Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Mireille Castanet

Showing results (31-40 of 47) with videos related to

Pageof 5
Sort By:
Human Reproduction (Oxford, England)|January 14, 2026
Fertility preservation and counselling in prepubertal and pubertal girls with Turner syndromeAlix Sage, Nathalie Rives, Romane Levadé, et al.
Human Mutation|December 19, 2009
NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome"Loïc Guillot, Aurore Carré, Gabor Szinnai, et al.
Hormone Research in Paediatrics|January 24, 2015
Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesisHelton Estrela Ramos, Magnus Régios Dias da Silva, Aurore Carré, et al.
Pediatric Research|August 31, 2006
High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosisSophie Guilmin-Crépon, Catherine Garel, Clarisse Baumann, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portionTaise Lima Oliveira Cerqueira, Aurore Carré, Lucie Chevrier, et al.
Nutrients|May 24, 2020
Early Effect of Supplemented Infant Formulae on Intestinal Biomarkers and Microbiota: A Randomized Clinical TrialMireille Castanet, Christos Costalos, Nadja Haiden, et al.
Hormone Research in Paediatrics|April 11, 2012
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndromeRaphaël Teissier, Loïc Guillot, Aurore Carré, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
European cystic fibrosis bone mineralisation guidelinesIsabelle Sermet-Gaudelus, Maria Luisa Bianchi, Michèle Garabédian, et al.
European Journal of Endocrinology|November 25, 2010
Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal careHelton Estrela Ramos, Melina Morandini, Aurore Carré, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2005
Management of Graves' disease during pregnancy: the key role of fetal thyroid gland monitoringDominique Luton, Isabelle Le Gac, Edith Vuillard, et al.
Pageof 5

Showing results (31-40 of 47) with videos related to

Sort By:
Pageof 5
Human Reproduction (Oxford, England)|January 14, 2026
Fertility preservation and counselling in prepubertal and pubertal girls with Turner syndromeAlix Sage, Nathalie Rives, Romane Levadé, et al.
Human Mutation|December 19, 2009
NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome"Loïc Guillot, Aurore Carré, Gabor Szinnai, et al.
Hormone Research in Paediatrics|January 24, 2015
Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesisHelton Estrela Ramos, Magnus Régios Dias da Silva, Aurore Carré, et al.
Pediatric Research|August 31, 2006
High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosisSophie Guilmin-Crépon, Catherine Garel, Clarisse Baumann, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 26, 2014
Functional characterization of the novel sequence variant p.S304R in the hinge region of TSHR in a congenital hypothyroidism patients and analogy with other formerly known mutations of this gene portionTaise Lima Oliveira Cerqueira, Aurore Carré, Lucie Chevrier, et al.
Nutrients|May 24, 2020
Early Effect of Supplemented Infant Formulae on Intestinal Biomarkers and Microbiota: A Randomized Clinical TrialMireille Castanet, Christos Costalos, Nadja Haiden, et al.
Hormone Research in Paediatrics|April 11, 2012
Multiplex Ligation-dependent Probe Amplification improves the detection rate of NKX2.1 mutations in patients affected by brain-lung-thyroid syndromeRaphaël Teissier, Loïc Guillot, Aurore Carré, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|June 11, 2011
European cystic fibrosis bone mineralisation guidelinesIsabelle Sermet-Gaudelus, Maria Luisa Bianchi, Michèle Garabédian, et al.
European Journal of Endocrinology|November 25, 2010
Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal careHelton Estrela Ramos, Melina Morandini, Aurore Carré, et al.
The Journal of Clinical Endocrinology and Metabolism|August 25, 2005
Management of Graves' disease during pregnancy: the key role of fetal thyroid gland monitoringDominique Luton, Isabelle Le Gac, Edith Vuillard, et al.
Pageof 5