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Udo Heinrich

Showing results (1-10 of 8) with videos related to

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Fertility and Sterility|March 2, 2002
Conception and spontaneous delivery after total hypophysectomyJoachim Volz, Udo Heinrich, Stefanie Volz-Köster
Hormone Research|July 24, 2003
Growth analysis in patients with 21-hydroxylase deficiency influence of glucocorticoid dosage, age at diagnosis, phenotype and genotype on growth and height outcomeAnca Grigorescu-Sido, Markus Bettendorf, Egbert Schulze, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Heterozygous nonsense mutation in exon 3 of the growth hormone receptor (GHR) in severe GH insensitivity (Laron syndrome) and the issue of the origin and function of the GHRd3 isoformJacques Pantel, Jürgen Grulich-Henn, Markus Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 31, 2002
Mutational analysis and genotype-phenotype correlation in patients with classic 21-hydroxylase deficiency from transylvania (north-west Romania)Anca Grigorescu-Sido, Egbert Schulze, Paula Grigorescu-Sido, et al.
The Journal of Clinical Endocrinology and Metabolism|July 28, 2005
21-Hydroxylase and 11beta-hydroxylase mutations in Romanian patients with classic congenital adrenal hyperplasiaAnca Grigorescu Sido, Matthias M Weber, Paula Grigorescu Sido, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Three new 46,XX male patients: a clinical, cytogenetic and molecular analysisAnca Grigorescu-Sido, Udo Heinrich, Paula Grigorescu-Sido, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 24, 2007
MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarismAnca Zimmermann, Jens-Peter Schenk, Paula Grigorescu Sido, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short statureGudrun A Rappold, Maki Fukami, Beate Niesler, et al.
Pageof 1

Showing results (1-10 of 8) with videos related to

Sort By:
Pageof 1
Fertility and Sterility|March 2, 2002
Conception and spontaneous delivery after total hypophysectomyJoachim Volz, Udo Heinrich, Stefanie Volz-Köster
Hormone Research|July 24, 2003
Growth analysis in patients with 21-hydroxylase deficiency influence of glucocorticoid dosage, age at diagnosis, phenotype and genotype on growth and height outcomeAnca Grigorescu-Sido, Markus Bettendorf, Egbert Schulze, et al.
The Journal of Clinical Endocrinology and Metabolism|April 8, 2003
Heterozygous nonsense mutation in exon 3 of the growth hormone receptor (GHR) in severe GH insensitivity (Laron syndrome) and the issue of the origin and function of the GHRd3 isoformJacques Pantel, Jürgen Grulich-Henn, Markus Bettendorf, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|December 31, 2002
Mutational analysis and genotype-phenotype correlation in patients with classic 21-hydroxylase deficiency from transylvania (north-west Romania)Anca Grigorescu-Sido, Egbert Schulze, Paula Grigorescu-Sido, et al.
The Journal of Clinical Endocrinology and Metabolism|July 28, 2005
21-Hydroxylase and 11beta-hydroxylase mutations in Romanian patients with classic congenital adrenal hyperplasiaAnca Grigorescu Sido, Matthias M Weber, Paula Grigorescu Sido, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|March 9, 2005
Three new 46,XX male patients: a clinical, cytogenetic and molecular analysisAnca Grigorescu-Sido, Udo Heinrich, Paula Grigorescu-Sido, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 24, 2007
MRI findings and genotype analysis in patients with childhood onset growth hormone deficiency--correlation with severity of hypopituitarismAnca Zimmermann, Jens-Peter Schenk, Paula Grigorescu Sido, et al.
The Journal of Clinical Endocrinology and Metabolism|March 13, 2002
Deletions of the homeobox gene SHOX (short stature homeobox) are an important cause of growth failure in children with short statureGudrun A Rappold, Maki Fukami, Beate Niesler, et al.
Pageof 1