[HTML][HTML] High levels of LIGHT/TNFSF14 in patients with prader–willi syndrome
MF Faienza, G Brunetti, D Fintini, G Grugni… - Journal of …, 2023 - Springer
Abstract Purpose/methods Prader–Willi syndrome (PWS) is a rare genetic disorder
displaying different clinical features, including obesity and bone impairment …
displaying different clinical features, including obesity and bone impairment …
High levels of LIGHT/TNFSF14 in patients with Prader-Willi syndrome
MF Faienza, G Brunetti, D Fintini… - Journal of …, 2023 - pubmed.ncbi.nlm.nih.gov
Purpose/methods Prader-Willi syndrome (PWS) is a rare genetic disorder displaying
different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a …
different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a …
High levels of LIGHT/TNFSF14 in patients with Prader–Willi syndrome
MF Faienza, G Brunetti, D Fintini, G Grugni… - JOURNAL OF …, 2023 - ricerca.uniba.it
Purpose/methods: Prader–Willi syndrome (PWS) is a rare genetic disorder displaying
different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a …
different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a …
[HTML][HTML] High levels of LIGHT/TNFSF14 in patients with Prader–Willi syndrome
MF Faienza, G Brunetti, D Fintini, G Grugni… - Journal of …, 2023 - ncbi.nlm.nih.gov
Results Median serum LIGHT levels were significantly increased in pediatric PWS with
respect to controls [255.82 (284.43) pg/ml vs 168.11 (76.23) pg/ml, p≤ 0.02] as well as in …
respect to controls [255.82 (284.43) pg/ml vs 168.11 (76.23) pg/ml, p≤ 0.02] as well as in …
High levels of LIGHT/TNFSF14 in patients with Prader-Willi syndrome.
MF Faienza, G Brunetti, D Fintini, G Grugni… - Journal of …, 2023 - europepmc.org
Results Median serum LIGHT levels were significantly increased in pediatric PWS with
respect to controls [255.82 (284.43) pg/ml vs 168.11 (76.23) pg/ml, p≤ 0.02] as well as in …
respect to controls [255.82 (284.43) pg/ml vs 168.11 (76.23) pg/ml, p≤ 0.02] as well as in …
[引用][C] High levels of LIGHT/TNFSF14 in patients with Prader–Willi syndrome
MF Faienza, G Brunetti, D Fintini, G Grugni… - Journal of …, 2023 - europepmc.org
Abstract Purpose/methods Prader–Willi syndrome (PWS) is a rare genetic disorder
displaying different clinical features, including obesity and bone impairment …
displaying different clinical features, including obesity and bone impairment …