Importance of therapeutic patient education in ichthyosis: results of a prospective single reference center study

od Dufresne, Helene, Hadj-Rabia, Smail, Taïeb, Charles, Bodemer, Christine
Izdano 2013

Incontinentia pigmenti burden scale: designing a family burden questionnaire

od Taieb, Charles, Hadj-Rabia, Smail, Monnet, Jacques, Bennani, Mohammed, Bodemer, Christine
izdano v Orphanet J Rare Dis (2019)

Family burden in inherited ichthyosis: creation of a specific questionnaire

od Dufresne, Hélène, Hadj-Rabia, Smail, Méni, Cécile, Sibaud, Vincent, Bodemer, Christine, Taïeb, Charles
Izdano 2013

Both recessive and dominant forms of anhidrotic/hypohidrotic ectodermal dysplasia map to chromosome 2q11-q13.

od Baala, L, Hadj Rabia, S, Zlotogora, J, Kabbaj, K, Chhoul, H, Munnich, A, Lyonnet, S, Sefiani, A
Izdano 1999

Early management of sight threatening retinopathy in incontinentia pigmenti

od Michel, Sarah, Reynaud, Clothilde, Daruich, Alejandra, Hadj-Rabia, Smail, Bremond-Gignac, Dominique, Bodemer, Christine, Robert, Matthieu P.
izdano v Orphanet J Rare Dis (2020)

Use of Epidermal Growth Factor Receptor Inhibitor Erlotinib to Treat Palmoplantar Keratoderma in Patients With Olmsted Syndrome Caused by TRPV3 Mutations

od Greco, Céline, Leclerc-Mercier, Stéphanie, Chaumon, Sarah, Doz, François, Hadj-Rabia, Smail, Molina, Thierry, Boucheix, Claude, Bodemer, Christine
izdano v JAMA Dermatol (2020)

Pseudo-engelures de l’enfant et SARS-CoV-2 : quel lien ?

od Fertitta, L., Welfringer, A., Polivka, L., Chhun, S., Ouedrani, A., Chatenoud, L., Hadj-Rabia, S., Sermet-Gaudelus, I., Bodemer, C.
izdano v Ann Dermatol Venereol (2020)

Immunological and virological profile of children with chilblain‐like lesions and SARS‐CoV‐2

od Fertitta, L., Welfringer‐Morin, A., Ouedrani, A., Polivka, L., Chhun, S., Chatenoud, L., Fourgeaud, J., Hadj‐Rabia, S., Temmam, S., Eloit, M., Sermet‐Gaudelus, I., Bodemer, C.
izdano v J Eur Acad Dermatol Venereol (2020)

Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study

od Sbidian Emilie, Hadj-Rabia Smaïl, Riccardi Vincent M, Valeyrie-Allanore Laurence L, Barbarot Sébastien, Chosidow Olivier, Ferkal Salah, Rodriguez Diana, Wolkenstein Pierre, Bastuji-Garin Sylvie
Izdano 2012-09-01

A novel form of syndromic cutis laxa with facial dysmorphism, cleft palate, and mental retardation

od Genevieve, D, Baumann, C, Huber, C, Faivre, L, Sanlaville, D, Bodemer, C, Hadj-Rabia, S, Assoumou, A, Verloes, A, Raqbi, F, Munnich, A, Cormier-Daire, V
Izdano 2004

Clinical characteristics predicting internal neurofibromas in 357 children with neurofibromatosis-1: results from a cross-selectional study

od Sbidian, Emilie, Hadj-Rabia, Smaïl, Riccardi, Vincent M, Valeyrie-Allanore, Laurence L, Barbarot, Sébastien, Chosidow, Olivier, Ferkal, Salah, Rodriguez, Diana, Wolkenstein, Pierre, Bastuji-Garin, Sylvie
Izdano 2012

Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1(MET)/APR-246

od Aberdam, Edith, Roux, Lauriane N., Secrétan, Philippe-Henri, Boralevi, Franck, Schlatter, Joël, Morice-Picard, Fanny, Sol, Stefano, Bodemer, Christine, Missero, Caterina, Cisternino, Salvatore, Aberdam, Daniel, Hadj-Rabia, Smail
izdano v Cell Death Dis (2020)

Mortality Associated with Neurofibromatosis 1: A Cohort Study of 1895 Patients in 1980-2006 in France

od Duong, Tu Anh, Sbidian, Emilie, Valeyrie-Allanore, Laurence, Vialette, Cédric, Ferkal, Salah, Hadj-Rabia, Smaïl, Glorion, Christophe, Lyonnet, Stanislas, Zerah, Michel, Kemlin, Isabelle, Rodriguez, Diana, Bastuji-Garin, Sylvie, Wolkenstein, Pierre
Izdano 2011

Homozygosity Mapping of a Locus for a Novel Syndromic Ichthyosis to Chromosome 3q27–q28

od 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
izdano v J Invest Dermatol (2002)

Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity

od Hadj-Rabia, Smail, Callewaert, Bert L, Bourrat, Emmanuelle, Kempers, Marlies, Plomp, Astrid S, Layet, Valerie, Bartholdi, Deborah, Renard, Marjolijn, Backer, Julie De, Malfait, Fransiska, Vanakker, Olivier M, Coucke, Paul J, De Paepe, Anne M, Bodemer, Christine
Izdano 2013

New splicing pathogenic variant in EBP causing extreme familial variability of Conradi–Hünermann–Happle Syndrome

od Pacault, Mathilde, Vincent, Marie, Besnard, Thomas, Kannengiesser, Caroline, Bénéteau, Claire, Barbarot, Sébastien, Latypova, Xénia, Belabbas, Khaldia, Lamazière, Antonin, Winer, Norbert, Joubert, Madeleine, Bézieau, Stéphane, Isidor, Bertrand, Mercier, Sandra, Nizon, Mathilde, Leclerc-Mercier, Stéphanie, Hadj-Rabia, Smail, Dufernez, Fabienne
izdano v Eur J Hum Genet (2018)

Multicentre consensus recommendations for skin care in inherited epidermolysis bullosa

od El Hachem, May, Zambruno, Giovanna, Bourdon-Lanoy, Eva, Ciasulli, Annalisa, Buisson, Christiane, Hadj-Rabia, Smail, Diociaiuti, Andrea, Gouveia, Carolina F, Hernández-Martín, Angela, de Lucas Laguna, Raul, Dolenc-Voljč, Mateja, Tadini, Gianluca, Salvatori, Guglielmo, De Ranieri, Cristiana, Leclerc-Mercier, Stephanie, Bodemer, Christine
Izdano 2014

More than keratitis, ichthyosis, and deafness: multisystem effects of lethal GJB2 mutations

od Lilly, Evelyn, Bunick, Christopher G., Maley, Alexander M., Zhang, Shali, Spraker, Mary K, Theos, Amy J, Vivar, Karina L, Seminario-Vidal, Lucia, Bennett, Adam E, Sidbury, Robert, Ogawa, Yasushi, Akiyama, Masashi, Binder, Barbara, Hadj-Rabia, Smail, Morotti, Raffaella A., Glusac, Earl J., Choate, Keith A., Richard, Gabriele, Milstone, Leonard M
izdano v J Am Acad Dermatol (2018)

Epithelial barrier dysfunction in desmoglein-1 deficiency

od Polivka, Laura, Hadj-Rabia, Smail, Bal, Elodie, Leclerc-Mercier, Stéphanie, Madrange, Marine, Hamel, Yamina, Bonnet, Damien, Mallet, Stéphanie, Lepidi, Hubert, Ovaert, Caroline, Barbet, Patrick, Dupont, Christophe, Neven, Bénédicte, Munnich, Arnold, Godsel, Lisa M., Campeotto, Florence, Weil, Robert, Laplantine, Emmanuel, Marchetto, Sylvie, Borg, Jean-Paul, Weis, William I., Casanova, Jean-Laurent, Puel, Anne, Green, Kathleen J., Bodemer, Christine, Smahi, Asma
izdano v J Allergy Clin Immunol (2018)

Mosaic Activating Mutations in GNA11 and GNAQ Are Associated with Phakomatosis Pigmentovascularis and Extensive Dermal Melanocytosis

od Thomas, Anna C., Zeng, Zhiqiang, Rivière, Jean-Baptiste, O’Shaughnessy, Ryan, Al-Olabi, Lara, St.-Onge, Judith, Atherton, David J., Aubert, Hélène, Bagazgoitia, Lorea, Barbarot, Sébastien, Bourrat, Emmanuelle, Chiaverini, Christine, Chong, W. Kling, Duffourd, Yannis, Glover, Mary, Groesser, Leopold, Hadj-Rabia, Smail, Hamm, Henning, Happle, Rudolf, Mushtaq, Imran, Lacour, Jean-Philippe, Waelchli, Regula, Wobser, Marion, Vabres, Pierre, Patton, E. Elizabeth, Kinsler, Veronica A.
izdano v J Invest Dermatol (2016)