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 *

122 related articles for article (PubMed ID: 11486910)

  • 1. Mevalonic aciduria and hyper-IgD syndrome: two sides of the same coin?
    Tsimaratos M; Kone-Paut I; Divry P; Philip N; Chabrol B
    J Inherit Metab Dis; 2001 Jun; 24(3):413-4. PubMed ID: 11486910
    [No Abstract]   [Full Text] [Related]  

  • 2. Mevalonate kinase deficiency in a child with periodic fever and without hyperimmunoglobulinaemia D.
    Di Rocco M; Caruso U; Waterham HR; Picco P; Loy A; Wanders RJ
    J Inherit Metab Dis; 2001 Jun; 24(3):411-2. PubMed ID: 11486909
    [No Abstract]   [Full Text] [Related]  

  • 3. Mevalonic aciduria in 12 unrelated patients with hyperimmunoglobulinaemia D and periodic fever syndrome.
    Poll-The BT; Frenkel J; Houten SM; Kuis W; Duran M; de Koning TJ; Dorland L; de Barse MM; Romeijn GJ; Wanders RJ; Waterham HR
    J Inherit Metab Dis; 2000 Jun; 23(4):363-6. PubMed ID: 10896295
    [No Abstract]   [Full Text] [Related]  

  • 4. Molecular basis of classical mevalonic aciduria and the hyperimmunoglobulinaemia D and periodic fever syndrome: high frequency of 3 mutations in the mevalonate kinase gene.
    Houten SM; Frenkel J; Kuis W; Wanders RJ; Poll-The BT; Waterham HR
    J Inherit Metab Dis; 2000 Jun; 23(4):367-70. PubMed ID: 10896296
    [No Abstract]   [Full Text] [Related]  

  • 5. Mevalonate kinase deficiency: Evidence for a phenotypic continuum.
    Simon A; Kremer HP; Wevers RA; Scheffer H; De Jong JG; Van Der Meer JW; Drenth JP
    Neurology; 2004 Mar; 62(6):994-7. PubMed ID: 15037710
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Hereditary periodic fever.
    Kelley RI; Takada I
    N Engl J Med; 2002 May; 346(18):1415-6; author reply 1415-6. PubMed ID: 11987326
    [No Abstract]   [Full Text] [Related]  

  • 7. [Identification of the gene for hyper-IgD syndrome: a model of modern genetics].
    Drenth JP; Waterham HR; Kuis W; Houten SM; Frenkel J; Wanders RJ; Poll-The BT; van der Meer JW
    Ned Tijdschr Geneeskd; 2000 Apr; 144(17):782-5. PubMed ID: 10800545
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mevalonate kinase deficiency: enlarging the clinical and biochemical spectrum.
    Prietsch V; Mayatepek E; Krastel H; Haas D; Zundel D; Waterham HR; Wanders RJ; Gibson KM; Hoffmann GF
    Pediatrics; 2003 Feb; 111(2):258-61. PubMed ID: 12563048
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Temperature dependence of mutant mevalonate kinase activity as a pathogenic factor in hyper-IgD and periodic fever syndrome.
    Houten SM; Frenkel J; Rijkers GT; Wanders RJ; Kuis W; Waterham HR
    Hum Mol Genet; 2002 Dec; 11(25):3115-24. PubMed ID: 12444096
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mevalonate kinase deficiencies: from mevalonic aciduria to hyperimmunoglobulinemia D syndrome.
    Haas D; Hoffmann GF
    Orphanet J Rare Dis; 2006 Apr; 1():13. PubMed ID: 16722536
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome.
    Houten SM; Koster J; Romeijn GJ; Frenkel J; Di Rocco M; Caruso U; Landrieu P; Kelley RI; Kuis W; Poll-The BT; Gibson KM; Wanders RJ; Waterham HR
    Eur J Hum Genet; 2001 Apr; 9(4):253-9. PubMed ID: 11313768
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [MVK gene abnormality and new approach to treatment of hyper IgD syndrome and periodic fever syndrome].
    Naruto T
    Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr; 30(2):86-9. PubMed ID: 17473510
    [TBL] [Abstract][Full Text] [Related]  

  • 13. High IgD could be a nonpathogenetic diagnostic marker of the hyper-IgD and periodic fever syndrome.
    de Dios García-Díaz J; Alvarez-Blanco MJ
    Ann Allergy Asthma Immunol; 2001 May; 86(5):587. PubMed ID: 11379812
    [No Abstract]   [Full Text] [Related]  

  • 14. Allogeneic bone marrow transplantation in mevalonic aciduria.
    Neven B; Valayannopoulos V; Quartier P; Blanche S; Prieur AM; Debré M; Rolland MO; Rabier D; Cuisset L; Cavazzana-Calvo M; de Lonlay P; Fischer A
    N Engl J Med; 2007 Jun; 356(26):2700-3. PubMed ID: 17596604
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mevalonate kinase deficiency in a dizygotic twin with mild mevalonic aciduria.
    Gibson KM; Hoffmann GF; Sweetman L; Buckingham B
    J Inherit Metab Dis; 1997 Jul; 20(3):391-4. PubMed ID: 9266363
    [No Abstract]   [Full Text] [Related]  

  • 16. Bile acid metabolism in three patients with mevalonic aciduria due to mevalonate kinase deficiency.
    Gibson KM; Stellaard F; Hoffmann GF; Rating D; Hrebicek M; Jakobs C
    Clin Chim Acta; 1993 Aug; 217(2):217-20. PubMed ID: 8261631
    [No Abstract]   [Full Text] [Related]  

  • 17. [Mevalonic aciduria].
    Yoshida I
    Ryoikibetsu Shokogun Shirizu; 1998; (18 Pt 1):305-9. PubMed ID: 9590053
    [No Abstract]   [Full Text] [Related]  

  • 18. Molecular analysis of MVK mutations and enzymatic activity in hyper-IgD and periodic fever syndrome.
    Cuisset L; Drenth JP; Simon A; Vincent MF; van der Velde Visser S; van der Meer JW; Grateau G; Delpech M;
    Eur J Hum Genet; 2001 Apr; 9(4):260-6. PubMed ID: 11313769
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hyper-IgD syndrome in a patient with IgA immunodeficiency.
    Smerla RG; Agrafiotou C; Fragoulis GE
    Clin Exp Rheumatol; 2018; 36(5):934. PubMed ID: 30148429
    [No Abstract]   [Full Text] [Related]  

  • 20. Hyperimmunoglobulinemia D and periodic fever syndrome (HIDS) in a child with normal serum IgD, but increased serum IgA concentration.
    Saulsbury FT
    J Pediatr; 2003 Jul; 143(1):127-9. PubMed ID: 12915839
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.