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Showing results (251-260 of 257) with videos related to

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Journal of Neuroendocrinology|May 11, 2011
The glucose-dependent insulinotropic polypeptide receptor is overexpressed amongst GNAS1 mutation-negative somatotropinomas and drives growth hormone (GH)-promoter activity in GH3 cellsG Occhi, M Losa, N Albiger, et al.
European Journal of Endocrinology|April 8, 2011
AME position statement on adrenal incidentalomaM Terzolo, A Stigliano, I Chiodini, 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 13, 2003
Diagnosis and complications of Cushing's syndrome: a consensus statementG Arnaldi, A Angeli, A B Atkinson, 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.
Journal of Human Hypertension|June 22, 2012
Prospective appraisal of the prevalence of primary aldosteronism in hypertensive patients presenting with atrial flutter or fibrillation (PAPPHY Study): rationale and study designG P Rossi, T M Seccia, V Gallina, et al.
Pageof 26

Showing results (251-260 of 257) with videos related to

Sort By:
Pageof 26
You have reached the last page of results.This site can display upto 257 results.
Journal of Neuroendocrinology|May 11, 2011
The glucose-dependent insulinotropic polypeptide receptor is overexpressed amongst GNAS1 mutation-negative somatotropinomas and drives growth hormone (GH)-promoter activity in GH3 cellsG Occhi, M Losa, N Albiger, et al.
European Journal of Endocrinology|April 8, 2011
AME position statement on adrenal incidentalomaM Terzolo, A Stigliano, I Chiodini, 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 13, 2003
Diagnosis and complications of Cushing's syndrome: a consensus statementG Arnaldi, A Angeli, A B Atkinson, 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.
Journal of Human Hypertension|June 22, 2012
Prospective appraisal of the prevalence of primary aldosteronism in hypertensive patients presenting with atrial flutter or fibrillation (PAPPHY Study): rationale and study designG P Rossi, T M Seccia, V Gallina, et al.
Pageof 26