Cargando…
Study of a supplement and a genetic test for lymphedema management
Malformations in the lymphatic vasculature, injury, surgery, trauma or toxic damage may lead to swelling of the limbs caused by inefficient lymphatic uptake and flow (lymphedema). Lymphedema can be congenital or acquired. Primary lymphedema is rare and caused by mutations in single genes, secondary...
Autores principales: | Michelini, Sandro, Cestari, Marina, Michelini, Serena, Camilleri, Giorgio, De Antoni, Luca, Nelson, Willy, Bertelli, Matteo |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mattioli 1885
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8023136/ https://www.ncbi.nlm.nih.gov/pubmed/33170163 http://dx.doi.org/10.23750/abm.v91i13-S.10658 |
Ejemplares similares
-
Dietary supplements in lymphedema
por: BONETTI, GABRIELE, et al.
Publicado: (2022) -
Low Efficacy of Genetic Tests for the Diagnosis of Primary Lymphedema Prompts Novel Insights into the Underlying Molecular Pathways
por: Bonetti, Gabriele, et al.
Publicado: (2022) -
Dietary supplements for lipedema
por: BONETTI, GABRIELE, et al.
Publicado: (2022) -
Imbalance between Expression of FOXC2 and Its lncRNA in Lymphedema-Distichiasis Caused by Frameshift Mutations
por: Missaglia, Sara, et al.
Publicado: (2021) -
FOXC2 Disease Mutations Identified in Lymphedema Distichiasis Patients Impair Transcriptional Activity and Cell Proliferation
por: Tavian, Daniela, et al.
Publicado: (2020)