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 *

232 related articles for article (PubMed ID: 8989455)

  • 21. Primary antibody deficiency syndromes.
    Wood P
    Ann Clin Biochem; 2009 Mar; 46(Pt 2):99-108. PubMed ID: 19151170
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Immunological and genetic bases of new primary immunodeficiencies.
    Maródi L; Notarangelo LD
    Nat Rev Immunol; 2007 Nov; 7(11):851-61. PubMed ID: 17960151
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Role of the vascular endothelial growth factor isoforms in retinal angiogenesis and DiGeorge syndrome.
    Stalmans I
    Verh K Acad Geneeskd Belg; 2005; 67(4):229-76. PubMed ID: 16334858
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Antibody deficiency diseases.
    Pan-Hammarström Q; Hammarström L
    Eur J Immunol; 2008 Feb; 38(2):327-33. PubMed ID: 18200502
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Autoimmune manifestations in primary immune deficiencies.
    Bussone G; Mouthon L
    Autoimmun Rev; 2009 Feb; 8(4):332-6. PubMed ID: 19028607
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Immunodeficiencies with autoimmune consequences.
    Notarangelo LD; Gambineri E; Badolato R
    Adv Immunol; 2006; 89():321-70. PubMed ID: 16682278
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Characterization of congenital anomalies in individuals with choanal atresia.
    Burrow TA; Saal HM; de Alarcon A; Martin LJ; Cotton RT; Hopkin RJ
    Arch Otolaryngol Head Neck Surg; 2009 Jun; 135(6):543-7. PubMed ID: 19528400
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Hereditary orotic aciduria: a defect of pyrimidine metabolism with cellular immunodeficiency.
    Girot R; Durandy A; Perignon JL; Griscelli C
    Birth Defects Orig Artic Ser; 1983; 19(3):313-6. PubMed ID: 6606448
    [No Abstract]   [Full Text] [Related]  

  • 29. Novel primary immunodeficiencies relevant to internal medicine: novel phenotypes.
    Maródi L; Casanova JL
    J Intern Med; 2009 Dec; 266(6):502-6. PubMed ID: 19930097
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Immunodeficiency and chromosome instability].
    Weemaes CM; Bakkeren JA; Hustinx TW; van Munster PJ; Scheres JM
    Tijdschr Kindergeneeskd; 1988 Oct; 56(5):209-12. PubMed ID: 3206518
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Antibody deficiency in Wolf-Hirschhorn syndrome.
    Hanley-Lopez J; Estabrooks LL; Stiehm R
    J Pediatr; 1998 Jul; 133(1):141-3. PubMed ID: 9672528
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Cellular and genetic basis of primary immune deficiencies.
    Verbsky JW; Grossman WJ
    Pediatr Clin North Am; 2006 Aug; 53(4):649-84. PubMed ID: 16872998
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Human primary immunodeficiency diseases: a perspective.
    Fischer A
    Nat Immunol; 2004 Jan; 5(1):23-30. PubMed ID: 14699405
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [Progress in pediatric neurology].
    Landrieu P
    Rev Neurol (Paris); 2000 Jul; 156(6-7):595-605. PubMed ID: 10891793
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [Functional disorders of the immune system].
    Schmolke B
    Z Lymphol; 1990 Aug; 14(1):1-16. PubMed ID: 2238798
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Immunology in the medical practice. XXXI. Hereditary immune deficiencies: relationship between clinical symptoms and abnormalities of the immune system].
    Vossen JM; Kuijpers TW
    Ned Tijdschr Geneeskd; 2000 Jul; 144(31):1474-80. PubMed ID: 10941433
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Molecular diagnosis of dysmorphic syndromes and inherited metabolic disorders in Thailand.
    Shotelersuk V
    J Med Assoc Thai; 2003 Jun; 86 Suppl 2():S129-34. PubMed ID: 12929979
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Immunodeficiency mutation databases (IDbases).
    Piirilä H; Väliaho J; Vihinen M
    Hum Mutat; 2006 Dec; 27(12):1200-8. PubMed ID: 17004234
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Molecular and phenotypic markers of hamartomatous polyposis syndromes in the gastrointestinal tract.
    Entius MM; Westerman AM; van Velthuysen ML; Wilson JH; Hamilton SR; Giardiello FM; Offerhaus GJ
    Hepatogastroenterology; 1999; 46(26):661-6. PubMed ID: 10370593
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Restricted immunoglobulin constant heavy G chain genes in primary immunodeficiencies.
    Oxelius VA; Ochs HD; Hammarström L
    Clin Immunol; 2008 Aug; 128(2):190-8. PubMed ID: 18502179
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.