186 related articles for article (PubMed ID: 27899390)
1. Hyper-IgD and periodic fever syndrome (HIDS) due to compound heterozygosity for G336S and V377I in a 44-year-old patient with a 27-year history of fever.
Schlabe S; Schwarze-Zander C; Lohse P; Rockstroh JK
BMJ Case Rep; 2016 Nov; 2016():. PubMed ID: 27899390
[TBL] [Abstract][Full Text] [Related]
2. [Periodic fever: the first Portuguese case-report of hyper-IgD syndrome (HIDS)].
Abreu TT
Acta Med Port; 2004; 17(5):391-4. PubMed ID: 16197847
[TBL] [Abstract][Full Text] [Related]
3. Clinical and molecular variability in childhood periodic fever with hyperimmunoglobulinaemia D.
Frenkel J; Houten SM; Waterham HR; Wanders RJ; Rijkers GT; Duran M; Kuijpers TW; van Luijk W; Poll-The BT; Kuis W
Rheumatology (Oxford); 2001 May; 40(5):579-84. PubMed ID: 11371670
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. MVK mutations and associated clinical features in Italian patients affected with autoinflammatory disorders and recurrent fever.
D'Osualdo A; Picco P; Caroli F; Gattorno M; Giacchino R; Fortini P; Corona F; Tommasini A; Salvi G; Specchia F; Obici L; Meini A; Ricci A; Seri M; Ravazzolo R; Martini A; Ceccherini I
Eur J Hum Genet; 2005 Mar; 13(3):314-20. PubMed ID: 15536479
[TBL] [Abstract][Full Text] [Related]
6. Favorable preliminary experience with etanercept in two patients with the hyperimmunoglobulinemia D and periodic fever syndrome.
Takada K; Aksentijevich I; Mahadevan V; Dean JA; Kelley RI; Kastner DL
Arthritis Rheum; 2003 Sep; 48(9):2645-51. PubMed ID: 13130485
[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. Overt and occult rheumatic diseases: the child with chronic fever.
Frenkel J; Kuis W
Best Pract Res Clin Rheumatol; 2002 Jul; 16(3):443-69. PubMed ID: 12387810
[TBL] [Abstract][Full Text] [Related]
9. [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]
10. [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]
11. 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]
12. 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]
13. Carrier frequency of the V377I (1129G>A) MVK mutation, associated with Hyper-IgD and periodic fever syndrome, in the Netherlands.
Houten SM; van Woerden CS; Wijburg FA; Wanders RJ; Waterham HR
Eur J Hum Genet; 2003 Feb; 11(2):196-200. PubMed ID: 12634869
[TBL] [Abstract][Full Text] [Related]
14. [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]
15. Hereditary periodic fever with systemic amyloidosis: is hyper-IgD syndrome really a benign disease?
Siewert R; Ferber J; Horstmann RD; Specker C; Heering PJ; Timmann C
Am J Kidney Dis; 2006 Sep; 48(3):e41-5. PubMed ID: 16931207
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
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. Location of the gene causing hyperimmunoglobulinemia D and periodic fever syndrome differs from that for familial Mediterranean fever. International Hyper-IgD Study Group.
Drenth JP; Mariman EC; Van der Velde-Visser SD; Ropers HH; Van der Meer JW
Hum Genet; 1994 Dec; 94(6):616-20. PubMed ID: 7989036
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
