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期刊名:Lymphology

缩写:LYMPHOLOGY

ISSN:0024-7766

e-ISSN:N/A

IF/分区:2.1/Q3

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共收录本刊相关文章索引1354
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
K Leela Praveen Kumar,G Manokaran K Leela Praveen Kumar
Genital lymphedema is a common problem seen by lymphology surgeons in India due to filarial infections. We have developed an innovative operative technique to correct this issue using native skin and have found the results in the first fift...
J Rothbauer,S Driver,L Callender J Rothbauer
Turner syndrome (TS) is a chromosomal condition affecting an estimated 1 in 2,500 girls where the second X chromosome is missing, or partially formed. This abnormality affects multiple body systems and can lead to short stature, cardiac, ne...
Observational Study Lymphology. 2015 Sep;48(3):139-52. DOI: 2015
J Weiss,T Daniel J Weiss
Evidence-based practice supports the use of validated outcome measures to assess the impact of lymphedema; however, condition-specific lymphedema assessment measures are needed. The Lymphedema Life Impact Scale (LLIS) was developed as a com...
G Morcaldi,T Bellini,C Rossi et al. G Morcaldi et al.
Cardio-facio-cutaneous (CFC) syndrome is a very rare and sporadic disease whose characteristics include dysmorphic facial appearance, ectodermal abnormalities, cardiac abnormalities, growth retardation and neurodevelopmental delay. This syn...
A Finnane,M Janda,S C Hayes A Finnane
Most studies evaluating lymphedema treatment effect focus on objective reductions in limb volume, with little attention given to subjective treatment outcomes. The objective of this work was to describe the range of lymphedema symptoms expe...
A Hecimovic,M Jakopovic,G Pavlisa et al. A Hecimovic et al.
Lymphangioleiomyomatosis (LAM) is a rare, progressive, diffuse cystic lung disease predominantly affecting women of child bearing age. Recently treatment with sirolimus was shown to stabilize lung function decline and improve quality of lif...
N F Liu,Z Yu,Y Luo et al. N F Liu et al.
Milroy disease is a congenital onset lymphedema linked to FLT4 gene mutations in the tyrosine kinase domain. So far, a total of 59 different FLT4 variants have been identified. Here, we report a novel FLT4 gene mutation in a Chinese family ...