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Radiology|May 1, 1996
Proton MR spectroscopy of the basal ganglia in healthy children and children with AIDSD Lu, S G Pavlakis, Y Frank, et al.Journal of Endocrinological Investigation|July 17, 2023
Calcitonin levels in autoimmune atrophic gastritis-related hypergastrinemiaS Censi, S Carducci, G Zoppini, et al.Endocrine|April 21, 2016
A multicenter experience on the prevalence of ARMC5 mutations in patients with primary bilateral macronodular adrenal hyperplasia: from genetic characterization to clinical phenotypeN M Albiger, D Regazzo, B Rubin, et al.The Journal of Clinical Psychiatry|November 15, 2011
Effect of antidepressant medication treatment on suicidal ideation and behavior in a randomized trial: an exploratory report from the Combining Medications to Enhance Depression Outcomes StudySidney Zisook, Ira M Lesser, Barry Lebowitz, et al.Annals of Neurology|January 23, 1999
Modulation by DLST of the genetic risk of Alzheimer's disease in a very elderly populationK F Sheu, A M Brown, V Haroutunian, et al.Journal of Psychiatric Practice|October 4, 2008
An open pilot study of the combination of escitalopram and bupropion-SR for outpatients with major depressive disorderAndrew F Leuchter, Ira M Lesser, Madhukar H Trivedi, et al.Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.The International Journal of Neuropsychopharmacology|July 10, 2008
What predicts attrition in second step medication treatments for depression?: a STAR*D ReportDiane Warden, A John Rush, Stephen R Wisniewski, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.Pageof 35