Iris Caramalho
Lisbon, Portugal
Last Updated: 09/26/2026
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Found 19 publications
Whole Exome Sequencing in Children With Type 1 Diabetes Before Age 6 Years Reveals Insights Into Disease Heterogeneity.
Journal: Journal of diabetes research
Published: February 28, 2024
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.
Journal: Frontiers in immunology
Published: September 22, 2023
Adoptive Transfer and Bone Marrow Chimera Models to Analyze Treg Function and Differentiation.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: September 30, 2022
Influence of the mesenchymal stromal cell source on the hematopoietic supportive capacity of umbilical cord blood-derived CD34+-enriched cells.
Journal: Stem cell research & therapy
Published: March 17, 2021
LRBA deficiency: a new genetic cause of monogenic lupus.
Journal: Annals of the rheumatic diseases
Published: October 01, 2019
The multifaceted Foxp3fgfp allele enhances spontaneous and therapeutic immune surveillance of cancer in mice.
Journal: European journal of immunology
Published: May 21, 2019
Children with type 1 diabetes of early age at onset - immune and metabolic phenotypes.
Journal: Journal of pediatric endocrinology & metabolism : JPEM
Published: February 24, 2019
MonoMAC Syndrome Caused by a Novel GATA2 Mutation Successfully Treated by Allogeneic Hematopoietic Stem Cell Transplantation.
Journal: Journal of clinical immunology
Published: June 22, 2018
Fatal CTLA-4 heterozygosity with autoimmunity and recurrent infections: a de novo mutation.
Journal: Clinical case reports
Published: April 25, 2017
Human naïve regulatory T-cells feature high steady-state turnover and are maintained by IL-7.
Journal: Oncotarget
Published: December 17, 2015
Bee venom enhances the differentiation of human regulatory T cells.
Journal: Allergy
Published: July 05, 2015
Last Updated: 09/26/2026