Rezultati pretrage - G. Lorette
- Prikaz rezultata 1 – 5 od 5
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1
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2
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3
Brain Magnetic Resonance Imaging in Patients With Cowden Syndrome od Catherine Lok, Valérie Viseux, M.-F. Avril, M.‐A. Richard, Catherine Gondry‐Jouet, H. Deramond, Caroline Desfossez-Tribout, Sandrine Courtade, M. Delaunay, F Piette, D. Legars, Brigitte Dréno, Philippe Saïag, Michel Longy, G. Lorette, L. Laroche, F. Caux
Izdano 2005Artigo -
4
Leg Ulcers and Hydroxyurea od Marie-Emmanuelle Sirieix, C. Debure, N. Baudot, Louis Dubertret, M Roux, P Morel, C. Françès, S. Loubeyres, C Beylot, Donald H. Lambert, P. Humbert, O Gauthier, M. Dandurand, B. Guillot, L. Vaillant, G Lorette, J.-M. Bonnetblanc, C. Lok, J P Denoeux
Izdano 1999Artigo -
5
Pediatric Mastocytosis Is a Clonal Disease Associated with D816V and Other Activating c-KIT Mutations od Christine Bodemer, Olivier Hermine, Fabienne Palmérini, Ying Yang, Catherine Grandpeix‐Guyodo, Phillip S. Leventhal, S. Hadj‐Rabia, Laurent Nasca, Sophie Georgin-Lavialle, Annick Cohen-Akenine, Jean-Marie Launay, Stéphane Barète, Frédéric Féger, Michel Arock, B. Catteau, B. Sans, J.F. Stalder, Francois Skowron, L. Thomas, G Lorette, P. Plantin, Pierre Bordigoni, Olivier Lortholary, Y. De Prost, Alain Moussy, Hagay Sobol, Patrice Dubreuil
Izdano 2009Artigo
Alati za pretragu:
Povezani predmeti
Medicine
Biology
Pathology
Biochemistry
Chemistry
Disease
Gene
Genetics
Internal medicine
Mutation
Surgery
Vascular disease
Adverse effect
Angioma
Asymptomatic
Atrophy
BK virus
Bioinformatics
Cancer research
Carcinoma
Cowden syndrome
Cutaneous Mastocytosis
Discovery and development of mTOR inhibitors
Exon
Genotype
Germline mutation
Haematopoiesis
Hemangioma
Hydroxycarbamide
Immunology