BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

147 related articles for article (PubMed ID: 36155879)

  • 1. Lymphoma as an Exclusion Criteria for CVID Diagnosis Revisited.
    Allain V; Grandin V; Meignin V; Bertinchamp R; Boutboul D; Fieschi C; Galicier L; Gérard L; Malphettes M; Bustamante J; Fusaro M; Lambert N; Rosain J; Lenoir C; Kracker S; Rieux-Laucat F; Latour S; de Villartay JP; Picard C; Oksenhendler E
    J Clin Immunol; 2023 Jan; 43(1):181-191. PubMed ID: 36155879
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The Rapidly Expanding Genetic Spectrum of Common Variable Immunodeficiency-Like Disorders.
    Ameratunga R; Edwards ESJ; Lehnert K; Leung E; Woon ST; Lea E; Allan C; Chan L; Steele R; Longhurst H; Bryant VL
    J Allergy Clin Immunol Pract; 2023 Jun; 11(6):1646-1664. PubMed ID: 36796510
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Exclusion of Patients with a Severe T-Cell Defect Improves the Definition of Common Variable Immunodeficiency.
    Bertinchamp R; Gérard L; Boutboul D; Malphettes M; Fieschi C; Oksenhendler E;
    J Allergy Clin Immunol Pract; 2016; 4(6):1147-1157. PubMed ID: 27522107
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Late-onset combined immune deficiency: a subset of common variable immunodeficiency with severe T cell defect.
    Malphettes M; Gérard L; Carmagnat M; Mouillot G; Vince N; Boutboul D; Bérezné A; Nove-Josserand R; Lemoing V; Tetu L; Viallard JF; Bonnotte B; Pavic M; Haroche J; Larroche C; Brouet JC; Fermand JP; Rabian C; Fieschi C; Oksenhendler E;
    Clin Infect Dis; 2009 Nov; 49(9):1329-38. PubMed ID: 19807277
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The outcome of patients with unclassified hypogammaglobulinemia in early childhood.
    Kutukculer N; Gulez N
    Pediatr Allergy Immunol; 2009 Nov; 20(7):693-8. PubMed ID: 19196447
    [TBL] [Abstract][Full Text] [Related]  

  • 6. [Adult-onset primary hypogammaglobulinemia].
    Fieschi C; Malphettes M; Galicier L; Oksenhendler E
    Presse Med; 2006 May; 35(5 Pt 2):887-94. PubMed ID: 16710162
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The Natural History of Untreated Primary Hypogammaglobulinemia in Adults: Implications for the Diagnosis and Treatment of Common Variable Immunodeficiency Disorders (CVID).
    Ameratunga R; Ahn Y; Steele R; Woon ST
    Front Immunol; 2019; 10():1541. PubMed ID: 31379811
    [No Abstract]   [Full Text] [Related]  

  • 8. Good syndrome: an adult-onset immunodeficiency remarkable for its high incidence of invasive infections and autoimmune complications.
    Malphettes M; Gérard L; Galicier L; Boutboul D; Asli B; Szalat R; Perlat A; Masseau A; Schleinitz N; Le Guenno G; Viallard JF; Bonnotte B; Thiercelin-Legrand MF; Sanhes L; Borie R; Georgin-Lavialle S; Fieschi C; Oksenhendler E;
    Clin Infect Dis; 2015 Jul; 61(2):e13-9. PubMed ID: 25828999
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Common variable immunodeficiency (CVID) in a family: an autosomal dominant mode of inheritance.
    Nijenhuis T; Klasen I; Weemaes CM; Preijers F; de Vries E; van der Meer JW
    Neth J Med; 2001 Sep; 59(3):134-9. PubMed ID: 11583829
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Non-Hodgkin lymphoma in pediatric patients with common variable immunodeficiency.
    Piquer Gibert M; Alsina L; Giner Muñoz MT; Cruz Martínez O; Ruiz Echevarria K; Dominguez O; Plaza Martín AM; Arostegui JI; de Valles G; Juan Otero M; Martin-Mateos MA
    Eur J Pediatr; 2015 Aug; 174(8):1069-76. PubMed ID: 25749928
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum.
    Driessen GJ; Dalm VA; van Hagen PM; Grashoff HA; Hartwig NG; van Rossum AM; Warris A; de Vries E; Barendregt BH; Pico I; Posthumus S; van Zelm MC; van Dongen JJ; van der Burg M
    Haematologica; 2013 Oct; 98(10):1617-23. PubMed ID: 23753020
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders.
    Ameratunga R; Ahn Y; Jordan A; Lehnert K; Brothers S; Woon ST
    Expert Rev Clin Immunol; 2018 Jul; 14(7):549-556. PubMed ID: 29806948
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia.
    Aghamohammadi A; Allahverdi A; Abolhassani H; Moazzami K; Alizadeh H; Gharagozlou M; Kalantari N; Sajedi V; Shafiei A; Parvaneh N; Mohammadpour M; Karimi N; Sadaghiani MS; Rezaei N
    Respirology; 2010 Feb; 15(2):289-95. PubMed ID: 20051045
    [TBL] [Abstract][Full Text] [Related]  

  • 14. In-depth blood immune profiling of Good syndrome patients.
    Torres-Valle A; Aragon L; Silva SL; Serrano C; Marcos M; Melero J; Bonroy C; Arenas-Caro PP; Casado DM; Olaizola PMR; Neirinck J; Hofmans M; de Arriba S; Jara M; Prieto C; Sousa AE; Prada Á; van Dongen JJM; Pérez-Andrés M; Orfao A
    Front Immunol; 2023; 14():1285088. PubMed ID: 38035080
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Common Variable Immunodeficiency-Associated Cancers: The Role of Clinical Phenotypes, Immunological and Genetic Factors.
    Bruns L; Panagiota V; von Hardenberg S; Schmidt G; Adriawan IR; Sogka E; Hirsch S; Ahrenstorf G; Witte T; Schmidt RE; Atschekzei F; Sogkas G
    Front Immunol; 2022; 13():742530. PubMed ID: 35250968
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Identification of patients with RAG mutations previously diagnosed with common variable immunodeficiency disorders.
    Buchbinder D; Baker R; Lee YN; Ravell J; Zhang Y; McElwee J; Nugent D; Coonrod EM; Durtschi JD; Augustine NH; Voelkerding KV; Csomos K; Rosen L; Browne S; Walter JE; Notarangelo LD; Hill HR; Kumánovics A
    J Clin Immunol; 2015 Feb; 35(2):119-24. PubMed ID: 25516070
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Parental consanguinity is associated with a severe phenotype in common variable immunodeficiency.
    Rivoisy C; Gérard L; Boutboul D; Malphettes M; Fieschi C; Durieu I; Tron F; Masseau A; Bordigoni P; Alric L; Haroche J; Hoarau C; Bérézné A; Carmagnat M; Mouillot G; Oksenhendler E;
    J Clin Immunol; 2012 Feb; 32(1):98-105. PubMed ID: 22002594
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [Common variable immunodeficiency disorders: Updated diagnostic criteria and genetics].
    Fieschi C; Viallard JF
    Rev Med Interne; 2021 Jul; 42(7):465-472. PubMed ID: 33875312
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Involvement of miR-142 and miR-155 in Non-Infectious Complications of CVID.
    Amato G; Vita F; Quattrocchi P; Minciullo PL; Pioggia G; Gangemi S
    Molecules; 2020 Oct; 25(20):. PubMed ID: 33081305
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common variable immunodeficiency: test indications and interpretations.
    Weiler CR; Bankers-Fulbright JL
    Mayo Clin Proc; 2005 Sep; 80(9):1187-200. PubMed ID: 16178499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.