Becker’s Naevus Syndrome with Breast Aplasia Due to Postzygotic Mutation of ACTB

por RAMSPACHER, Jeanne, CARMIGNAC, Virginie, VABRES, Pierre, MAZEREEUW-HAUTIER, Juliette
Publicado 2022

Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome

por ALBLUWI, Shatha, MAZA, Aude, SEVERINO-FREIRE, Maella, TOURNIER, Emilie, MAZEREEUW-HAUTIER, Juliette
Publicado 2020

Segmental schwannomatosis: characteristics in 12 patients

por Alaidarous, Abdulqader, Parfait, Beatrice, Ferkal, Salah, Cohen, Joëlle, Wolkenstein, Pierre, Mazereeuw-Hautier, Juliette
Publicado 2019

Angiolymphoid hyperplasia with eosinophilia treated with low-dose methotrexate

por Alaidarous, Abdulqader, Bouissou, Xavier, Mazereeuw-Hautier, Juliette, Bulai-Livideanu, Cristina, Lamant, Laurence, Paul, Carle
Publicado 2015

Alitretinoin reduces erythema in inherited ichthyosis

por Onnis, Giuliana, Chiaverini, Christine, Hickman, Geoffroy, Dreyfus, Isabelle, Fischer, Judith, Bourrat, Emmanuelle, Mazereeuw-Hautier, Juliette
Publicado 2018

Prevalence and risk factors of vitamin D deficiency in inherited ichthyosis: A French prospective observational study performed in a reference center

por Frascari, Flora, Dreyfus, Isabelle, Rodriguez, Lauriane, Gennero, Isabelle, Ezzedine, Khaled, Salles, Jean-Pierre, Mazereeuw-Hautier, Juliette
Publicado 2014

Botulinum toxin injections as an effective treatment for patients with intertriginous Hailey-Hailey or Darier disease: an open-label 6-month pilot interventional study

por Dreyfus, Isabelle, Maza, Aude, Rodriguez, Lauriane, Merlos, Margot, Texier, Hélène, Rousseau, Vanessa, Sommet, Agnès, Mazereeuw-Hautier, Juliette
Publicado 2021

Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases

por MAZEREEUW-HAUTIER, Juliette, BOURRAT, Emmanuelle, TOURNIER, Emilie, BATTISTELLA, Maxime, BERNABEU-WITTEL, José, BARBAROT, Sébastien, HERNANDEZ-MARTIN, Angela
Publicado 2021

Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis

por MAZEREEUW-HAUTIER, Juliette, SEVERINO-FREIRE, Maella, GASTON, Véronique, TEXIER, Hélène, VINCENT, Marie, AUBERT, Hélène, MORICE-PICARD, Fanny, JONCA, Nathalie
Publicado 2020

TOPICOP©: A New Scale Evaluating Topical Corticosteroid Phobia among Atopic Dermatitis Outpatients and Their Parents

por Moret, Leïla, Anthoine, Emmanuelle, Aubert-Wastiaux, Hélène, Le Rhun, Anne, Leux, Christophe, Mazereeuw-Hautier, Juliette, Stalder, Jean-François, Barbarot, Sébastien
Publicado 2013

Azathioprine Hypersensitivity Syndrome: Two Cases of Febrile Neutrophilic Dermatosis Induced by Azathioprine

por Aleissa, Majed, Nicol, Perrine, Godeau, Marion, Tournier, Emilie, de Bellissen, Frederic, Robic, Marie-Angèle, Livideanu, Cristina Bulai, Mazereeuw-Hautier, Juliette, Paul, Carle
Publicado 2017

Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis

por Komlosi, Katalin, Claris, Olivier, Collardeau-Frachon, Sophie, Kopp, Julia, Hausser, Ingrid, Mazereeuw-Hautier, Juliette, Jonca, Nathalie, Zimmer, Andreas D., Sanlaville, Damien, Fischer, Judith
Publicado 2021

Health care transition for patients with vascular malformations: a French multicenter cross-sectional study

por Vermersch, Camille, Boccara, Olivia, Chiaverini, Christine, Mazereeuw-Hautier, Juliette, Sigg, Nina, Mallet, Stéphanie, Vabres, Pierre, Herbreteau, Denis, Le Touze, Anne, Maruani, Annabel, Leducq, Sophie
Publicado 2021

Prevalence of inherited ichthyosis in France: a study using capture-recapture method

por Dreyfus, Isabelle, Chouquet, Cécile, Ezzedine, Khaled, Henner, Sophie, Chiavérini, Christine, Maza, Aude, Pascal, Sandrine, Rodriguez, Lauriane, Vabres, Pierre, Martin, Ludovic, Mallet, Stéphanie, Barbarot, Sébastien, Dupuis, Jérôme, Mazereeuw-Hautier, Juliette
Publicado 2014

Perialar intertrigo in children and adolescents: A multicenter prospective study of 41 cases

por Sanchez, Adrien, Mahe, Emmanuel, Miquel, Juliette, Abasq, Claire, Phan, Alice, Mazereeuw‐Hautier, Juliette, Lemille, Juliette, Maruani, Annabel, Bonniaud, Bertille, Plantin, Patrice, Mallet, Stéphanie, Martin, Hélène, Hubiche, Thomas, Chiaverini, Christine, Lacour, Jean‐Philippe
Publicado 2022

Treatment of voluminous and complicated superficial slow-flow vascular malformations with sirolimus (PERFORMUS): protocol for a multicenter phase 2 trial with a randomized observat...

por Maruani, Annabel, Boccara, Olivia, Bessis, Didier, Guibaud, Laurent, Vabres, Pierre, Mazereeuw-Hautier, Juliette, Barbarot, Sébastien, Chiaverini, Christine, Blaise, Sophie, Droitcourt, Catherine, Mallet, Stéphanie, Martin, Ludovic, Lorette, Gérard, Woillard, Jean-Baptiste, Jonville-Bera, Annie-Pierre, Rollin, Jérome, Gruel, Yves, Herbreteau, Denis, Goga, Dominique, le Touze, Anne, Leducq, Sophie, Gissot, Valérie, Morel, Baptiste, Tavernier, Elsa, Giraudeau, Bruno
Publicado 2018

Topical sirolimus 0.1% for treating cutaneous microcystic lymphatic malformations in children and adults (TOPICAL): protocol for a multicenter phase 2, within-person, randomized, d...

por Leducq, Sophie, Caille, Agnès, Barbarot, Sébastien, Bénéton, Nathalie, Bessis, Didier, Boccara, Olivia, Bursztejn, Anne-Claire, Chiaverini, Christine, Dompmartin, Anne, Droitcourt, Catherine, Gissot, Valérie, Goga, Dominique, Guibaud, Laurent, Herbreteau, Denis, Le Touze, Anne, Léauté-Labrèze, Christine, Lorette, Gérard, Mallet, Stéphanie, Martin, Ludovic, Mazereeuw-Hautier, Juliette, Phan, Alice, Plantin, Patrice, Quéré, Isabelle, Vabres, Pierre, Bourgoin, Hélène, Giraudeau, Bruno, Maruani, Annabel
Publicado 2019

Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients

por Hotz, Alrun, Kopp, Julia, Bourrat, Emmanuelle, Oji, Vinzenz, Komlosi, Katalin, Giehl, Kathrin, Bouadjar, Bakar, Bygum, Anette, Tantcheva-Poor, Iliana, Hellström Pigg, Maritta, Has, Cristina, Yang, Zhou, Irvine, Alan D., Betz, Regina C., Zambruno, Giovanna, Tadini, Gianluca, Süßmuth, Kira, Gruber, Robert, Schmuth, Matthias, Mazereeuw-Hautier, Juliette, Jonca, Natalie, Guez, Sophie, Brena, Michela, Hernandez-Martin, Angela, van den Akker, Peter, Bolling, Maria C., Hannula-Jouppi, Katariina, Zimmer, Andreas D., Alter, Svenja, Vahlquist, Anders, Fischer, Judith
Publicado 2021

Severe Phenotype in Patients with Large Deletions of NF1

por Pacot, Laurence, Vidaud, Dominique, Sabbagh, Audrey, Laurendeau, Ingrid, Briand-Suleau, Audrey, Coustier, Audrey, Maillard, Théodora, Barbance, Cécile, Morice-Picard, Fanny, Sigaudy, Sabine, Glazunova, Olga O., Damaj, Lena, Layet, Valérie, Quelin, Chloé, Gilbert-Dussardier, Brigitte, Audic, Frédérique, Dollfus, Hélène, Guerrot, Anne-Marie, Lespinasse, James, Julia, Sophie, Vantyghem, Marie-Christine, Drouard, Magali, Lackmy, Marilyn, Leheup, Bruno, Alembik, Yves, Lemaire, Alexia, Nitschké, Patrick, Petit, Florence, Dieux Coeslier, Anne, Mutez, Eugénie, Taieb, Alain, Fradin, Mélanie, Capri, Yline, Nasser, Hala, Ruaud, Lyse, Dauriat, Benjamin, Bourthoumieu, Sylvie, Geneviève, David, Audebert-Bellanger, Séverine, Nizon, Mathilde, Stoeva, Radka, Hickman, Geoffroy, Nicolas, Gaël, Mazereeuw-Hautier, Juliette, Jannic, Arnaud, Ferkal, Salah, Parfait, Béatrice, Vidaud, Michel, Wolkenstein, Pierre, Pasmant, Eric
Publicado 2021