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Primus E Mullis

Showing results (81-90 of 97) with videos related to

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The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasiaChrista E Flück, Alexander Maret, Delphine Mallet, et al.
European Journal of Endocrinology|December 3, 2005
Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretionSouzan Salemi, Shida Yousefi, Kurt Baltensperger, et al.
European Journal of Endocrinology|February 19, 2013
Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GHVibor Petkovic, Maria Consolata Miletta, Annemieke M Boot, et al.
Plos One|June 8, 2011
Characterization of novel StAR (steroidogenic acute regulatory protein) mutations causing non-classic lipoid adrenal hyperplasiaChrista E Flück, Amit V Pandey, Bernhard Dick, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 2005
Isolated autosomal dominant growth hormone deficiency: an evolving pituitary deficit? A multicenter follow-up studyPrimus E Mullis, Iain C A F Robinson, Souzan Salemi, et al.
European Journal of Endocrinology|August 21, 2015
Human 3β-hydroxysteroid dehydrogenase deficiency seems to affect fertility but may not harbor a tumor risk: lesson from an experiment of natureMarie-Anne Burckhardt, Sameer S Udhane, Nesa Marti, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2007
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiencyVibor Petkovic, Didier Lochmatter, James Turton, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 17, 2014
Radiometrical, hormonal and biological correlates of skeletal growth in the female rat from birth to senescenceEmilio del Pozo, Marco Janner, Andrew R Mackenzie, et al.
Hormone Research in Paediatrics|February 14, 2015
Natural history of growth hormone deficiency in a pediatric cohortEva Deillon, Michael Hauschild, Mohamed Faouzi, et al.
Clinical Endocrinology|October 27, 2011
Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiencyMaria Consolata Miletta, Ursina A Scheidegger, Mara Giordano, et al.
Pageof 10

Showing results (81-90 of 97) with videos related to

Sort By:
Pageof 10
The Journal of Clinical Endocrinology and Metabolism|June 30, 2005
A novel mutation L260P of the steroidogenic acute regulatory protein gene in three unrelated patients of Swiss ancestry with congenital lipoid adrenal hyperplasiaChrista E Flück, Alexander Maret, Delphine Mallet, et al.
European Journal of Endocrinology|December 3, 2005
Variability of isolated autosomal dominant GH deficiency (IGHD II): impact of the P89L GH mutation on clinical follow-up and GH secretionSouzan Salemi, Shida Yousefi, Kurt Baltensperger, et al.
European Journal of Endocrinology|February 19, 2013
Short stature in two siblings heterozygous for a novel bioinactive GH mutant (GH-P59S) suggesting that the mutant also affects secretion of the wild-type GHVibor Petkovic, Maria Consolata Miletta, Annemieke M Boot, et al.
Plos One|June 8, 2011
Characterization of novel StAR (steroidogenic acute regulatory protein) mutations causing non-classic lipoid adrenal hyperplasiaChrista E Flück, Amit V Pandey, Bernhard Dick, et al.
The Journal of Clinical Endocrinology and Metabolism|January 27, 2005
Isolated autosomal dominant growth hormone deficiency: an evolving pituitary deficit? A multicenter follow-up studyPrimus E Mullis, Iain C A F Robinson, Souzan Salemi, et al.
European Journal of Endocrinology|August 21, 2015
Human 3β-hydroxysteroid dehydrogenase deficiency seems to affect fertility but may not harbor a tumor risk: lesson from an experiment of natureMarie-Anne Burckhardt, Sameer S Udhane, Nesa Marti, et al.
The Journal of Clinical Endocrinology and Metabolism|August 30, 2007
Exon splice enhancer mutation (GH-E32A) causes autosomal dominant growth hormone deficiencyVibor Petkovic, Didier Lochmatter, James Turton, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|April 17, 2014
Radiometrical, hormonal and biological correlates of skeletal growth in the female rat from birth to senescenceEmilio del Pozo, Marco Janner, Andrew R Mackenzie, et al.
Hormone Research in Paediatrics|February 14, 2015
Natural history of growth hormone deficiency in a pediatric cohortEva Deillon, Michael Hauschild, Mohamed Faouzi, et al.
Clinical Endocrinology|October 27, 2011
Association of the (CA)n repeat polymorphism of insulin-like growth factor-I and -202 A/C IGF-binding protein-3 promoter polymorphism with adult height in patients with severe growth hormone deficiencyMaria Consolata Miletta, Ursina A Scheidegger, Mara Giordano, et al.
Pageof 10