Hadj-Rabia, Smail
Hôpital Necker-Enfants Malades · Université Paris Cité · Assistance Publique – Hôpitaux de Paris
6 papers on CoChatORCID 0000-0001-6801-7106
Most cited papers
- Verified
Pediatric mastocytosis is a clonal disease associated with D816V and other activating c-KIT mutations
Bodemer, C., Hermine, O., Palmérini, F., Yang, Y., Grandpeix-Guyodo, C., Leventhal, P. S., Hadj-Rabia, S., Nasca, L., Georgin-Lavialle, S., Cohen-Akenine, A., et al. (2010) · Journal of Investigative Dermatology
Mast cells and histamineGastrointestinal Tumor Research and Treatment
Cited by 397
- Verified
Only four genes (EDA1, EDAR, EDARADD, and WNT10A) account for 90% of hypohidrotic/anhidrotic ectodermal dysplasia cases
Cluzeau, C., Hadj-Rabia, S., Jambou, M., Mansour, S., Guigue, P., Masmoudi, S., Bal, E., Chassaing, N., Vincent, M.-C., Viot, G., et al. (2011) · Human Mutation
dental development and anomaliesGenetic and rare skin diseases.
Cited by 311
- Verified
Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus
Bal, E., Baala, L., Cluzeau, C., El Kerch, F., Ouldim, K., Hadj-Rabia, S., Bodemer, C., Munnich, A., Courtois, G., Sefiani, A., et al. (2007) · Human Mutation
dental development and anomaliesGenetic and rare skin diseases.
Cited by 100
- Verified
Molecular Pathway-Based Classification of Ectodermal Dysplasias: First Five-Yearly Update
Peschel, N., Wright, J. T., Koster, M. I., Clarke, A. J., Tadini, G., Fete, M., Hadj-Rabia, S., Sybert, V. P., Norderyd, J., Maier-Wohlfart, S., et al. (2022) · Genes
dental development and anomaliesGenetic and rare skin diseases.
Cited by 60
- Verified
Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of KIT. A prospective study
Meni, C., Georgin-Lavialle, S., Le Saché de Peufeilhoux, L., Jais, J. P., Hadj-Rabia, S., Bruneau, J., Fraitag, S., Hanssens, K., Dubreuil, P., Hermine, O., et al. (2018) · British Journal of Dermatology
Mast cells and histamineHistiocytic Disorders and Treatments
Cited by 34
- Verified
Improvement of epidermal covering on AEC patients with severe skin erosions by PRIMA-1MET/APR-246
Aberdam, E., Roux, L. N., Secrétan, P.-H., Boralevi, F., Schlatter, J., Morice-Picard, F., Sol, S., Bodemer, C., Missero, C., Cisternino, S., et al. (2020) · Cell Death & Disease
Genetic and rare skin diseases.Skin and Cellular Biology Research
Cited by 26
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