These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

72 related articles for article (PubMed ID: 926354)

  • 21. [Compensated or minor anomalies of the immune system].
    Vel'tishchev IuE
    Sov Med; 1988; (7):46-50. PubMed ID: 3147516
    [No Abstract]   [Full Text] [Related]  

  • 22. Combined immunodeficiency associated with increased apoptosis of lymphocytes and radiosensitivity fibroblasts.
    Peake J; Waugh A; Le Deist F; Priestley A; Rieux-Laucat F; Foray N; Capulas E; Singleton BK; de Villartay JP; Cant A; Malaise EP; Fischer A; Hivroz C; Jeggo PA
    Cancer Res; 1999 Jul; 59(14):3454-60. PubMed ID: 10416610
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Immunodeficiency. Detection of immune deficiency states by the primary care physician.
    Straub DL; Hulett AC; Dockhorn RJ
    J Kans Med Soc; 1978 Jul; 79(7):311-6. PubMed ID: 307585
    [No Abstract]   [Full Text] [Related]  

  • 24. [Severe familial combined immunodeficiency with presence of B-lymphocytes and lymphoid dissociation. Attempted immunological reconstitution].
    Allergol Immunopathol (Madr); 1977; 5(3):179-88. PubMed ID: 302086
    [No Abstract]   [Full Text] [Related]  

  • 25. Two siblings with autosomal recessive form of severe combined immune deficiency disease.
    Ninomiya T; Nishikawa K; Miyao M
    Nihon Ketsueki Gakkai Zasshi; 1976 Feb; 39(1):73-8. PubMed ID: 989233
    [No Abstract]   [Full Text] [Related]  

  • 26. [Analysis of leukocyte adhesion deficiency].
    Kobayashi K
    Hokkaido Igaku Zasshi; 1991 May; 66(3):241-6. PubMed ID: 1885153
    [No Abstract]   [Full Text] [Related]  

  • 27. Inherited disorders of lymphocyte development and function.
    Fischer A
    Curr Opin Immunol; 1996 Aug; 8(4):445-7. PubMed ID: 8794017
    [No Abstract]   [Full Text] [Related]  

  • 28. Malignancy in children with and without genetically-determined immunodeficiencies.
    Spector BD; Perry GS; Gajl-Peczalska KJ; Coccia P; Nesbit ME; Kersey JH
    Birth Defects Orig Artic Ser; 1978; 14(6A):85-9. PubMed ID: 365263
    [No Abstract]   [Full Text] [Related]  

  • 29. Pleiotropic defects in lymphocyte activation caused by caspase-8 mutations lead to human immunodeficiency.
    Chun HJ; Zheng L; Ahmad M; Wang J; Speirs CK; Siegel RM; Dale JK; Puck J; Davis J; Hall CG; Skoda-Smith S; Atkinson TP; Straus SE; Lenardo MJ
    Nature; 2002 Sep; 419(6905):395-9. PubMed ID: 12353035
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Severe combined immunodeficiency and adenosine deaminase deficiency.
    Parkman R; Gelfand EW; Rosen FS; Sanderson A; Hirschhorn R
    N Engl J Med; 1975 Apr; 292(14):714-9. PubMed ID: 1089883
    [TBL] [Abstract][Full Text] [Related]  

  • 31. [Cellular immunologic examination in suspected immunodeficiency. Presentation of a laboratory material].
    Egeland T; Mellbye OJ
    Tidsskr Nor Laegeforen; 1987 Nov; 107(31):2759-62. PubMed ID: 3424315
    [No Abstract]   [Full Text] [Related]  

  • 32. Cutaneous graft-versus-host-like histology in childhood. Importance of clonality analysis in differential diagnosis. A case report.
    D'hauw A; Seyger MM; Groenen PJ; Weemaes CM; Warris A; Blokx WA
    Br J Dermatol; 2008 May; 158(5):1153-6. PubMed ID: 18341659
    [No Abstract]   [Full Text] [Related]  

  • 33. A familial aggregate of common variable immunodeficiency, Hodgkin disease and other malignancies in Newfoundland--I. Clinical features.
    Marshall WH; Buehler SK; Crumley J; Salmon D; Landre MF; Fraser GR
    Clin Invest Med; 1979; 2(4):153-9. PubMed ID: 583571
    [No Abstract]   [Full Text] [Related]  

  • 34. Cellular immune deficiency in two siblings with hereditary orotic aciduria.
    Girot R; Hamet M; Perignon JL; Guesnu M; Fox RM; Cartier P; Durandy A; Griscelli C
    N Engl J Med; 1983 Mar; 308(12):700-4. PubMed ID: 6828110
    [No Abstract]   [Full Text] [Related]  

  • 35. [Bone marrow transplantation in genetic diseases].
    Torres Gómez A
    An Esp Pediatr; 1989 Sep; 31 Suppl 39():109-13. PubMed ID: 2490308
    [No Abstract]   [Full Text] [Related]  

  • 36. Genetic analysis of the human CD3-epsilon gene in a T cell receptor/CD3 immunodeficiency.
    Soudais C; De Villartay JP; Le Deist F; Fischer A; Lisowska-Grospierre B
    Immunodeficiency; 1993; 4(1-4):117-9. PubMed ID: 8167684
    [No Abstract]   [Full Text] [Related]  

  • 37. [Griscelli syndrome].
    Svenningsen P; Petersen BL; Ryder LP; Broholm H; Møller-Hansen KJ; Glenthøj JP; Heilmann CJ; Müller KG
    Ugeskr Laeger; 2004 Feb; 166(7):600-2. PubMed ID: 15005046
    [No Abstract]   [Full Text] [Related]  

  • 38. X-linked immunodeficiency diseases.
    Lederman HM; Mak H; Pepple JM; Winkelstein JA
    Johns Hopkins Med J; 1980 Jul; 147(1):33-9. PubMed ID: 7189803
    [No Abstract]   [Full Text] [Related]  

  • 39. [Immune system and immunodeficiency].
    Sapin MR
    Klin Med (Mosk); 1999; 77(1):5-11. PubMed ID: 10097498
    [No Abstract]   [Full Text] [Related]  

  • 40. [Various hereditary immune deficiencies linked to the X-chromosome].
    Ivanovskaia TE; Gurevich PS; Katasonova LP; Parsegova TS; Talalaev AG
    Arkh Patol; 1986; 48(5):53-9. PubMed ID: 3741177
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 4.