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Adelbert A Roscher

Showing results (11-20 of 39) with videos related to

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Clinical Chemistry|December 21, 2004
Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 21-hydroxylase deficiencySiegfried Kösel, Siegfried Burggraf, Ralph Fingerhut, et al.
Journal of Experimental & Clinical Cancer Research : CR|January 15, 2016
The leukemogenic fusion gene MLL-AF9 alters microRNA expression pattern and inhibits monoblastic differentiation via miR-511 repressionKatrin K Fleischmann, Philipp Pagel, Julia von Frowein, et al.
Annals of Neurology|October 29, 2002
Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivationEsther M Maier, Stefan Kammerer, Ania C Muntau, et al.
Preventive Medicine|January 31, 2002
Very high compliance in an expanded MS-MS-based newborn screening program despite written parental consentBernhard Liebl, Uta Nennstiel-Ratzel, Rüdiger von Kries, et al.
Preventive Medicine|January 31, 2002
Expanded newborn screening in Bavaria: tracking to achieve requested repeat testingBernhard Liebl, Uta Nennstiel-Ratzel, Rüdiger von Kries, et al.
Clinical Chemistry|May 25, 2002
Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasiaNils Krone, Andreas Braun, Stefanie Weinert, et al.
Biological Chemistry|October 1, 2003
Kinin-B1 receptors in ischaemia-induced pancreatitis: functional importance and cellular localisationJoachim F Kuebler, Elisabeth Schremmer-Danninger, Kanti D Bhoola, et al.
The New England Journal of Medicine|December 27, 2002
Tetrahydrobiopterin as an alternative treatment for mild phenylketonuriaAnia C Muntau, Wulf Röschinger, Matthias Habich, et al.
Clinical Chemistry|February 28, 2002
Age-related reference values for serum selenium concentrations in infants and childrenAnia C Muntau, Monika Streiter, Matthias Kappler, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 25, 2006
Disease manifestations and X inactivation in heterozygous females with Fabry diseaseEsther M Maier, Stephanie Osterrieder, Catharina Whybra, et al.
Pageof 4

Showing results (11-20 of 39) with videos related to

Sort By:
Pageof 4
Clinical Chemistry|December 21, 2004
Rapid second-tier molecular genetic analysis for congenital adrenal hyperplasia attributable to steroid 21-hydroxylase deficiencySiegfried Kösel, Siegfried Burggraf, Ralph Fingerhut, et al.
Journal of Experimental & Clinical Cancer Research : CR|January 15, 2016
The leukemogenic fusion gene MLL-AF9 alters microRNA expression pattern and inhibits monoblastic differentiation via miR-511 repressionKatrin K Fleischmann, Philipp Pagel, Julia von Frowein, et al.
Annals of Neurology|October 29, 2002
Symptoms in carriers of adrenoleukodystrophy relate to skewed X inactivationEsther M Maier, Stefan Kammerer, Ania C Muntau, et al.
Preventive Medicine|January 31, 2002
Very high compliance in an expanded MS-MS-based newborn screening program despite written parental consentBernhard Liebl, Uta Nennstiel-Ratzel, Rüdiger von Kries, et al.
Preventive Medicine|January 31, 2002
Expanded newborn screening in Bavaria: tracking to achieve requested repeat testingBernhard Liebl, Uta Nennstiel-Ratzel, Rüdiger von Kries, et al.
Clinical Chemistry|May 25, 2002
Multiplex minisequencing of the 21-hydroxylase gene as a rapid strategy to confirm congenital adrenal hyperplasiaNils Krone, Andreas Braun, Stefanie Weinert, et al.
Biological Chemistry|October 1, 2003
Kinin-B1 receptors in ischaemia-induced pancreatitis: functional importance and cellular localisationJoachim F Kuebler, Elisabeth Schremmer-Danninger, Kanti D Bhoola, et al.
The New England Journal of Medicine|December 27, 2002
Tetrahydrobiopterin as an alternative treatment for mild phenylketonuriaAnia C Muntau, Wulf Röschinger, Matthias Habich, et al.
Clinical Chemistry|February 28, 2002
Age-related reference values for serum selenium concentrations in infants and childrenAnia C Muntau, Monika Streiter, Matthias Kappler, et al.
Acta Paediatrica (Oslo, Norway : 1992). Supplement|May 25, 2006
Disease manifestations and X inactivation in heterozygous females with Fabry diseaseEsther M Maier, Stephanie Osterrieder, Catharina Whybra, et al.
Pageof 4