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R J Auchus

Showing results (31-40 of 36) with videos related to

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World Journal of Surgery|November 15, 2017
Refining the Definitions of Biochemical and Clinical Cure for Primary Aldosteronism Using the Primary Aldosteronism Surgical Outcome (PASO) Classification SystemB S Miller, A F Turcu, A T Nanba, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 23, 2010
What we still do not know about adrenal vein sampling for primary aldosteronismR J Auchus, F H Wians, M E Anderson, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 13, 2017
Functional characterization of the G162R and D216H genetic variants of human CYP17A1C P Capper, J Liu, L R McIntosh, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Clinical Genetics|April 26, 2008
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblingsY Miyoshi, M Akagi, A K Agarwal, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 15, 2014
Catecholamine-resistant hypotension and myocardial performance following patent ductus arteriosus ligationS Noori, P McNamara, A Jain, et al.
Pageof 4

Showing results (31-40 of 36) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 36 results.
World Journal of Surgery|November 15, 2017
Refining the Definitions of Biochemical and Clinical Cure for Primary Aldosteronism Using the Primary Aldosteronism Surgical Outcome (PASO) Classification SystemB S Miller, A F Turcu, A T Nanba, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme|April 23, 2010
What we still do not know about adrenal vein sampling for primary aldosteronismR J Auchus, F H Wians, M E Anderson, et al.
The Journal of Steroid Biochemistry and Molecular Biology|December 13, 2017
Functional characterization of the G162R and D216H genetic variants of human CYP17A1C P Capper, J Liu, L R McIntosh, et al.
The Journal of Clinical Endocrinology and Metabolism|March 30, 2006
A novel point mutation in P450c17 (CYP17) causing combined 17alpha-hydroxylase/17,20-lyase deficiencyA M Brooke, N F Taylor, J H Shepherd, et al.
Clinical Genetics|April 26, 2008
Severe mandibuloacral dysplasia caused by novel compound heterozygous ZMPSTE24 mutations in two Japanese siblingsY Miyoshi, M Akagi, A K Agarwal, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|August 15, 2014
Catecholamine-resistant hypotension and myocardial performance following patent ductus arteriosus ligationS Noori, P McNamara, A Jain, et al.
Pageof 4