Mireille Castanet

Mireille Castanet

UNVERIFIED PROFILE

Are you Mireille Castanet?   Register this Author

Register author
Mireille Castanet

Mireille Castanet

Publications by authors named "Mireille Castanet"

Are you Mireille Castanet?   Register this Author

38Publications

595Reads

11Profile Views

Paracrine Regulation of Aldosterone Secretion in Physiological and Pathophysiological Conditions.

Vitam Horm 2019 1;109:303-339. Epub 2018 Dec 1.

Laboratory of Neuronal and Neuroendocrine Differentiation and Communication, Normandie University, UNIROUEN, INSERM, Rouen, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/bs.vh.2018.10.001DOI Listing
April 2019

Hyperinsulinemic Hypoglycemia in a Neonate.

Clin Chem 2019 Feb;65(2):351-353

Department of Metabolic Biochemistry, Rouen University Hospital, Rouen, France;

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1373/clinchem.2018.292326DOI Listing
February 2019

Molecular characterization of a recurrent 10.9 kb CYP24A1 deletion in Idiopathic Infantile Hypercalcemia.

Eur J Med Genet 2018 Nov 10:103577. Epub 2018 Nov 10.

CHU de Caen, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism, Caen, F-14000, France; Université Caen Normandie, Medical School, Caen, F14000, France; BioTARGEN, Université Caen Normandie, Caen, F14000, France.

View Article

Download full-text PDF

Source
https://linkinghub.elsevier.com/retrieve/pii/S17697212183026
Publisher Site
http://dx.doi.org/10.1016/j.ejmg.2018.11.011DOI Listing
November 2018

Temporal and spatial distribution of mast cells and steroidogenic enzymes in the human fetal adrenal.

Mol Cell Endocrinol 2016 10 11;434:69-80. Epub 2016 Jun 11.

INSERM U982, Laboratory of Differentiation & Neuronal and Neuroendocrine Communication, Institute for Research and Innovation in Biomedicine, University of Rouen, Mont-Saint-Aignan, France. Electronic address:

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.mce.2016.06.015DOI Listing
October 2016

Metallic Profile of Whole Blood and Plasma in a Series of 99 Healthy Children.

J Anal Toxicol 2015 Nov-Dec;39(9):707-13. Epub 2015 Aug 10.

Laboratoire de Toxicologie, ABTE ToxEMAC EA 4651, Faculté de Médecine et de Pharmacie, 22 boulevard Gambetta, 76183 Rouen Cedex 1, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1093/jat/bkv088DOI Listing
August 2016

Molecular insights into the possible role of Kir4.1 and Kir5.1 in thyroid hormone biosynthesis.

Horm Res Paediatr 2015 22;83(2):141-7. Epub 2015 Jan 22.

INSERM U1016, Université Paris Descartes, Sorbonne Paris Cité, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000369251DOI Listing
December 2015

Natural history and management of congenital hypothyroidism with in situ thyroid gland.

Horm Res Paediatr 2015 28;83(2):102-10. Epub 2015 Jan 28.

Service d'Endocrinologie, Gynécologie et Diabétologie Pédiatrique, Hôpital Universitaire Necker-Enfants Malades, AP-HP, Paris, France.

View Article

Download full-text PDF

Source
https://www.karger.com/Article/FullText/362234
Publisher Site
http://dx.doi.org/10.1159/000362234DOI Listing
December 2015

Pharmacokinetic study of metopimazine by oral route in children.

Pharmacol Res Perspect 2015 Jun 1;3(3):e00130. Epub 2015 Jun 1.

CIC INSERM 204, Department of Pediatrics, Rouen University Hospital Charles Nicolle, 76031, Rouen, France.

View Article

Download full-text PDF

Source
http://doi.wiley.com/10.1002/prp2.130
Publisher Site
http://dx.doi.org/10.1002/prp2.130DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4492748PMC
June 2015

A novel FOXE1 mutation (R73S) in Bamforth-Lazarus syndrome causing increased thyroidal gene expression.

Thyroid 2014 Apr 23;24(4):649-54. Epub 2014 Jan 23.

1 Research Center for Growth and Signaling (INSERM U845), Université Paris Descartes , Sorbonne Paris Cité, Paris, France .

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1089/thy.2013.0417DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3993030PMC
April 2014

Lightwood syndrome revisited with a novel mutation in CYP24 and vitamin D supplement recommendations.

J Pediatr 2013 Oct 14;163(4):1208-10. Epub 2013 Jun 14.

Department of Pediatrics, National Reference Center for Rare Calcium and Phosphorus Metabolism Diseases, Rouen University Hospital and CIC INSERM 204, Rouen University Faculty of Medicine, Rouen, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.jpeds.2013.04.056DOI Listing
October 2013

European cystic fibrosis bone mineralisation guidelines.

J Cyst Fibros 2011 Jun;10 Suppl 2:S16-23

Pôle de Pediatric Multidisciplinaire, Hôpital Necker, Université René Descartes, 75015 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/S1569-1993(11)60004-0DOI Listing
June 2011

Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care.

Eur J Endocrinol 2011 Feb 23;164(2):309-14. Epub 2010 Nov 23.

INSERM U845 Pediatric Endocrinology and Gynecology, Centre des Maladies Endocriniennes Rares de la Croissance, AP-HP, Necker-Enfants Malades Hospital, Université Paris Descartes, 75743 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1530/EJE-10-0679DOI Listing
February 2011

Maternal isodisomy for chromosome 9 causing homozygosity for a novel FOXE1 mutation in syndromic congenital hypothyroidism.

J Clin Endocrinol Metab 2010 Aug 19;95(8):4031-6. Epub 2010 May 19.

University of Cambridge, Metabolic Research Laboratories, Institute of Metabolic Science, Department of Medicine, Level 4, Box 289, Addenbrooke's Hospital, Cambridge CB2 0QQ, United Kingdom.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2010-0275DOI Listing
August 2010

Spectrum of Human Foxe1/TTF2 Mutations.

Horm Res Paediatr 2010 6;73(6):423-9. Epub 2010 May 6.

Faculty of Medicine René Descartes, Paris V, Site Necker, Institut National de la Santé et de la Recherche Médicale (INSERM) U845 and Pediatric Endocrine Unit, Assistance Publique - Hôpitaux de PARIS (AP-HP), Hôpital Necker Enfants-Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000281438DOI Listing
July 2010

Epidemiology of thyroid dysgenesis: the familial component.

Horm Res Paediatr 2010 9;73(4):231-7. Epub 2010 Mar 9.

Paediatric Endocrinology Unit and INSERM U363, Hôpital Necker Enfants-Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000284386DOI Listing
June 2010

New cases of isolated congenital central hypothyroidism due to homozygous thyrotropin beta gene mutations: a pitfall to neonatal screening.

Thyroid 2010 Jun;20(6):639-45

Centre des Maladies Endocriniennes Rares de la Croissance, Hôpital Necker Enfants-Malade, Assistance Publique-Hôpitaux de PARIS, Institut National de la Santé et de la Recherche Médicale U845 and Pediatric Endocrine Unit, Université Paris Descartes, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1089/thy.2009.0462DOI Listing
June 2010

Experience with intraamniotic thyroxine treatment in nonimmune fetal goitrous hypothyroidism in 12 cases.

J Clin Endocrinol Metab 2009 Oct 8;94(10):3731-9. Epub 2009 Sep 8.

Department of Pediatrics, Clemenceau Hospital, Caen, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2008-2681DOI Listing
October 2009

Update on cystic fibrosis-related bone disease: a special focus on children.

Paediatr Respir Rev 2009 Sep 17;10(3):134-42. Epub 2009 Jul 17.

Centre de Référence et de Compétence en Mucoviscidose, Hopital Necker-Enfants Malades, INSERM U 845, Université René Descartes, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1016/j.prrv.2009.05.001DOI Listing
September 2009

Clinical description of infants with congenital hypothyroidism and iodide organification defects.

Horm Res 2008 5;70(4):240-8. Epub 2008 Sep 5.

Pediatric Endocrinology Unit, Hôpital Necker-Enfants Malades, AP-HP and University Paris Descartes, Faculty Necker, INSERM U845, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000151597DOI Listing
December 2008

Predictors of autoimmune hyperthyroidism relapse in children after discontinuation of antithyroid drug treatment.

J Clin Endocrinol Metab 2008 Oct 15;93(10):3817-26. Epub 2008 Jul 15.

Institut National de la Santé et de la Recherche Médicale U690, Hôpital Robert Debré, 75019 Paris, France.

View Article

Download full-text PDF

Source
https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
Publisher Site
http://dx.doi.org/10.1210/jc.2008-0842DOI Listing
October 2008

Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesis.

Hum Genet 2007 Dec 24;122(5):467-76. Epub 2007 Aug 24.

Faculty of Medicine René Descartes, Paris V, Site Necker, Institut National de la Santé et de la Recherche Médicale U845 and Pediatric Endocrine Unit Assistance Publique-Hôpitaux de PARIS, Hôpital Necker Enfants-Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1007/s00439-007-0420-5DOI Listing
December 2007

Familial forms of thyroid dysgenesis.

Endocr Dev 2007 ;10:15-28

Paediatric Endocrinology Unit and INSERM U845, Hôpital Necker-Enfants Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000106817DOI Listing
October 2007

High proportion of pituitary abnormalities and other congenital defects in children with congenital nasal pyriform aperture stenosis.

Pediatr Res 2006 Oct 28;60(4):478-84. Epub 2006 Aug 28.

Pediatric Endocrinology and Diabetes Unit, Centre de Référence Maladies Endocriniennes Rares de la Croissance, Hôpital Robert Debré, Assistance Publique-Hôpitaux de Paris, Paris VII University, 75019 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1203/01.pdr.0000238380.03683.cbDOI Listing
October 2006

Congenital hyperthyroidism: the fetus as a patient.

Horm Res 2006 30;65(5):235-42. Epub 2006 Mar 30.

INSERM 0363, AP-HP, Paris Descartes University, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000092454DOI Listing
June 2006

Insulin allergy and extensive lipoatrophy in child with type 1 diabetes.

Horm Res 2006 14;65(5):253-60. Epub 2006 Mar 14.

Inserm U 690 'Diabète de l'enfant et développement', Robert Debré Hospital, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000092515DOI Listing
June 2006

Management of Graves' disease during pregnancy: the key role of fetal thyroid gland monitoring.

J Clin Endocrinol Metab 2005 Nov 23;90(11):6093-8. Epub 2005 Aug 23.

Department of Perinatology, Multidisciplinary Center for Prenatal Diagnosis, Robert Debré Hospital, 75019 Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1210/jc.2004-2555DOI Listing
November 2005

Molecular mechanisms of thyroid dysgenesis.

Horm Res 2004 ;62 Suppl 3:14-21

Paediatric Endocrinology, Hôpital Necker-Enfants Malades, Paris, France.

View Article

Download full-text PDF

Source
http://dx.doi.org/10.1159/000080494DOI Listing
June 2005