Torthaí cuardaigh - Marie Gonzalès

Beachtaigh na torthaí
  1. 1
    Twin-to-Twin Transfusion Syndrome

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

    Foilsithe / Cruthaithe 2000
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  2. 2
    Influence of infused cell dose and HLA match on engraftment after double-unit cord blood allografts

    Influence of infused cell dose and HLA match on engraftment after double-unit cord blood allografts de réir Sharon Avery, Weiji Shi, Marissa Lubin, Anne Marie Gonzales, Glenn Heller, Hugo Castro‐Malaspina, Sergio Giralt, Nancy A. Kernan, Andromachi Scaradavou, Juliet N. Barker

    Foilsithe / Cruthaithe 2010
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  3. 3
    Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome

    Temporal bone anomaly proposed as a major criteria for diagnosis of CHARGE syndrome de réir Jeanne Amiel, Tania Attié‐Bitach, R�mi Marianowski, Valérie Cormier‐Daire, V�ronique Abadie, Damien Bonnet, Marie Gonzalès, Sophie Chemouny, Françis Brunelle, Arnold Münnich, Y Manac'h, Stanislas Lyonnet

    Foilsithe / Cruthaithe 2001
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  4. 4
    Quantitative assessment of T cell repertoire recovery after hematopoietic stem cell transplantation

    Quantitative assessment of T cell repertoire recovery after hematopoietic stem cell transplantation de réir Jeroen W. J. van Heijst, Izaskun Ceberio, Lauren Lipuma, Dane Samilo, Gloria Wasilewski, Anne Marie Gonzales, Jimmy Nieves, Marcel R.M. van den Brink, Miguel‐Angel Perales, Eric G. Pamer

    Foilsithe / Cruthaithe 2013
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  5. 5
    Characteristics and Outcomes of Breast Cancer in Women With and Without a History of Radiation for Hodgkin's Lymphoma: A Multi-Institutional, Matched Cohort Study

    Characteristics and Outcomes of Breast Cancer in Women With and Without a History of Radiation for Hodgkin's Lymphoma: A Multi-Institutional, Matched Cohort Study de réir Elena B. Elkin, Michelle L. Klem, Anne Marie Gonzales, Nicole Ishill, David C. Hodgson, Andrea K. Ng, Lawrence B. Marks, Joanne B. Weidhaas, Gary M. Freedman, Robert C. Miller, Louis S. Constine, Sten Myrehaug, Joachim Yahalom

    Foilsithe / Cruthaithe 2011
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  6. 6
    Mutations in GLDN , Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis

    Mutations in GLDN , Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis de réir Jérôme Maluenda, Constance Manso, Loïc Quevarec, Alexandre Vivanti, Florent Marguet, Marie Gonzalès, Fabien Guimiot, Florence Petit, Annick Toutain, Sandra Whalen, R Grigorescu, Anne Dieux Coeslier, Marta Gut, Marta Gut, Annie Laquerrière, Jérôme Devaux, Judith Melki

    Foilsithe / Cruthaithe 2016
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  7. 7
    Phylogeography Analysis Reveals Rabies Epidemiology, Evolution, and Transmission in the Philippines

    Phylogeography Analysis Reveals Rabies Epidemiology, Evolution, and Transmission in the Philippines de réir Liang Zhang, Jeffrey L. Cruz, Yao Tian, Yuyang Wang, Jianfeng Jiang, Riva Marie Gonzales, Rachel R Azul, Rainelda C. Dela Peña, Sheng Sun, Yan Liu, Tao Jiang, Li‐Qun Fang, Changchun Tu, Wenjie Gong, Ye Feng

    Foilsithe / Cruthaithe 2025
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  8. 8
    Serious Infection Risk and Immune Recovery after Double-Unit Cord Blood Transplantation Without Antithymocyte Globulin

    Serious Infection Risk and Immune Recovery after Double-Unit Cord Blood Transplantation Without Antithymocyte Globulin de réir Craig S. Sauter, Michelle Abboud, Xiaoyu Jia, Glenn Heller, Anne-Marie Gonzales, Marissa Lubin, Rebecca Hawke, Miguel‐Angel Perales, Marcel R.M. van den Brink, Sergio Giralt, Genovefa A. Papanicolaou, Andromachi Scaradavou, Trudy N. Small, Juliet N. Barker

    Foilsithe / Cruthaithe 2011
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  9. 9
    A Novel Reduced-Intensity Conditioning Regimen Induces a High Incidence of Sustained Donor-Derived Neutrophil and Platelet Engraftment after Double-Unit Cord Blood Transplantation

    A Novel Reduced-Intensity Conditioning Regimen Induces a High Incidence of Sustained Donor-Derived Neutrophil and Platelet Engraftment after Double-Unit Cord Blood Transplantation de réir Doris M. Ponce, Craig S. Sauter, Sean M. Devlin, Marissa Lubin, Anne Marie Gonzales, Nancy A. Kernan, Andromachi Scaradavou, Sergio Giralt, Jenna D. Goldberg, Guenther Koehne, Miguel‐Angel Perales, James W. Young, Hugo Castro‐Malaspina, Ann A. Jakubowski, Esperanza B. Papadopoulos, Juliet N. Barker

    Foilsithe / Cruthaithe 2013
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  10. 10
    Frequent Human Herpesvirus-6 Viremia But Low Incidence of Encephalitis in Double-Unit Cord Blood Recipients Transplanted Without Antithymocyte Globulin

    Frequent Human Herpesvirus-6 Viremia But Low Incidence of Encephalitis in Double-Unit Cord Blood Recipients Transplanted Without Antithymocyte Globulin de réir Amanda Olson, Parastoo B. Dahi, Junting Zheng, Sean M. Devlin, Marissa Lubin, Anne Marie Gonzales, Sergio Giralt, Miguel‐Angel Perales, Esperanza B. Papadopoulos, Doris M. Ponce, James W. Young, Nancy A. Kernan, Andromachi Scaradavou, Richard J. O’Reilly, Trudy N. Small, Genovefa A. Papanicolaou, Juliet N. Barker

    Foilsithe / Cruthaithe 2014
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  11. 11
    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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  12. 12
    Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

    Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract de réir Laurence Heidet, Vincent Morinière, C. Henry, Lara De Tomasi, Madeline Louise Reilly, Camille Humbert, Olivier Alibeu, Cécile Fourrage, Christine Bôle‐Feysot, Patrick Nitschké, Frédéric Torès, Marc Bras, Marc Jeanpierre, Christine Piétrement, Dominique Gaillard, Marie Gonzalès, Robert Novo, Élise Schaefer, J. Roume, Jéléna Martinovic, Valérie Malan, Rémi Salomon, Sophie Saunier, Corinne Antignac, Marc Jeanpierre

    Foilsithe / Cruthaithe 2017
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  13. 13
    Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly

    Identification of Mutations in TMEM5 and ISPD as a Cause of Severe Cobblestone Lissencephaly de réir Sandrine Vuillaumier‐Barrot, C. Bouchet-Séraphin, M. Chelbi, Louise Devisme, Samuel Quentin, Steven Gazal, Annie Laquerrière, Catherine Fallet‐Bianco, Philippe Loget, Sylvie Odent, Dominique Carles, Anne Bazin, Jacqueline Aziza, Alix Clémenson, Fabien Guimiot, Maryse Bonnière, Sophie Monnot, Christine Bôle‐Feysot, Jean‐Pierre Bernard, Laurence Lœuillet, Marie Gonzalès, Koryna Socha, Bernard Grandchamp, Tania Attié‐Bitach, Férechté Encha‐Razavi, Nathalie Seta

    Foilsithe / Cruthaithe 2012
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  14. 14
    Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development

    Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development de réir Damien Sanlaville, Heather Etchevers, Marie Gonzalès, Jéléna Martinovic, Mathieu Clément‐Ziza, Anne‐Lise Delezoide, M. C. Aubry, Anna Pelet, Sophie Chemouny, Corinne Cruaud, Sophie Audollent, Chantal Esculpavit, Géraldine Goudefroye, Catherine Ozilou, C. Fredouille, Nicole Joyé, N. Morichon-Delvallez, Yves Dumez, Jean Weissenbach, Arnold Münnich, Jeanne Amiel, Férechté Encha‐Razavi, Stanislas Lyonnet, Michel Vekemans, Tania Attié‐Bitach

    Foilsithe / Cruthaithe 2005
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  15. 15
    Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway

    Mutational Spectrum in Holoprosencephaly Shows That FGF is a New Major Signaling Pathway de réir Christèle Dubourg, Wilfrid Carré, Houda Hamdi‐Rozé, Charlotte Mouden, J. Roume, Benmansour Abdelmajid, Daniel Amram, Clarisse Baumann, Nicolas Chassaing, Christine Coubes, Laurence Faivre-Olivier, Emmanuelle Ginglinger, Marie Gonzalès, Annie Levy‐Mozziconacci, Sally Ann Lynch, Sophie Naudion, Laurent Pasquier, Amélie Poidvin, Fabienne Prieur, Pierre Sarda, Annick Toutain, Valérie Dupé, Linda Akloul, Sylvie Odent, Marie de Tayrac, Véronique David

    Foilsithe / Cruthaithe 2016
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  16. 16
    Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling

    Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling de réir Thomas Eggermann, Frédéric Brioude, Silvia Russo, Maria Lombardi, Jet Bliek, Eamonn R. Maher, Lidia Larizza, Dirk Prawitt, Irène Netchine, Marie Gonzalès, Karen Grønskov, Zeynep Tümer, David Monk, M. Mannens, Krystyńa Chrzańowska, Malgorzata Krajewska Walasek, Matthias Begemann, Lukas Soellner, Katja Eggermann, Jair Tenorio, Julián Nevado, Gudrun E. Moore, Deborah Mackay, I. Karen Temple, Gabriele Gillessen‐Kaesbach, Tsutomu Ogata, Rosanna Weksberg, Elizabeth M. Algar, Pablo Lapunzina

    Foilsithe / Cruthaithe 2015
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  17. 17
    Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome

    Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome de réir Houda Karmous‐Benailly, Jéléna Martinovic, Marie‐Claire Gubler, Yoann Sirot, Laure Clech, Catherine Ozilou, Joëlle Augé, Nora Brahimi, Heather Etchevers, Eric Detrait, Chantal Esculpavit, Sophie Audollent, Géraldine Goudefroye, Marie Gonzalès, Julia Tantau, Philippe Loget, Madeleine Joubert, Dominique Gaillard, Corinne Jeanne‐Pasquier, Anne‐Lise Delezoide, Marie-Odile Peter, Ghislaine Plessis, Brigitte Simon‐Bouy, Hélène Dollfus, Martine Le Merrer, Arnold Münnich, Férechté Encha‐Razavi, Michel Vekemans, Tania Attié‐Bitach

    Foilsithe / Cruthaithe 2005
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  18. 18
    Reduced Late Mortality Risk Contributes to Similar Survival after Double-Unit Cord Blood Transplantation Compared with Related and Unrelated Donor Hematopoietic Stem Cell Transplantation

    Reduced Late Mortality Risk Contributes to Similar Survival after Double-Unit Cord Blood Transplantation Compared with Related and Unrelated Donor Hematopoietic Stem Cell Transplan... de réir Doris M. Ponce, Junting Zheng, Anne Marie Gonzales, Marissa Lubin, Glenn Heller, Hugo Castro‐Malaspina, Sergio Giralt, Katharine C. Hsu, Ann A. Jakubowski, Robert R. Jenq, Guenther Koehne, Esperanza B. Papadopoulos, Miguel‐Angel Perales, Marcel R.M. van den Brink, James W. Young, Farid Boulad, Nancy A. Kernan, Rachel Kobos, Susan E. Prockop, Andromachi Scaradavou, Trudy N. Small, Richard J. O’Reilly, Juliet N. Barker

    Foilsithe / Cruthaithe 2011
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  19. 19
    Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios

    Renal Tubular Dysgenesis, a Not Uncommon Autosomal Recessive Disorder Leading to Oligohydramnios de réir Mireille Lacoste, Yi Cai, Liliane Guicharnaud, FrancCOMBINING CEDILLAoise Mounier, Yves Dumez, Raymonde Bouvier, FreCombining Acute AccentdeCombining Acute Accentrique Dijoud, Marie Gonzalès, Jane Chatten, Anne‐Lise Delezoide, Laurent Daniel, Madeleine Joubert, Nicole Laurent, Jacqueline Aziza, Tahya Sellami, H. Ben Amar, C Jarnet, Anne Marie Frances, Farida DaiCombining Diaeresiskha-Dahmane, Aurore Coulomb, Thomas J. Neuhaus, B. Foliguet, Pierre Chenal, Pascale Marcorelles, Jean Marie Gasc, Pierre Corvol, Marie‐Claire Gubler

    Foilsithe / Cruthaithe 2006
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  20. 20
    <i>CC2D2A</i>mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

    <i>CC2D2A</i>mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation de réir Soumaya Mougou-Zerelli, Sophie Thomas, Emmanuelle Szenker‐Ravi, Sophie Audollent, Nadia Elkhartoufi, Candice Babarit, Stéphane Romano, Rémi Salomon, Jeanne Amiel, Chantal Esculpavit, Marie Gonzalès, Estelle Escudier, Bruno Leheup, Philippe Loget, Sylvie Odent, J. Roume, Marion Gérard, Anne-Lise Delezoide, Suonavy Khung, Sophie Patrier, Marie-Pierre Cordier, Raymonde Bouvier, Jéléna Martinovic, Marie‐Claire Gubler, Nathalie Boddaert, Arnold Münnich, Férechté Encha‐Razavi, Enza Maria Valente, Ali Saâd, Sophie Saunier, Michel Vekemans, Tania Attié‐Bitach

    Foilsithe / Cruthaithe 2009
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