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 *

106 related articles for article (PubMed ID: 15604887)

  • 21. Heritable defects of the human TLR signalling pathways.
    Puel A; Yang K; Ku CL; von Bernuth H; Bustamante J; Santos OF; Lawrence T; Chang HH; Al-Mousa H; Picard C; Casanova JL
    J Endotoxin Res; 2005; 11(4):220-4. PubMed ID: 16176658
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Molecular diagnosis of primary immunodeficiencies].
    García Rodríguez MC; López Granados E; Cambronero Martínez R; Ferreira Cerdán A; Fontán Casariego G
    Allergol Immunopathol (Madr); 2001; 29(3):107-13. PubMed ID: 11434883
    [TBL] [Abstract][Full Text] [Related]  

  • 23. X-linked immunodeficiencies.
    Ochs HD; Notarangelo LD
    Curr Allergy Asthma Rep; 2004 Sep; 4(5):339-48. PubMed ID: 15283872
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies.
    D'Assante R; Fusco A; Palamaro L; Giardino G; Gallo V; Cirillo E; Pignata C
    Int Rev Immunol; 2016; 35(1):25-38. PubMed ID: 25774666
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Human IκBα Gain of Function: a Severe and Syndromic Immunodeficiency.
    Boisson B; Puel A; Picard C; Casanova JL
    J Clin Immunol; 2017 Jul; 37(5):397-412. PubMed ID: 28597146
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Mendelian traits causing susceptibility to mucocutaneous fungal infections in human subjects.
    Engelhardt KR; Grimbacher B
    J Allergy Clin Immunol; 2012 Feb; 129(2):294-305; quiz 306-7. PubMed ID: 22284928
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Autosomal dominant anhidrotic ectodermal dysplasias at the EDARADD locus.
    Bal E; Baala L; Cluzeau C; El Kerch F; Ouldim K; Hadj-Rabia S; Bodemer C; Munnich A; Courtois G; Sefiani A; Smahi A
    Hum Mutat; 2007 Jul; 28(7):703-9. PubMed ID: 17354266
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Recurrent CXCR4 sequence variation in a girl with WHIM syndrome.
    Alapi K; Erdos M; Kovács G; Maródi L
    Eur J Haematol; 2007 Jan; 78(1):86-8. PubMed ID: 17087743
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The hyperimmunoglobulin E syndrome--clinical manifestation diversity in primary immune deficiency.
    Szczawinska-Poplonyk A; Kycler Z; Pietrucha B; Heropolitanska-Pliszka E; Breborowicz A; Gerreth K
    Orphanet J Rare Dis; 2011 Nov; 6():76. PubMed ID: 22085750
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Molecular genetics of X-linked primary immunodeficiencies: advances in diagnosis and prevention].
    Carbonara A; Brusco A; Carbonara C
    Ann Ital Med Int; 1996; 11(3):180-6. PubMed ID: 8998263
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Severe congenital neutropenia: new genes explain an old disease.
    Bohn G; Welte K; Klein C
    Curr Opin Rheumatol; 2007 Nov; 19(6):644-50. PubMed ID: 17917547
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Diagnosis and treatment in anhidrotic ectodermal dysplasia with immunodeficiency.
    Kawai T; Nishikomori R; Heike T
    Allergol Int; 2012 Jun; 61(2):207-17. PubMed ID: 22635013
    [TBL] [Abstract][Full Text] [Related]  

  • 33. STAT mutations as program switchers: turning primary immunodeficiencies into autoimmune diseases.
    Lorenzini T; Dotta L; Giacomelli M; Vairo D; Badolato R
    J Leukoc Biol; 2017 Jan; 101(1):29-38. PubMed ID: 27803128
    [TBL] [Abstract][Full Text] [Related]  

  • 34. The range of defects associated with nuclear factor kappaB essential modulator.
    Uzel G
    Curr Opin Allergy Clin Immunol; 2005 Dec; 5(6):513-8. PubMed ID: 16264331
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Pulmonary complications of primary immunodeficiencies.
    Buckley RH
    Paediatr Respir Rev; 2004; 5 Suppl A():S225-33. PubMed ID: 14980276
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Signal transducer and activator of transcription gain-of-function primary immunodeficiency/immunodysregulation disorders.
    Consonni F; Dotta L; Todaro F; Vairo D; Badolato R
    Curr Opin Pediatr; 2017 Dec; 29(6):711-717. PubMed ID: 28914637
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Dysregulatory syndromes: the role of signal transducers and activators of transcription.
    Bezrodnik L; Gaillard MI; Caldirola MS
    Curr Opin Pediatr; 2018 Dec; 30(6):821-828. PubMed ID: 30407975
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Familial occurrence of warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome.
    Siedlar M; Rudzki Z; Strach M; Trzyna E; Pituch-Noworolska A; Błaut-Szlósarczyk A; Bukowska-Strakova K; Lenart M; Grodzicki T; Zembala M
    Arch Immunol Ther Exp (Warsz); 2008; 56(6):419-25. PubMed ID: 19043667
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Description and outcome of a cohort of 8 patients with WHIM syndrome from the French Severe Chronic Neutropenia Registry.
    Beaussant Cohen S; Fenneteau O; Plouvier E; Rohrlich PS; Daltroff G; Plantier I; Dupuy A; Kerob D; Beaupain B; Bordigoni P; Fouyssac F; Delezoide AL; Devouassoux G; Nicolas JF; Bensaid P; Bertrand Y; Balabanian K; Chantelot CB; Bachelerie F; Donadieu J
    Orphanet J Rare Dis; 2012 Sep; 7():71. PubMed ID: 23009155
    [TBL] [Abstract][Full Text] [Related]  

  • 40. X-linked immunodeficiencies.
    Conley ME
    Curr Opin Genet Dev; 1994 Jun; 4(3):401-6. PubMed ID: 7919918
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.