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 *

233 related articles for article (PubMed ID: 32618442)

  • 41. Optic nerve and retinal features in uveitis associated with juvenile systemic granulomatous disease (Blau syndrome).
    Carreño E; Guly CM; Chilov M; Hinchcliffe A; Arostegui JI; Lee RW; Dick AD; Ramanan AV
    Acta Ophthalmol; 2015 May; 93(3):253-7. PubMed ID: 25209167
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Familial Blau syndrome without uveitis caused by a novel mutation in the nucleotide-binding oligomerization domain-containing protein 2 gene with good response to infliximab.
    Toral-López J; González-Huerta LM; Martín-Del Campo M; Messina-Baas O; Cuevas-Covarrubias SA
    Pediatr Dermatol; 2018 May; 35(3):e180-e183. PubMed ID: 29570830
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Blau syndrome: a case report from Palestine.
    Iriqat S; Safieh MA; Fatouleh M; Alkaiyat A
    Pediatr Rheumatol Online J; 2021 Aug; 19(1):138. PubMed ID: 34465352
    [TBL] [Abstract][Full Text] [Related]  

  • 44. Using genes to triangulate the pathophysiology of granulomatous autoinflammatory disease: NOD2, PLCG2 and LACC1.
    Szymanski AM; Ombrello MJ
    Int Immunol; 2018 Apr; 30(5):205-213. PubMed ID: 29538758
    [TBL] [Abstract][Full Text] [Related]  

  • 45. A Chinese girl of Blau syndrome with renal arteritis and a literature review.
    Zeng Q; Liu H; Li G; Li Y; Guan W; Zhang T; Gong Y; Zhang X; Lv Q; Wu B; Xu H; Sun L
    Pediatr Rheumatol Online J; 2023 Mar; 21(1):23. PubMed ID: 36915122
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Case Report: Methotrexate and hydroxychloroquine in combination for the treatment of NOD2-mutation-associated Blau syndrome.
    Jensen ME; Harrell K; McBride JD
    Front Immunol; 2023; 14():1279329. PubMed ID: 37868966
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Unique Variant of NOD2 Pediatric Granulomatous Arthritis With Severe 1,25-Dihydroxyvitamin D-Mediated Hypercalcemia and Generalized Osteosclerosis.
    Whyte MP; Lim E; McAlister WH; Gottesman GS; Trinh L; Veis DJ; Bijanki VN; Boden MG; Nenninger A; Mumm S; Buchbinder D
    J Bone Miner Res; 2018 Nov; 33(11):2071-2080. PubMed ID: 29933504
    [TBL] [Abstract][Full Text] [Related]  

  • 48. NOD2 gene-associated pediatric granulomatous arthritis: clinical diversity, novel and recurrent mutations, and evidence of clinical improvement with interleukin-1 blockade in a Spanish cohort.
    Aróstegui JI; Arnal C; Merino R; Modesto C; Antonia Carballo M; Moreno P; García-Consuegra J; Naranjo A; Ramos E; de Paz P; Rius J; Plaza S; Yagüe J
    Arthritis Rheum; 2007 Nov; 56(11):3805-13. PubMed ID: 17968944
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Ultrasonographic assessment reveals detailed distribution of synovial inflammation in Blau syndrome.
    Ikeda K; Kambe N; Takei S; Nakano T; Inoue Y; Tomiita M; Oyake N; Satoh T; Yamatou T; Kubota T; Okafuji I; Kanazawa N; Nishikomori R; Shimojo N; Matsue H; Nakajima H
    Arthritis Res Ther; 2014 Apr; 16(2):R89. PubMed ID: 24713464
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Effective treatment of TNFα inhibitors in Chinese patients with Blau syndrome.
    Chen J; Luo Y; Zhao M; Wu D; Yang Y; Zhang W; Shen M
    Arthritis Res Ther; 2019 Nov; 21(1):236. PubMed ID: 31718710
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Ocular manifestations of Blau syndrome.
    Suresh S; Tsui E
    Curr Opin Ophthalmol; 2020 Nov; 31(6):532-537. PubMed ID: 33009086
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Incomplete penetrance of NOD2 C483W mutation underlining Blau syndrome.
    Chang SY; Kambe N; Fan WL; Huang JL; Lee WI; Wu CY
    Pediatr Rheumatol Online J; 2022 Oct; 20(1):86. PubMed ID: 36192768
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Mutations of NOD2 gene and clinical features in Chinese Blau syndrome patients].
    Wang W; Wei M; Song H; Qiu Z
    Zhonghua Er Ke Za Zhi; 2014 Dec; 52(12):896-901. PubMed ID: 25619344
    [TBL] [Abstract][Full Text] [Related]  

  • 54. A Case of Blau Syndrome with NOD2 E383K Mutation.
    Harada J; Nakajima T; Kanazawa N
    Pediatr Dermatol; 2016 Nov; 33(6):e385-e387. PubMed ID: 27339507
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Early onset sarcoidosis (Blau syndrome): erosive and often misdiagnosed.
    Ellis JC; Faber BG; Uri IF; J Emerson S
    Rheumatology (Oxford); 2020 May; 59(5):1179-1180. PubMed ID: 31620796
    [No Abstract]   [Full Text] [Related]  

  • 56. NOD2/CARD15 gene mutation identified in a Chinese family with Blau syndrome.
    Xiang H; Zhang T; Chen M; Zhou X; Li Z; Yan N; Li S; Han Y; Gong Q; Liu X
    Mol Vis; 2012; 18():617-23. PubMed ID: 22509093
    [TBL] [Abstract][Full Text] [Related]  

  • 57. Novel NOD2 Mutation in Early-Onset Inflammatory Bowel Phenotype.
    Girardelli M; Loganes C; Pin A; Stacul E; Decleva E; Vozzi D; Baj G; De Giacomo C; Tommasini A; Bianco AM
    Inflamm Bowel Dis; 2018 May; 24(6):1204-1212. PubMed ID: 29697845
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Granulomatous skin involvement in a patient with an unusual NOD2 mutation.
    Kuye IO; Adisa M; Nazarian RM; Arvikar SL; Smith GP
    Australas J Dermatol; 2017 May; 58(2):142-144. PubMed ID: 26768519
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Blau syndrome-associated uveitis and the NOD2 gene.
    Pillai P; Sobrin L
    Semin Ophthalmol; 2013; 28(5-6):327-32. PubMed ID: 24010719
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Nod2-Nodosome in a Cell-Free System: Implications in Pathogenesis and Drug Discovery for Blau Syndrome and Early-Onset Sarcoidosis.
    Iwasaki T; Kaneko N; Ito Y; Takeda H; Sawasaki T; Heike T; Migita K; Agematsu K; Kawakami A; Morikawa S; Mokuda S; Kurata M; Masumoto J
    ScientificWorldJournal; 2016; 2016():2597376. PubMed ID: 27403452
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 12.