150 related articles for article (PubMed ID: 10896295)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. 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]
7. 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]
8. [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]
9. 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]
10. 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]
11. Molecular mechanisms of amyloidosis.
van der Hilst JC; Simon A; Drenth JP
N Engl J Med; 2003 Nov; 349(19):1872-3; author reply 1872-3. PubMed ID: 14606469
[No 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. 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]
14. Increased urinary leukotriene E(4) during febrile attacks in the hyperimmunoglobulinaemia D and periodic fever syndrome.
Frenkel J; Willemsen MA; Weemaes CM; Dorland L; Mayatepek E
Arch Dis Child; 2001 Aug; 85(2):158-9. PubMed ID: 11466192
[TBL] [Abstract][Full Text] [Related]
15. Hyper-IgD syndrome and familial Hibernian fever are true periodic fever syndromes.
Drenth JP; Powell RJ
J Pediatr; 2000 Sep; 137(3):438-9. PubMed ID: 10969277
[No Abstract] [Full Text] [Related]
16. Inefficacy of etanercept in a child with hyper-IgD syndrome and periodic fever.
Marchetti F; Barbi E; Tommasini A; Oretti C; Ventura A
Clin Exp Rheumatol; 2004; 22(6):791-2. PubMed ID: 15638064
[No Abstract] [Full Text] [Related]
17. 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]
18. Biochemical and genetic aspects of mevalonate kinase and its deficiency.
Houten SM; Wanders RJ; Waterham HR
Biochim Biophys Acta; 2000 Dec; 1529(1-3):19-32. PubMed ID: 11111075
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]