検索結果 - Anne‐Lise Delezoide

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  1. 1
    Undersulfation of Proteoglycans Synthesized by Chondrocytes from a Patient with Achondrogenesis Type 1B Homozygous for an L483P Substitution in the Diastrophic Dysplasia Sulfate Transporter

    Undersulfation of Proteoglycans Synthesized by Chondrocytes from a Patient with Achondrogenesis Type 1B Homozygous for an L483P Substitution in the Diastrophic Dysplasia Sulfate Tr... 著者: Antonio Rossi, Jacky Bonaventure, Anne‐Lise Delezoide, Giuseppe Cetta, Andrea Superti‐Furga

    出版事項 1996
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  2. 2
    Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia

    Fibroblast Growth Factor Receptor 3 Mutations Promote Apoptosis but Do Not Alter Chondrocyte Proliferation in Thanatophoric Dysplasia 著者: Laurence Legeai‐Mallet, Catherine Benoist-Lasselin, Anne‐Lise Delezoide, Arnold Münnich, Jacky Bonaventure

    出版事項 1998
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    Artigo
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  3. 3
    Biometry of Face and Brain in Fetuses with Trisomy 21

    Biometry of Face and Brain in Fetuses with Trisomy 21 著者: Anne-Marie Guihard-Costa, Suonavy Khung, Kathy Delbecque, Françoise Ménez, Anne‐Lise Delezoide

    出版事項 2005
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  4. 4
    Negative Fetal FSH/LH Regulation in Late Pregnancy Is Associated with Declined Kisspeptin/KISS1R Expression in the Tuberal Hypothalamus

    Negative Fetal FSH/LH Regulation in Late Pregnancy Is Associated with Declined Kisspeptin/KISS1R Expression in the Tuberal Hypothalamus 著者: Fabien Guimiot, L. Chevrier, Sophie Dreux, Didier Chevenne, Alain Caraty, Anne Lise Delezoïde, Nicolás de Roux

    出版事項 2012
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  5. 5
    Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions

    Defective migration of neuroendocrine GnRH cells in human arrhinencephalic conditions 著者: Luís Teixeira, Fabien Guimiot, Catherine Dodé, Catherine Fallet‐Bianco, Robert P. Millar, Anne‐Lise Delezoide, Jean‐Pierre Hardelin

    出版事項 2010
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  6. 6
    Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification

    Spatio-temporal expression of FGFR 1, 2 and 3 genes during human embryo-fetal ossification 著者: Anne‐Lise Delezoide, Catherine Benoist-Lasselin, Laurence Legeai‐Mallet, Martine Le Merrer, Arnold Münnich, Michel Vekemans, Jacky Bonaventure

    出版事項 1998
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  7. 7
    Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1)

    Missense FGFR3 mutations create cysteine residues in thanatophoric dwarfism type I (TD1) 著者: François Rousseau, Vincent El Ghouzzi, Anne‐Lise Delezoide, Laurence Legeai‐Mallet, M Le Merrer, A Munnich, Jacky Bonaventure

    出版事項 1996
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  8. 8
    Absence of Functional Type 1 Parathyroid Hormone (PTH)/PTH-Related Protein Receptors in Humans Is Associated with Abnormal Breast Development and Tooth Impaction1

    Absence of Functional Type 1 Parathyroid Hormone (PTH)/PTH-Related Protein Receptors in Humans Is Associated with Abnormal Breast Development and Tooth Impaction1 著者: John J. Wysolmerski, Sarah Cormier, William M. Philbrick, Pamela Dann, Jianping Zhang, J. Roume, Anne‐Lise Delezoide, Caroline Silve

    出版事項 2001
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  9. 9
    Low Renal Mineralocorticoid Receptor Expression at Birth Contributes to Partial Aldosterone Resistance in Neonates

    Low Renal Mineralocorticoid Receptor Expression at Birth Contributes to Partial Aldosterone Resistance in Neonates 著者: Lætitia Martinerie, Say Viengchareun, Anne‐Lise Delezoide, Francis Jaubert, Martine Sinico, Sophie Prévôt, Pascal Boileau, Geri Méduri, Marc Lombès

    出版事項 2009
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  10. 10
    Paradoxic Activation of the Renin-Angiotensin System in Twin-Twin Transfusion Syndrome: An Explanation for Cardiovascular Disturbances in the Recipient

    Paradoxic Activation of the Renin-Angiotensin System in Twin-Twin Transfusion Syndrome: An Explanation for Cardiovascular Disturbances in the Recipient 著者: D. Mahieu‐Caputo, A. Meulemans, Jéléna Martinovic, Marie‐Claire Gubler, Anne‐Lise Delezoide, Françoise Müller, Patrick Madélénat, Nicholas M. Fisk, Marc Dommergues

    出版事項 2005
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  11. 11
    Twin-to-Twin Transfusion Syndrome

    Twin-to-Twin Transfusion Syndrome 著者: D. Mahieu‐Caputo, Marc Dommergues, Anne‐Lise Delezoide, Mireille Lacoste, Yi Cai, Françoise Narcy, Dominique Jolly, Marie Gonzalès, Yves Dumez, Marie‐Claire Gubler

    出版事項 2000
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  12. 12
    Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus

    Sodium/Iodide Symporter (NIS) Gene Expression Is the Limiting Step for the Onset of Thyroid Function in the Human Fetus 著者: Gabor Szinnai, Ludovic Lacroix, Aurore Carré, Fabien Guimiot, Monique Talbot, Jéléna Martinovic, Anne‐Lise Delezoide, Michel Vekemans, Stefan Michiels, Bernard Caillou, Martin Schlumberger, Jean‐Michel Bidart, Michel Polak

    出版事項 2006
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  13. 13
    Dynamics of Thymus-Colonizing Cells during Human Development

    Dynamics of Thymus-Colonizing Cells during Human Development 著者: Rima Haddad, Fabien Guimiot, Emmanuelle Six, Frédéric Jourquin, Niclas Setterblad, Edmond Kahn, Micaël Yagello, Cécile Schiffer, Isabelle André‐Schmutz, Marina Cavazzana, Jean Claude Gluckman, Anne‐Lise Delezoide, Françoise Pflumio, Bruno Canque

    出版事項 2006
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  14. 14
    Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease

    Genotype–phenotype correlations in fetuses and neonates with autosomal recessive polycystic kidney disease 著者: Érick Denamur, Anne‐Lise Delezoide, Corinne Alberti, Agnès Bourillon, Marie‐Claire Gubler, Raymonde Bouvier, Olivier Pascaud, Jacques Élion, Bernard Grandchamp, Laurence Michel‐Calemard, Pascale Missy, Isabelle Zaccaria, Hervé Le Nagard, Bénédicte Gérard, Chantal Loirat

    出版事項 2009
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  15. 15
    Hippocampal Radial Glial Subtypes and Their Neurogenic Potential in Human Fetuses and Healthy and Alzheimer’s Disease Adults

    Hippocampal Radial Glial Subtypes and Their Neurogenic Potential in Human Fetuses and Healthy and Alzheimer’s Disease Adults 著者: Sara Cipriani, Isidró Ferrer, Eleonora Aronica, Gábor G. Kovács, Catherine Verney, Jeannette Nardelli, Suonavy Khung, Anne‐Lise Delezoide, Ivan Milenković, Sowmyalakshmí Rasika, Philippe Manivet, Jean‐Louis Bénifla, Nicolas Deriot, Pierre Gressèns, Homa Adle‐Biassette

    出版事項 2018
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  16. 16
    Phenotypic spectrum of<i>STRA6</i>mutations: from Matthew-Wood syndrome to non-lethal anophthalmia

    Phenotypic spectrum of<i>STRA6</i>mutations: from Matthew-Wood syndrome to non-lethal anophthalmia 著者: Nicolas Chassaing, Christelle Golzio, Sylvie Odent, Léopoldine Lequeux, Adeline Vigouroux, Jelena Martinovic-Bouriel, Francesco Danilo Tiziano, L. Masini, F. Piro, G Maragliano, Anne‐Lise Delezoide, Tania Attié‐Bitach, Sylvie Manouvrier‐Hanu, Heather Etchevers, Patrick Calvas

    出版事項 2009
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  17. 17
    DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III

    DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III 著者: Nathalie Dagoneau, Marie Goulet, David Geneviève, Yves Sznajer, Jéléna Martinovic, Sarah Smithson, Céline Huber, Geneviève Baujat, Elisabeth Flori, Laura Tecco, Denise P. Cavalcanti, Anne‐Lise Delezoide, Valérie Serre, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire

    出版事項 2009
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  18. 18
    Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia

    Exome Sequencing Identifies INPPL1 Mutations as a Cause of Opsismodysplasia 著者: Céline Huber, Eissa Faqeih, Deborah Bartholdi, Christine Bôle‐Feysot, Zvi Borochowitz, Denise P. Cavalcanti, Amandine Frigo, Patrick Nitschké, J. Roume, Heloísa G. dos Santos, Stavit Shalev, Andrea Superti‐Furga, Anne‐Lise Delezoide, Martine Le Merrer, Arnold Münnich, Valérie Cormier‐Daire

    出版事項 2012
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  19. 19
    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects

    RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects 著者: Marc Jeanpierre, G. Macé, Mélanie Parisot, Vincent Morinière, A. Pawtowsky, Max E. Benabou, Jéléna Martinovic, Jeanne Amiel, Tania Attié‐Bitach, Anne‐Lise Delezoide, Philippe Loget, Patricia Blanchet, Dominique Gaillard, M. Gonzalés, Wassila Carpentier, Patrick Nitschké, Frédéric Torès, Laurence Heidet, Corinne Antignac, Rémi Salomon

    出版事項 2011
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  20. 20
    Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry

    Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry 著者: Sarah Beaussant-Cohen, Odile Fenneteau, Emmanuel Plouvier, Pierre‐Simon Rohrlich, G Daltroff, Isabelle Plantier, A. Dupuy, Delphine Kérob, Blandine Beaupain, Pierre Bordigoni, Fanny Fouyssac, Anne‐Lise Delezoide, Gilles Devouassoux, Jean‐François Nicolas, Philippe Bensaïd, Yves Bertrand, Karl Balabanian, Christine bellanne Chantelot, Françoise Bachelerie, Jean Donadieu

    出版事項 2012
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