Lymphohistiocytosis, Hemophagocytic research, articles, guidelines & medical evidence database search.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 19 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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Research
The current outbreak of Kaposi's sarcoma and opportunistic infections.
Haverkos H W, Curran J W
CA: a cancer journal for clinicians Vol 32(6)
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Date 01 Dec 1982
Research
Munc13-4 is essential for cytolytic granules fusion and is mutated in a form of familial hemophagocytic lymphohistiocytosis (FHL3).
Feldmann Jérôme, Callebaut Isabelle, Raposo Graça, Certain Stéphanie, Bacq Delphine ...
Cell Vol 115(4)
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Date 14 Nov 2003
Research
Microbiota-Dependent Sequelae of Acute Infection Compromise Tissue-Specific Immunity.
Fonseca Denise Morais da, Hand Timothy W, Han Seong-Ji, Gerner Michael Y, Glatman Zaretsky Arielle ...
Cell Vol 163(2)
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Date 08 Oct 2015
Research
Generalized lymphoproliferative disease in mice, caused by a point mutation in the Fas ligand.
Takahashi T, Tanaka M, Brannan C I, Jenkins N A, Copeland N G ...
Cell Vol 76(6)
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Date 25 Mar 1994
Research
Avian reticuloendotheliosis virus: identification of the hematopoietic target cell for transformation.
Lewis R B, McClure J, Rup B, Niesel D W, Garry R F ...
Cell Vol 25(2)
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Date 01 Aug 1981
Research
bcl-2-immunoglobulin transgenic mice demonstrate extended B cell survival and follicular lymphoproliferation.
McDonnell T J, Deane N, Platt F M, Nunez G, Jaeger U ...
Cell Vol 57(1)
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Date 07 Apr 1989
Research
Germline HAVCR2 mutations altering TIM-3 characterize subcutaneous panniculitis-like T cell lymphomas with hemophagocytic lymphohistiocytic syndrome.
Gayden Tenzin, Sepulveda Fernando E, Khuong-Quang Dong-Anh, Pratt Jonathan, Valera Elvis T ...
Nature genetics Vol 50(12)
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Date 01 Dec 2018
Research
Mutations in RAB27A cause Griscelli syndrome associated with haemophagocytic syndrome.
Ménasché G, Pastural E, Feldmann J, Certain S, Ersoy F ...
Nature genetics Vol 25(2)
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Date 01 Jun 2000
Research
Somatic RHOA mutation in angioimmunoblastic T cell lymphoma.
Sakata-Yanagimoto Mamiko, Enami Terukazu, Yoshida Kenichi, Shiraishi Yuichi, Ishii Ryohei ...
Nature genetics Vol 46(2)
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Date 01 Feb 2014
Research
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study Group.
Drenth J P, Cuisset L, Grateau G, Vasseur C, van de Velde-Visser S D ...
Nature genetics Vol 22(2)
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Date 01 Jun 1999
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