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Hormone Research in Paediatrics
|
May 11, 2010
Spectrum of Human Foxe1/TTF2 Mutations
Mireille Castanet, Michel Polak
Endocrine Development
|
August 9, 2007
Familial forms of thyroid dysgenesis
Mireille Castanet, Michel Polak, Juliane Léger
The Journal of Pediatrics
|
June 18, 2013
Lightwood syndrome revisited with a novel mutation in CYP24 and vitamin D supplement recommendations
Mireille Castanet, Eric Mallet, Marie-Laure Kottler
Hormone Research in Paediatrics
|
March 11, 2010
Epidemiology of thyroid dysgenesis: the familial component
Mireille Castanet, Daniela Marinovic, Michel Polak, et al.
Paediatric Respiratory Reviews
|
August 5, 2009
Update on cystic fibrosis-related bone disease: a special focus on children
Isabelle Sermet-Gaudelus, Mireille Castanet, George Retsch-Bogart, et al.
Endocrine Development
|
June 11, 2018
Fertility Preservation in Klinefelter Syndrome Patients during the Transition Period
Nathalie Rives, Aurélie Rives, Christine Rondanino, et al.
Hormone Research
|
April 4, 2006
Congenital hyperthyroidism: the fetus as a patient
Michel Polak, Isabelle Legac, Edith Vuillard, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 17, 2008
Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment
Florentia Kaguelidou, Corinne Alberti, Mireille Castanet, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 28, 2020
Role of Mast Cells in the Control of Aldosterone Secretion
Antoine-Guy Lopez, Céline Duparc, Alexandre Naccache, et al.
Vitamins and Hormones
|
January 26, 2019
Paracrine Regulation of Aldosterone Secretion in Physiological and Pathophysiological Conditions
Hervé Lefebvre, Céline Duparc, Alexandre Naccache, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 47) with videos related to
Sort By:
Page
of 5
Hormone Research in Paediatrics
|
May 11, 2010
Spectrum of Human Foxe1/TTF2 Mutations
Mireille Castanet, Michel Polak
Endocrine Development
|
August 9, 2007
Familial forms of thyroid dysgenesis
Mireille Castanet, Michel Polak, Juliane Léger
The Journal of Pediatrics
|
June 18, 2013
Lightwood syndrome revisited with a novel mutation in CYP24 and vitamin D supplement recommendations
Mireille Castanet, Eric Mallet, Marie-Laure Kottler
Hormone Research in Paediatrics
|
March 11, 2010
Epidemiology of thyroid dysgenesis: the familial component
Mireille Castanet, Daniela Marinovic, Michel Polak, et al.
Paediatric Respiratory Reviews
|
August 5, 2009
Update on cystic fibrosis-related bone disease: a special focus on children
Isabelle Sermet-Gaudelus, Mireille Castanet, George Retsch-Bogart, et al.
Endocrine Development
|
June 11, 2018
Fertility Preservation in Klinefelter Syndrome Patients during the Transition Period
Nathalie Rives, Aurélie Rives, Christine Rondanino, et al.
Hormone Research
|
April 4, 2006
Congenital hyperthyroidism: the fetus as a patient
Michel Polak, Isabelle Legac, Edith Vuillard, et al.
The Journal of Clinical Endocrinology and Metabolism
|
July 17, 2008
Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment
Florentia Kaguelidou, Corinne Alberti, Mireille Castanet, et al.
Hormone and Metabolic Research = Hormon- Und Stoffwechselforschung = Hormones Et Metabolisme
|
March 28, 2020
Role of Mast Cells in the Control of Aldosterone Secretion
Antoine-Guy Lopez, Céline Duparc, Alexandre Naccache, et al.
Vitamins and Hormones
|
January 26, 2019
Paracrine Regulation of Aldosterone Secretion in Physiological and Pathophysiological Conditions
Hervé Lefebvre, Céline Duparc, Alexandre Naccache, et al.
Page
of 5