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3. Review of hemophagocytic lymphohistiocytosis (HLH) in children with focus on Japanese experiences. Ishii E, Ohga S, Imashuku S, Kimura N, Ueda I, Morimoto A, Yamamoto K, Yasukawa M. Crit Rev Oncol Hematol; 2005 Mar; 53(3):209-23. PubMed ID: 15718147 [Abstract] [Full Text] [Related]
4. 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 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
7. An unusual cause of multiple organ dysfunction syndrome in the pediatric intensive care unit: hemophagocytic lymphohistiocytosis. Karapinar B, Yilmaz D, Balkan C, Akin M, Ay Y, Kvakli K. Pediatr Crit Care Med; 2009 May; 10(3):285-90. PubMed ID: 19433941 [Abstract] [Full Text] [Related]
8. Malignancy-associated hemophagocytic lymphohistiocytosis in pediatric cases: a multicenter study from Turkey. Celkan T, Berrak S, Kazanci E, Ozyürek E, Unal S, Uçar C, Yilmaz S, Gürgey A. Turk J Pediatr; 2009 May; 51(3):207-13. PubMed ID: 19817262 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. 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 [Abstract] [Full Text] [Related]
11. Bone marrow changes mimicking myelodysplasia in patients with hemophagocytic lymphohistiocytosis. Imashuku S, Kitazawa K, Ishii M, Kataoka S, Asami K, Ishii E, Fukushima K, Sako M, Matsubayashi T, Teramura GT, Hibi S. Int J Hematol; 2000 Oct; 72(3):353-7. PubMed ID: 11185994 [Abstract] [Full Text] [Related]
12. Rapid LightCycler assay for identification of the perforin codon 374 Trp --> stop mutation in patients and families with hemophagocytic lymphohistiocytosis (HLH). zur Stadt U, Kabisch H, Janka G, Schneider EM. Med Pediatr Oncol; 2003 Jul; 41(1):26-9. PubMed ID: 12764739 [Abstract] [Full Text] [Related]
14. Hemophagocytic lymphohistiocytosis. Report of 122 children from the International Registry. FHL Study Group of the Histiocyte Society. Aricò M, Janka G, Fischer A, Henter JI, Blanche S, Elinder G, Martinetti M, Rusca MP. Leukemia; 1996 Feb; 10(2):197-203. PubMed ID: 8637226 [Abstract] [Full Text] [Related]
15. Mutations in the perforin gene in children with hemophagocytic lymphohistiocytosis. Lu G, Xie ZD, Shen KL, Ye LJ, Wu RH, Liu CY, Jin YK, Yang S. Chin Med J (Engl); 2009 Dec 05; 122(23):2851-5. PubMed ID: 20092789 [Abstract] [Full Text] [Related]
16. Perforin deficiency and familial hemophagocytic lymphohistiocytosis. Zipursky A. Pediatr Res; 2001 Jan 05; 49(1):3. PubMed ID: 11134481 [No Abstract] [Full Text] [Related]
17. [Familial hemophagocytic lymphohistiocytosis]. Vucković N, Vucković D, Klem I. Med Pregl; 1991 Jan 05; 44(5-6):254-7. PubMed ID: 1808490 [Abstract] [Full Text] [Related]
18. Non-familial haemophagocytic lymphohistiocytosis in children. Hoh MC, Lin HP. Med J Malaysia; 1997 Jun 05; 52(2):146-50. PubMed ID: 10968072 [Abstract] [Full Text] [Related]
19. 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 05; 22(7):863-8. PubMed ID: 17715280 [Abstract] [Full Text] [Related]
20. [Diagnostic image (137) An infant with fever and pancytopenia. Hemophagocytic lymphohistiocytosis]. Verhallen-Dantuma JT, Buysse CM. Ned Tijdschr Geneeskd; 2003 May 03; 147(18):861. PubMed ID: 12756877 [Abstract] [Full Text] [Related] Page: [Next] [New Search]