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P Mulatero

Showing results (1-10 of 50) with videos related to

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Minerva Endocrinologica|January 1, 1992
[Primary dexamethasone-suppressible hyperaldosteronism and hyperprolactinemia]F Veglio, G Pinna, F Rabbia, et al.
Minerva Medica|November 8, 2003
Recent advances in diagnosis and treatment of primary aldosteronismF Veglio, F Morello, F Rabbia, et al.
Annali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|January 1, 1996
[The L-arginine/nitric oxide metabolic pathway. Its physiopathology and clinical implications]G Mengozzi, F Veglio, D Schiavone, et al.
Hypertension (Dallas, Tex. : 1979)|December 24, 1997
Dopamine D3 receptor in peripheral mononuclear cells of essential hypertensivesA Ricci, E Bronzetti, P Mulatero, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1994
Inhibition of lysozyme synthesis by dexamethasone in human mononuclear leukocytes: an index of glucocorticoid sensitivityM Panarelli, C D Holloway, P Mulatero, et al.
American Journal of Hypertension|May 8, 1999
Vasoactive hormones induce nitric oxide synthase mRNA expression and nitric oxide production in human endothelial cells and monocytesM Schena, P Mulatero, D Schiavone, et al.
Journal of Human Hypertension|September 15, 2007
Characteristics of the patients referred to a Hypertension Unit between 1989 and 2003G Leotta, F Rabbia, A Canadè, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasiaS Portrat, P Mulatero, K M Curnow, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 2, 2010
Confirmatory tests in the diagnosis of primary aldosteronismP Mulatero, S Monticone, C Bertello, et al.
Journal of Human Hypertension|October 9, 2015
ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesionsP Mulatero, F Schiavi, T A Williams, et al.
Pageof 5

Showing results (1-10 of 50) with videos related to

Sort By:
Pageof 5
Minerva Endocrinologica|January 1, 1992
[Primary dexamethasone-suppressible hyperaldosteronism and hyperprolactinemia]F Veglio, G Pinna, F Rabbia, et al.
Minerva Medica|November 8, 2003
Recent advances in diagnosis and treatment of primary aldosteronismF Veglio, F Morello, F Rabbia, et al.
Annali Italiani Di Medicina Interna : Organo Ufficiale Della Societa Italiana Di Medicina Interna|January 1, 1996
[The L-arginine/nitric oxide metabolic pathway. Its physiopathology and clinical implications]G Mengozzi, F Veglio, D Schiavone, et al.
Hypertension (Dallas, Tex. : 1979)|December 24, 1997
Dopamine D3 receptor in peripheral mononuclear cells of essential hypertensivesA Ricci, E Bronzetti, P Mulatero, et al.
The Journal of Clinical Endocrinology and Metabolism|April 1, 1994
Inhibition of lysozyme synthesis by dexamethasone in human mononuclear leukocytes: an index of glucocorticoid sensitivityM Panarelli, C D Holloway, P Mulatero, et al.
American Journal of Hypertension|May 8, 1999
Vasoactive hormones induce nitric oxide synthase mRNA expression and nitric oxide production in human endothelial cells and monocytesM Schena, P Mulatero, D Schiavone, et al.
Journal of Human Hypertension|September 15, 2007
Characteristics of the patients referred to a Hypertension Unit between 1989 and 2003G Leotta, F Rabbia, A Canadè, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Deletion hybrid genes, due to unequal crossing over between CYP11B1 (11beta-hydroxylase) and CYP11B2(aldosterone synthase) cause steroid 11beta-hydroxylase deficiency and congenital adrenal hyperplasiaS Portrat, P Mulatero, K M Curnow, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|February 2, 2010
Confirmatory tests in the diagnosis of primary aldosteronismP Mulatero, S Monticone, C Bertello, et al.
Journal of Human Hypertension|October 9, 2015
ARMC5 mutation analysis in patients with primary aldosteronism and bilateral adrenal lesionsP Mulatero, F Schiavi, T A Williams, et al.
Pageof 5