BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

364 related articles for article (PubMed ID: 29665027)

  • 21. Genetic features of late onset primary hemophagocytic lymphohistiocytosis in adolescence or adulthood.
    Wang Y; Wang Z; Zhang J; Wei Q; Tang R; Qi J; Li L; Ye L; Wang J; Ye L
    PLoS One; 2014; 9(9):e107386. PubMed ID: 25233452
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genetic predisposition to hemophagocytic lymphohistiocytosis: Report on 500 patients from the Italian registry.
    Cetica V; Sieni E; Pende D; Danesino C; De Fusco C; Locatelli F; Micalizzi C; Putti MC; Biondi A; Fagioli F; Moretta L; Griffiths GM; Luzzatto L; Aricò M
    J Allergy Clin Immunol; 2016 Jan; 137(1):188-196.e4. PubMed ID: 26342526
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Prevalence of type 5 familial hemophagocytic lymphohistiocytosis in Korea and novel mutations in STXBP2.
    Seo JY; Lee KO; Yoo KH; Sung KW; Koo HH; Kim SH; Kang HJ; Park KD; Shin HY; Baek HJ; Kook H; Lyu CJ; Song JS; Lee MJ; Kim JY; Lim YT; Koh KN; Im HJ; Seo JJ; Kim HJ;
    Clin Genet; 2016 Feb; 89(2):222-7. PubMed ID: 26451869
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Munc18-2 deficiency causes familial hemophagocytic lymphohistiocytosis type 5 and impairs cytotoxic granule exocytosis in patient NK cells.
    Côte M; Ménager MM; Burgess A; Mahlaoui N; Picard C; Schaffner C; Al-Manjomi F; Al-Harbi M; Alangari A; Le Deist F; Gennery AR; Prince N; Cariou A; Nitschke P; Blank U; El-Ghazali G; Ménasché G; Latour S; Fischer A; de Saint Basile G
    J Clin Invest; 2009 Dec; 119(12):3765-73. PubMed ID: 19884660
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A case report of novel mutation in PRF1 gene, which causes familial autosomal recessive hemophagocytic lymphohistiocytosis.
    Bordbar MR; Modarresi F; Farazi Fard MA; Dastsooz H; Shakib Azad N; Faghihi MA
    BMC Med Genet; 2017 May; 18(1):49. PubMed ID: 28468610
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Severe adult hemophagocytic lymphohistiocytosis (HLHa) correlates with HLH-related gene variants.
    Bloch C; Jais JP; Gil M; Boubaya M; Lepelletier Y; Bader-Meunier B; Mahlaoui N; Garcelon N; Lambotte O; Launay D; Larroche C; Lazaro E; Liffermann F; Lortholary O; Michel M; Michot JM; Morel P; Cheminant M; Suarez F; Terriou L; Urbanski G; Viallard JF; Alcais A; Fischer A; de Saint Basile G; Hermine O;
    J Allergy Clin Immunol; 2024 Jan; 153(1):256-264. PubMed ID: 37678575
    [TBL] [Abstract][Full Text] [Related]  

  • 27. The expanding spectrum of hemophagocytic lymphohistiocytosis.
    Filipovich AH
    Curr Opin Allergy Clin Immunol; 2011 Dec; 11(6):512-6. PubMed ID: 21971331
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Angeborene hämophagozytische Lymphohistiozytose (HLH).
    Pachlopnik Schmid J; de Saint Basile G
    Klin Padiatr; 2010 Nov; 222(6):345-50. PubMed ID: 20458667
    [TBL] [Abstract][Full Text] [Related]  

  • 29. [Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in Chinese children: a primary study on clinical characteristics and gene mutations].
    Liu R; Shi X; Li J; Hu T; Cao J; Sun Y; Tong C; Liu H
    Zhonghua Yi Xue Za Zhi; 2014 Jul; 94(25):1941-6. PubMed ID: 25253006
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Case Report: Characterizing the Role of the STXBP2-R190C Monoallelic Mutation Found in a Patient With Hemophagocytic Syndrome and Langerhans Cell Histiocytosis.
    Viñas-Giménez L; Rincón R; Colobran R; de la Cruz X; Celis VP; Dapena JL; Alsina L; Sayós J; Martínez-Gallo M
    Front Immunol; 2021; 12():723836. PubMed ID: 34630398
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hypomorphic mutations in PRF1, MUNC13-4, and STXBP2 are associated with adult-onset familial HLH.
    Zhang K; Jordan MB; Marsh RA; Johnson JA; Kissell D; Meller J; Villanueva J; Risma KA; Wei Q; Klein PS; Filipovich AH
    Blood; 2011 Nov; 118(22):5794-8. PubMed ID: 21881043
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Familial Hemophagocytic Lymphohistiocytosis secondary to UNC13D mutation: a report of two cases.
    Sadeghi P; Esslami GG; Rokni-Zadeh H; Changi-Ashtiani M; Mohsenipour R
    BMC Pediatr; 2022 Nov; 22(1):667. PubMed ID: 36401200
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Identification of a novel nonsense mutation in SH2D1A in a patient with X-linked lymphoproliferative syndrome type 1: a case report.
    Lyu X; Guo Z; Li Y; Fan R; Song Y
    BMC Med Genet; 2018 Apr; 19(1):60. PubMed ID: 29649976
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Spectrum, and clinical and functional implications of UNC13D mutations in familial haemophagocytic lymphohistiocytosis.
    Rudd E; Bryceson YT; Zheng C; Edner J; Wood SM; Ramme K; Gavhed S; Gürgey A; Hellebostad M; Bechensteen AG; Ljunggren HG; Fadeel B; Nordenskjöld M; Henter JI
    J Med Genet; 2008 Mar; 45(3):134-41. PubMed ID: 17993578
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Characterization of PRF1, STX11 and UNC13D genotype-phenotype correlations in familial hemophagocytic lymphohistiocytosis.
    Horne A; Ramme KG; Rudd E; Zheng C; Wali Y; al-Lamki Z; Gürgey A; Yalman N; Nordenskjöld M; Henter JI
    Br J Haematol; 2008 Oct; 143(1):75-83. PubMed ID: 18710388
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Prognostic Factors and Long-Term Outcome in 52 Turkish Children With Hemophagocytic Lymphohistiocytosis.
    Kaya Z; Bay A; Albayrak M; Kocak U; Yenicesu I; Gursel T
    Pediatr Crit Care Med; 2015 Jul; 16(6):e165-73. PubMed ID: 25901543
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Comparison of Th1/Th2 cytokine profiles between primary and secondary haemophagocytic lymphohistiocytosis.
    Chen Y; Wang Z; Luo Z; Zhao N; Yang S; Tang Y
    Ital J Pediatr; 2016 May; 42(1):50. PubMed ID: 27209435
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Atypical familial hemophagocytic lymphohistiocytosis due to mutations in UNC13D and STXBP2 overlaps with primary immunodeficiency diseases.
    Rohr J; Beutel K; Maul-Pavicic A; Vraetz T; Thiel J; Warnatz K; Bondzio I; Gross-Wieltsch U; Schündeln M; Schütz B; Woessmann W; Groll AH; Strahm B; Pagel J; Speckmann C; Janka G; Griffiths G; Schwarz K; zur Stadt U; Ehl S
    Haematologica; 2010 Dec; 95(12):2080-7. PubMed ID: 20823128
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Frequency and spectrum of disease-causing variants in 1892 patients with suspected genetic HLH disorders.
    Gadoury-Levesque V; Dong L; Su R; Chen J; Zhang K; Risma KA; Marsh RA; Sun M
    Blood Adv; 2020 Jun; 4(12):2578-2594. PubMed ID: 32542393
    [TBL] [Abstract][Full Text] [Related]  

  • 40. The Spectrum of Clinical, Immunological, and Molecular Findings in Familial Hemophagocytic Lymphohistiocytosis: Experience From India.
    Shabrish S; Kelkar M; Yadav RM; Bargir UA; Gupta M; Dalvi A; Aluri J; Kulkarni M; Shinde S; Sawant-Desai S; Kambli P; Hule G; Setia P; Jodhawat N; Gaikwad P; Dhawale A; Nambiar N; Gowri V; Pandrowala A; Taur P; Raj R; Uppuluri R; Sharma R; Kini P; Sivasankaran M; Munirathnam D; Vedam R; Vignesh P; Banday A; Rawat A; Aggarwal A; Poddar U; Girish M; Chaudhary A; Sampagar A; Jayaraman D; Chaudhary N; Shah N; Jijina F; Chandrakla S; Kanakia S; Arora B; Sen S; Lokeshwar M; Desai M; Madkaikar M
    Front Immunol; 2021; 12():612583. PubMed ID: 33746956
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 19.