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Primus E Mullis

Showing results (71-80 of 97) with videos related to

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Clinical Endocrinology|October 27, 2015
A 2-year multicentre, open-label, randomized, controlled study of growth hormone (Genotropin®) treatment in very young children born small for gestational age: Early Growth and Neurodevelopment (EGN) StudyJean De Schepper, Johan Vanderfaeillie, Primus-E Mullis, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|May 7, 2011
A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type II combined with bioinactive GH syndromeVibor Petkovic, Andrée Eblé, Amit V Pandey, et al.
Hormone Research in Paediatrics|March 1, 2013
Towards optimal treatment with growth hormone in short children and adolescents: evidence and thesesMichael B Ranke, Anders Lindberg, Primus E Mullis, et al.
International Journal of Endocrinology|November 7, 2013
Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn (2+) for Normal Growth and DevelopmentMaria Consolata Miletta, Andreas Bieri, Kristin Kernland, et al.
Thyroid : Official Journal of the American Thyroid Association|August 22, 2003
Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and ArgentinaJohnny Deladoëy, Jean-Marc Vuissoz, Horacio M Domené, et al.
Endocrinology|October 14, 2006
Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosisSouzan Salemi, Shida Yousefi, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|February 17, 2005
Short stature caused by a biologically inactive mutant growth hormone (GH-C53S)Amélie Besson, Souzan Salemi, Johnny Deladoëy, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2007
Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiencyBarbara Räz, Marco Janner, Vibor Petkovic, et al.
The Journal of Endocrinology|May 1, 2009
Role of DNA methylation in the tissue-specific expression of the CYP17A1 gene for steroidogenesis in rodentsElika Missaghian, Petra Kempná, Bernhard Dick, et al.
The Journal of Clinical Endocrinology and Metabolism|December 3, 2009
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and actionVibor Petkovic, Michela Godi, Amit V Pandey, et al.
Pageof 10

Showing results (71-80 of 97) with videos related to

Sort By:
Pageof 10
Clinical Endocrinology|October 27, 2015
A 2-year multicentre, open-label, randomized, controlled study of growth hormone (Genotropin®) treatment in very young children born small for gestational age: Early Growth and Neurodevelopment (EGN) StudyJean De Schepper, Johan Vanderfaeillie, Primus-E Mullis, et al.
Growth Hormone & IGF Research : Official Journal of the Growth Hormone Research Society and the International IGF Research Society|May 7, 2011
A novel GH-1 gene mutation (GH-P59L) causes partial GH deficiency type II combined with bioinactive GH syndromeVibor Petkovic, Andrée Eblé, Amit V Pandey, et al.
Hormone Research in Paediatrics|March 1, 2013
Towards optimal treatment with growth hormone in short children and adolescents: evidence and thesesMichael B Ranke, Anders Lindberg, Primus E Mullis, et al.
International Journal of Endocrinology|November 7, 2013
Transient Neonatal Zinc Deficiency Caused by a Heterozygous G87R Mutation in the Zinc Transporter ZnT-2 (SLC30A2) Gene in the Mother Highlighting the Importance of Zn (2+) for Normal Growth and DevelopmentMaria Consolata Miletta, Andreas Bieri, Kristin Kernland, et al.
Thyroid : Official Journal of the American Thyroid Association|August 22, 2003
Congenital secondary hypothyroidism due to a mutation C105Vfs114X thyrotropin-beta mutation: genetic study of five unrelated families from Switzerland and ArgentinaJohnny Deladoëy, Jean-Marc Vuissoz, Horacio M Domené, et al.
Endocrinology|October 14, 2006
Isolated autosomal dominant growth hormone deficiency: stimulating mutant GH-1 gene expression drives GH-1 splice-site selection, cell proliferation, and apoptosisSouzan Salemi, Shida Yousefi, Didier Lochmatter, et al.
The Journal of Clinical Endocrinology and Metabolism|February 17, 2005
Short stature caused by a biologically inactive mutant growth hormone (GH-C53S)Amélie Besson, Souzan Salemi, Johnny Deladoëy, et al.
The Journal of Clinical Endocrinology and Metabolism|November 22, 2007
Influence of growth hormone (GH) receptor deletion of exon 3 and full-length isoforms on GH response and final height in patients with severe GH deficiencyBarbara Räz, Marco Janner, Vibor Petkovic, et al.
The Journal of Endocrinology|May 1, 2009
Role of DNA methylation in the tissue-specific expression of the CYP17A1 gene for steroidogenesis in rodentsElika Missaghian, Petra Kempná, Bernhard Dick, et al.
The Journal of Clinical Endocrinology and Metabolism|December 3, 2009
Growth hormone (GH) deficiency type II: a novel GH-1 gene mutation (GH-R178H) affecting secretion and actionVibor Petkovic, Michela Godi, Amit V Pandey, et al.
Pageof 10