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Author

Vassilis Lougaris

Observed name: V Lougaris
OpenAlex ID: A5113487293
Relevance of biallelic versus monoallelic TNFRSF13B mutations in distinguishing disease-causing from risk-increasing TNFRSF13B variants in antibody deficiency syndromes
2008 · Ulrich Salzer, Chiara Bacchelli, et al. · Blood · 286
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Disseminated cryptosporidium infection in an infant with hyper-IgM syndrome caused by CD40 deficiency
2003 · Necil Kutukculer, Daniele Moratto, et al. · The Journal of Pediatrics · 78
Molecular analysis of the pre-BCR complex in a large cohort of patients affected by autosomal-recessive agammaglobulinemia
2007 · S Ferrari, R Zuntini, et al. · Genes and Immunity · 49
Screening of functional and positional candidate genes in families with common variable immunodeficiency
2008 · Ulrich Salzer, Carla Neumann, et al. · BMC Immunology · 38
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Mutations of the X-linked lymphoproliferative disease gene SH2D1A mimicking common variable immunodeficiency
2002 · Annarosa Soresina, Vassilis Lougaris, et al. · European Journal of Pediatrics · 37
Burden of Skin Disease in Selective IgA Deficiency and Common Variable Immunodeficiency.
2015 · G Gualdi, V Lougaris, et al. · PubMed · 22
Diagnostic criteria of hypogammaglobulinemia in infancy
2009 · V Lougaris, A Soresina, et al. · Hematology Meeting Reports · 1
Outcomes of splenectomy in patients with common variable immunodeficiency (CVID): a survey of 45 patients (vol 172, pg 63, 2013)
2013 · Gabriel K. Wong, Sigune Goldacker, et al. · Clinical & Experimental Immunology
Deleterious Lrba Mutations in a Novel Syndrome of Immune Deficiency and Autoimmunity
2012 · Gabriela López‐Herrera, Giacomo Tampella, et al. · Data Archiving and Networked Services (DANS)
Mutations in Lrba Are Associated With a Syndrome of Immune Deficiency and Autoimmunity
2012 · Gabriela López‐Herrera, Giacomo Tampella, et al. · Journal of Clinical Immunology
Works count: 10
Citation count: 511
H-index: 6
I10-index: 6
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