Results 161 to 170 of about 55,553 (186)
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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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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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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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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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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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Two new ketene derivatives from the endophytic fungus Daldinia eschscholtzii J11
Phytochemistry Letters, 2023Song-Mei Lu +5 more
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J11 Simulation of Spherically Propagating Hydrogen Laminar Flames
The Proceedings of Conference of Kyushu Branch, 2008Hiromasa NAKAGAWA +3 more
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J11 Effects of mechanical load on tissue formation in cultured cartilage
The Proceedings of Conference of Kyushu Branch, 2011Tomohiro Shimizu +2 more
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