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 *

188 related articles for article (PubMed ID: 20442642)

  • 1. Pathology of the liver in familial hemophagocytic lymphohistiocytosis.
    Chen JH; Fleming MD; Pinkus GS; Pinkus JL; Nichols KE; Mo JQ; Perez-Atayde AR
    Am J Surg Pathol; 2010 Jun; 34(6):852-67. PubMed ID: 20442642
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Down-regulation of CD5 expression on activated CD8+ T cells in familial hemophagocytic lymphohistiocytosis with perforin gene mutations.
    Wada T; Sakakibara Y; Nishimura R; Toma T; Ueno Y; Horita S; Tanaka T; Nishi M; Kato K; Yasumi T; Ohara O; Yachie A
    Hum Immunol; 2013 Dec; 74(12):1579-85. PubMed ID: 24051121
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Late-onset cases of familial hemophagocytic lymphohistiocytosis with missense perforin gene mutations.
    Ueda I; Kurokawa Y; Koike K; Ito S; Sakata A; Matsumora T; Fukushima T; Morimoto A; Ishii E; Imashuku S
    Am J Hematol; 2007 Jun; 82(6):427-32. PubMed ID: 17266056
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Perforin gene analaysis in an Iranian family with familial hemophagocytic lymphohistiocytosis.
    Galehdari H; Mohammadi E; Andashti B; Naderi A; Molavi MA
    Iran J Immunol; 2007 Jun; 4(2):122-6. PubMed ID: 17652853
    [TBL] [Abstract][Full Text] [Related]  

  • 5. A neurologic presentation of familial hemophagocytic lymphohistiocytosis which mimicked septic emboli to the brain.
    Turtzo LC; Lin DD; Hartung H; Barker PB; Arceci R; Yohay K
    J Child Neurol; 2007 Jul; 22(7):863-8. PubMed ID: 17715280
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Correlation between phenotypic heterogeneity and gene mutational characteristics in familial hemophagocytic lymphohistiocytosis (FHL).
    Ueda I; Ishii E; Morimoto A; Ohga S; Sako M; Imashuku S
    Pediatr Blood Cancer; 2006 Apr; 46(4):482-8. PubMed ID: 16365863
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Novel spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis in ethnic Omani patients.
    Muralitharan S; Wali YA; Dennison D; Lamki ZA; Zachariah M; Nagwa el B; Pathare A; Krishnamoorthy R
    Am J Hematol; 2007 Dec; 82(12):1099-102. PubMed ID: 17674359
    [TBL] [Abstract][Full Text] [Related]  

  • 8. An inframe perforin gene deletion in familial hemophagocytic lymphohistiocytosis is associated with perforin expression.
    Muralitharan S; Al Lamki Z; Dennison D; Christie BS; Wali YA; Zachariah M; Romana M; Bayoumi R; Krishnamoorthy R
    Am J Hematol; 2005 Jan; 78(1):59-63. PubMed ID: 15609274
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A teenage boy with late onset hemophagocytic lymphohistiocytosis with predominant neurologic disease and perforin deficiency.
    Beaty AD; Weller C; Levy B; Vogler C; Ferguson WS; Bicknese A; Knutsen AP
    Pediatr Blood Cancer; 2008 May; 50(5):1070-2. PubMed ID: 18074390
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Central nervous system involvement in a case of familial hemophagocytic lymphohistiocytosis with perforin mutation.
    Akbayram S; Akgun C; Dogan M; Caksen H; Okur H; Oner AF
    Genet Couns; 2011; 22(3):281-5. PubMed ID: 22029169
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genotype-phenotype study of familial haemophagocytic lymphohistiocytosis due to perforin mutations.
    Trizzino A; zur Stadt U; Ueda I; Risma K; Janka G; Ishii E; Beutel K; Sumegi J; Cannella S; Pende D; Mian A; Henter JI; Griffiths G; Santoro A; Filipovich A; Aricò M;
    J Med Genet; 2008 Jan; 45(1):15-21. PubMed ID: 17873118
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Novel mutation of the perforin gene and maternal uniparental disomy 10 in a patient with familial hemophagocytic lymphohistiocytosis.
    Al-Jasmi F; Abdelhaleem M; Stockley T; Lee KS; Clarke JT
    J Pediatr Hematol Oncol; 2008 Aug; 30(8):621-4. PubMed ID: 18799942
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Clinical and molecular aspects of Turkish familial hemophagocytic lymphohistiocytosis patients with perforin mutations.
    Okur H; Balta G; Akarsu N; Oner A; Patiroglu T; Bay A; Sayli T; Unal S; Gurgey A
    Leuk Res; 2008 Jun; 32(6):972-5. PubMed ID: 18190960
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Hemophagocytic lymphohistiocytosis: when the immune system runs amok.
    Janka G
    Klin Padiatr; 2009 Sep; 221(5):278-85. PubMed ID: 19707989
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Biology and treatment of familial hemophagocytic lymphohistiocytosis: importance of perforin in lymphocyte-mediated cytotoxicity and triggering of apoptosis.
    Henter JI
    Med Pediatr Oncol; 2002 May; 38(5):305-9. PubMed ID: 11979453
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Clinical aspects, immunologic assessment, and genetic analysis in Taiwanese children with hemophagocytic lymphohistiocytosis.
    Lee WI; Chen SH; Hung IJ; Yang CP; Jaing TH; Chen CJ; Li SP; Huang JL
    Pediatr Infect Dis J; 2009 Jan; 28(1):30-4. PubMed ID: 19057461
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Mutations of the hemophagocytic lymphohistiocytosis-associated gene UNC13D in a patient with systemic juvenile idiopathic arthritis.
    Hazen MM; Woodward AL; Hofmann I; Degar BA; Grom A; Filipovich AH; Binstadt BA
    Arthritis Rheum; 2008 Feb; 58(2):567-70. PubMed ID: 18240215
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Familial haemophagocytic lymphohistiocytosis caused by perforin deficit can be successfully treated by haematopoietic stem cell transplantation--the first diagnosed case in the Czech Republic].
    Spísek R; Mejstríková E; Formánková R; Zizková H; Vávra V; Hrusák O; Sedivá A; Sedlácek P; Starý J
    Cas Lek Cesk; 2006; 145(1):50-4. PubMed ID: 16468242
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Fatal sibling cases of familial hemophagocytic lymphohistiocytosis (FHL) with MUNC13-4 mutations: case reports.
    Nakao T; Shimizu T; Fukushima T; Saito M; Okamoto M; Sugiura M; Yamamoto K; Ueda I; Imashuku S; Kobayashi C; Koike K; Tsuchida M; Sumazaki R; Matsui A
    Pediatr Hematol Oncol; 2008; 25(3):171-80. PubMed ID: 18432499
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.