Zoekresultaten - P. Vabres

Verfijn jouw resultaten
  1. 1
    Efficacy and tolerability of methotrexate in severe childhood alopecia areata

    Efficacy and tolerability of methotrexate in severe childhood alopecia areata door M. Royer, Christine Bodemer, P. Vabres, C. Pajot, S. Barbarot, C. Paul, J. Mazereeuw‐Hautier

    Gepubliceerd in 2011
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  2. 2
    Dacarbazine-Mediated Upregulation of NKG2D Ligands on Tumor Cells Activates NK and CD8 T Cells and Restrains Melanoma Growth

    Dacarbazine-Mediated Upregulation of NKG2D Ligands on Tumor Cells Activates NK and CD8 T Cells and Restrains Melanoma Growth door Alice Hervieu, Cédric Rébé, Frédérique Végran, Fanny Chalmin, Mélanie Bruchard, P. Vabres, Lionel Apétoh, François Ghiringhelli, Grégoire Mignot

    Gepubliceerd in 2012
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  3. 3
    The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome Xq

    The Gene for Bazex-Dupré-Christol Syndrome Maps to Chromosome Xq door P. Vabres, Didier Lacombe, Linda G. Rabinowitz, Gérard Aubert, Carol E. Anderson, Alain Taı̈eb, Jean‐Louis Bonafé, M. C. Hors‐Cayla

    Gepubliceerd in 1995
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  4. 4
    Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity

    Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity door F. Caux, Henri Plauchu, Frédéric Chibon, Laurence Faivre, Olivier Fain, P. Vabres, Françoise Bonnet, Zied Ben Selma, L. Laroche, Marion Gérard, Michel Longy

    Gepubliceerd in 2007
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  5. 5
    Integrating longitudinal serum IL-17 and IL-23 follow-up, along with autoantibodies variation, contributes to predict bullous pemphigoid outcome

    Integrating longitudinal serum IL-17 and IL-23 follow-up, along with autoantibodies variation, contributes to predict bullous pemphigoid outcome door J. Plée, Sébastien Le Jan, Jérôme Giustiniani, Coralie Barbe, P. Joly, C. Bédane, P. Vabres, F. Truchetet, F. Aubin, Frank Antonicelli, Philippe Bernard

    Gepubliceerd in 2015
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  6. 6
    Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease

    Claudin-1 gene mutations in neonatal sclerosing cholangitis associated with ichthyosis: A tight junction disease door S. Hadj‐Rabia, Lekbir Baala, P. Vabres, Dominique Hamel‐Teillac, Emmanuel Jacquemin, Monique Fabrè, Stanislas Lyonnet, Y. De Prost, Arnold Münnich, Michelle Hadchouel, Asma Smahi

    Gepubliceerd in 2004
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  7. 7
    Next-Generation Sequencing of Nevus Spilus–Type Congenital Melanocytic Nevus: Exquisite Genotype–Phenotype Correlation in Mosaic RASopathies

    Next-Generation Sequencing of Nevus Spilus–Type Congenital Melanocytic Nevus: Exquisite Genotype–Phenotype Correlation in Mosaic RASopathies door Veronica A. Kinsler, Sven Krengel, Jean‐Baptiste Rivière, Regula Waelchli, Carolina Chapusot, Lara Al-Olabi, Laurence Faivre, Holger A. Haenssle, Lisa Weibel, G. Jeudy, P. Vabres

    Gepubliceerd in 2014
    Volledige tekst Volledige tekst
    Carta
    Toevoegen aan favorieten
    Bewaard in:
  8. 8
    Prevalence of inherited ichthyosis in France: a study using capture-recapture method

    Prevalence of inherited ichthyosis in France: a study using capture-recapture method door I. Dreyfus, Cécile Chouquet, Khaled Ezzedine, Sophie Henner, C. Chiavérini, Aude Maza, Sandrine Pascal, Lauriane Rodriguez, P. Vabres, Ludovic Martin, S. Mallet, S. Barbarot, Jérôme A. Dupuis, J. Mazereeuw‐Hautier

    Gepubliceerd in 2014
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  9. 9
    Etiologies and prognostic factors of leukocytoclastic vasculitis with skin involvement

    Etiologies and prognostic factors of leukocytoclastic vasculitis with skin involvement door Kévin Bouiller, S. Audia, H. Devilliers, Evelyne Collet, Marie Hélène Aubriot, V. Leguy‐Seguin, S. Berthier, Philippe Bonniaud, P. Chavanet, J.-F. Besancenot, P. Vabres, Laurent Martin, Maxime Samson, Bernard Bonnotte

    Gepubliceerd in 2016
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  10. 10
    Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex

    Pain and quality of life evaluation in patients with localized epidermolysis bullosa simplex door Jennifer Brun, C. Chiavérini, Caroline Devos, Stéphanie Leclerc‐Mercier, J. Mazereeuw‐Hautier, E. Bourrat, A. Maruani, S. Mallet, C. Abasq, Alice Phan, P. Vabres, Ludovic Martin, Christine Bodemer, S. Lagrange, J.‐P. Lacour

    Gepubliceerd in 2017
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  11. 11
    Alpelisib for treatment of patients with PIK3CA-related overgrowth spectrum (PROS)

    Alpelisib for treatment of patients with PIK3CA-related overgrowth spectrum (PROS) door Guillaume Canaud, Juan Carlos López‐Gutiérrez, Alan D. Irvine, P. Vabres, Jordan R. Hansford, Nii Ankrah, Fabrice Branle, Athanasia Papadimitriou, Antonia Ridolfi, P.R. O'Connell, Stuart Turner, Denise M. Adams

    Gepubliceerd in 2023
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  12. 12
    Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment

    Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment door E. Castela, Meri K. Tulić, Aurore Rozières, E. Bourrat, Jean‐François Nicolas, Jean Kanitakis, P. Vabres, D. Bessis, J. Mazereeuw‐Hautier, Fanny Morice‐Picard, David Baty, F. Bérard, J.‐P. Lacour, Thierry Passeron, C. Chiavérini

    Gepubliceerd in 2018
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  13. 13
    Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations

    Molecular apocrine differentiation is a common feature of breast cancer in patients with germline PTEN mutations door Guillaume Banneau, Mickaël Guedj, Gaëtan MacGrogan, Isabelle de Mascarel, Valérie Velasco, Renaud Schiappa, Valérie Bonadona, Albert David, Catherine Dugast, Brigitte Gilbert‐Dussardier, Olivier Ingster, P. Vabres, F. Caux, Aurélien de Reyniès, Richard Iggo, Nicolas Sévenet, Françoise Bonnet, Michel Longy

    Gepubliceerd in 2010
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  14. 14
    Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation

    Genotypes and Phenotypes of 162 Families with a <b><i>Glomulin</i></b> Mutation door Pascal Brouillard, Laurence M. Boon, Nicole Revençu, J. Berg, A. Dompmartin, Josée Dubois, Maria C. Garzón, Simon Holden, Loshan Kangesu, Christine Labrèze, Sally Ann Lynch, C McKeown, Raimundas Meškauskas, I. Quéré, Samira Syed, P. Vabres, Michel Wassef, John B. Mulliken, Miikka Vikkula

    Gepubliceerd in 2013
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  15. 15
    SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia

    SPRED1, a RAS MAPK pathway inhibitor that causes Legius syndrome, is a tumour suppressor downregulated in paediatric acute myeloblastic leukaemia door Éric Pasmant, Brigitte Gilbert‐Dussardier, Arnaud Petit, Bérengère de Laval, Armelle Luscan, Aurélia Gruber, Hélène Lapillonne, Caroline Deswarte, P. Goussard, Ingrid Laurendeau, Benjamin Uzan, Françoise Pflumio, Françoise Brizard, P. Vabres, I Naguibvena, S. Fasola, Frédéric Millot, Françoise Porteu, Dominique Vidaud, Judith Landman‐Parker, Paola Ballerini

    Gepubliceerd in 2014
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  16. 16
    Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma

    Autosomal-recessive SASH1 variants associated with a new genodermatosis with pigmentation defects, palmoplantar keratoderma and skin carcinoma door Jean- Benoît Courcet, Siham Chafai Elalaoui, Laurence Duplomb, Mariam Tajir, Jean‐Baptiste Rivière, Julien Thévenon, Nadège Gigot, Nathalie Marle, Bernard Aral, Yannis Duffourd, Alain Sarasin, Valeria Naim, Emilie Courcet-Degrolard, Marie Hélène Aubriot-Lorton, Laurent Martin, Jamal Eddin Abrid, Christel Thauvin, Abdelaziz Sefiani, P. Vabres, Laurence Faivre

    Gepubliceerd in 2014
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  17. 17
    Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy

    Lamin A and ZMPSTE24 (FACE-1) defects cause nuclear disorganization and identify restrictive dermopathy as a lethal neonatal laminopathy door Claire Navarro, Annachiara De Sandre‐Giovannoli, Rafaëlle Bernard, Irène Boccaccio, Amandine Boyer, David Geneviève, S. Hadj‐Rabia, C. Gaudy‐Marqueste, Henk Sillevis Smitt, P. Vabres, Laurence Bonhomme‐Faivre, Alain Verloès, Ton van Essen, Elisabeth Flori, Raoul C. M. Hennekam, Frits A. Beemer, Nicole Laurent, Martine Le Merrer, Pierre Cau, Nicolas Lévy

    Gepubliceerd in 2004
    Volledige tekst Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  18. 18
    A standard of care for individuals with <scp><i>PIK3CA</i></scp>‐related disorders: An international expert consensus statement

    A standard of care for individuals with <scp><i>PIK3CA</i></scp>‐related disorders: An international expert consensus statement door Sofia Douzgou, Myfanwy Rawson, Eulàlia Baselga, Moise Danielpour, Laurence Faivre, Alon Kashanian, Kim M. Keppler‐Noreuil, Paul Kuentz, Grazia M.S. Mancini, Marie‐Cécile Manière, Víctor Martínez‐Glez, Victoria Parker, Robert K. Semple, Siddharth Srivastava, P. Vabres, Marie‐Claire Y. de Wit, John M. Graham, Jill Clayton‐Smith, Ghayda Mirzaa, Leslie G. Biesecker

    Gepubliceerd in 2021
    Volledige tekst
    Revisão
    Toevoegen aan favorieten
    Bewaard in:
  19. 19
    Sirolimus (Rapamycin) for Slow-Flow Malformations in Children

    Sirolimus (Rapamycin) for Slow-Flow Malformations in Children door A. Maruani, Elsa Tavernier, O. Boccara, J. Mazereeuw‐Hautier, Sophie Leducq, D. Bessis, Laurent Guibaud, P. Vabres, Virginie Carmignac, S. Mallet, S. Barbarot, C. Chiavérini, C. Droitcourt, A.‐C. Bursztejn, Céline Lengellé, Jean‐Baptiste Woillard, Denis Herbreteau, Anne Le Touze, Aline Joly, C. Léauté‐Labrèze, Julie Powell, Hélène Bourgoin, Valérie Gissot, Bruno Giraudeau, Baptiste Morel

    Gepubliceerd in 2021
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:
  20. 20
    Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

    Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis door Anna Thomas, Zhiqiang Zeng, Jean‐Baptiste Rivière, Ryan F.L. O’Shaughnessy, Lara Al-Olabi, Judith St.-Onge, David J. Atherton, H. Aubert, Lorea Bagazgoitia, S. Barbarot, E. Bourrat, C. Chiavérini, W.K. Chong, Yannis Duffourd, Mary Glover, Leopold Groesser, S. Hadj‐Rabia, Henning Hamm, Rudolf Happle, Imran Mushtaq, J.‐P. Lacour, Regula Waelchli, Marion Wobser, P. Vabres, E. Elizabeth Patton, Veronica A. Kinsler

    Gepubliceerd in 2016
    Volledige tekst
    Artigo
    Toevoegen aan favorieten
    Bewaard in:

Zoekinstrumenten: