BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

161 related articles for article (PubMed ID: 25619352)

  • 1. [Report of a child with neonatal-onset multisystem inflammatory disease and review of the literature].
    Guan N; Li B; Wu Y
    Zhonghua Er Ke Za Zhi; 2014 Dec; 52(12):932-6. PubMed ID: 25619352
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Clinical characteristics of Chinese neonates with neonatal-onset multisystem inflammatory disease: a case report and literature review.
    Zhao C; Liu C; Li X
    Front Immunol; 2023; 14():1291345. PubMed ID: 38250066
    [TBL] [Abstract][Full Text] [Related]  

  • 3. A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases.
    Aróstegui JI; Lopez Saldaña MD; Pascal M; Clemente D; Aymerich M; Balaguer F; Goel A; Fournier del Castillo C; Rius J; Plaza S; López Robledillo JC; Juan M; Ibañez M; Yagüe J
    Arthritis Rheum; 2010 Apr; 62(4):1158-66. PubMed ID: 20131270
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Necrotizing Funisitis as an Intrauterine manifestation of Cryopyrin-Associated Periodic Syndrome: a case report and review of the literature.
    Yokoi K; Minamiguchi S; Honda Y; Kobayashi M; Kobayashi S; Nishikomori R
    Pediatr Rheumatol Online J; 2021 May; 19(1):77. PubMed ID: 34059097
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Case Report: Infantile Urticaria as a Herald of Neonatal Onset Multisystem Inflammatory Disease With a Novel Mutation in NLRP3.
    Patrick AE; Lyons EM; Ishii L; Boyd AS; Choi JM; Dewan AK; Markle JG
    Front Immunol; 2021; 12():775140. PubMed ID: 34868041
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Successful management of cryopyrin-associated periodic syndrome with canakinumab in infancy.
    Kanariou M; Tantou S; Varela I; Raptaki M; Petropoulou C; Nikas I; Valari M
    Pediatrics; 2014 Nov; 134(5):e1468-73. PubMed ID: 25349319
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID).
    Nair SB; Chavan PP; Athalye AS; Aksentijevich I; Khubchandani RP
    Clin Rheumatol; 2019 Feb; 38(2):403-406. PubMed ID: 30066283
    [TBL] [Abstract][Full Text] [Related]  

  • 8. De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseases.
    Aksentijevich I; Nowak M; Mallah M; Chae JJ; Watford WT; Hofmann SR; Stein L; Russo R; Goldsmith D; Dent P; Rosenberg HF; Austin F; Remmers EF; Balow JE; Rosenzweig S; Komarow H; Shoham NG; Wood G; Jones J; Mangra N; Carrero H; Adams BS; Moore TL; Schikler K; Hoffman H; Lovell DJ; Lipnick R; Barron K; O'Shea JJ; Kastner DL; Goldbach-Mansky R
    Arthritis Rheum; 2002 Dec; 46(12):3340-8. PubMed ID: 12483741
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Neonatal-onset multisystem inflammatory disease (NOMID) due to a novel S331R mutation of the CIAS1 gene and response to interleukin-1 receptor antagonist treatment.
    Boschan C; Witt O; Lohse P; Foeldvari I; Zappel H; Schweigerer L
    Am J Med Genet A; 2006 Apr; 140(8):883-6. PubMed ID: 16532456
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Severe cryopyrin-associated periodic syndrome first characterized by early childhood-onset sensorineural hearing loss - Case report and literature review.
    Hui A; Johnson LB; Greemberg R; Penney L; Ramsey SE
    Int J Pediatr Otorhinolaryngol; 2019 May; 120():68-72. PubMed ID: 30772614
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Cryopyrin-associated periodic syndrome in Australian children and adults: Epidemiological, clinical and treatment characteristics.
    Mehr S; Allen R; Boros C; Adib N; Kakakios A; Turner PJ; Rogers M; Zurynski Y; Singh-Grewal D
    J Paediatr Child Health; 2016 Sep; 52(9):889-95. PubMed ID: 27650144
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A Novel Mutation in the Pyrin Domain of the NOD-like Receptor Family Pyrin Domain Containing Protein 3 in Muckle-Wells Syndrome.
    Hu J; Zhu Y; Zhang JZ; Zhang RG; Li HM
    Chin Med J (Engl); 2017 Mar; 130(5):586-593. PubMed ID: 28229991
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Urticaria, fever, and hypofibrinogenemia.
    Mohr V; Schulz A; Lohse P; Schumann C; Debatin KM; Schuetz C
    Arthritis Rheumatol; 2014 May; 66(5):1377. PubMed ID: 24782193
    [No Abstract]   [Full Text] [Related]  

  • 14. [Cryopyrin-associated periodic syndromes].
    Quartier P; Rodrigues F; Georgin-Lavialle S
    Rev Med Interne; 2018 Apr; 39(4):287-296. PubMed ID: 29111302
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Early canakinumab therapy for the sensorineural deafness in a family with Muckle-Wells syndrome due to a novel mutation of NLRP3 gene.
    Iida Y; Wakiguchi H; Okazaki F; Nakamura T; Yasudo H; Kubo M; Sugahara K; Yamashita H; Suehiro Y; Okayama N; Hashimoto K; Iwamoto N; Kawakami A; Aoki Y; Takada H; Ohga S; Hasegawa S
    Clin Rheumatol; 2019 Mar; 38(3):943-948. PubMed ID: 30338413
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Current status of understanding the pathogenesis and management of patients with NOMID/CINCA.
    Goldbach-Mansky R
    Curr Rheumatol Rep; 2011 Apr; 13(2):123-31. PubMed ID: 21538043
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Chronic Infantile Neurological Cutaneous and Articular (CINCA) syndrome: a review.
    Finetti M; Omenetti A; Federici S; Caorsi R; Gattorno M
    Orphanet J Rare Dis; 2016 Dec; 11(1):167. PubMed ID: 27927236
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Gene mutations and clinical phenotypes in 15 Chinese children with cryopyrin-associated periodic syndrome (CAPS).
    Li C; Tan X; Zhang J; Li S; Mo W; Han T; Kuang W; Zhou Y; Deng J
    Sci China Life Sci; 2017 Dec; 60(12):1436-1444. PubMed ID: 29285715
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Identification of Interleukin-1β-Producing Monocytes That Are Susceptible to Pyronecrotic Cell Death in Patients With Neonatal-Onset Multisystem Inflammatory Disease.
    Edwan JH; Goldbach-Mansky R; Colbert RA
    Arthritis Rheumatol; 2015 Dec; 67(12):3286-97. PubMed ID: 26245468
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Neonatal urticaria: Could it be CAPS?
    Cutts L; Parslew R; Eustace K
    Pediatr Dermatol; 2018 Nov; 35(6):e420-e421. PubMed ID: 30187963
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.