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Expert Review of Endocrinology & Metabolism
|
February 13, 2019
Molecular pathogenesis of renal pseudohypoaldosteronism type 1
Felix G Riepe
Nature Reviews. Endocrinology
|
November 10, 2010
Adrenal gland: Congenital adrenal hyperplasia: new treatment guidelines
Felix G Riepe
Endocrine Development
|
February 9, 2013
Pseudohypoaldosteronism
Felix G Riepe
Hormone Research
|
July 3, 2009
Clinical and molecular features of type 1 pseudohypoaldosteronism
Felix G Riepe
Reviews in Endocrine & Metabolic Disorders
|
September 22, 2007
Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Felix G Riepe, Wolfgang G Sippell
American Journal of Nephrology
|
February 24, 2007
Exclusion of serum- and glucocorticoid-induced kinase 1 (SGK1) as a candidate gene for genetically heterogeneous renal pseudohypoaldosteronism type I in eight families
Felix G Riepe, Paul-Martin Holterhus
European Journal of Pediatrics
|
May 24, 2005
Disproportionate stature but normal height in hypochondroplasia
Felix G Riepe, Nils Krone, Wolfgang G Sippell
Hormone Research in Paediatrics
|
January 19, 2013
Implementation of a liquid chromatography tandem mass spectrometry assay for eight adrenal C-21 steroids and pediatric reference data
Alexandra E Kulle, Maik Welzel, Paul-Martin Holterhus, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Longitudinal study of plasma pregnenolone and 17-hydroxypregnenolone in full-term and preterm neonates at birth and during the early neonatal period
Felix G Riepe, Philip Mahler, Wolfgang G Sippell, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
January 30, 2004
The increased lysis of fetal cells in the mother after pregnancies complicated by pre-eclampsia or HELLP syndrome is not the result of a specific anti-fetal cytotoxicity of the mother
Thomas Brune, Tanja Hornung, Hans-Georg Koch, et al.
Page
of 6
Search research articles
Search
Showing results (1-10 of 60) with videos related to
Sort By:
Page
of 6
Expert Review of Endocrinology & Metabolism
|
February 13, 2019
Molecular pathogenesis of renal pseudohypoaldosteronism type 1
Felix G Riepe
Nature Reviews. Endocrinology
|
November 10, 2010
Adrenal gland: Congenital adrenal hyperplasia: new treatment guidelines
Felix G Riepe
Endocrine Development
|
February 9, 2013
Pseudohypoaldosteronism
Felix G Riepe
Hormone Research
|
July 3, 2009
Clinical and molecular features of type 1 pseudohypoaldosteronism
Felix G Riepe
Reviews in Endocrine & Metabolic Disorders
|
September 22, 2007
Recent advances in diagnosis, treatment, and outcome of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Felix G Riepe, Wolfgang G Sippell
American Journal of Nephrology
|
February 24, 2007
Exclusion of serum- and glucocorticoid-induced kinase 1 (SGK1) as a candidate gene for genetically heterogeneous renal pseudohypoaldosteronism type I in eight families
Felix G Riepe, Paul-Martin Holterhus
European Journal of Pediatrics
|
May 24, 2005
Disproportionate stature but normal height in hypochondroplasia
Felix G Riepe, Nils Krone, Wolfgang G Sippell
Hormone Research in Paediatrics
|
January 19, 2013
Implementation of a liquid chromatography tandem mass spectrometry assay for eight adrenal C-21 steroids and pediatric reference data
Alexandra E Kulle, Maik Welzel, Paul-Martin Holterhus, et al.
The Journal of Clinical Endocrinology and Metabolism
|
September 6, 2002
Longitudinal study of plasma pregnenolone and 17-hydroxypregnenolone in full-term and preterm neonates at birth and during the early neonatal period
Felix G Riepe, Philip Mahler, Wolfgang G Sippell, et al.
American Journal of Reproductive Immunology (New York, N.Y. : 1989)
|
January 30, 2004
The increased lysis of fetal cells in the mother after pregnancies complicated by pre-eclampsia or HELLP syndrome is not the result of a specific anti-fetal cytotoxicity of the mother
Thomas Brune, Tanja Hornung, Hans-Georg Koch, et al.
Page
of 6