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F Waldhauser

Showing results (61-70 of 73) with videos related to

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Neuroendocrinology|October 1, 1984
Bioavailability of oral melatonin in humansF Waldhauser, M Waldhauser, H R Lieberman, et al.
Pediatric Blood & Cancer|July 22, 2004
Pineal gland abnormalities in Langerhans cell histiocytosisN Grois, H Prosch, F Waldhauser, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Glycated plasma proteins in normal and diabetic mothers and their offspringsA Pollak, A Lischka, W Bartl, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2009
Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effectS Kleinle, R Lang, G F Fischer, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countriesJ Kovács, F Votava, G Heinze, et al.
Hormone Research|October 13, 2001
Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency. Results of a multicenter studyG Hargitai, J Sólyom, T Battelino, et al.
Hormone Research|June 18, 2002
Congenital adrenal hyperplasia: lessons from a multinational studyH Frisch, F Waldhauser, J Lebl, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutationS M Baumgartner-Parzer, E Schulze, W Waldhäusl, et al.
Neuroendocrinology|August 1, 1987
A pharmacological dose of melatonin increases PRL levels in males without altering those of GH, LH, FSH, TSH, testosterone or cortisolF Waldhauser, H R Lieberman, H J Lynch, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Pageof 8

Showing results (61-70 of 73) with videos related to

Sort By:
Pageof 8
Neuroendocrinology|October 1, 1984
Bioavailability of oral melatonin in humansF Waldhauser, M Waldhauser, H R Lieberman, et al.
Pediatric Blood & Cancer|July 22, 2004
Pineal gland abnormalities in Langerhans cell histiocytosisN Grois, H Prosch, F Waldhauser, et al.
Acta Endocrinologica. Supplementum|January 1, 1986
Glycated plasma proteins in normal and diabetic mothers and their offspringsA Pollak, A Lischka, W Bartl, et al.
The Journal of Clinical Endocrinology and Metabolism|September 24, 2009
Duplications of the functional CYP21A2 gene are primarily restricted to Q318X alleles: evidence for a founder effectS Kleinle, R Lang, G F Fischer, et al.
The Journal of Clinical Endocrinology and Metabolism|July 10, 2001
Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countriesJ Kovács, F Votava, G Heinze, et al.
Hormone Research|October 13, 2001
Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency. Results of a multicenter studyG Hargitai, J Sólyom, T Battelino, et al.
Hormone Research|June 18, 2002
Congenital adrenal hyperplasia: lessons from a multinational studyH Frisch, F Waldhauser, J Lebl, et al.
The Journal of Clinical Endocrinology and Metabolism|October 16, 2001
Mutational spectrum of the steroid 21-hydroxylase gene in Austria: identification of a novel missense mutationS M Baumgartner-Parzer, E Schulze, W Waldhäusl, et al.
Neuroendocrinology|August 1, 1987
A pharmacological dose of melatonin increases PRL levels in males without altering those of GH, LH, FSH, TSH, testosterone or cortisolF Waldhauser, H R Lieberman, H J Lynch, et al.
Human Genetics|July 1, 1995
Clinical phenotype of nephrogenic diabetes insipidus in females heterozygous for a vasopressin type 2 receptor mutationA F van Lieburg, M A Verdijk, F Schoute, et al.
Pageof 8