Results 21 to 30 of about 65,861 (304)

Abnormal lymphatic S1P signaling aggravates lymphatic dysfunction and tissue inflammation

open access: yes, 2023
BACKGROUNDLymphedema is a global health problem with no effective drug treatment. Enhanced T cell immunity and abnormal lymphatic endothelial cell (LEC) signaling are promising therapeutic targets for this condition. Sphingosine-1-phosphate (S1P) mediates a key signaling pathway required for normal LEC function, and altered S1P signaling in LECs could ...
Dongeon Kim   +17 more
openaire   +2 more sources

Utilizing lymphatic cell markers to visualize human lymphatic abnormalities [PDF]

open access: yesJournal of Biophotonics, 2017
In vivo visualization of the human lymphatic system is limited by the mode of delivery of tracing agents, depth of field and size of the area examined, and specificity of the cell markers used to distinguish lymphatic endothelium from the blood vessels and the surrounding tissues.
openaire   +3 more sources

Clinical evaluation of endolymphatic radiotherapy in malignant lymphoma [PDF]

open access: yes, 1974
By endolymphatic injection of radioisotope 131I.Lipiodol, so.called endolymphatic radiotherapy, we treated 10 cases with malignant lymphoma and found a marked tumor reduction to normal size in all the 10 cases we tried.
Irino, Shozo   +3 more
core   +1 more source

Prenatal Ultrasound Diagnosis of Klippel–Trenaunay Syndrome

open access: yesDiagnostics, 2023
Klippel–Trenaunay syndrome (KTS) is a very rare vascular malformation syndrome also referred to as a capillary–lymphatic–venous malformation with unknown aetiology.
Nicolae Gică   +6 more
doaj   +1 more source

Neurotrophic keratitis in a patient with disseminated lymphangiomatosis. [PDF]

open access: yes, 2009
INTRODUCTION: Neurotrophic keratitis, a degenerative corneal disease caused by trigeminal nerve impairment, has many etiologies and remains very difficult to treat.
Charukamnoetkanok, Puwat   +2 more
core   +2 more sources

Case report: Noonan syndrome with protein-losing enteropathy

open access: yesFrontiers in Genetics, 2023
Background: Noonan syndrome (NS) is characterized by typical facial features, short stature, congenital heart defects and other comorbidities. Lymphedema and chylous pleural effusions are also common in NS, but protein-losing enteropathy (PLE) is rarely ...
Yang Ou   +6 more
doaj   +1 more source

Peripheral vascular malformations : modern imaging [PDF]

open access: yes, 2018
Currently the major aim in peripheral vascular malformation diagnosis, crucial for subsequent management and treatment, is to identify its haemodynamic characteristics.

core   +1 more source

Regulating Retinoic Acid Availability during Development and Regeneration: The Role of the CYP26 Enzymes. [PDF]

open access: yes, 2020
This review focuses on the role of the Cytochrome p450 subfamily 26 (CYP26) retinoic acid (RA) degrading enzymes during development and regeneration. Cyp26 enzymes, along with retinoic acid synthesising enzymes, are absolutely required for RA homeostasis
Roberts, C
core   +2 more sources

Non-immune fetal hydrops: etiology and outcome according to gestational age at diagnosis. [PDF]

open access: yes, 2020
OBJECTIVE: Fetal hydrops is associated with increased perinatal morbidity and mortality. The etiology and outcome of fetal hydrops may differ according to the gestational age at diagnosis.
A. Bhide   +12 more
core   +2 more sources

Hydrops fetalis due to abnormal lymphatics. [PDF]

open access: yesArchives of Disease in Childhood, 1987
A case of generalised lymphatic abnormality that presented with hydrops fetalis is described. This seems to be the first such case reported.
K P, Windebank   +3 more
openaire   +2 more sources

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