27 results on '"Severino‐Freire, Maella"'
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2. Neuropsychiatric, cognitive and sexual impairment in mastocytosis patients
3. Severe gynaecological involvement in Proteus Syndrome
4. cLFM‐Qol : A specific quality of life measurement tool for children from 11 to 15 years with low‐flow malformations
5. Non‐occupational allergic contact dermatitis from epoxy resin in children's games
6. Élaboration et validation d’une échelle dédiée à évaluer spécifiquement l’atteinte cutanée mastocytaire
7. Rôle de la recherche de la mutation KIT cutanée pour le diagnostic de mastocytose
8. Programme d’accompagnement pour la pathologie mastocytaire
9. Le fardeau de la pathologie mastocytaire : étude observationnelle, prospective
10. Apport de la cytométrie de flux médullaire pour le diagnostic de mastocytose systémique
11. Efficacité à très long terme du dupilumab dans la dermatite atopique de l’adulte, en vie réelle : résultats d’une cohorte prospective
12. Non‐occupational allergic contact dermatitis from epoxy resin in children's games.
13. Neuropsychiatric, cognitive and sexual impairment in mastocytosis patients
14. Neuropsychiatric, Cognitive and Sexual Impairment in Mastocytosis Patients
15. A case of merkel leptomeningeal evolution after complete remission upon anti–PD-1 treatment
16. Changements (« switchs ») de biothérapies dans le psoriasis de l’enfant : résultats de la cohorte BiPe
17. Étude multicentrique, rétrospective de l’association des dermatoses bulleuses auto-immunes avec une hémophilie acquise
18. Identification of mutations in SDR9C7 in three patients with autosomal recessive congenital ichthyosis
19. PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-O-acylceramide synthesis and skin permeability barrier
20. O01 Clinical aspects of psoriasis flares and risk factors for developing a post-infectious flare in children with SARS-CoV-2 infection: data from the Chi-PsoCov registry.
21. PNPLA1 defects in patients with autosomal recessive congenital ichthyosis and KO mice sustain PNPLA1 irreplaceable function in epidermal omega-Oacylceramide synthesis and skin permeability barrier.
22. Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis.
23. Keratitis-Ichthyosis-Deafness Syndrome: Early Death Caused by the GJB2 Mutation p.Gly12Arg.
24. Mosaic Focal Dermal Hypoplasia (Goltz Syndrome) in Two Female Patients.
25. Extensive Post-zygotic Mosaicism of KRT1 or KRT10 Mutation Mimicking Classical Epidermolytic Ichthyosis.
26. Cardio-facio-cutaneous Syndrome with Severe Inflammatory Cutaneous Lesions: Dramatic Effect of Dupilumab.
27. Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome.
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