7 results on '"Kaustio, Meri"'
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2. Relevance of Coding Variation in FLG And DOCK8 in Finnish Pediatric Patients with Early-Onset Moderate-To-Severe Atopic Dermatitis
3. 49 Early-Onset Common Variable Immunodeficiency in a Patient with Heterozygous Variants in Interferon Response-Associated Genes TRAF3 and IRF4
4. Autoimmunity, hypogammaglobulinemia, lymphoproliferation, and mycobacterial disease in patients with activating mutations in STAT3
5. Long-term follow up of families with pathogenic NFKB1 variants reveals incomplete penetrance and frequent inflammatory sequelae
6. Constant B cell lymphocytosis since early age in a patient with CARD11 mutation: A 20-year follow-up
7. Dominant NFKB1 Mutations Cause Antibody Deficiency and Autoinflammatory Episodes
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