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名词信息
中 文 名:
丝虫病性乳糜尿
英 文 名:
filarial chyluria
中文又称:
丝虫性乳糜尿
中文曾称:
名词来源:
所属专业:
心血管外科
所属类别:
疾病诊断名词
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Pubmed相关的文献
filarial chyluria
相关文献:
Rare Cases of Filarial Chyluria in Children.
Srivastava S, Tiwari V, Sen M.
Int Med Case Rep J. 2022 Mar 30;15:135-139. doi: 10.2147/IMCRJ.S339207. eCollection 2022.
PMID:35386532
Filarial chyluria.
Kohli V, Gulati S, Kumar L.
Indian Pediatr. 1994 Apr;31(4):451-4.
PMID:7875869
An occult filarial infection presenting as chyluria with proteinuria: a case report and review of literature.
Saha M, Ray S, Goswami M, Kundu S, Saha P, Saha A, Maitra S, Talukdar A.
BMJ Case Rep. 2012 Jun 1;2012:bcr0120125635. doi: 10.1136/bcr.01.2012.5635.
PMID:22669920
Chyluria in non-filarial endemic areas: an internist's perspective.
Tan Y.
BMJ Case Rep. 2017 Oct 4;2017:bcr2017220772. doi: 10.1136/bcr-2017-220772.
PMID:28978586
Filarial chyluria.
SHETH SC, SHAH UK.
Indian J Child Health. 1962 Sep;11:431-4.
PMID:13977219
Chyluria in pregnancy: Etiology, diagnosis, and management perspective.
Purkait B, Garg G, Singh M, Sharma A, Pandey S, Sankhwar SN.
Saudi J Kidney Dis Transpl. 2019 Mar-Apr;30(2):309-314. doi: 10.4103/1319-2442.256837.
PMID:31031366
Chyluria Associated With Nephrotic-Range Proteinuria.
Kaur A, Kandari S, Saini S, Dhoot DK, Kandari A.
Cureus. 2022 Jul 9;14(7):e26690. doi: 10.7759/cureus.26690. eCollection 2022 Jul.
PMID:35959171
Filarial chyluria as a rare cause of urinary retention.
Hagiya H, Terasaka T, Kimura K, Satou A, Asano K, Waseda K, Hanayama Y, Takahashi T, Aoe M, Iio K, Watanabe T, Kondo E, Otsuka F.
Intern Med. 2014;53(17):2001-5. doi: 10.2169/internalmedicine.53.2572. Epub 2014 Sep 1.
PMID:25175138
Hematuria without chyluria: It could still be due to filarial etiology.
Nag VL, Sen M, Dash NR, Bansal R, Kumar M, Maurya AK.
Trop Parasitol. 2016 Jul-Dec;6(2):151-154. doi: 10.4103/2229-5070.190834.
PMID:27722105
Genetic association of MBL-2 gene polymorphisms with Filarial chyluria.
Pant S, Goel A, Gangwar PK, Agarwal J, Singh AK, Sankhwar SN, Gupta P.
Bioinformation. 2019 Dec 10;15(11):806-811. doi: 10.6026/97320630015806. eCollection 2019.
PMID:31902980
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