C. Méni

Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations

Sandra Mercier, Sébastien Küry, Emmanuelle Salort‐Campana et al. · Orphanet Journal of Rare Diseases · 2015 · 48 citations · Full text

Family burden in inherited ichthyosis: creation of a specific questionnaire

H. Dufresne, S. Hadj‐Rabia, C. Méni et al. · Orphanet Journal of Rare Diseases · 2013 · 48 citations · Full text

JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study

Marie‐Louise Frémond, Marie Hully, Benjamin Fournier et al. · Journal of Clinical Immunology · 2023 · 35 citations · Full text

Paediatric mastocytosis: long-term follow-up of 53 patients with whole sequencing of<i>KIT</i>. A prospective study

C. Méni, Sophie Georgin‐Lavialle, L. Le Sachè de Peufeilhoux et al. · British Journal of Dermatology · 2018 · 34 citations

Treatment of Neurofibromas with a Carbon Dioxide Laser: A Retrospective Cross-Sectional Study of 106 Patients

C. Méni, É. Sbidian, J.C. Moreno et al. · Dermatology · 2015 · 33 citations