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 *

164 related articles for article (PubMed ID: 29600537)

  • 1. Hyper-immunoglobulin D syndrome with novel mutations in an afebrile infant.
    Cadmus SD; Green R; Carrasco R; Levy ML; Diaz LZ
    Pediatr Dermatol; 2018 Jul; 35(4):482-485. PubMed ID: 29600537
    [TBL] [Abstract][Full Text] [Related]  

  • 2. "Hyper-IgD syndrome" or "mevalonate kinase deficiency": an old syndrome needing a new name?
    Celsi F; Tommasini A; Crovella S
    Rheumatol Int; 2014 Mar; 34(3):423-4. PubMed ID: 23412692
    [No Abstract]   [Full Text] [Related]  

  • 3. Hyper-IgD and periodic fever syndrome: a new MVK mutation (p.R277G) associated with a severe phenotype.
    Santos JA; Aróstegui JI; Brito MJ; Neves C; Conde M
    Gene; 2014 Jun; 542(2):217-20. PubMed ID: 24656624
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Perinatal manifestation of mevalonate kinase deficiency and efficacy of anakinra.
    Peciuliene S; Burnyte B; Gudaitiene R; Rusoniene S; Drazdiene N; Liubsys A; Utkus A
    Pediatr Rheumatol Online J; 2016 Mar; 14(1):19. PubMed ID: 27012807
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. [Mevalonate kinase deficiency in 2016].
    Galeotti C; Georgin-Lavialle S; Sarrabay G; Touitou I; Koné-Paut I
    Rev Med Interne; 2018 Apr; 39(4):265-270. PubMed ID: 27659743
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Mevalonate kinase genotype in children with recurrent fevers and high serum IgD level.
    Stabile A; Compagnone A; Napodano S; Raffaele CG; Patti M; Rigante D
    Rheumatol Int; 2013 Dec; 33(12):3039-42. PubMed ID: 23239036
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. [A 6-year-old girl diagnosed with mevalonate kinase deficiency who had hydrops fetalis and neonatal-onset cholestasis].
    Yamashita Y; Matsumoto S; Hiramoto R; Komori I; Tanaka T; Nishikomori R; Heike T; Umetsu S; Inui A
    Nihon Rinsho Meneki Gakkai Kaishi; 2017; 40(2):131-137. PubMed ID: 28603204
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A possibly new autoinflammatory disease due to compound heterozygous phosphomevalonate kinase gene mutation.
    Yıldız Ç; Gezgin Yıldırım D; Inci A; Tümer L; Cengiz Ergin FB; Sunar Yayla ENS; Esmeray Şenol P; Karaçayır N; Eğritaş Gürkan Ö; Okur I; Ezgü FS; Bakkaloğlu SA
    Joint Bone Spine; 2023 Jan; 90(1):105490. PubMed ID: 36410683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Intermittent neutropenia as an early feature of mild mevalonate kinase deficiency.
    Parvaneh N; Ziaee V; Moradinejad MH; Touitou I
    J Clin Immunol; 2014 Jan; 34(1):123-6. PubMed ID: 24177804
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The challenge of autoinflammatory syndromes: with an emphasis on hyper-IgD syndrome.
    van der Meer JW; Simon A
    Rheumatology (Oxford); 2016 Dec; 55(suppl 2):ii23-ii29. PubMed ID: 27856657
    [TBL] [Abstract][Full Text] [Related]  

  • 14. [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]  

  • 15. A restrospective survey of patients's journey before the diagnosis of mevalonate kinase deficiency.
    Berody S; Galeotti C; Koné-Paut I; Piram M
    Joint Bone Spine; 2015 Jul; 82(4):240-4. PubMed ID: 25677409
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Mevalonate kinase deficiency nomenclature.
    Stoffels M; van der Meer JW; Simon A
    Rheumatol Int; 2014 Feb; 34(2):295-6. PubMed ID: 23921621
    [No Abstract]   [Full Text] [Related]  

  • 17. Mevalonate kinase deficiency (hyper-IgD syndrome) overlap mutation familial Mediterranean fever.
    Flores Robles BJ; Peiró Callizo ME; Sanabria Sanchinel AA; Fernández Díaz C
    Reumatol Clin; 2017; 13(1):57. PubMed ID: 27079959
    [No Abstract]   [Full Text] [Related]  

  • 18. Mevalonate kinase deficiency (hyper IgD syndrome with periodic fever)--different faces with separate treatments: two cases and review of the literature.
    Gençpınar P; Makay BB; Gattorno M; Caroli F; Ünsal E
    Turk J Pediatr; 2012; 54(6):641-4. PubMed ID: 23692791
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Hyperimmunoglobulinemia D and periodic fever syndrome].
    Agbo-kpati KP; Condor R; Hollenberg H; Chalvon Demersay A; Cuisset L; Quartier P
    Arch Pediatr; 2014 Jul; 21(7):765-7. PubMed ID: 24935455
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Severe early-onset colitis revealing mevalonate kinase deficiency.
    Levy M; Arion A; Berrebi D; Cuisset L; Jeanne-Pasquier C; Bader-Meunier B; Jung C
    Pediatrics; 2013 Sep; 132(3):e779-83. PubMed ID: 23979089
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.