Giuliana Giardino
Address:
Via S.Pansini, 5
Research Interests:
Pediatrics, Immunology, Primary Immunodeficiencies
Biography:
Publications:
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches.
 - Risk factors predisposing to the development of hypogammaglobulinemia and infections post-Rituximab.
 - DiGeorge-like syndrome in a child with a 3p12.3 deletion involving MIR4273 gene born to a mother with gestational diabetes mellitus.
 - Unbalanced Immune System: Immunodeficiencies and Autoimmunity.
 - Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype.
 - Clinical heterogeneity of dominant chronic mucocutaneous candidiasis disease: presenting as treatment-resistant candidiasis and chronic lung disease.
 - Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.
 - Severe combined immunodeficiency-an update.
 - Novel STAT1 gain-of-function mutation and suppurative infections.
 - B cells from nuclear factor kB essential modulator deficient patients fail to differentiate to antibody secreting cells in response to TLR9 ligand.
 - Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects.
 - Insight into IKBKG/NEMO locus: Report of new mutations and complex genomic rearrangements leading to incontinentia pigmenti disease.