Torthaí cuardaigh - Christine Piétrement

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  1. 1
    Carbamylation-Derived Products: Bioactive Compounds and Potential Biomarkers in Chronic Renal Failure and Atherosclerosis

    Carbamylation-Derived Products: Bioactive Compounds and Potential Biomarkers in Chronic Renal Failure and Atherosclerosis de réir Stéphane Jaisson, Christine Piétrement, Philippe Gillery

    Foilsithe / Cruthaithe 2011
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    Revisão
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  2. 2
    Chronic Increase of Urea Leads to Carbamylated Proteins Accumulation in Tissues in a Mouse Model of CKD

    Chronic Increase of Urea Leads to Carbamylated Proteins Accumulation in Tissues in a Mouse Model of CKD de réir Christine Piétrement, Laëtitia Gorisse, Stéphane Jaisson, Philippe Gillery

    Foilsithe / Cruthaithe 2013
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  3. 3
    Distinct Expression Patterns of Different Subunit Isoforms of the V-ATPase in the Rat Epididymis1

    Distinct Expression Patterns of Different Subunit Isoforms of the V-ATPase in the Rat Epididymis1 de réir Christine Piétrement, G-H. Sun-Wada, N. Da Silva, Mary McKee, Vladimir Marshansky, Dennis Brown, Masamitsu Futai, Sylvie Breton

    Foilsithe / Cruthaithe 2005
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  4. 4
    Protein carbamylation is a hallmark of aging

    Protein carbamylation is a hallmark of aging de réir Laëtitia Gorisse, Christine Piétrement, Vincent Vuiblet, Christian E.H. Schmelzer, Martin Köhler, Laurent Duca, Laurent Debelle, Paul Fornès, Stéphane Jaisson, Philippe Gillery

    Foilsithe / Cruthaithe 2015
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  5. 5
    Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3

    Relapsing encephalopathy with cerebellar ataxia are caused by variants involving p.Arg756 in ATP1A3 de réir Pascal Sabouraud, Audrey Riquet, Marie‐Aude Spitz, Kumaran Deiva, Soňa Nevšímalová, Cyril Mignot, Gaëtan Lesca, Nathalie Bednarek, Diane Doummar, Christine Piétrement, Vincent Laugel

    Foilsithe / Cruthaithe 2019
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  6. 6
    Hypertension in Children and Adolescents: A Position Statement From a Panel of Multidisciplinary Experts Coordinated by the French Society of Hypertension

    Hypertension in Children and Adolescents: A Position Statement From a Panel of Multidisciplinary Experts Coordinated by the French Society of Hypertension de réir Béatrice Bouhanick, P. Sosner, Karine Brochard, Claire Mounier‐Véhier, Geneviève Plu‐Bureau, Sébastien Hascoët, Bruno Ranchin, Christine Piétrement, Lætitia Martinerie, Jean Marc Boivin, J. P. Fauvel, Justine Bacchetta

    Foilsithe / Cruthaithe 2021
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  7. 7
    Role of NHERF1, Cystic Fibrosis Transmembrane Conductance Regulator, and cAMP in the Regulation of Aquaporin 9

    Role of NHERF1, Cystic Fibrosis Transmembrane Conductance Regulator, and cAMP in the Regulation of Aquaporin 9 de réir Christine Piétrement, Nicolas Da Silva, Claudia Silberstein, Marianne F. James, Mireille Marsolais, Alfred N. Van Hoek, Dennis Brown, Núria M. Pastor‐Soler, Nadia A. Ameen, Raynald Laprade, Vijaya Ramesh, Sylvie Breton

    Foilsithe / Cruthaithe 2007
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  8. 8
    Acute Neurological Involvement in Diarrhea-Associated Hemolytic Uremic Syndrome

    Acute Neurological Involvement in Diarrhea-Associated Hemolytic Uremic Syndrome de réir Sylvie Nathanson, Thérèsa Kwon, Monique Elmaleh, Marina Charbit, Emma Allain Launay, Jérôme Harambat, Muriel Brun, Bruno Ranchin, Isabel Bandı́n, Sylvie Cloarec, Guylhène Bourdat-Michel, Christine Piétrement, Gérard Champion, Tim Ulinski, Georges Deschênes

    Foilsithe / Cruthaithe 2010
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  9. 9
    C5 nephritic factors drive the biological phenotype of C3 glomerulopathies

    C5 nephritic factors drive the biological phenotype of C3 glomerulopathies de réir Maria-Chiara Marinozzi, Sophie Chauvet, Moglie Le Quintrec, Morgane Mignotet, Florent Petitprez, Christophe Legendre, Mathilde Cailliez, Georges Deschênes, Michel Fischbach, Alexandre Karras, François Nobili, Christine Piétrement, Marie‐Agnès Dragon‐Durey, Fádi Fakhouri, Lubka T. Roumenina, Véronique Frémeaux‐Bacchi

    Foilsithe / Cruthaithe 2017
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  10. 10
    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome

    Prevalence of Novel MAGED2 Mutations in Antenatal Bartter Syndrome de réir Anne Debost‐Legrand, Cyrielle Tréard, Isabelle Roncelin, Sophie Dreux, Aurélia Bertholet‐Thomas, Françoise Broux, Bruno Daniele, Stéphane Decramer, Georges Deschênes, D. Djeddi, Vincent Guigonis, Nadine Jay, Tackwa Khalifeh, Brigitte Llanas, Denis Morin, G Morin, François Nobili, Christine Piétrement, Amélie Ryckewaert, Rémi Salomon, Isabelle Vrillon, Anne Blanchard, Rosa Vargas‐Poussou

    Foilsithe / Cruthaithe 2017
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  11. 11
    Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study

    Clinical characteristics and outcomes of childhood-onset ANCA-associated vasculitis: a French nationwide study de réir Anne‐Sylvia Sacri, T. Chambaraud, Bruno Ranchin, Benoît Florkin, H. See, Stéphane Decramer, Hugues Flodrops, Tim Ulinski, Emma Allain‐Launay, Olivia Boyer, Olivier Dunand, Michel Fischbach, É. Hachulla, Christine Piétrement, P. Le Pogamp, JL Stéphan, Alexandre Bélot, Hubert Nivet, François Nobili, Loı̈c Guillevin, Pierre Quartier, Georges Deschênes, Rémi Salomon, Marie Essig, J. Harambat

    Foilsithe / Cruthaithe 2015
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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
    A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts

    A big-data approach to producing descriptive anthropometric references: a feasibility and validation study of paediatric growth charts de réir Barbara Heude, Pauline Scherdel, A. Werner, Morgane Le Guern, Nathalie Gelbert, Déborah Walther, Michel Arnould, M. Bellaïche, Bertrand Chevallier, J Cheymol, Emmanuel Jobez, Sylvie Nguyen, Christine Piétrement, Rachel Reynaud, Jean‐François Salaün, Babak Khoshnood, Jennifer Zeitlin, Jean Maccario, Gérard Bréart, Jean-Christophe Thalabard, Marie‐Aline Charles, Jérémie Botton, Bruno Frandji, Martin Chalumeau

    Foilsithe / Cruthaithe 2019
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  14. 14
    Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus

    Haploinsufficiency in PTPN2 leads to early-onset systemic autoimmunity from Evans syndrome to lupus de réir Marie Jeanpierre, Jade Cognard, Maud Tusseau, Quentin Riller, Linh‐Chi Bui, Jérémy Berthelet, Audrey Laurent, Étienne Crickx, Marianna Parlato, Marie–Claude Stolzenberg, Felipe Suárez, Guy Leverger, Nathalie Aladjidi, Sophie Collardeau‐Frachon, Christine Piétrement, Marion Malphettes, Antoine Froissart, Christine Bôle‐Feysot, Nicolas Cagnard, Fernando Rodrigues‐Lima, Thierry Walzer, Frédéric Rieux‐Laucat, Alexandre Bélot, Anne‐Laure Mathieu

    Foilsithe / Cruthaithe 2024
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  15. 15
    Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability

    Mutations of CEP83 Cause Infantile Nephronophthisis and Intellectual Disability de réir Marion Failler, Heon Yung Gee, Pauline Krug, Kwangsic Joo, Jan Halbritter, Lilya Belkacem, Emilie Filhol, Jonathan D. Porath, Daniela A. Braun, Markus Schueler, Amandine Frigo, Olivier Alibeu, Cécile Masson, Karine Brochard, Bruno Hurault de Ligny, Robert Novo, Christine Piétrement, Hülya Kayserili, Rémi Salomon, Marie‐Claire Gubler, Edgar A. Otto, Corinne Antignac, Joon Kim, Alexandre Benmerah, Friedhelm Hildebrandt, Sophie Saunier

    Foilsithe / Cruthaithe 2014
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  16. 16
    Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations

    Mainzer-Saldino Syndrome Is a Ciliopathy Caused by IFT140 Mutations de réir Isabelle Perrault, Sophie Saunier, Sylvain Hanein, Emilie Filhol, Albane A. Bizet, Felicity Collins, Mustafa A. Salih, S. Gerber, Nathalie Delphin, Karine Bigot, Christophe Orssaud, Eduardo Silva, Véronique Baudouin, Machteld M. Oud, Nora Shannon, Martine Le Merrer, Olivier Roche, Christine Piétrement, Jamal Goumid, Clarisse Baumann, Christine Bôle‐Feysot, Patrick Nitschké, Mohammed Zahrate, Philip L. Beales, Heleen H. Arts, Arnold Münnich, Josseline Kaplan, Corinne Antignac, Valérie Cormier‐Daire, Jean‐Michel Rozet

    Foilsithe / Cruthaithe 2012
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  17. 17
    Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice

    Mutations in GREB1L Cause Bilateral Kidney Agenesis in Humans and Mice de réir Lara De Tomasi, Pierre David, Camille Humbert, Flora Silbermann, Christelle Arrondel, Frédéric Torès, Stéphane Fouquet, Audrey Desgrange, Olivier Niel, Christine Bôle‐Feysot, Patrick Nitschké, J. Roume, Marie‐Pierre Cordier, Christine Piétrement, Bertrand Isidor, Philippe Khau Van Kien, Marie Gonzalès, Marie‐Hélène Saint‐Frison, Jéléna Martinovic, Robert Novo, Juliette Piard, Christelle Cabrol, Ishwar C. Verma, Ratna Dua Puri, Hubert Journel, Jacqueline Aziza, Laurent Gavard, Marie-Hélène Saïd-Menthon, Laurence Heidet, Sophie Saunier, Marc Jeanpierre

    Foilsithe / Cruthaithe 2017
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