Expanding the clinical spectrum of hereditary fibrosing poikiloderma with tendon contractures, myopathy and pulmonary fibrosis due to FAM111B mutations
2015 · Orphanet Journal of Rare Diseases · 48 citations
https://doi.org/10.1186/s13023-015-0352-4
C
C. Méni
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11
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11
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C. Méni is an academic researcher from Hôpital Necker-Enfants Malades. The author has contributed to research in topics: Mast cells and histamine & Urticaria and Related Conditions & Food Allergy and Anaphylaxis Research. The author has an h-index of 11, co-authored 45 publications.
ORCID: 0000-0003-2272-378XPapers by this author
worksFamily burden in inherited ichthyosis: creation of a specific questionnaire
2013 · Orphanet Journal of Rare Diseases · 48 citations
https://doi.org/10.1186/1750-1172-8-28
JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study
2023 · Journal of Clinical Immunology · 35 citations
https://doi.org/10.1007/s10875-023-01500-z
Pathophysiologic implications of elevated prevalence of hereditary alpha-tryptasemia in all mastocytosis subtypes
2023 · Journal of Allergy and Clinical Immunology · 30 citations
https://doi.org/10.1016/j.jaci.2023.08.015
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