Showing results (81-90 of 87) with videos related to
Sort By:
Pageof 9
You have reached the last page of results.This site can display upto 87 results.
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.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 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.European Journal of Endocrinology|May 19, 2012
Predictors of morbidity and mortality in acromegaly: an Italian surveyM Arosio, G Reimondo, E Malchiodi, et al.Journal of Endocrinological Investigation|May 18, 2021
Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patientsS Garelli, M Dalla Costa, C Sabbadin, et al.Pageof 9