Search Results - Hanitra Randrianaivo

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  1. 1
    Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome

    Expanding the clinical spectrum of B4GALT7 deficiency: homozygous p.R270C mutation with founder effect causes Larsen of Reunion Island syndrome by François Cartault, Patrick Munier, Marie‐Line Jacquemont, Jeannine Vellayoudom, Bérénice Doray, Christine Payet, Hanitra Randrianaivo, J.-M. Laville, Arnold Münnich, Valérie Cormier‐Daire

    Published 2014
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  2. 2
    Multidisciplinary Prospective Study of Mother-to-Child Chikungunya Virus Infections on the Island of La Réunion

    Multidisciplinary Prospective Study of Mother-to-Child Chikungunya Virus Infections on the Island of La Réunion by Patrick Gérardin, G. Barau, Alain Michault, Marc Bintner, Hanitra Randrianaivo, G. Choker, Y. Lenglet, Yasmina Touret, A. Bouveret, Philippe Grivard, K. Le Roux, Séverine Blanc, Isabelle Schuffenecker, Thérèse Couderc, Fernando Arenzana‐Seisdedos, Marc Lecuit, Pierre‐Yves Robillard

    Published 2008
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  3. 3
    Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study

    Beta-Blocker Use in Pregnancy and Risk of Specific Congenital Anomalies: A European Case-Malformed Control Study by Jorieke E. H. Bergman, L. Renée Lutke, Rijk O. B. Gans, Marie‐Claude Addor, Ingeborg Barišić, Clara Cavero‐Carbonell, Ester Garne, Miriam Gatt, Kari Klungsøyr, Nathalie Lelong, Catherine Lynch, Olatz Mokoroa, Vera Nelen, Amanda J. Neville, Anna Pierini, Hanitra Randrianaivo, Anke Rißmann, David Tucker, Awi Wiesel, Helen Dolk, Maria Loane, Marian K. Bakker

    Published 2017
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  4. 4
    Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease

    Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease by Marie‐Pierre Audrézet, Christine Corbiere, Saïd Lebbah, Vincent Morinière, Françoise Broux, Férielle Louillet, Michel Fischbach, Ariane Zaloszyc, Sylvie Cloarec, Élodie Merieau, Véronique Baudouin, Georges Deschênes, G. Roussey, Sandrine Maestri, Chiara Visconti, Olivia Boyer, Carine Abel, Annie Lahoche, Hanitra Randrianaivo, Lucie Bessenay, Djalila Mekahli, Inès Ouertani, Stéphane Decramer, Amélie Ryckenwaert, Émilie Cornec-Le Gall, Rémi Salomon, Claude Férec, Laurence Heidet

    Published 2015
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  5. 5
    Epidemiology of hypospadias in Europe: a registry-based study

    Epidemiology of hypospadias in Europe: a registry-based study by Jorieke E. H. Bergman, Maria Loane, Martine Vrijheid, Anna Pierini, Rien J.M. Nijman, Marie‐Claude Addor, Ingeborg Barišić, Judit Béres, Paula Braz, J. L. S. Budd, Virginia Delaney, Miriam Gatt, Babak Khoshnood, Kari Klungsøyr, Carmen Martos, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Annette Queißer‐Luft, Hanitra Randrianaivo, Anke Rißmann, Catherine Rounding, David Tucker, Diana Wellesley, Nataliia Zymak‐Zakutnia, Marian K. Bakker, Hermien E. K. de Walle

    Published 2015
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  6. 6
    Prevalence of microcephaly in Europe: population based study

    Prevalence of microcephaly in Europe: population based study by Joan K. Morris, Judith Rankin, Ester Garne, Maria Loane, Ruth Greenlees, Marie‐Claude Addor, Larraitz Arriola, Ingeborg Barišić, Jorieke E. H. Bergman, Melinda Csáky‐Szunyogh, Carlos Matias Dias, Elizabeth S. Draper, Miriam Gatt, Babak Khoshnood, Kari Klungsøyr, Jennifer J. Kurinczuk, Catherine Lynch, Robert McDonnell, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Anna Pierini, Hanitra Randrianaivo, Anke Rißmann, David Tucker, Christine Verellen‐Dumoulin, Hermien E. K. de Walle, Diana Wellesley, Awi Wiesel, Helen Dolk

    Published 2016
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  7. 7
    Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data

    Estimating Global Burden of Disease due to congenital anomaly: an analysis of European data by Breidge Boyle, Marie‐Claude Addor, Larraitz Arriola, Ingeborg Barišić, Fabrizio Bianchi, Melinda Csáky‐Szunyogh, Hermien E. K. de Walle, Carlos Matias Dias, Elizabeth S. Draper, Miriam Gatt, Ester Garne, Martin Haeusler, Karin Källén, Anna Latos‐Bieleńska, Bob McDonnell, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Annette Queißer-Wahrendorf, Hanitra Randrianaivo, Judith Rankin, Anke Rißmann, Annukka Ritvanen, Catherine Rounding, David Tucker, Christine Verellen‐Dumoulin, Diana Wellesley, Ben Wreyford, Natalia Zymak-Zakutnia, Helen Dolk

    Published 2017
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  8. 8
    Trends in congenital anomalies in Europe from 1980 to 2012

    Trends in congenital anomalies in Europe from 1980 to 2012 by Joan K. Morris, Anna Springett, Ruth Greenlees, Maria Loane, Marie-Claude Addor, Larraitz Arriola, Ingeborg Barišić, Jorieke E. H. Bergman, Melinda Csáky‐Szunyogh, Carlos Matias Dias, Elizabeth S. Draper, Ester Garne, Miriam Gatt, Babak Khoshnood, Kari Klungsøyr, Catherine Lynch, Robert McDonnell, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Anna Pierini, Annette Queißer‐Luft, Hanitra Randrianaivo, Judith Rankin, Anke Rißmann, Jennifer J. Kurinczuk, David Tucker, Christine Verellen‐Dumoulin, Diana Wellesley, Helen Dolk

    Published 2018
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  9. 9
    Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study

    Epidemiology of septo-optic dysplasia with focus on prevalence and maternal age – A EUROCAT study by Ester Garne, Anke Rißmann, Marie-Claude Addor, Ingeborg Barišić, Jorieke E. H. Bergman, Paula Braz, Clara Cavero‐Carbonell, Elizabeth S. Draper, Miriam Gatt, Martin Haeusler, Kari Klungsøyr, Jennifer J. Kurinczuk, Nathalie Lelong, Karen Luyt, Catherine Lynch, Mary O’Mahony, Olatz Mokoroa, Vera Nelen, Amanda J. Neville, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Florence Rouget, Bruno Schaub, David Tucker, Christine Verellen‐Dumoulin, Diana Wellesley, Awi Wiesel, Nataliia Zymak‐Zakutnia, Monica Lanzoni, Joan K. Morris

    Published 2018
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  10. 10
    Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study

    Epidemiology of congenital cerebral anomalies in Europe: a multicentre, population-based EUROCAT study by Joan K. Morris, Diana Wellesley, Ingeborg Barišić, Marie‐Claude Addor, Jorieke E. H. Bergman, Paula Braz, Clara Cavero‐Carbonell, Elizabeth S. Draper, Miriam Gatt, Martin Haeusler, Kari Klungsøyr, Jennifer J. Kurinczuk, Natalie Lelong, Karen Luyt, Catherine Lynch, Mary O’Mahony, Olatz Mokoroa, Vera Nelen, Amanda J. Neville, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Anke Rißmann, Florence Rouget, Bruno Schaub, David Tucker, Christine Verellen‐Dumoulin, Awi Wiesel, Natalia Zymak-Zakutnia, Monica Lanzoni, Ester Garne

    Published 2019
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  11. 11
    Spectrum of the Mutations in Bernard-Soulier Syndrome

    Spectrum of the Mutations in Bernard-Soulier Syndrome by Anna Savoia, Shinji Kunishima, Daniela De Rocco, Barbara Zieger, Margaret L. Rand, Núria Pujol‐Moix, Ümran Çalışkan, Hüseyin Tokgöz, Alessandro Pecci, Patrizia Noris, Alok Srivastava, Christopher Wård, Marie‐Christine Morel‐Kopp, Marie‐Christine Alessi, Sylvia Bellucci, Philippe Beurrier, Emmanuel de Maistre, Rémi Favier, Nathalie Hézard, Marie-Françoise Hurtaud-Roux, Véronique Latger‐Cannard, Cécile Lavenu‐Bombled, Valérie Proulle, Sandrine Meunier, Claude Négrier, Alan T. Nurden, Hanitra Randrianaivo, Fabrizio Fabris, Helen Platokouki, Nurit Rosenberg, Basma HadjKacem, Paula G. Heller, Mehran Karimi, Carlo L. Balduini, Annalisa Pastore, François Lanza

    Published 2014
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  12. 12
    Paper 6: EUROCAT member registries: Organization and activities

    Paper 6: EUROCAT member registries: Organization and activities by Ruth Greenlees, Amanda J. Neville, Marie‐Claude Addor, Emmanuelle Amar, Larraitz Arriola, Marian K. Bakker, Ingeborg Barišić, Patricia A. Boyd, Elisa Calzolari, Bérénice Doray, Elizabeth S. Draper, Dan J. Stein, Ester Garne, Miriam Gatt, Martin Haeusler, Karin Källén, Babak Khoshnood, Anna Latos‐Bieleńska, María‐Luisa Martínez‐Frías, Anna Materna‐Kiryluk, Carlos Matias Dias, Bob McDonnell, Carmel Mullaney, Vera Nelen, Mary O’Mahony, Anna Pierini, Annette Queißer‐Luft, Hanitra Randrianaivo–Ranjatoélina, Judith Rankin, Anke Rißmann, Annukka Ritvanen, Joaquín Salvador, A Šípek, David Tucker, Christine Verellen‐Dumoulin, Diana Wellesley, Wladimir Wertelecki

    Published 2011
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  13. 13
    Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study

    Spectrum of congenital anomalies among VACTERL cases: a EUROCAT population-based study by Romy van de Putte, Iris A.L.M. van Rooij, Carlo Marcelis, Michel Guo, Han G. Brunner, Marie‐Claude Addor, Clara Cavero‐Carbonell, Carlos Matias Dias, Elizabeth S. Draper, Larraitz Etxebarriarteun, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Jenny J. Kurinczuk, Monica Lanzoni, Anna Latos‐Bieleńska, Karen Luyt, Mary O’Mahony, Nicola Miller, Carmel Mullaney, Vera Nelen, Amanda J. Neville, Isabelle Perthus, Anna Pierini, Hanitra Randrianaivo, Judith Rankin, Anke Rißmann, Florence Rouget, Bruno Schaub, David Tucker, Diana Wellesley, Awi Wiesel, Nataliia Zymak‐Zakutnia, Maria Loane, Ingeborg Barišić, Hermien E. K. de Walle, Nel Roeleveld, Jorieke E. H. Bergman

    Published 2019
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  14. 14
    Treacher Collins syndrome: a clinical and molecular study based on a large series of patients

    Treacher Collins syndrome: a clinical and molecular study based on a large series of patients by Marie Vincent, David Geneviève, Agnès Ostertag, Sandrine Marlin, Didier Lacombe, Dominique Martin–Coignard, Christine Coubes, Albert David, Stanislas Lyonnet, Catheline Vilain, Anne Dieux‐Coëslier, Sylvie Manouvrier, Bertrand Isidor, Marie‐Line Jacquemont, Sophie Julia, Valérie Layet, Sophie Naudion, Sylvie Odent, Laurent Pasquier, Sybille Pelras, Nicole Philip, Geneviève Pierquin, Fabienne Prieur, Nisrine Aboussair, Tania Attié‐Bitach, Geneviève Baujat, Patricia Blanchet, Catherine Blanchet, Hélène Dollfus, Bérénice Doray, Élise Schaefer, Patrick Edery, Fabienne Giuliano, Alice Goldenberg, Cyril Goizet, Agnès Guichet, Christian Herlin, Laëtitia Lambert, Bruno Leheup, Jéléna Martinovic, Sandra Mercier, Cyril Mignot, Marie‐Laure Moutard, M. Laguía Pérez, Lucile Pinson, Jacques Puechberty, Marjolaine Willems, Hanitra Randrianaivo, Kateline Szaskon, Annick Toutain, Alain Verloès, Jacqueline Vigneron, Elodie Sanchez, Pierre Sarda, Jean Laplanche, Corinne Collet

    Published 2015
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