivatives from the endophytic fungus Daldinia eschscholtzii J11

Phytochemistry Letters, 2023
Song-Mei Lu, Cheng-Juan Liao, Yuan Xu, Teng-Yuan Gui, He-Lin Sui, Min Zhou   +5 more
openaire   +1 more source