Výsledky vyhledávání - Bernard Bénichou

  • Zobrazuji výsledky 1 - 7 z 7
Upřesnit hledání
  1. 1
    Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis.

    Class II-antigen-negative patient and mutant B-cell lines represent at least three, and probably four, distinct genetic defects defined by complementation analysis. Autor Bernard Bénichou, Jack L. Strominger

    Vydáno 1991
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  2. 2
    Evaluation of a low dose, after a standard therapeutic dose, of agalsidase beta during enzyme replacement therapy in patients with Fabry disease

    Evaluation of a low dose, after a standard therapeutic dose, of agalsidase beta during enzyme replacement therapy in patients with Fabry disease Autor Jean-Claude Lubanda, Ene Anijalg, Vladimı́r Bzdúch, Beth L. Thurberg, Bernard Bénichou, Anna Tylki‐Szymańska

    Vydáno 2009
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  3. 3
    Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy.

    Large deletion of the peroxisomal acyl-CoA oxidase gene in pseudoneonatal adrenoleukodystrophy. Autor B. Fournier, Jean Marie Saudubray, Bernard Bénichou, Stanislas Lyonnet, A Munnich, Hans Clevers, Bwee Tien Poll‐The

    Vydáno 1994
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  4. 4
    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28

    Mapping of X-Linked Myxomatous Valvular Dystrophy to Chromosome Xq28 Autor Florence Kyndt, Jean‐Jacques Schott, Jean‐Noël Trochu, Florence Baranger, O. Herbert, Valerie E. Scott, Édith Fressinaud, Albert David, Jean‐Paul Moisan, Jean-Brieuc Bouhour, Hervé Le Marec, Bernard Bénichou

    Vydáno 1998
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  5. 5
    Identification and characterization of a spinal muscular atrophy-determining gene

    Identification and characterization of a spinal muscular atrophy-determining gene Autor Suzie Lefebvre, Lydie Bürglen, Sophie Reboullet, Olivier Clermont, Philippe Burlet, Louis Viollet, Bernard Bénichou, Corinne Cruaud, Philippe Millasseau, Massimo Zeviani, Denis Le Paslier, J Frézal, Daniel Cohen, Jean Weissenbach, Arnold Münnich, Judith Melki

    Vydáno 1995
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  6. 6
    Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial

    Characterization of Early Disease Status in Treatment-Naive Male Paediatric Patients with Fabry Disease Enrolled in a Randomized Clinical Trial Autor Frits A. Wijburg, Bernard Bénichou, Daniel G. Bichet, Lorne A. Clarke, Gabriela Dostálová, Alejandro Fainboim, Andreas Fellgiebel, Cassiano Mateus Forcelini, Kristina An Haack, Robert J. Hopkin, Michael Mauer, Behzad Najafian, C. Ronald Scott, Suma P. Shankar, Beth L. Thurberg, Camilla Tøndel, Anna Tylki‐Szymańska, Uma Ramaswami

    Vydáno 2015
    Získat plný text Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:
  7. 7
    Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial

    Low-dose agalsidase beta treatment in male pediatric patients with Fabry disease: A 5-year randomized controlled trial Autor Uma Ramaswami, Daniel G. Bichet, Lorne A. Clarke, Gabriela Dostálová, Alejandro Fainboim, Andreas Fellgiebel, Cassiano Mateus Forcelini, Kristina An Haack, Robert J. Hopkin, Michael Mauer, Behzad Najafian, C. Ronald Scott, Suma P. Shankar, Beth L. Thurberg, Camilla Tøndel, Anna Tylki‐Szymańska, Bernard Bénichou, Frits A. Wijburg

    Vydáno 2019
    Získat plný text
    Artigo
    Přidat do oblíbených
    Uloženo v:

Vyhledávací nástroje: