Որոնման արդյունքները - Mireille Castanet
- Ցուցադրվում են 1 - 19 արդյունքները 19
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Spectrum of Human <i>Foxe1/TTF2</i> Mutations Mireille Castanet, Michel Polak
Հրապարակվել է 2010Revisão -
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Nineteen Years of National Screening for Congenital Hypothyroidism: Familial Cases with Thyroid Dysgenesis Suggest the Involvement of Genetic Factors Mireille Castanet, Michel Polak, Catherine Bonaïti‐Pellié, Stanislas Lyonnet, Paul Czernichow, Juliane Léger
Հրապարակվել է 2001Artigo -
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Experience with Intraamniotic Thyroxine Treatment in Nonimmune Fetal Goitrous Hypothyroidism in 12 Cases Virginie Ribault, Mireille Castanet, Anne‐Marie Bertrand, Jean Guibourdenche, Edith Vuillard, Dominique Luton, Michel Polak
Հրապարակվել է 2009Artigo -
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A Novel<i>FOXE1</i>Mutation (R73S) in Bamforth–Lazarus Syndrome Causing Increased Thyroidal Gene Expression Aurore Carré, Rasha T. Hamza, Dulanjalee Kariyawasam, Loïc Guillot, Raphaël Teissier, Elodie Tron, Mireille Castanet, Corinne Dupuy, Mohamed El Kholy, Michel Polak
Հրապարակվել է 2013Artigo -
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<i>NKX2-1</i>mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in “Brain-Lung-Thyroid Syndrome” Loïc Guillot, Aurore Carré, Gabor Szinnai, Mireille Castanet, Elodie Tron, Francis Jaubert, Isabelle Broutin, François Counil, Delphine Feldmann, Annick Clement, Michel Polak, Ralph Epaud
Հրապարակվել է 2009Artigo -
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European cystic fibrosis bone mineralisation guidelines Isabelle Sermet‐Gaudelus, Maria Luisa Bianchi, Michèle Garabédian, Robert M. Aris, Alison Morton, Dana S. Hardin, Sarah Elkin, Juliet Compston, S.P. Conway, Mireille Castanet, Susan Wolfe, Charles Haworth
Հրապարակվել է 2011Artigo -
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Early Effect of Supplemented Infant Formulae on Intestinal Biomarkers and Microbiota: A Randomized Clinical Trial Mireille Castanet, Christos Costalos, Nadja Haiden, Jean‐Michel Hascoët, Bernard Berger, Norbert Sprenger, Dominik Grathwohl, Harald Brüssow, Nanda de Groot, Philippe Steenhout, Sophie Pecquet, Jalil Benyacoub, Jean‐Charles Picaud
Հրապարակվել է 2020Artigo -
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Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations Helton Estrela Ramos, Aurore Carré, L. Chevrier, Gabor Szinnai, Elodie Tron, Taíse Lima Oliveira Cerqueira, Juliane Léger, S Cabrol, Olivia Puel, C Queinnec, Nicolás de Roux, Loïc Guillot, Mireille Castanet, Michel Polak
Հրապարակվել է 2014Artigo -
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Unbalanced Expression of 11p15 Imprinted Genes in Focal Forms of Congenital Hyperinsulinism Jean‐Christophe Fournet, Christine Mayaud, Pascale de Lonlay, M S Gross-Morand, Virginie Verkarre, Mireille Castanet, Martine Devillers, Jacques Rahier, Françis Brunelle, Jean‐Jacques Robert, Claire Nihoul‐Feketé, Jean‐Marie Saudubray, Claudine Junien
Հրապարակվել է 2001Artigo -
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Pregnancy in women heterozygous for MCT8 mutations: risk of maternal hypothyroxinemia and fetal care Helton Estrela Ramos, Mélina Morandini, Aurore Carré, Elodie Tron, Corinne Floch, Laurent Mandelbrot, Nathalie Neri, Benoit De Sarcus, Albane Simon, Jean‐Paul Bonnefont, Jeanne Amiel, Isabelle Desguerre, Vassili Valayannopoulos, Mireille Castanet, Michel Polak
Հրապարակվել է 2010Artigo -
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Management of Graves’ Disease during Pregnancy: The Key Role of Fetal Thyroid Gland Monitoring Dominique Luton, Isabelle Le Gac, Edith Vuillard, Mireille Castanet, Jean Guibourdenche, Michèle Noël, Marie‐Elisabeth Toubert, Juliane Léger, C. Boissinot, Marie‐Hélène Schlageter, Cathérine Garel, Brigitte Tébeka, Jean‐François Oury, Paul Czernichow, Michel Polak
Հրապարակվել է 2005Artigo -
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Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper Justine Bacchetta, Thomas Édouard, Gilles Laverny, Julie Bernardor, Aurélia Bertholet‐Thomas, Mireille Castanet, C. Garnier, Isabelle Gennero, J. Harambat, Alexandre Lapillonne, Arnaud Molin, C. Naud, Jean‐Pierre Salles, Sophie Laborie, Patrick Tounian, Agnès Linglart
Հրապարակվել է 2022Artigo -
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Five new TTF1/NKX2.1 mutations in brain-lung-thyroid syndrome: rescue by PAX8 synergism in one case Aurore Carré, Gabor Szinnai, Mireille Castanet, Sylvia Sura‐Trueba, Elodie Tron, Isabelle Broutin, Pascal Barat, Cyril Goizet, Didier Lacombe, M.L. Moutard, C. Raybaud, C. Raynaud-Ravni, Serge Romana, H Ythier, Juliane Léger, Mirosław P. Polak
Հրապարակվել է 2009Artigo -
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Mutations in the selenocysteine insertion sequence–binding protein 2 gene lead to a multisystem selenoprotein deficiency disorder in humans Erik Schoenmakers, Maura Agostini, Catherine Mitchell, Nadia Schoenmakers, Laura V. Papp, Odelia Rajanayagam, Raja Padidela, Lourdes Ceron‐Gutierrez, Rainer Döffinger, Claudia Prevosto, Jian’an Luan, Sergio Montaño, Jun Lu, Mireille Castanet, Nicholas J. Clemons, Matthijs Groeneveld, Perrine Castets, Mahsa Karbaschi, Sri W. Aitken, Adrian Dixon, Jane Williams, Irene Campi, Margaret Blount, H. Burton, Francesco Muntoni, Dominic G. O’Donovan, Andrew Dean, A Jane Warren, Charlotte Brierley, David Baguley, Pascale Guicheney, Rebecca C. Fitzgerald, Alasdair Coles, Hill Gaston, Pamela Todd, Arne Holmgren, Kum Kum Khanna, Marcus S. Cooke, Robert K. Semple, David Halsall, Nicholas J. Wareham, John W. R. Schwabe, L. Grasso, Paolo Beck‐Peccoz, Arthur Ogunko, Mehul Dattani, Mark Gurnell, Krishna Chatterjee
Հրապարակվել է 2010Artigo
Որոնման գործիքներ:
Առնչվող խորագիր
Medicine
Internal medicine
Biology
Genetics
Endocrinology
Thyroid
Gene
Mutation
Congenital hypothyroidism
Pediatrics
Pregnancy
Fetus
Anatomy
Environmental health
Missense mutation
Population
Thyroid function
Agenesis
Biochemistry
Dysgenesis
Euthyroid
Gastroenterology
Gene expression
Graves' disease
Gynecology
Immunology
Lung
Obstetrics
Pathology
Thyroid function tests