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 *

179 related articles for article (PubMed ID: 15674660)

  • 1. Hyperimmunoglobulinemia D syndrome in an Arab child.
    Hammoudeh M
    Clin Rheumatol; 2005 Feb; 24(1):92-4. PubMed ID: 15674660
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Periodic fever in children with hyperimmunoglobulinemia D and mevalonate kinase mutations.
    Grose C
    Pediatr Infect Dis J; 2005 Jun; 24(6):573-4. PubMed ID: 15933578
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features.
    Livneh A; Drenth JP; Klasen IS; Langevitz P; George J; Shelton DA; Gumucio DL; Pras E; Kastner DL; Pras M; van der Meer JW
    J Rheumatol; 1997 Aug; 24(8):1558-63. PubMed ID: 9263151
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [Hereditary periodic fever].
    Lamprecht P; Timmann C; Ahmadi-Simab K; Gross WL
    Internist (Berl); 2004 Aug; 45(8):904-11. PubMed ID: 15243709
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular analysis of the MVK and TNFRSF1A genes in patients with a clinical presentation typical of the hyperimmunoglobulinemia D with periodic fever syndrome: a low-penetrance TNFRSF1A variant in a heterozygous MVK carrier possibly influences the phenotype of hyperimmunoglobulinemia D with periodic fever syndrome or vice versa.
    Stojanov S; Lohse P; Lohse P; Hoffmann F; Renner ED; Zellerer S; Kéry A; Shin YS; Haas D; Hoffmann GF; Belohradsky BH
    Arthritis Rheum; 2004 Jun; 50(6):1951-8. PubMed ID: 15188372
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Identification of a novel mevalonate kinase gene mutation in combination with the common MVK V377I substitution and the low-penetrance TNFRSF1A R92Q mutation.
    Hoffmann F; Lohse P; Stojanov S; Shin YS; Renner ED; Kéry A; Zellerer S; Belohradsky BH
    Eur J Hum Genet; 2005 Apr; 13(4):510-2. PubMed ID: 15657603
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Molecular analysis of the mevalonate kinase gene in a cohort of patients with the hyper-igd and periodic fever syndrome: its application as a diagnostic tool.
    Simon A; Cuisset L; Vincent MF; van Der Velde-Visser SD; Delpech M; van Der Meer JW; Drenth JP
    Ann Intern Med; 2001 Sep; 135(5):338-43. PubMed ID: 11529697
    [TBL] [Abstract][Full Text] [Related]  

  • 9. [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]  

  • 10. Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins.
    Hospach T; Lohse P; Heilbronner H; Dannecker GE; Lohse P
    Arthritis Rheum; 2005 Nov; 52(11):3606-10. PubMed ID: 16255052
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Hereditary recurrent fever syndromes].
    Grateau G
    Bull Acad Natl Med; 2005 Jun; 189(6):1235-46; discussion 1246-8. PubMed ID: 16433446
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.
    Drenth JP; Cuisset L; Grateau G; Vasseur C; van de Velde-Visser SD; de Jong JG; Beckmann JS; van der Meer JW; Delpech M
    Nat Genet; 1999 Jun; 22(2):178-81. PubMed ID: 10369262
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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]  

  • 14. Tendonitis in variant hyperimmunoglobulinaemia D and periodic fever syndrome--a rare disease with a new symptom.
    Armbrust S; Drenth JP; Schröder C; Domning E; Poeschl E; Wiersbitzky SK
    Eur J Pediatr; 2005 Jun; 164(6):391-4. PubMed ID: 15770507
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Diagnostic value of serum immunoglobulinaemia D level in patients with a clinical suspicion of hyper IgD syndrome.
    Ammouri W; Cuisset L; Rouaghe S; Rolland MO; Delpech M; Grateau G; Ravet N
    Rheumatology (Oxford); 2007 Oct; 46(10):1597-600. PubMed ID: 17804452
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Autoinflammatory diseases: the hereditary periodic fever syndromes.
    Fietta P
    Acta Biomed; 2004 Aug; 75(2):92-9. PubMed ID: 15481697
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Hyperimmunoglobulinaemia D syndrome: a rare cause of prolonged fever and treatment with anti-interleukin 1 agent.
    Aygun D; Sahin S; Cokugras H; Kasapcopur O
    BMJ Case Rep; 2016 May; 2016():. PubMed ID: 27190114
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Summaries for patients. Can genetics help diagnose the hyper-IgD and periodic fever syndrome.
    Ann Intern Med; 2001 Sep; 135(5):S-36. PubMed ID: 11556290
    [No Abstract]   [Full Text] [Related]  

  • 19. [Periodic fever due to hyper-IgD syndrome].
    Wauters IM; Linskens RK; Stehouwer CD
    Ned Tijdschr Geneeskd; 2000 Apr; 144(17):809-11. PubMed ID: 10800552
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.