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Journal Abstract Search
780 related items for PubMed ID: 24583560
1. [Flow cytometry in the diagnosis of hemophagocytic lymphohistiocytosis in a case with fatal outcome]. Pállinger E, Erdélyi D, Kovács G, Kriván G, Korponay Z, Fekete G, Szabó A, Falus A, Dérfalvi B. Orv Hetil; 2014 Mar 09; 155(10):389-95. PubMed ID: 24583560 [Abstract] [Full Text] [Related]
2. [Screening for cytotoxic defects with flow cytometric detection of CD107α on natural killer cells and cytotoxic lymphocyte cells]. Wang J, Liu Z, Jiang LP, An YF, Zhao XD. Zhonghua Er Ke Za Zhi; 2012 May 09; 50(5):386-91. PubMed ID: 22883044 [Abstract] [Full Text] [Related]
3. Perforin and CD107a testing is superior to NK cell function testing for screening patients for genetic HLH. Rubin TS, Zhang K, Gifford C, Lane A, Choo S, Bleesing JJ, Marsh RA. Blood; 2017 Jun 01; 129(22):2993-2999. PubMed ID: 28270454 [Abstract] [Full Text] [Related]
4. 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 01; 22(7):863-8. PubMed ID: 17715280 [Abstract] [Full Text] [Related]
5. 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 01; 46(4):482-8. PubMed ID: 16365863 [Abstract] [Full Text] [Related]
6. 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 01; 74(12):1579-85. PubMed ID: 24051121 [Abstract] [Full Text] [Related]
7. Hemophagocytic lymphohistiocytosis: when the immune system runs amok. Janka G. Klin Padiatr; 2009 Sep 01; 221(5):278-85. PubMed ID: 19707989 [Abstract] [Full Text] [Related]
8. The syndrome of hemophagocytic lymphohistiocytosis in primary immunodeficiencies: implications for differential diagnosis and pathogenesis. Bode SF, Ammann S, Al-Herz W, Bataneant M, Dvorak CC, Gehring S, Gennery A, Gilmour KC, Gonzalez-Granado LI, Groß-Wieltsch U, Ifversen M, Lingman-Framme J, Matthes-Martin S, Mesters R, Meyts I, van Montfrans JM, Pachlopnik Schmid J, Pai SY, Soler-Palacin P, Schuermann U, Schuster V, Seidel MG, Speckmann C, Stepensky P, Sykora KW, Tesi B, Vraetz T, Waruiru C, Bryceson YT, Moshous D, Lehmberg K, Jordan MB, Ehl S, Inborn Errors Working Party of the EBMT. Haematologica; 2015 Jul 01; 100(7):978-88. PubMed ID: 26022711 [Abstract] [Full Text] [Related]
9. Hemophagocytic lymphohistiocytosis and related disorders. Filipovich AH. Curr Opin Allergy Clin Immunol; 2006 Dec 01; 6(6):410-5. PubMed ID: 17088644 [Abstract] [Full Text] [Related]
11. Familial hemophagocytic lymphohistiocytosis in a 6-week-old male infant. Jakovljević G, Kardum-Skelin I, Rogosić S, Culić S, Stepan J, Gagro A, Skarić I, Mikecin L, Bonevski A, Barisić I, Nakić M. Coll Antropol; 2010 Jun 01; 34(2):631-4. PubMed ID: 20698142 [Abstract] [Full Text] [Related]
17. Perforin gene mutation in familial haemophagocytic lymphohistiocytosis: the first reported case from Hong Kong. Chiang GP, Li CK, Lee V, Cheng FW, Leung AW, Imashuku S, Imamura T, Shing MM. Hong Kong Med J; 2014 Aug 01; 20(4):339-42. PubMed ID: 25104007 [Abstract] [Full Text] [Related]
18. 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 01; 34(6):852-67. PubMed ID: 20442642 [Abstract] [Full Text] [Related]
19. Adult cancer-related hemophagocytic lymphohistiocytosis - a challenging diagnosis: a case report. Hust MA, Blechacz BRA, Bonilla DL, Daver N, Rojas-Hernandez CM. J Med Case Rep; 2017 Jun 27; 11(1):172. PubMed ID: 28651636 [Abstract] [Full Text] [Related]