Results 161 to 170 of about 4,722 (204)
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J11 Can Music Therapy Improve The Quality Of Life In Huntington's Disease?
Journal of Neurology, Neurosurgery & Psychiatry, 2014Background 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 +3 more
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J11 Contemporary dance improves motor function and body perception in huntington disease
Clinical therapeutics, 2018Background 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 +7 more
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MPEC 2023-J11 : DAILY ORBIT UPDATE (2023 May 2)
2023The 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.
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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.
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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
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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
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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.
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MPEC 2026-J11 : OBSERVATIONS AND ORBITS OF COMETS AND A/ OBJECTS
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
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 +4 more
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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 +4 more
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Éclampsie retardée : leçons à tirer d’un cas survenu à j11 post-partum
Gynécologie Obstétrique & Fertilité, 2008We 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 +4 more
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High mass flow rate in a BAL outflow of quasar SDSS J1130 + 0411
Monthly Notices of the Royal Astronomical Society, 2022Nahum Arav, Doyee Byun, Gwen Walker
exaly

