Malignant Superficial Mesenchymal Tumors in Children

Por Philippe Drabent, Sylvie Fraitag
Publicado em 2022-04-01

Kaposi varicelliform eruption in a patient with epidermolysis bullosa simplex generalized severe

Por Huguen, Johanna, Fraitag, Sylvie, Misery, Laurent, Abasq-Thomas, Claire
Publicado no JAAD Case Rep (2016)

Efficacy and safety of the peripheral kappa agonist fedotozine versus placebo in the treatment of functional dyspepsia

Por Read, N, Abitbol, J, Bardhan, K, Whorwell, P, Fraitag, B
Publicado em 1997

Pharmacological modulators of autophagy activate a parallel noncanonical pathway driving unconventional LC3 lipidation

Por Jacquin, Elise, Leclerc-Mercier, Stéphanie, Judon, Celine, Blanchard, Emmanuelle, Fraitag, Sylvie, Florey, Oliver
Publicado no Autophagy (2017)

Probable DRESS syndrome induced by IL-1 inhibitors

Por Polivka, L., Diana, J. S., Soria, A., Bodemer, C., Quartier, P., Fraitag, S., Bader-Meunier, B.
Publicado no Orphanet J Rare Dis (2017)

Validation of a specific quality of life questionnaire for functional digestive disorders

Por Chassany, O, Marquis, P, Scherrer, B, Read, N, Finger, T, Bergmann, J, Fraitag, B, Geneve, J, Caulin, C
Publicado em 1999

Mucor irregularis-associated cutaneous mucormycosis: Case report and review

Por Rammaert, Blandine, Angebault, Cécile, Scemla, Anne, Fraitag, Sylvie, Lerolle, Nathalie, Lecuit, Marc, Bougnoux, Marie-Elisabeth, Lortholary, Olivier
Publicado em 2014

Cytophagic histiocytic panniculitis: is it a macrophage activation syndrome in situ?

Por Bader-Meunier, B, Fraitag, S, Janssen, CEI, de Saint Basile, G, Brochard, K, Brousse, N, Bodemer, C, Wouters, C
Publicado em 2011

Molecular characterization of subcutaneous panniculitis-like T-cell lymphoma reveals upregulation of immunosuppression- and autoimmunity-associated genes

Por Maliniemi, Pilvi, Hahtola, Sonja, Ovaska, Kristian, Jeskanen, Leila, Väkevä, Liisa, Jäntti, Kirsi, Stadler, Rudolf, Michonneau, David, Fraitag, Sylvie, Hautaniemi, Sampsa, Ranki, Annamari
Publicado no Orphanet J Rare Dis (2014)

Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibr...

Por Hovnanian, A, Rochat, A, Bodemer, C, Petit, E, Rivers, C A, Prost, C, Fraitag, S, Christiano, A M, Uitto, J, Lathrop, M, Barrandon, Y, de Prost, Y
Publicado em 1997

Granulomatous inflammation in cartilage-hair hypoplasia: risks and benefits of anti-TNF alpha monoclonal antibodies

Por Moshous, D, Meyts, I, Fraitag, S, Janssen, C, Debré, M, Suarez, F, Toelen, J, De Boeck, K, Roskams, T, Deschildre, A, Picard, C, Bodemer, C, Wouters, C, Fischer, A
Publicado em 2011

New somatic BRAF splicing mutation in Langerhans cell histiocytosis

Por Héritier, Sébastien, Hélias-Rodzewicz, Zofia, Chakraborty, Rikhia, Sengal, Amel G., Bellanné-Chantelot, Christine, Thomas, Caroline, Moreau, Anne, Fraitag, Sylvie, Allen, Carl E., Donadieu, Jean, Emile, Jean-François
Publicado no Mol Cancer (2017)

Detection of t(2;5)(p23;q35) translocation by reverse transcriptase polymerase chain reaction and in situ hybridization in CD30-positive primary cutaneous lymphoma and lymphomatoid...

Por Beylot-Barry, M., Lamant, L., Vergier, B., de Muret, A., Fraitag, S., Delord, B., Dubus, P., Vaillant, L., Delaunay, M., MacGrogan, G., Beylot, C., de Mascarel, A., Delsol, G., Merlio, J. P.
Publicado em 1996

Unusual cutaneous features associated with a heterozygous gain-of-function mutation in IFIH1: overlap between Aicardi–Goutières and Singleton–Merten syndromes

Por Bursztejn, A.-C., Briggs, T.A., del Toro Duany, Y., Anderson, B.H., O’Sullivan, J., Williams, S.G., Bodemer, C., Fraitag, S., Gebhard, F., Leheup, B., Lemelle, I., Oojageer, A., Raffo, E., Schmitt, E., Rice, G.I., Hur, S., Crow, Y.J.
Publicado no Br J Dermatol (2015)

Phenotypic and Genotypic Characteristics of Mastocytosis According to the Age of Onset

Por Lanternier, Fanny, Cohen-Akenine, Annick, Palmerini, Fabienne, Feger, Frédéric, Yang, Ying, Zermati, Yael, Barète, Stéphane, Sans, Beatrix, Baude, Cédric, Ghez, David, Suarez, Felipe, Delarue, Richard, Casassus, Philippe, Bodemer, Christine, Catteau, Adeline, Soppelsa, Frédérique, Hanssens, Katia, Arock, Michel, Sobol, Hagay, Fraitag, Sylvie, Canioni, Danièle, Moussy, Alain, Launay, Jean Marie, Dubreuil, Patrice, Hermine, Olivier, Lortholary, Olivier
Publicado em 2008

Masitinib for treatment of severely symptomatic indolent systemic mastocytosis: a randomised, placebo-controlled, phase 3 study

Por Lortholary, Olivier, Chandesris, Marie Olivia, Livideanu, Cristina Bulai, Paul, Carle, Guillet, Gérard, Jassem, Ewa, Niedoszytko, Marek, Barete, Stéphane, Verstovsek, Srdan, Grattan, Clive, Damaj, Gandhi, Canioni, Danielle, Fraitag, Sylvie, Lhermitte, Ludovic, Lavialle, Sophie Georgin, Frenzel, Laurent, Afrin, Lawrence B, Hanssens, Katia, Agopian, Julie, Gaillard, Raphael, Kinet, Jean-Pierre, Auclair, Christian, Mansfield, Colin, Moussy, Alain, Dubreuil, Patrice, Hermine, Olivier
Publicado no Lancet (2017)

Revised classification of histiocytoses and neoplasms of the macrophage-dendritic cell lineages

Por Emile, Jean-François, Abla, Oussama, Fraitag, Sylvie, Horne, Annacarin, Haroche, Julien, Donadieu, Jean, Requena-Caballero, Luis, Jordan, Michael B., Abdel-Wahab, Omar, Allen, Carl E., Charlotte, Frédéric, Diamond, Eli L., Egeler, R. Maarten, Fischer, Alain, Herrera, Juana Gil, Henter, Jan-Inge, Janku, Filip, Merad, Miriam, Picarsic, Jennifer, Rodriguez-Galindo, Carlos, Rollins, Barret J., Tazi, Abdellatif, Vassallo, Robert, Weiss, Lawrence M.
Publicado no Blood (2016)

Imaging Mass Spectrometry assists in the classification of diagnostically challenging Atypical Spitzoid Neoplasms

Por Lazova, Rossitza, Seeley, Erin H., Kutzner, Heinz, Scolyer, Richard A., Scott, Glynis, Cerroni, Lorenzo, Fried, Isabella, Kozovska, Milena E., Rosenberg, Arlene S., Prieto, Victor G., Shehata, Bahig M., Durham, Megan M., Henry, Gina, Rodriguez-Peralto, Jose L., Riveiro-Falkenbach, Erica, Schaefer, Jochen T., Danialan, Richard, Fraitag, Sylvie, Vollenweider-Roten, Sonja, Sepehr, Alireza, Sangueza, Martin, Hijazi, Nouf, Corredoira, Yamile, Kowal, Rachel, Harris, Olga M., Bravo, Francisco, Boyd, Alan S., Gueorguieva, Ralitza, Caprioli, Richard M.
Publicado no J Am Acad Dermatol (2016)

Deep Dermatophytosis and Inherited CARD9 Deficiency

Por Lanternier, Fanny, Pathan, Saad, Vincent, Quentin B., Liu, Luyan, Cypowyj, Sophie, Prando, Carolina, Migaud, Mélanie, Taibi, Lynda, Ammar-Khodja, Aomar, Stambouli, Omar Boudghene, Guellil, Boumediene, Jacobs, Frederique, Goffard, Jean-Christophe, Schepers, Kinda, del Marmol, Véronique, Boussofara, Lobna, Denguezli, Mohamed, Larif, Molka, Bachelez, Hervé, Michel, Laurence, Lefranc, Gérard, Hay, Rod, Jouvion, Gregory, Chretien, Fabrice, Fraitag, Sylvie, Bougnoux, Marie-Elisabeth, Boudia, Merad, Abel, Laurent, Lortholary, Olivier, Casanova, Jean-Laurent, Picard, Capucine, Grimbacher, Bodo, Puel, Anne
Publicado em 2013

Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations

Por Wang, Yi, Ma, Cindy S., Ling, Yun, Bousfiha, Aziz, Camcioglu, Yildiz, Jacquot, Serge, Payne, Kathryn, Crestani, Elena, Roncagalli, Romain, Belkadi, Aziz, Kerner, Gaspard, Lorenzo, Lazaro, Deswarte, Caroline, Chrabieh, Maya, Patin, Etienne, Vincent, Quentin B., Müller-Fleckenstein, Ingrid, Fleckenstein, Bernhard, Ailal, Fatima, Quintana-Murci, Lluis, Fraitag, Sylvie, Alyanakian, Marie-Alexandra, Leruez-Ville, Marianne, Picard, Capucine, Puel, Anne, Bustamante, Jacinta, Boisson-Dupuis, Stéphanie, Malissen, Marie, Malissen, Bernard, Abel, Laurent, Hovnanian, Alain, Notarangelo, Luigi D., Jouanguy, Emmanuelle, Tangye, Stuart G., Béziat, Vivien, Casanova, Jean-Laurent
Publicado no J Exp Med (2016)