Results 11 to 20 of about 52,438 (270)

A review of factors that influence individual compliance with mass drug administration for elimination of lymphatic filariasis. [PDF]

open access: yes, 2013
BACKGROUND: The success of programs to eliminate lymphatic filariasis (LF) depends in large part on their ability to achieve and sustain high levels of compliance with mass drug administration (MDA). This paper reports results from a comprehensive review
Fischer, Peter U   +2 more
core   +18 more sources

Economic Costs and Benefits of a Community-Based Lymphedema Management Program for Lymphatic Filariasis in Odisha State, India [PDF]

open access: yes, 2016
Lymphatic filariasis afflicts 68 million people in 73 countries, including 17 million persons living with chronic lymphedema. The Global Program to Eliminate Lymphatic Filariasis aims to stop new infections and to provide care for persons already ...
Addiss, David   +4 more
core   +2 more sources

Upgradation of Lymph Supermicrosurgical Skills through Lymphatic Venous Anastomosis

open access: yesJournal of Plastic and Reconstructive Surgery, 2022
Supermicrosurgery, a technique involving the dissection and anastomosis of small vessels, has revolutionized the field of lymphedema treatment. However, in a lymphatic venous anastomosis, an arduous technique is required to manipulate the 0.1-0.8-mm ...
Hirofumi Imai   +4 more
doaj  

How to Dissect Lymphatics under Loupes for Line Production System for Multiple Lymphaticovenular Anastomosis

open access: yesJournal of Reconstructive Microsurgery Open, 2020
Background A surgical line production system using loupes to dissect lymphatics and veins is a cost-effective way of performing multiple lymphaticovenular anastomoses.
Tarek Elsayed Mohamed Eldahshoury   +7 more
doaj   +1 more source

Mutations in GATA2 cause primary lymphedema associated with a predisposition to acute myeloid leukemia (Emberger syndrome). [PDF]

open access: yes, 2011
We report an allelic series of eight mutations in GATA2 underlying Emberger syndrome, an autosomal dominant primary lymphedema associated with a predisposition to acute myeloid leukemia.
C Preudhomme   +32 more
core   +1 more source

A rare truncal collateral lymph drainage pathway seen on indocyanine green lymphography in patients with secondary lower limb lymphedema

open access: yesJournal of Vascular Surgery Cases and Innovative Techniques, 2023
Objective: Although collateral lymphatic vessels are known to develop in patients with lymphedema, little is known about their significance. In this study, we investigated truncal collateral lymphatic drainage pathways in patients with lower limb ...
Solji Roh, MD   +5 more
doaj  

Supermicrosurgical lymphatic venous anastomosis for intractable lymphocele after great saphenous vein harvesting graft

open access: yesJournal of Vascular Surgery Cases and Innovative Techniques, 2022
Lymphoceles result from either trauma to the lymphatic vessels or after vein graft harvest, which occurs in 10% to 16% of patients. When a lymphocele persists despite conservative treatment, patients can experience undue distress.
Hirofumi Imai, MD   +4 more
doaj  

Self-reported symptoms of arm lymphedema and health-related quality of life among female breast cancer survivors

open access: yesScientific Reports, 2021
We examined cross-sectional associations between arm lymphedema symptoms and health-related quality of life (HRQoL) in the Health, Eating, Activity and Lifestyle (HEAL) Study.
Kayo Togawa   +9 more
doaj   +1 more source

Using the Indocyanine Green (ICG) Lymphography to Screen Breast Cancer Patients at High Risk for Lymphedema

open access: yesDiagnostics, 2022
Background: Indocyanine green (ICG) lymphography is a newer technique for diagnosing lymphedema. Our study aimed to find whether the abnormality of ICG lymphography can predict the occurrence of early lymphedema and then select candidates at high risk of
Miao Liu   +5 more
doaj   +1 more source

A novel KIF11 mutation in a Turkish patient with microcephaly, lymphedema, and chorioretinal dysplasia from a consanguineous family. [PDF]

open access: yes, 2012
Microcephaly–lymphedema–chorioretinal dysplasia (MLCRD) syndrome is a rare syndrome that was first described in 1992. Characteristic craniofacial features include severe microcephaly, upslanting palpebral fissures, prominent ears, a broad nose, and a ...
Atlihan, F   +6 more
core   +1 more source

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