Torthaí cuardaigh - Marie-Claude Addor

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  1. 1
    Congenital hydrocephalus – prevalence, prenatal diagnosis and outcome of pregnancy in four European regions

    Congenital hydrocephalus – prevalence, prenatal diagnosis and outcome of pregnancy in four European regions de réir Ester Garne, Maria Loane, Marie‐Claude Addor, Patricia A. Boyd, Ingeborg Barišić, Helen Dolk

    Foilsithe / Cruthaithe 2009
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  2. 2
    Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome

    Ubiquitin Ligases of the N-End Rule Pathway: Assessment of Mutations in UBR1 That Cause the Johanson-Blizzard Syndrome de réir Cheol-Sang Hwang, Maja Sukalo, Olga Batygin, Marie-Claude Addor, Han G. Brunner, Antonio Pérez Aytés, Julia Mayerle, Hyun Kyu Song, Alexander Varshavsky, Martin Zenker

    Foilsithe / Cruthaithe 2011
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  3. 3
    Metformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control study

    Metformin exposure in first trimester of pregnancy and risk of all or specific congenital anomalies: exploratory case-control study de réir Joanne Given, Maria Loane, Ester Garne, Marie-Claude Addor, Marian K. Bakker, Bénédicte Bertaut-Nativel, Miriam Gatt, Kari Klungsøyr, Nathalie Lelong, Margery Morgan, Amanda J. Neville, Anna Pierini, Anke Rißmann, Helen Dolk

    Foilsithe / Cruthaithe 2018
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  4. 4
    Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe

    Rare chromosome abnormalities, prevalence and prenatal diagnosis rates from population-based congenital anomaly registers in Europe de réir Diana Wellesley, Helen Dolk, Patricia A. Boyd, Ruth Greenlees, Martin Haeusler, Vera Nelen, Ester Garne, Babak Khoshnood, Bérénice Doray, Anke Rißmann, Carmel Mullaney, Elisa Calzolari, Marian K. Bakker, Joaquín Salvador, Marie‐Claude Addor, Elizabeth S. Draper, Judith Rankin, David Tucker

    Foilsithe / Cruthaithe 2012
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  5. 5
    The changing epidemiology of Ebstein’s anomaly and its relationship with maternal mental health conditions: a European registry-based study

    The changing epidemiology of Ebstein’s anomaly and its relationship with maternal mental health conditions: a European registry-based study de réir Breidge Boyle, Ester Garne, Maria Loane, Marie‐Claude Addor, Larraitz Arriola, Clara Cavero‐Carbonell, Miriam Gatt, Nathalie Lelong, Catherine Lynch, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Anna Pierini, Anke Rißmann, David Tucker, Natalia Zymak-Zakutnia, Helen Dolk

    Foilsithe / Cruthaithe 2016
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  6. 6
    Selective serotonin reuptake inhibitor antidepressant use in first trimester pregnancy and risk of specific congenital anomalies: a European register-based study

    Selective serotonin reuptake inhibitor antidepressant use in first trimester pregnancy and risk of specific congenital anomalies: a European register-based study de réir Anthony Wemakor, Karen Casson, Ester Garne, Marian K. Bakker, Marie‐Claude Addor, Larraitz Arriola, Miriam Gatt, Babak Khoshnood, Kari Klungsøyr, Vera Nelen, M. O'Mahoney, Anna Pierini, Anke Rißmann, David Tucker, Breidge Boyle, Lolkje de Jong‐van den Berg, Helen Dolk

    Foilsithe / Cruthaithe 2015
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  7. 7
    Toward the effective surveillance of hypospadias.

    Toward the effective surveillance of hypospadias. de réir Helen Dolk, Martine Vrijheid, J. E. Scott, Marie‐Claude Addor, Bev Botting, Catherine De Vigan, Hermien E. K. de Walle, Ester Garne, Maria Loane, Anna Pierini, Sixto García‐Miñaúr, Nigel Physick, Romano Tenconi, Awi Wiesel, Elisa Calzolari, David H. Stone

    Foilsithe / Cruthaithe 2003
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  8. 8
    Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe

    Meckel–Gruber Syndrome: a population-based study on prevalence, prenatal diagnosis, clinical features, and survival in Europe de réir Ingeborg Barišić, Ljubica Boban, Maria Loane, Ester Garne, Diana Wellesley, Elisa Calzolari, Helen Dolk, Marie‐Claude Addor, Jorieke E. H. Bergman, Paula Braz, Elizabeth S. Draper, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Anna Pierini, Annette Queißer‐Luft, Judith Rankin, Anke Rißmann, Christine Verellen‐Dumoulin

    Foilsithe / Cruthaithe 2014
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  9. 9
    Use of asthma medication during pregnancy and risk of specific congenital anomalies: A European case-malformed control study

    Use of asthma medication during pregnancy and risk of specific congenital anomalies: A European case-malformed control study de réir Ester Garne, Anne Vinkel Hansen, Joan K. Morris, Louise Zaupper, Marie‐Claude Addor, Ingeborg Barišić, Miriam Gatt, Nathalie Lelong, Kari Klungsøyr, Mary O’Mahony, Vera Nelen, Amanda J. Neville, Anna Pierini, David Tucker, Hermien E. K. de Walle, Awi Wiesel, Maria Loane, Helen Dolk

    Foilsithe / Cruthaithe 2015
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  10. 10
    Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB

    Multicentric Carpotarsal Osteolysis Is Caused by Mutations Clustering in the Amino-Terminal Transcriptional Activation Domain of MAFB de réir Andreas Zankl, Emma L. Duncan, Paul Leo, Graeme R. Clark, Evgeny A. Glazov, Marie-Claude Addor, Troels Herlin, Chong Ae Kim, Bruno Leheup, Jim McGill, Steven McTaggart, Stephan Mittas, Anna L. Mitchell, Geert Mortier, Stephen P. Robertson, Marie Schroeder, Paulien A. Terhal, Matthew A. Brown

    Foilsithe / Cruthaithe 2012
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  11. 11
    Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Information Services

    Use of GLP1 receptor agonists in early pregnancy and reproductive safety: a multicentre, observational, prospective cohort study based on the databases of six Teratology Informatio... de réir Kim Dao, Svetlana Shechtman, Corinna Weber‐Schoendorfer, Orna Diav‐Citrin, Reem Hegla Murad, Maya Berlin, Ariela Hazan, Jonathan L. Richardson, Georgios Eleftheriou, Valentin Rousson, Léonore Diezi, David Haefliger, Ana Paula Simões‐Wüst, Marie‐Claude Addor, David Baud, Faïza Lamine, Alice Panchaud, Thierry Buclin, François Girardin, Ursula Winterfeld

    Foilsithe / Cruthaithe 2024
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  12. 12
    Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe

    Prevalence, prenatal diagnosis and clinical features of oculo-auriculo-vertebral spectrum: a registry-based study in Europe de réir Ingeborg Barišić, Ljubica Odak, Maria Loane, Ester Garne, Diana Wellesley, Elisa Calzolari, Helen Dolk, Marie‐Claude Addor, Larraitz Arriola, Jorieke E. H. Bergman, Sebastiano Bianca, Bérénice Doray, Babak Khoshnood, Kari Klungsøyr, Bob McDonnell, Anna Pierini, Judith Rankin, Anke Rißmann, Catherine Rounding, Annette Queißer‐Luft, Gioacchino Scarano, David Tucker

    Foilsithe / Cruthaithe 2014
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  13. 13
    Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly

    Mutations in tubulin genes are frequent causes of various foetal malformations of cortical development including microlissencephaly de réir Catherine Fallet‐Bianco, Annie Laquerrière, Karine Poirier, Ferechté Razavi, Fabien Guimiot, Patrícia Dias, Laurence Lœuillet, Karine Lascelles, Chérif Beldjord, Nathalie Carion, Aurélie Toussaint, Nicole Revençu, Marie‐Claude Addor, Benoît Lhermitte, Marie Gonzalès, Jelena Martinovich, Bettina Bessières, Maryse Marcy-Bonnière, Frédérique Jossic, Pascale Marcorelles, Philippe Loget, Jamel Chelly, Nadia Bahi‐Buisson

    Foilsithe / Cruthaithe 2014
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  14. 14
    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 de réir 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

    Foilsithe / Cruthaithe 2017
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  15. 15
    Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening

    Twenty-year trends in the prevalence of Down syndrome and other trisomies in Europe: impact of maternal age and prenatal screening de réir Maria Loane, Joan K. Morris, Marie‐Claude Addor, Larraitz Arriola, J. L. S. Budd, Bérénice Doray, Ester Garne, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Anna Latos‐Bieleńska, Bob McDonnell, Carmel Mullaney, Mary O’Mahony, Annette Queißer-Wahrendorf, Judith Rankin, Anke Rißmann, Catherine Rounding, Joaquín Salvador, David Tucker, Diana Wellesley, Lyubov Yevtushok, Helen Dolk

    Foilsithe / Cruthaithe 2012
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  16. 16
    Holt Oram syndrome: a registry-based study in Europe

    Holt Oram syndrome: a registry-based study in Europe de réir Ingeborg Barišić, Ljubica Boban, Ruth Greenlees, Ester Garne, Diana Wellesley, Elisa Calzolari, Marie‐Claude Addor, Larraitz Arriola, Jorieke E. H. Bergman, Paula Braz, J. L. S. Budd, Miriam Gatt, Martin Haeusler, Babak Khoshnood, Kari Klungsøyr, Bob McDonnell, Vera Nelen, Anna Pierini, Annette Queißer-Wahrendorf, Judith Rankin, Anke Rißmann, Catherine Rounding, David Tucker, Christine Verellen‐Dumoulin, Helen Dolk

    Foilsithe / Cruthaithe 2014
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  17. 17
    Congenital clubfoot in Europe: A population‐based study

    Congenital clubfoot in Europe: A population‐based study de réir Hao Wang, Ingeborg Barišić, Maria Loane, Marie‐Claude Addor, Linda M. Bailey, Miriam Gatt, Kari Klungsøyr, Olatz Mokoroa, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Anna Pierini, Anke Rißmann, Christine Verellen‐Dumoulin, Hermien E. K. de Walle, Awi Wiesel, Katarzyna Wiśniewska, Lolkje T.W. de Jong‐van den Berg, Helen Dolk, Babak Khoshnood, Ester Garne

    Foilsithe / Cruthaithe 2019
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  18. 18
    Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization

    Subtelomeric deletion of chromosome 10p15.3: Clinical findings and molecular cytogenetic characterization de réir Cheryl DeScipio, Laura K. Conlin, Jill A. Rosenfeld, James Tepperberg, Romela Pasion, Ankita Patel, Marie McDonald, Swaroop Aradhya, Darlene Ho, Jennifer Goldstein, Marianne McGuire, Surabhi Mulchandani, Līvija Medne, Rosemarie Rupps, Alvaro Serrano, Erik C. Thorland, Anne Chun‐Hui Tsai, Yvonne Hilhorst‐Hofstee, Claudia Ruivenkamp, Hilde Van Esch, Marie‐Claude Addor, Danielle Martinet, Thornton B.A. Mason, Dinah Clark, Nancy B. Spinner, Ian D. Krantz

    Foilsithe / Cruthaithe 2012
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  19. 19
    Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies

    Lamotrigine use in pregnancy and risk of orofacial cleft and other congenital anomalies de réir Helen Dolk, Hao Wang, Maria Loane, Joan K. Morris, Ester Garne, Marie‐Claude Addor, Larraitz Arriola, Marian K. Bakker, Ingeborg Barišić, Bérénice Doray, Miriam Gatt, Karin Källén, Babak Khoshnood, Kari Klungsøyr, Anna‐Maria Lahesmaa‐Korpinen, Anna Latos‐Bieleńska, Jan P. Mejnartowicz, Vera Nelen, Amanda J. Neville, Mary O’Mahony, Anna Pierini, Anke Rißmann, David Tucker, Diana Wellesley, Awi Wiesel, Lolkje T.W. de Jong‐van den Berg

    Foilsithe / Cruthaithe 2016
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  20. 20
    Epidemiology of hypospadias in Europe: a registry-based study

    Epidemiology of hypospadias in Europe: a registry-based study de réir 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

    Foilsithe / Cruthaithe 2015
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