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G Riepe

Showing results (41-50 of 109) with videos related to

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Hormone Research|January 22, 2008
A case of 11beta-hydroxylase deficiency detected in a newborn screening program by second-tier LC-MS/MSM Peter, N Janzen, S Sander, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|October 23, 2002
What can we learn from explanted endovascular devices?G Riepe, C Heintz, E Kaiser, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 14, 2011
Critical points in the management of pseudohypoaldosteronism type 1Tülay Güran, Serpil Değirmenci, İpek K Bulut, et al.
Hormone Research in Paediatrics|December 12, 2018
Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation - A Case Report and Review of the Literature: Implications for the PathomechanismStella A Nagel, Michaela F Hartmann, Felix G Riepe, et al.
Archives of Pediatrics & Adolescent Medicine|May 18, 2001
Special feature: picture of the month. Infantile scurvyF G Riepe, D Eichmann, H C Oppermann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneityFelix G Riepe, Nils Krone, Michel Morlot, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor geneFelix G Riepe, Nils Krone, Michel Morlot, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 15, 2005
The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutionsNils Krone, Felix G Riepe, Joachim Grötzinger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interactionFelix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Tissue Viability|August 12, 2010
A practice-oriented recommendation for treatment of critically colonised and locally infected wounds using polihexanideJ Dissemond, V Gerber, A Kramer, et al.
Pageof 11

Showing results (41-50 of 109) with videos related to

Sort By:
Pageof 11
Hormone Research|January 22, 2008
A case of 11beta-hydroxylase deficiency detected in a newborn screening program by second-tier LC-MS/MSM Peter, N Janzen, S Sander, et al.
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|October 23, 2002
What can we learn from explanted endovascular devices?G Riepe, C Heintz, E Kaiser, et al.
Journal of Clinical Research in Pediatric Endocrinology|July 14, 2011
Critical points in the management of pseudohypoaldosteronism type 1Tülay Güran, Serpil Değirmenci, İpek K Bulut, et al.
Hormone Research in Paediatrics|December 12, 2018
Gonadotropin- and Adrenocorticotropic Hormone-Independent Precocious Puberty of Gonadal Origin in a Patient with Adrenal Hypoplasia Congenita Due to DAX1 Gene Mutation - A Case Report and Review of the Literature: Implications for the PathomechanismStella A Nagel, Michaela F Hartmann, Felix G Riepe, et al.
Archives of Pediatrics & Adolescent Medicine|May 18, 2001
Special feature: picture of the month. Infantile scurvyF G Riepe, D Eichmann, H C Oppermann, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Identification of a novel mutation in the human mineralocorticoid receptor gene in a german family with autosomal-dominant pseudohypoaldosteronism type 1: further evidence for marked interindividual clinical heterogeneityFelix G Riepe, Nils Krone, Michel Morlot, et al.
The Journal of Clinical Endocrinology and Metabolism|May 6, 2004
Autosomal-dominant pseudohypoaldosteronism type 1 in a Turkish family is associated with a novel nonsense mutation in the human mineralocorticoid receptor geneFelix G Riepe, Nils Krone, Michel Morlot, et al.
Journal of Molecular Medicine (Berlin, Germany)|April 15, 2005
The residue E351 is essential for the activity of human 21-hydroxylase: evidence from a naturally occurring novel point mutation compared with artificial mutants generated by single amino acid substitutionsNils Krone, Felix G Riepe, Joachim Grötzinger, et al.
The Journal of Clinical Endocrinology and Metabolism|May 1, 2008
Functional and structural consequences of a novel point mutation in the CYP21A2 gene causing congenital adrenal hyperplasia: potential relevance of helix C for P450 oxidoreductase-21-hydroxylase interactionFelix G Riepe, Olaf Hiort, Joachim Grötzinger, et al.
Journal of Tissue Viability|August 12, 2010
A practice-oriented recommendation for treatment of critically colonised and locally infected wounds using polihexanideJ Dissemond, V Gerber, A Kramer, et al.
Pageof 11