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 *

261 related articles for article (PubMed ID: 30574935)

  • 1. 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]  

  • 2. 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]  

  • 3. 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]  

  • 4. Molecular diagnostic yield for Blau syndrome in previously diagnosed juvenile idiopathic arthritis with uveitis or cutaneous lesions.
    Zhong Z; Dai L; Ding J; Gao Y; Su G; Zhu Y; Deng Y; Li F; Gao Y; Yang P
    Rheumatology (Oxford); 2024 Sep; 63(SI2):SI260-SI268. PubMed ID: 37941393
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Exacerbation of symptoms in Blau syndrome/early-onset sarcoidosis following delivery.
    Mizawa M; Makino T; Nakamura T; Yamaguchi S; Taki H; Shimizu T
    Eur J Dermatol; 2015; 25(6):620-2. PubMed ID: 26712281
    [No Abstract]   [Full Text] [Related]  

  • 6. Blau syndrome with a rare mutation in exon 9 of
    Velickovic J; Silan F; Bir FD; Silan C; Albuz B; Ozdemir O
    Autoimmunity; 2019; 52(7-8):256-263. PubMed ID: 31556326
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Blau Syndrome With Delayed Cutaneous Manifestations: A Case Report.
    Panah E; Garfield E; Zahirsha Z; Muhlbauer A; Lake E; Speiser J
    Am J Dermatopathol; 2024 Jun; 46(6):381-382. PubMed ID: 38648024
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A novel mutation in early-onset sarcoidosis/Blau syndrome: an association with Propionibacterium acnes.
    Okazaki F; Wakiguchi H; Korenaga Y; Nakamura T; Yasudo H; Uchi S; Yanai R; Asano N; Hoshii Y; Tanabe T; Izawa K; Honda Y; Nishikomori R; Uchida K; Eishi Y; Ohga S; Hasegawa S
    Pediatr Rheumatol Online J; 2021 Feb; 19(1):18. PubMed ID: 33602264
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Blau syndrome with pulmonary nodule in a child.
    Su J; Liu D
    Australas J Dermatol; 2021 May; 62(2):217-220. PubMed ID: 33742458
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Blau syndrome: Lessons learned in a tertiary care centre at Chandigarh, North India.
    Kumrah R; Pilania RK; Menia NK; Rawat A; Sharma J; Gupta A; Vignesh P; Jindal AK; Rikhi R; Agarwal A; Gupta V; Singh S; Suri D
    Front Immunol; 2022; 13():932919. PubMed ID: 36189202
    [TBL] [Abstract][Full Text] [Related]  

  • 12. A case of infantile Takayasu arteritis with a p.D382E NOD2 mutation: an unusual phenotype of Blau syndrome/early-onset sarcoidosis?
    Inoue Y; Kawaguchi Y; Shimojo N; Yamaguchi K; Morita Y; Nakano T; Arima T; Tomiita M; Kohno Y
    Mod Rheumatol; 2013 Jul; 23(4):837-9. PubMed ID: 22821420
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. 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]  

  • 15. Proteomic Profiling of Tears in Blau Syndrome Patients in Identification of Potential Disease Biomarkers.
    Galozzi P; Bindoli S; Baggio C; Battisti I; Leonardi A; Basso D; Arrigoni G; Sfriso P
    Int J Mol Sci; 2024 Aug; 25(15):. PubMed ID: 39125957
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. 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]  

  • 20. 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]  

    [Next]    [New Search]
    of 14.