Search Results - "Prost, Yves"

Adjuvant treatment with the bacterial lysate (OM-85) improves management of atopic dermatitis: A randomized study by Bodemer, Christine, Guillet, Gerard, Cambazard, Frederic, Boralevi, Franck, Ballarini, Stefania, Milliet, Christian, Bertuccio, Paola, La Vecchia, Carlo, Bach, Jean-François, de Prost, Yves

“…Environmental factors play a major role on atopic dermatitis (AD) which shows a constant rise in prevalence in western countries over the last decades. The…”
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Connective tissue nevi: An entity revisited by Saussine, Anne, MD, Marrou, Karine, MD, Delanoé, Phillippe, MD, Bodak, Nathalie, MD, Hamel, Dominique, MD, Picard, Arnaud, MD, Sassolas, Bruno, MD, de Prost, Yves, MD, PhD, Lemerrer, Martine, MD, Fraitag, Sylvie, MD, Bodemer, Christine, MD, PhD

“…Background Connective tissue nevi (CTN) may be isolated, either sporadic or hereditary, or syndromic as in the Buschke-Ollendorff syndrome. Few publications…”
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Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases by Cluzeau, Céline, Hadj-Rabia, Smail, Jambou, Marguerite, Mansour, Sourour, Guigue, Philippe, Masmoudi, Sahben, Bal, Elodie, Chassaing, Nicolas, Vincent, Marie-Claire, Viot, Géraldine, Clauss, François, Manière, Marie-Cécile, Toupenay, Steve, Le Merrer, Martine, Lyonnet, Stanislas, Cormier-Daire, Valérie, Amiel, Jeanne, Faivre, Laurence, de Prost, Yves, Munnich, Arnold, Bonnefont, Jean-Paul, Bodemer, Christine, Smahi, Asma

“…Hypohidrotic and anhidrotic ectodermal dysplasia (HED/EDA) is a rare genodermatosis characterized by abnormal development of sweat glands, teeth, and hair…”
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Cutaneous findings in sporadic and familial autosomal dominant hyper-IgE syndrome: A retrospective, single-center study of 21 patients diagnosed using molecular analysis by Olaiwan, Amani, MD, Chandesris, Marie-Olivia, MD, Fraitag, Sylvie, MD, Lortholary, Olivier, MD, PhD, Hermine, Olivier, MD, PhD, Fischer, Alain, MD, PhD, de Prost, Yves, MD, PhD, Picard, Capucine, MD, PhD, Bodemer, Christine, MD, PhD

“…Background Recent identification of STAT3 mutations in autosomal dominant (AD) hyper-IgE syndrome (HIES) has improved the clinical, genetic, and molecular…”
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Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations by Hadj-Rabia, Smaïl, MD, PhD, Rimella, Aude, MD, Smahi, Asma, PhD, Fraitag, Sylvie, MD, Hamel-Teillac, Dominique, MD, Bonnefont, Jean-Paul, MD, PhD, de Prost, Yves, MD, PhD, Bodemer, Christine, MD, PhD

“…Background Incontinentia pigmenti (IP) is a multisystem disorder, in which cutaneous symptoms can be accompanied by dental, ocular, and central nervous system…”
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Cutaneous B-cell lymphoblastic lymphoma in children: A rare diagnosis by Boccara, Olivia, MD, Laloum-Grynberg, Etty, MD, Jeudy, Géraldine, MD, Aubriot-Lorton, Marie-Hélène, MD, Vabres, Pierre, MD, PhD, de Prost, Yves, MD, PhD, Pacquement, Hélène, MD, Brousse, Nicole, MD, PhD, Fraitag, Sylvie, MD, Bodemer, Christine, MD, PhD

“…Background Lymphoblastic lymphoma (LBL) is a rare malignant neoplasm usually occurring in the mediastinum of children and adolescents. The B-cell…”
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Scalp nodules as a presenting sign of fibrodysplasia ossificans progressiva: A register-based study by Piram, Maryam, MD, Le Merrer, Martine, MD, Bughin, Valérie, De Prost, Yves, MD, PhD, Fraitag, Sylvie, MD, Bodemer, Christine, MD, PhD

“…Background Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by progressive ossification of soft tissues. Clinical diagnosis…”
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Efficacy and safety of pimecrolimus cream in the long-term management of atopic dermatitis in children by Wahn, Ulrich, Bos, Jan D, Goodfield, Mark, Caputo, Ruggero, Papp, Kim, Manjra, Ahmed, Dobozy, Attila, Paul, Carle, Molloy, Stephen, Hultsch, Thomas, Graeber, Michael, Cherill, Robert, de Prost, Yves

“…Pimecrolimus cream (SDZ ASM 981), a nonsteroid inhibitor of inflammatory cytokines, is effective in atopic dermatitis (AD). We assessed whether early treatment…”
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Mutations in SPINK5 , encoding a serine protease inhibitor, cause Netherton syndrome by Taïeb, Alain, Wilkinson, John, Irvine, Alan D, Rochat, Ariane, Bodemer, Christine, Hovnanian, Alain, Ali, Mohsin, Chavanas, Stéphane, Hamel-Teillac, Dominique, Barrandon, Yann, Bonafé, Jean-Louis, Harper, John I, de Prost, Yves

“…We describe here eleven different mutations in SPINK5, encoding the serine protease inhibitor LEKTI, in 13 families with Netherton syndrome (NS, MIM256500)…”
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Characterization of 18 New Mutations in COL7A1 in Recessive Dystrophic Epidermolysis Bullosa Provides Evidence for Distinct Molecular Mechanisms Underlying Defective Anchoring Fibril Formation by Hovnanian, Alain, Rochat, Ariane, Bodemer, Christine, Petit, Elisabeth, Rivers, Caroline A., Prost, Catherine, Fraitag, Sylvie, Christiano, Angela M., Uitto, Jouni, Lathrop, Mark, Barrandon, Yann, Prost, Yves de

“…We have characterized 21 mutations in the type VII collagen gene (COL7A1) encoding the anchoring fibrils, 18 of which were not previously reported, in patients…”
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Localization of the Netherton Syndrome Gene to Chromosome 5q32, by Linkage Analysis and Homozygosity Mapping by Chavanas, Stéphane, Garner, Chad, Bodemer, Christine, Ali, Mohsin, Teillac, Dominique Hamel, Wilkinson, John, Bonafé, Jean-Louis, Paradisi, Mauro, Kelsell, David P., Ansai, Shin-ichi, Mitsuhashi, Yoshihiko, Larrègue, Marc, Leigh, Irene M., Harper, John I., Taïeb, Alain, Prost, Yves de, Cardon, Lon R., Hovnanian, Alain

“…Netherton syndrome (NS [MIM 256500]) is a rare and severe autosomal recessive disorder characterized by congenital ichthyosis, a specific hair-shaft defect…”
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Wells' syndrome after primoinfection by parvovirus B19 in a child by Toulon, Antoine, MD, Bourdon-Lanoy, Eva, MD, Hamel, Dominique, MD, Fraitag, Sylvie, MD, Leruez-Ville, Mariane, MD, de Prost, Yves, MD, Hadj-Rabia, Smaïl, MD, PhD

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Netherton Syndrome: Disease Expression and Spectrum of SPINK5 Mutations in 21 Families by Bitoun, Emmanuelle, Chavanas, Stéphane, Irvine, Alan D., Lonie, Lorne, Bodemer, Christine, Paradisi, Mauro, Hamel-Teillac, Dominique, Ansai, Shin-ichi, Mitsuhashi, Yoshihiko, Taïeb, Alain, de Prost, Yves, Zambruno, Giovanna, Harper, John I., Hovnanian, Alain

“…Netherton syndrome is a severe autosomal recessive skin disorder characterized by congenital erythroderma, a specific hair-shaft abnormality, and atopic…”
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Proceedings of the 4th Georg Rajka International Symposium on Atopic Dermatitis, Arcachon, France, September 15-17, 2005 by Taïeb (Bordeaux, France), A., Giannetti (Modena, Italy), A., Thestrup-Pedersen (Aarhus, Denmark), K., Ring (Munich, Germany), J., Taïeb, Alain, Hanifin, Jon, Cooper, Kevin, Bos, Jan D., Imokawa, Genji, David, Tim J., Ring, Johannes, Gelmetti, Carlo, Kapp, Alexander, Furue, Masutaka, de Prost, Yves, Darsow, Ulf, Werfel, Thomas, Atherton, David, Oranje, Arnold P.

“…The 4th Georg Rajka International Symposium on Atopic Dermatitis presented a comprehensive view of our current understanding and management of atopic…”
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Pediatric Mastocytosis Is a Clonal Disease Associated with D816V and Other Activating c-KIT Mutations by Bodemer, Christine, Hermine, Olivier, Palmérini, Fabienne, Yang, Ying, Grandpeix-Guyodo, Catherine, Leventhal, Phillip S., Hadj-Rabia, Smail, Nasca, Laurent, Georgin-Lavialle, Sophie, Cohen-Akenine, Annick, Launay, Jean-Marie, Barete, Stéphane, Feger, Frédéric, Arock, Michel, Catteau, Benoît, Sans, Beatrix, Stalder, Jean François, Skowron, Francois, Thomas, Luc, Lorette, Gérard, Plantin, Patrice, Bordigoni, Pierre, Lortholary, Olivier, Prost, Yves de, Moussy, Alain, Sobol, Hagay, Dubreuil, Patrice

“…Adult mastocytosis is an incurable clonal disease associated with c-KIT mutations, mostly in exon 17 (D816V). In contrast, pediatric mastocytosis often…”
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Presence of Chimeric Maternally Derived Keratinocytes in Cutaneous Inflammatory Diseases of Children: The Example of Pityriasis Lichenoides by Khosrotehrani, Kiarash, Guegan, Sarah, Fraitag, Sylvie, Oster, Michèle, de Prost, Yves, Bodemer, Christine, Aractingi, Selim

“…During pregnancy, maternal cells may enter the fetal circulation and persist until adulthood. The fate of these cells remains unknown. As unexplained…”
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Identification of new RECQL4 mutations in Caucasian Rothmund-Thomson patients and analysis of sensitivity to a wide range of genotoxic agents by Cabral, Rosa Estela Caseira, Queille, Sophie, Bodemer, Christine, de Prost, Yves, Neto, Januario Bispo Cabral, Sarasin, Alain, Daya-Grosjean, Leela

“…Rothmund-Thomson syndrome (RTS), a rare recessive autosomal disorder, presents genome instability and clinical heterogeneity with growth deficiency, skin and…”
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Epigallocatechin Gallate's Protective Effect against MMP7 in Recessive Dystrophic Epidermolysis Bullosa Patients by Changotade, Sylvie Igondjo-Tchen, Assoumou, Antoine, Guéniche, Farida, Fioretti, Florence, Séguier, Sylvie, de Prost, Yves, Bodemer, Christine, Godeau, Gaston, Senni, Karim

“…The analysis of phenotype–genotype correlations of patients suffering from recessive dystrophic epidermolysis bullosa (RDEB) evidenced intrafamilial and…”
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Homozygosity Mapping of a Locus for a Novel Syndromic Ichthyosis to Chromosome 3q27–q28 by Baala, Lekbir, Hadj-Rabia, Smaïl, Hamel-Teillac, Dominique, Hadchouel, Michelle, Prost, Catherine, Leal, Suzanne M., Jacquemin, Emmanuel, Sefiani, Abdelaziz, de Prost, Yves, Courtois, Gilles, Munnich, Arnold, Lyonnet, Stanislas, Vabres, Pierre

“…Ichthyosis is a heterogeneous group of skin disorders characterized by abnormal epidermal scaling. Occasionally, extracutaneous features are associated. A…”
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Hair and Skin Disorders as Signs of Mitochondrial Disease by Bodemer, Christine, Rotig, Agnes, Rustin, Pierre, Cormier, Valerie, Niaudet, Patrick, Saudubray, Jean-Marie, Rabier, Denis, Munnich, Arnold, de Prost, Yves

“…To compare and explore the skin manifestations of mitochondrial disorders in 14 children with puzzling and unexpected cutaneous presentations. One hundred…”
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