Access the latest scientific research and medical evidence related to Lymphedema treatment, diagnosis and symptoms, quickly and easily with doctorAsyou.
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All Pubmed data courtesy of the U.S. National Library of Medicine. Library last updated 18 December 2020.
Clinical trials databases last updated 1 December 2020 (clinicaltrials.gov) and 1 December 2020 (ictrp)
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4835 Abstracts
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
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
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
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
Missense mutations interfere with VEGFR-3 signalling in primary lymphoedema.
Karkkainen M J, Ferrell R E, Lawrence E C, Kimak M A, Levinson K L ...
Nature genetics Vol 25(2)
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Date 01 Jun 2000
Research
Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome).
Ostergaard Pia, Simpson Michael A, Connell Fiona C, Steward Colin G, Brice Glen ...
Nature genetics Vol 43(10)
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Date 04 Sep 2011
Research
Mutations in CCBE1 cause generalized lymph vessel dysplasia in humans.
Alders Marielle, Hogan Benjamin M, Gjini Evisa, Salehi Faranak, Al-Gazali Lihadh ...
Nature genetics Vol 41(12)
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Date 01 Dec 2009
Research
Autosomal recessive lissencephaly with cerebellar hypoplasia is associated with human RELN mutations.
Hong S E, Shugart Y Y, Huang D T, Shahwan S A, Grant P E ...
Nature genetics Vol 26(1)
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Date 01 Sep 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
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