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25. Mutual alteration of NOD2-associated Blau syndrome and IFNγR1 deficiency. Parackova Z; Bloomfield M; Vrabcova P; Zentsova I; Klocperk A; Milota T; Svaton M; Casanova JL; Bustamante J; Fronkova E; Sediva A J Clin Immunol; 2020 Jan; 40(1):165-178. PubMed ID: 31760574 [TBL] [Abstract][Full Text] [Related]
26. [Clinical features of Blau syndrome and early-onset sarcoidosis and associating CARD15/NOD2 gene mutations]. Kanazawa N Nihon Rinsho Meneki Gakkai Kaishi; 2007 Apr; 30(2):123-32. PubMed ID: 17473515 [TBL] [Abstract][Full Text] [Related]
27. Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism. Mensa-Vilaro A; Cham WT; Tang SP; Lim SC; González-Roca E; Ruiz-Ortiz E; Ariffin R; Yagüe J; Aróstegui JI Arthritis Rheumatol; 2016 Apr; 68(4):1039-44. PubMed ID: 26606664 [TBL] [Abstract][Full Text] [Related]
28. Co-existence of Blau syndrome and NAID? Diagnostic challenges associated with presence of multiple pathogenic variants in NOD2 gene: a case report. Dziedzic M; Marjańska A; Bąbol-Pokora K; Urbańczyk A; Grześk E; Młynarski W; Kołtan S Pediatr Rheumatol Online J; 2017 Jul; 15(1):57. PubMed ID: 28750667 [TBL] [Abstract][Full Text] [Related]
29. Ocular Features in Chinese Patients with Blau Syndrome. Wu S; Zhong L; Sun Z; Zhu T; Song H; Sui R Ocul Immunol Inflamm; 2020; 28(1):79-85. PubMed ID: 30806112 [No Abstract] [Full Text] [Related]
31. Role of NOD2 Pathway Genes in Sarcoidosis Cases with Clinical Characteristics of Blau Syndrome. Bello GA; Adrianto I; Dumancas GG; Levin AM; Iannuzzi MC; Rybicki BA; Montgomery C Am J Respir Crit Care Med; 2015 Nov; 192(9):1133-5. PubMed ID: 26517420 [No Abstract] [Full Text] [Related]
32. Identification of a novel missense mutation in the NOD2 gene in a Chinese child with early-onset sarcoidosis. Wang X; Zhang X; Zhang W; Sun J Indian J Dermatol Venereol Leprol; 2018; 84(5):645. PubMed ID: 29067935 [No Abstract] [Full Text] [Related]
33. Clinical Profile in Genetically Proven Blau Syndrome: A Case Series from South India. Babu K; Rao AP Ocul Immunol Inflamm; 2021 Feb; 29(2):250-256. PubMed ID: 32293936 [No Abstract] [Full Text] [Related]
34. Blau Syndrome: A Systemic Granulomatous Disease of Cutaneous Onset and Phenotypic Complexity. Rose CD Pediatr Dermatol; 2017 Mar; 34(2):216-218. PubMed ID: 27874205 [No Abstract] [Full Text] [Related]
35. Lipogranulomatous subconjunctival nodules: a novel presentation in Blau syndrome. Ahmad M; Hermanson ME; Enzenauer R; Palestine A; Lin C; Meeks N; McCourt E J AAPOS; 2017 Jun; 21(3):249-251. PubMed ID: 28532706 [TBL] [Abstract][Full Text] [Related]
36. Computational model to analyze and characterize the functional mutations of NOD2 protein causing inflammatory disorder - Blau syndrome. Thirumal Kumar D; Udhaya Kumar S; Nishaat Laeeque AS; Apurva Abhay S; Bithia R; Magesh R; Kumar M; Zayed H; George Priya Doss C Adv Protein Chem Struct Biol; 2020; 120():379-408. PubMed ID: 32085886 [TBL] [Abstract][Full Text] [Related]
38. Mutational analysis of human NOD1 and NOD2 NACHT domains reveals different modes of activation. Zurek B; Proell M; Wagner RN; Schwarzenbacher R; Kufer TA Innate Immun; 2012 Feb; 18(1):100-11. PubMed ID: 21310790 [TBL] [Abstract][Full Text] [Related]
39. Tofacitinib, a suppressor of NOD2 expression, is a potential treatment for Blau syndrome. Ueki Y; Takimoto-Ito R; Saito MK; Tanizaki H; Kambe N Front Immunol; 2023; 14():1211240. PubMed ID: 37415984 [TBL] [Abstract][Full Text] [Related]
40. Whole-exome sequencing in three children with sporadic Blau syndrome, one of them co-presenting with recurrent polyserositis. Córdova-Fletes C; Rangel-Sosa MM; Martínez-Jacobo LA; Becerra-Solano LE; Arellano-Valdés CA; Tlacuilo-Parra JA; Galán-Huerta KA; Rivas-Estilla AM; Hernandez-Orozco AA; García-Ortiz JE Autoimmunity; 2020 Sep; 53(6):344-352. PubMed ID: 32597225 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]