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 *

302 related articles for article (PubMed ID: 25416713)

  • 21. [Early-onset sarcoidosis/Blau syndrome].
    Kambe N; Satoh T; Nakano M; Nakamura Y; Matsue H
    Nihon Rinsho Meneki Gakkai Kaishi; 2011; 34(5):378-81. PubMed ID: 22041425
    [TBL] [Abstract][Full Text] [Related]  

  • 22. A Novel Pathogenic
    Rodrigues FG; Petrushkin H; Webster AR; Bickerstaff M; Moraitis E; Rowczenio D; Aróstegui JI; Westcott M
    Ophthalmic Genet; 2021 Dec; 42(6):753-764. PubMed ID: 34251956
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Two Chinese pedigrees of Blau syndrome with thirteen affected members.
    Wu D; Shen M
    Clin Rheumatol; 2018 Jan; 37(1):265-270. PubMed ID: 28721627
    [TBL] [Abstract][Full Text] [Related]  

  • 24. [The present and the prospect of study on Blau syndrome/early-onset sarcoidosis].
    Nakano M; Kambe N
    Nihon Rinsho; 2013 Apr; 71(4):737-41. PubMed ID: 23678609
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel nucleotide oligomerisation domain 2 mutation in a family with Blau syndrome: Phenotype and function.
    Ong LT; Nachbur U; Rowczenio D; Ziegler JB; Fischer E; Lin MW
    Innate Immun; 2017 Oct; 23(7):578-583. PubMed ID: 28836875
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Blau arteritis resembling Takayasu disease with a novel NOD2 mutation.
    Khubchandani RP; Hasija R; Touitou I; Khemani C; Wouters CH; Rose CD
    J Rheumatol; 2012 Sep; 39(9):1888-92. PubMed ID: 22859352
    [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. 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]  

  • 29. Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis.
    Zhong Z; Ding J; Su G; Liao W; Gao Y; Zhu Y; Deng Y; Li F; Du L; Gao Y; Yang P
    Ophthalmology; 2022 Jul; 129(7):821-828. PubMed ID: 35314268
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Familial Blau syndrome:First molecularly confirmed report from India.
    Janarthanan M; Poddar C; Sudharshan S; Seabra L; Crow YJ
    Indian J Ophthalmol; 2019 Jan; 67(1):165-167. PubMed ID: 30574935
    [TBL] [Abstract][Full Text] [Related]  

  • 31. A Novel NOD2-associated Mutation and Variant Blau Syndrome: Phenotype and Molecular Analysis.
    Ebrahimiadib N; Samra KA; Domina AM; Stiles ER; Ewer R; Bocian CP; Foster CS
    Ocul Immunol Inflamm; 2018; 26(1):57-64. PubMed ID: 27419275
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Clinical and genetic aspects of Blau syndrome: a 25-year follow-up of one family and a literature review.
    Punzi L; Furlan A; Podswiadek M; Gava A; Valente M; De Marchi M; Peserico A
    Autoimmun Rev; 2009 Jan; 8(3):228-32. PubMed ID: 18718560
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. 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]  

  • 35. Gene mutations and clinical phenotypes in Chinese children with Blau syndrome.
    Li C; Zhang J; Li S; Han T; Kuang W; Zhou Y; Deng J; Tan X
    Sci China Life Sci; 2017 Jul; 60(7):758-762. PubMed ID: 28639104
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Blau syndrome associated with a CARD15/NOD2 mutation.
    Snyers B; Dahan K
    Am J Ophthalmol; 2006 Dec; 142(6):1089-92. PubMed ID: 17157607
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Immunophenotyping in peripheral blood mononuclear cells, aqueous humour and vitreous in a Blau syndrome patient caused by a novel NOD2 mutation.
    Jimenez-Martinez MC; Cruz F; Groman-Lupa S; Zenteno JC
    Int J Immunogenet; 2011 Jun; 38(3):233-42. PubMed ID: 21320290
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Sporadic Blau syndrome with onset of widespread granulomatous dermatitis in the newborn period.
    Stoevesandt J; Morbach H; Martin TM; Zierhut M; Girschick H; Hamm H
    Pediatr Dermatol; 2010; 27(1):69-73. PubMed ID: 20199415
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 16.