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Peculiar hyper-IgM syndrome. Case report / Sindrom hiper-IgM atipic. Prezentare de caz

Romanian Journal of Laboratory Medicine, 01 August 2015, Vol.23(3), pp.341-345 [Peer Reviewed Journal]

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Inherited MST1 deficiency underlies susceptibility to EV-HPV infections

PLoS ONE, 01 January 2012, Vol.7(8), p.e44010 [Peer Reviewed Journal]

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Copy number variations and founder effect underlying complete IL-10Rβ deficiency in Portuguese kindreds

PLoS ONE, 01 January 2018, Vol.13(10), p.e0205826 [Peer Reviewed Journal]

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OL-EDA-ID Syndrome: a Novel Hypomorphic NEMO Mutation Associated with a Severe Clinical Presentation and Transient HLH

Journal of Clinical Immunology, 2017, Vol.37(1), pp.7-11 [Peer Reviewed Journal]

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Variant of X-Linked Chronic Granulomatous Disease Revealed by a Severe Burkholderia cepacia Invasive Infection in an Infant

Case Reports in Immunology, 01 January 2013, Vol.2013 [Peer Reviewed Journal]

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Human Adaptive Immunity Rescues an Inborn Error of Innate Immunity

Cell, 2017, Vol.168(5), pp.789-800.e10 [Peer Reviewed Journal]

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B‐cell subpopulations in children: National reference values

Immunity, Inflammation and Disease, Nov 2014, pp.131-140 [Peer Reviewed Journal]

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PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunity

Journal of Allergy and Clinical Immunology, 2015, Vol.135(6), pp.1578-1588 [Peer Reviewed Journal]

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IRAK4 Deficiency in a Patient with Recurrent Pneumococcal Infections: Case Report and Review of the Literature

Frontiers in Pediatrics, 01 April 2017, Vol.5 [Peer Reviewed Journal]

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Autoimmune Lymphoproliferative Syndrome-FAS Patients Have an Abnormal Regulatory T Cell (Treg) Phenotype but Display Normal Natural Treg-Suppressive Function on T Cell Proliferation

Frontiers in Immunology, 01 April 2018, Vol.9 [Peer Reviewed Journal]

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  1. Picard, Capucine
  2. Picard, C
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