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of 64
pro vyhledávání: '"X. Lataste"'
Autor:
X. Lataste
The recognition of the dopaminergic properties of some ergot derivatives has initiated new therapeutical approaches in endocrinology as well as in neurology. The pharmacological characterization of the different ergot derivatives during the last deca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b577e8ff886b42623dbdf27a80317a00
http://doc.rero.ch/record/291215/files/S0317167100046266.pdf
http://doc.rero.ch/record/291215/files/S0317167100046266.pdf
Publikováno v:
Movement Disorders. 7:239-243
A selective dopamine D1-receptor agonist, CY 208-243, was administered to 23 de novo patients who had had Parkinson disease (PD) for less than or equal to 3 months. The drug was first used as monotherapy and then in some patients in combination with
Autor:
M Hoyer, Olivier Rascol, X Lataste, C Lücking, D Hirt, Werner Poewe, Urpo K. Rinne, H Teräväinen, E Dupont, N Fabre
Publikováno v:
Clinical Neuropharmacology. 13:303-311
The antiparkinsonian efficacy and tolerability of CQA 206-291, a novel ergoline derivative with potent dopamine agonist properties, were studied during 2 months of treatment in 72 parkinsonian patients. In 36 de novo patients (patients who have not p
Autor:
A. Azcona, X. Lataste
Publikováno v:
Drugs. 40:52-57
Calcium-related mechanisms are an integral part of metabolic reactions during acute cerebral infarction. In an animal model of stroke, the calcium antagonist isradipine was shown to protect neurons against ischaemia. In order to improve the neurologi
Autor:
A. Floesser, I. Bruenig-Traebert, Daniela Eser, M. Merz, Rainer Rupprecht, K. Kucher, R. Zaninelli, C. Schuele, A. Krebs-Brown, X. Lataste
Publikováno v:
European Neuropsychopharmacology. 16:S248-S249
Publikováno v:
Neurology. 44(11 Suppl 9)
The therapeutic profile of a new antispastic drug cannot be defined solely on the basis of placebo-controlled studies. Its potential advantages must be evaluated in comparison with existing drugs. This review compares the efficacy and tolerability of
Publikováno v:
Psychopharmacology. 112(1)
The selective 5HT3 antagonist tropisetron was studied in 91 outpatients meeting DSM-III criteria for Generalized Anxiety Disorder. Following a placebo washout period of up to 1 week, one of three active treatments (tropisetron 0.5 mg, 5 mg, or 25 mg
Autor:
X. Lataste
Publikováno v:
International journal of sports medicine. 13
The concept of blood-brain barrier has moved over the past years from a passive and relatively immutable structure to a more dynamic interface between blood and brain tissue. The transport mechanisms regulating this adaptative interface might be cons
Autor:
André Rascol, Geneviève Durrieu, Jean-Michel Senard, O. Rascol, Jean-Louis Montastruc, M. A. Tran, X. Lataste
Publikováno v:
Neurology. 40:707-707
We found blood pressure (BP), heart rate (HR), plasma norepinephrine (NE), and epinephrine (E) levels in the lying and the standing positions to be similar in never-treated parkinsonian patients (stages 1 and 2) and age-matched controls. CY 208-243,
Autor:
R. Markstein, A. M. Bonnet, Yves Agid, X. Lataste, C. D. Marsden, Temlett Ja, Niall Quinn, Peter Jenner, E. Pourcher
Publikováno v:
Movement Disorders. 4:261-265
The effect of stimulation of cerebral dopamine D-1 receptors by CY 208-243 on motor disability was tested in MPTP-treated parkinsonian marmosets and patients with Parkinson's disease. CY 208-243 (0.5-1.25 mg/kg s.c.) produced a dose-related reversal