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TITLE: The rare DRB1*04:08-DQ8 haplotype is the main HLA class II genetic driver and discriminative factor of Early-onset Type 1 diabetes in the Portuguese population  Full Text
AUTHORS: Caramalho, Iris; Matoso, Paula; Ligeiro, Dario; Paixao, Tiago; Sobral, Daniel; Fitas, Ana Laura; Limbert, Catarina; Demengeot, Jocelyne; Penha Goncalves, Carlos;
PUBLISHED: 2024, SOURCE: FRONTIERS IN IMMUNOLOGY, VOLUME: 14
INDEXED IN: Scopus WOS CrossRef: 1 Handle
IN MY: ORCID
2
TITLE: Adoptive Transfer and Bone Marrow Chimera Models to Analyze Treg Function and Differentiation
AUTHORS: da Silva Domingues, V; Caramalho, I; Bergman, ML; Demengeot, J;
PUBLISHED: 2023, SOURCE: Methods in Molecular Biology, VOLUME: 2559
INDEXED IN: Scopus CrossRef: 1
IN MY: ORCID
4
TITLE: The rare DRB1*04-DQ8 haplotype is the main discriminative HLA class II genetic driver of Early-Onset Type 1 Diabetes in the Portuguese population
AUTHORS: Iris Caramalho; Paula Matoso; Dário Ligeiro; Tiago Paixão; Daniel Sobral; Ana Laura Fitas; Catarina Limbert; Jocelyne Demengeot; Carlos Penha-Gonçalves;
PUBLISHED: 2023
INDEXED IN: CrossRef
IN MY: ORCID
5
TITLE: Influence of the mesenchymal stromal cell source on the hematopoietic supportive capacity of umbilical cord blood-derived CD34(+)-enriched cells  Full Text
AUTHORS: Bucar, S; Branco, ADD; Mata, MF; Milhano, JC; Caramalho, I; Cabral, JMS; Fernandes Platzgummer, A; da Silva, CL;
PUBLISHED: 2021, SOURCE: STEM CELL RESEARCH & THERAPY, VOLUME: 12, ISSUE: 1
INDEXED IN: WOS CrossRef: 8
IN MY: ORCID
6
TITLE: The multifaceted Foxp3(fgfp) allele enhances spontaneous and therapeutic immune surveillance of cancer in mice  Full Text
AUTHORS: Almeida Santos, J; Bergman, ML; Cabral, IA; Correia, V; Caramalho, I; Demengeot, J;
PUBLISHED: 2020, SOURCE: EUROPEAN JOURNAL OF IMMUNOLOGY, VOLUME: 50, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 3
IN MY: ORCID
7
TITLE: LRBA deficiency: a new genetic cause of monogenic lupus
AUTHORS: Liphaus, BL; Caramalho, I; Rangel Santos, A; Silva, CA; Demengeot, J; Carneiro Sampaio, MMS;
PUBLISHED: 2020, SOURCE: ANNALS OF THE RHEUMATIC DISEASES, VOLUME: 79, ISSUE: 3
INDEXED IN: Scopus WOS CrossRef: 11
IN MY: ORCID
8
TITLE: MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation  Full Text
AUTHORS: Moraes Fontes, MF; Caramalho, I; Hsu, AP; Holland, SM; Abecasis, M;
PUBLISHED: 2019, SOURCE: JOURNAL OF CLINICAL IMMUNOLOGY, VOLUME: 39, ISSUE: 1
INDEXED IN: Scopus WOS CrossRef: 2
IN MY: ORCID
9
TITLE: Expansion of FOXP3(+) regulatory CD4 T cells upon exposure to hymenoptera venom during the beekeeping season  Full Text
AUTHORS: Santos, MCP; Serra Caetano, A; Pedro, E; Melo, A; Caramalho, I; Barbosa, MP; Victorino, RMM; Sousa, AE;
PUBLISHED: 2019, SOURCE: ALLERGY, VOLUME: 74, ISSUE: 6
INDEXED IN: Scopus WOS CrossRef: 5
IN MY: ORCID
10
TITLE: Children with type 1 diabetes of early age at onset - immune and metabolic phenotypes
AUTHORS: Luis, MS; Alcafache, M; Ferreira, S; Fitas, AL; Pereira, JS; Caramalho, I; Lopes, L; Limbert, C;
PUBLISHED: 2019, SOURCE: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, VOLUME: 32, ISSUE: 9
INDEXED IN: Scopus WOS CrossRef: 7
IN MY: ORCID
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