Хайлтын үр дүнгүүд - D Droz

  • 12-н 1 - 12 үр дүнгүүдийг харуулж байна
Үр дүнг сайжруулах
  1. 1
    Characterization of mononuclear cell subsets in renal cellular interstitial infiltrates

    Characterization of mononuclear cell subsets in renal cellular interstitial infiltrates -н Anne Boucher, D Droz, E Adafer, Laure‐Hélène Noël

    Хэвлэсэн 1986
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    Artigo
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  2. 2
    Renal Vascular Lesions in Lupus Nephritis

    Renal Vascular Lesions in Lupus Nephritis -н Éric Descombes, D Droz, Ludovic Drouet, Jean‐Pierre Grünfeld, Philippe Lesavre

    Хэвлэсэн 1997
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    Artigo
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  3. 3
    Light-chain deposition disease: Its relation with AL-type amyloidosis

    Light-chain deposition disease: Its relation with AL-type amyloidosis -н D Ganeval, Laure‐Hélène Noël, Jean‐Louis Preud'homme, D Droz, Jean‐Pierre Grünfeld

    Хэвлэсэн 1984
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    Artigo
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  4. 4
    Orodental phenotype and genotype findings in all subtypes of hypophosphatasia

    Orodental phenotype and genotype findings in all subtypes of hypophosphatasia -н Amélie Reibel, Marie‐Cécile Manière, François Clauss, D Droz, Yves Alembik, Étienne Mornet, Agnès Bloch‐Zupan

    Хэвлэсэн 2009
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    Artigo
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  5. 5
    The Intrarenal Vascular Lesions Associated with Primary Antiphospholipid Syndrome

    The Intrarenal Vascular Lesions Associated with Primary Antiphospholipid Syndrome -н Dominique Nochy, Éric Daugas, D Droz, Hélène Beaufils, Jean‐Pierre Grünfeld, Jean‐Charles Piette, J Bariéty, Gary S. Hill

    Хэвлэсэн 1999
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    Artigo
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  6. 6
    Tenofovir‐Related Nephrotoxicity in Human Immunodeficiency Virus–Infected Patients: Three Cases of Renal Failure, Fanconi Syndrome, and Nephrogenic Diabetes Insipidus

    Tenofovir‐Related Nephrotoxicity in Human Immunodeficiency Virus–Infected Patients: Three Cases of Renal Failure, Fanconi Syndrome, and Nephrogenic Diabetes Insipidus -н Alexandre Karras, Matthieu Lafaurie, André Furco, A. Bourgarit, D Droz, D. Séréni, Christophe Legendre, Frank Martinez, Jean‐Michel Molina

    Хэвлэсэн 2003
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    Artigo
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  7. 7
    Early renal changes in hemizygous and heterozygous patients with Fabry's disease

    Early renal changes in hemizygous and heterozygous patients with Fabry's disease -н Marie‐Claire Gubler, G. Lenoir, Jean‐Pierre Grünfeld, André Ulmann, D Droz, Renée Habib, C. Naizot, E Adafer, C. Grandhomme

    Хэвлэсэн 1978
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    Artigo
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  8. 8
    Renal involvement in von Hippel-Lindau disease

    Renal involvement in von Hippel-Lindau disease -н Dominique Chauveau, C Duvic, Yves Chrétien, François Paraf, D Droz, P Melki, O. Hélénon, Richard J. Kahnoski, Jean‐Pierre Grünfeld

    Хэвлэсэн 1996
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    Artigo
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  9. 9
    PROPHYLACTIC USE OF OKT3 MONOCLONAL ANTIBODY IN CADAVER KIDNEY RECIPIENTS UTILIZATION OF OKT3 AS THE SOLE IMMUNOSUPPRESSIVE AGENT

    PROPHYLACTIC USE OF OKT3 MONOCLONAL ANTIBODY IN CADAVER KIDNEY RECIPIENTS UTILIZATION OF OKT3 AS THE SOLE IMMUNOSUPPRESSIVE AGENT -н P Vigeral, N Chkoff, Lucienne Chatenoud, Henry de Holanda Campos, Hugo Lacombe, D Droz, Gideon Goldstein, Jean‐François Bach, H Kreis

    Хэвлэсэн 1986
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    Artigo
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  10. 10
    Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family

    Hereditary renal amyloidosis caused by a new variant lysozyme W64R in a French family -н Sophie Valleix, Séverine Drunat, Jean-Baptiste Philit, D. Adoué, Jean‐Charles Piette, D Droz, Brigitte MacGregor, Denis Canet, Marc Delpech, Gilles Grateau

    Хэвлэсэн 2002
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    Artigo
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  11. 11
    Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC

    Mutations of the VHL gene in sporadic renal cell carcinoma: Definition of a risk factor for VHL patients to develop an RCC -н Catherine Gallou, Dominique Joly, A. M�jean, F. Staroz, Natacha Martin, Georges Tarlet, Marie-Thérèse Orfanelli, Raymonde Bouvier, D Droz, Y. Chr�tien, J.M. Mar�chal, Richard J. Kahnoski, Claudine Junien, Christophe B�roud

    Хэвлэсэн 1999
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    Artigo
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  12. 12
    A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement

    A targeted next-generation sequencing assay for the molecular diagnosis of genetic disorders with orodental involvement -н Megana Prasad, Véronique Geoffroy, Serge Vicaire, Bernard Jost, Michaël Dumas, Stéphanie Le Gras, Marzena Switala, Barbara Gasse, Virginie Laugel-Haushalter, Marie Paschaki, Bruno Leheup, D Droz, Amelie Dalstein, Adeline Loing, Bruno Grollemund, Michèle Muller‐Bolla, Séréna Lopez-Cazaux, Maryline Minoux, Sophie Jung, Frédéric Obry, Vincent Vogt, Jean‐Luc Davideau, Tiphaine Davit‐Béal, Anne-Sophie Kaiser, Ute Moog, Béatrice Richard, Jean-Jacques Morrier, Jean‐Pierre Duprez, Sylvie Odent, Isabelle Bailleul‐Forestier, M. Rousset, Laure Merametdijan, Annick Toutain, Clara Joseph, Fabienne Giuliano, Jean-Christophe Dahlet, Aymeric Courval, Mustapha El Alloussi, Samir Laouina, S. Soskin, Nathalie Guffon, Anne Dieux, Bérénice Doray, Stephanie Feierabend, Emmanuelle Ginglinger, Benjamin Fournier, Muriel De La Dure‐Molla, Yves Alembik, C Tardieu, François Clauss, Ariane Berdal, Corinne Stoetzel, M.C. Manière, Hélène Dollfus, Agnès Bloch‐Zupan

    Хэвлэсэн 2015
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    Artigo
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