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The French national registry of primary immunodeficiency diseases.

Clinical immunology (Orlando, Fla.), May 2010, Vol.135(2), pp.264-272 [Peer Reviewed Journal]

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Onset of autoimmune lymphoproliferative syndrome (ALPS) in humans as a consequence of genetic defect accumulation

Journal of Clinical Investigation, 4 January 2011, Vol.121(1), pp.106-112 [Peer Reviewed Journal]

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A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation.

Blood, November 3, 2011, Vol.118(18), pp.4798-4807 [Peer Reviewed Journal]

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Clinical picture and treatment of 2212 patients with common variable immunodeficiency.

The Journal of allergy and clinical immunology, July 2014, Vol.134(1), pp.116-126 [Peer Reviewed Journal]

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Evidence of innate lymphoid cell redundancy in humans

Nature Immunology, Nov 2016, Vol.17(11), pp.1291-1299 [Peer Reviewed Journal]

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Corrigendum: Evidence of innate lymphoid cell redundancy in humans

Nature Immunology, Dec 2016, Vol.17(12), p.1479 [Peer Reviewed Journal]

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Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) study.

The Journal of allergy and clinical immunology, April 2017, Vol.139(4), pp.1275-1281.e7 [Peer Reviewed Journal]

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Autoimmune and inflammatory manifestations occur frequently in patients with primary immunodeficiencies.

The Journal of allergy and clinical immunology, November 2017, Vol.140(5), pp.1388-1393.e8 [Peer Reviewed Journal]

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Type I interferon-mediated autoinflammation due to DNase II deficiency.

Nature communications, December 19, 2017, Vol.8(1), p.2176 [Peer Reviewed Journal]

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Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency.

The Journal of pediatrics, March 2018, Vol.194, pp.211-217.e5 [Peer Reviewed Journal]

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by this Author/Contributor:

  1. Neven, Bénédicte
  2. Picard, Capucine
  3. Michel, Gérard
  4. Fischer, Alain
  5. Blanche, Stéphane

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