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Swiss Medical Weekly
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July 22, 2010
Metabolic control of type 1 diabetic patients followed at the University Children's Hospital in Berne: have we reached the goal?
Paolo Tonella, Christa E Flück, Primus E Mullis
Hormone Research in Paediatrics
|
September 12, 2012
Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency
Marco Janner, Christa E Flück, Primus E Mullis
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 4, 2003
New GH-1 gene mutations: expanding the spectrum of causes of isolated growth hormone deficiency
Primus E Mullis, Johnny Deladoëy, Priscilla S Dannies
Hormone Research
|
September 11, 2002
Molecular and cellular basis of isolated dominant-negative growth hormone deficiency, IGHD type II: insights on the secretory pathway of peptide hormones
Primus E Mullis, Johnny Deladoëy, Priscilla S Dannies
Endocrine Development
|
November 28, 2012
From endoplasmic reticulum to secretory granules: role of zinc in the secretory pathway of growth hormone
Vibor Petkovic, Maria Consolata Miletta, Primus-E Mullis
Biochemical and Biophysical Research Communications
|
August 25, 2010
Altered heme catabolism by heme oxygenase-1 caused by mutations in human NADPH cytochrome P450 reductase
Amit V Pandey, Christa E Flück, Primus E Mullis
Archives of Medical Research
|
March 11, 2004
Agreement between HbA1c measured by DCA 2000 and by HPLC: effects of fetal hemoglobin concentrations
Peter Diem, Manuela Wälchli, Primus E Mullis, et al.
Molecular and Cellular Endocrinology
|
September 12, 2009
Modeling of human P450 oxidoreductase structure by in silico mutagenesis and MD simulation
Christa E Flück, Primus E Mullis, Amit V Pandey
Therapeutische Umschau. Revue Therapeutique
|
March 28, 2014
[In Process Citation]
Andreas Bieri, Matthias Kamber, Martin Sterchi, et al.
Biochemical and Biophysical Research Communications
|
September 21, 2010
Reduction in hepatic drug metabolizing CYP3A4 activities caused by P450 oxidoreductase mutations identified in patients with disordered steroid metabolism
Christa E Flück, Primus E Mullis, Amit V Pandey
Page
of 10
Search research articles
Search
Showing results (11-20 of 97) with videos related to
Sort By:
Page
of 10
Swiss Medical Weekly
|
July 22, 2010
Metabolic control of type 1 diabetic patients followed at the University Children's Hospital in Berne: have we reached the goal?
Paolo Tonella, Christa E Flück, Primus E Mullis
Hormone Research in Paediatrics
|
September 12, 2012
Impact of estrogen replacement throughout childhood on growth, pituitary-gonadal axis and bone in a 46,XX patient with CYP19A1 deficiency
Marco Janner, Christa E Flück, Primus E Mullis
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
January 4, 2003
New GH-1 gene mutations: expanding the spectrum of causes of isolated growth hormone deficiency
Primus E Mullis, Johnny Deladoëy, Priscilla S Dannies
Hormone Research
|
September 11, 2002
Molecular and cellular basis of isolated dominant-negative growth hormone deficiency, IGHD type II: insights on the secretory pathway of peptide hormones
Primus E Mullis, Johnny Deladoëy, Priscilla S Dannies
Endocrine Development
|
November 28, 2012
From endoplasmic reticulum to secretory granules: role of zinc in the secretory pathway of growth hormone
Vibor Petkovic, Maria Consolata Miletta, Primus-E Mullis
Biochemical and Biophysical Research Communications
|
August 25, 2010
Altered heme catabolism by heme oxygenase-1 caused by mutations in human NADPH cytochrome P450 reductase
Amit V Pandey, Christa E Flück, Primus E Mullis
Archives of Medical Research
|
March 11, 2004
Agreement between HbA1c measured by DCA 2000 and by HPLC: effects of fetal hemoglobin concentrations
Peter Diem, Manuela Wälchli, Primus E Mullis, et al.
Molecular and Cellular Endocrinology
|
September 12, 2009
Modeling of human P450 oxidoreductase structure by in silico mutagenesis and MD simulation
Christa E Flück, Primus E Mullis, Amit V Pandey
Therapeutische Umschau. Revue Therapeutique
|
March 28, 2014
[In Process Citation]
Andreas Bieri, Matthias Kamber, Martin Sterchi, et al.
Biochemical and Biophysical Research Communications
|
September 21, 2010
Reduction in hepatic drug metabolizing CYP3A4 activities caused by P450 oxidoreductase mutations identified in patients with disordered steroid metabolism
Christa E Flück, Primus E Mullis, Amit V Pandey
Page
of 10