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International Journal of Molecular Medicine|July 30, 1999
Identification of LMX1B gene point mutations in italian patients affected with Nail-Patella syndromeM Seri, S Melchionda, S Dreyer, et al.Neurophysiologie Clinique = Clinical Neurophysiology|December 1, 1991
[Topographical analysis of endogenous evoked potentials in depressed old people and in patients with Alzheimer's type dementia]M H de Brionne, B Gueguen, M C Bourdel, et al.La Nouvelle Presse Medicale|April 17, 1982
[3H-Imipramine binding to human platelets. A peripheral index in depressive syndromes (author's transl)]E Zarifian, D Sechter, F Bouchami, et al.Biological Psychiatry|March 1, 1987
Changes in [3H]5-HT uptake and [3H]imipramine binding in platelets after chlorimipramine in healthy volunteers. Comparison with maprotiline and amineptineM F Poirier, A M Galzin, H Loo, et al.Human Immunology|April 21, 1998
Repertoire breadth of human CD4+ T cells specific for HIV gp120 and p66 (primary antigens) or for PPD and tetanus toxoid (secondary antigens)G Li Pira, L Oppezzi, M Seri, et al.Psychopharmacology|January 1, 1988
Short-term lithium administration to healthy volunteers produces long-lasting pronounced changes in platelet serotonin uptake but not imipramine bindingM F Poirier, A M Galzin, C Pimoule, et al.Journal of Affective Disorders|March 17, 2004
Phenomenological and comorbid features associated in obsessive-compulsive disorder: influence of age of onsetB Millet, F Kochman, T Gallarda, et al.Retina (Philadelphia, Pa.)|March 9, 2002
Factors associated with reduced visual acuity during long-term follow-up of patients with idiopathic central serous chorioretinopathyRoy H Loo, Ingrid U Scott, Harry W Flynn, et al.The American Journal of Psychiatry|January 1, 1990
Striatal D2 dopaminergic receptors assessed with positron emission tomography and [76Br]bromospiperone in untreated schizophrenic patientsJ L Martinot, P Peron-Magnan, J D Huret, et al.Arthritis and Rheumatism|January 13, 2011
Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A geneM A Pelagatti, A Meini, R Caorsi, et al.Pageof 18