检索结果 - Coulomb‐l'Hermine, Aurore

Pulmonary sarcoid-like granulomatous disease in an 11-month-old girl 由 Nathan, Nadia, Pautrat, Jade, Coulomb l'Hermine, Aurore, Corvol, Harriet

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Expression of Epstein-Barr Virus-Induced Gene 3, an Interleukin-12 p40-Related Molecule, throughout Human Pregnancy: Involvement of Syncytiotrophoblasts and Extravillous Trophoblas... 由 Devergne, Odile, Coulomb-L’Herminé, Aurore, Capel, Francis, Moussa, Marlène, Capron, Frédérique

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Pulmonary Fibrosis in Children 由 Nathan, Nadia, Sileo, Chiara, Thouvenin, Guillaume, Berdah, Laura, Delestrain, Céline, Manali, Effrosyne, Papiris, Spyros, Léger, Pierre-Louis, Ducou le Pointe, Hubert, Coulomb l’Hermine, Aurore, Clement, Annick

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Stromal cell-derived factor 1 (SDF-1) and antenatal human B cell lymphopoiesis: Expression of SDF-1 by mesothelial cells and biliary ductal plate epithelial cells 由 Coulomb-L’Herminé, Aurore, Amara, Ali, Schiff, Claudine, Durand-Gasselin, Ingrid, Foussat, Arnaud, Delaunay, Thierry, Chaouat, Gérard, Capron, Frédérique, Ledee, Nathalie, Galanaud, Pierre, Arenzana-Seisdedos, Fernando, Emilie, Dominique

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Bi-allelic missense ABCA3 mutations in a patient with childhood ILD who reached adulthood 由 Manali, Effrosyni D., Legendre, Marie, Nathan, Nadia, Kannengiesser, Caroline, Coulomb-L'Hermine, Aurore, Tsiligiannis, Theofanis, Tomos, Pericles, Griese, Matthias, Borie, Raphael, Clement, Annick, Amselem, Serge, Crestani, Bruno, Papiris, Spyros A.

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Chronic Intestinal Pseudo-Obstruction and Lymphoproliferative Syndrome as a Novel Phenotype Associated With Tetratricopeptide Repeat Domain 7A Deficiency 由 El-Daher, Marie-Thérèse, Lemale, Julie, Bruneau, Julie, Leveau, Claire, Guerin, Frédéric, Lambert, Nathalie, Diana, Jean-Sébastien, Neven, Bénédicte, Sepulveda, Fernando E., Coulomb-L'Hermine, Aurore, Molina, Thierry, Picard, Capucine, Fischer, Alain, de Saint Basile, Geneviève

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The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol 由 Vujanić, Gordan M., Gessler, Manfred, Ooms, Ariadne H. A. G., Collini, Paola, Coulomb-l’Hermine, Aurore, D’Hooghe, Ellen, de Krijger, Ronald R., Perotti, Daniela, Pritchard-Jones, Kathy, Vokuhl, Christian, van den Heuvel-Eibrink, Marry M., Graf, Norbert

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Publisher Correction: The UMBRELLA SIOP–RTSG 2016 Wilms tumour pathology and molecular biology protocol 由 Vujanić, Gordan M., Gessler, Manfred, Ooms, Ariadne H. A. G., Collini, Paola, Coulomb-l’Hermine, Aurore, D’Hooghe, Ellen, de Krijger, Ronald R., Perotti, Daniela, Pritchard-Jones, Kathy, Vokuhl, Christian, van den Heuvel-Eibrink, Marry M., Graf, Norbert

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Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling 由 Lepelley, Alice, Martin-Niclós, Maria José, Le Bihan, Melvin, Marsh, Joseph A., Uggenti, Carolina, Rice, Gillian I., Bondet, Vincent, Duffy, Darragh, Hertzog, Jonny, Rehwinkel, Jan, Amselem, Serge, Boulisfane-El Khalifi, Siham, Brennan, Mary, Carter, Edwin, Chatenoud, Lucienne, Chhun, Stéphanie, Coulomb l’Hermine, Aurore, Depp, Marine, Legendre, Marie, Mackenzie, Karen J., Marey, Jonathan, McDougall, Catherine, McKenzie, Kathryn J., Molina, Thierry Jo, Neven, Bénédicte, Seabra, Luis, Thumerelle, Caroline, Wislez, Marie, Nathan, Nadia, Manel, Nicolas, Crow, Yanick J., Frémond, Marie-Louise

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Characteristics and outcome of pediatric renal cell carcinoma patients registered in the International Society of Pediatric Oncology (SIOP) 93‐01, 2001 and UK‐IMPORT database: A re... 由 van der Beek, Justine N., Hol, Janna A., Coulomb‐l'Hermine, Aurore, Graf, Norbert, van Tinteren, Harm, Pritchard‐Jones, Kathy, Houwing, Maite E., de Krijger, Ronald R., Vujanic, Gordan M., Dzhuma, Kristina, Schenk, Jens‐Peter, Littooij, Annemieke S., Ramírez‐Villar, Gema L., Murphy, Dermot, Ray, Satyajit, Al‐Saadi, Reem, Gessler, Manfred, Godzinski, Jan, Ruebe, Christian, Collini, Paola, Verschuur, Arnaud C., Frisk, Tony, Vokuhl, Christian, Hulsbergen‐van de Kaa, Christina A., de Camargo, Beatriz, Sandstedt, Bengt, Selle, Barbara, Tytgat, Godelieve A. M., van den Heuvel‐Eibrink, Marry M.

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