User profiles for "author:Massimo Russo"
Massimo RussoTecnologo Verified email at ingv.it Cited by 924 |
[HTML][HTML] The role of NLRP3 inflammasome in the pathogenesis of traumatic brain injury
Traumatic brain injury (TBI) represents an important problem of global health. The damage
related to TBI is first due to the direct injury and then to a secondary phase in which …
related to TBI is first due to the direct injury and then to a secondary phase in which …
[HTML][HTML] Current options and future perspectives in the treatment of dyslipidemia
S Muscoli, M Ifrim, M Russo, F Candido… - Journal of clinical …, 2022 - mdpi.com
Low-density lipoprotein cholesterol (LDL-C) plays a crucial role in the development of
atherosclerosis. Statin therapy is the standard treatment for lowering LDL-C in primary and …
atherosclerosis. Statin therapy is the standard treatment for lowering LDL-C in primary and …
[HTML][HTML] Targeting the tumor microenvironment: a close up of tumor-associated macrophages and neutrophils
The importance of the tumor microenvironment (TME) in dynamically regulating cancer
progression and influencing the therapeutic outcome is widely accepted and appreciated …
progression and influencing the therapeutic outcome is widely accepted and appreciated …
Magma degassing as a trigger of bradyseismic events: The case of Phlegrean Fields (Italy)
Phlegrean Fields is an active and densely populated caldera near Naples (Italy). Two major
unrest episodes characterized its recent history, each leading to remarkable ground uplift …
unrest episodes characterized its recent history, each leading to remarkable ground uplift …
Hospital-acquired malnutrition in children with mild clinical conditions
A Campanozzi, M Russo, A Catucci, I Rutigliano… - Nutrition, 2009 - Elsevier
OBJECTIVE: Little is known about the incidence and risk factors of hospital-acquired
malnutrition in children with mild illness (grade 1 clinical conditions) and its timing of …
malnutrition in children with mild illness (grade 1 clinical conditions) and its timing of …
Geochemical evidence for the existence of high-temperature hydrothermal brines at Vesuvio volcano, Italy
A high-temperature hydrothermal system is present underneath the crater area of Vesuvio
volcano. It is suggested that NaCl brines reside in the high-temperature reservoir and …
volcano. It is suggested that NaCl brines reside in the high-temperature reservoir and …
Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study
D Adams, M Polydefkis, A González-Duarte… - The Lancet …, 2021 - thelancet.com
Background Hereditary transthyretin-mediated amyloidosis is a rare, inherited, progressive
disease caused by mutations in the transthyretin (TTR) gene. We assessed the safety and …
disease caused by mutations in the transthyretin (TTR) gene. We assessed the safety and …
Factors predicting survival in ALS: a multicenter Italian study
The aim of this multicenter, retrospective study is to investigate the role of clinical
characteristics and therapeutic intervention on ALS prognosis. The study included patients …
characteristics and therapeutic intervention on ALS prognosis. The study included patients …
ATTRv amyloidosis Italian Registry: clinical and epidemiological data
M Russo, L Obici, I Bartolomei, F Cappelli, M Luigetti… - Amyloid, 2020 - Taylor & Francis
Introduction ATTRv amyloidosis is worldwide spread with endemic foci in Portugal and
Sweden, Japan, Brazil, Maiorca, and Cyprus. A national Registry was developed to …
Sweden, Japan, Brazil, Maiorca, and Cyprus. A national Registry was developed to …
[HTML][HTML] Transthyretin-related familial amyloid polyneuropathy (TTR-FAP): a single-center experience in Sicily, an Italian endemic area
A Mazzeo, M Russo, G Di Bella… - Journal of …, 2015 - content.iospress.com
Background: Familial amyloid polyneuropathy related to transthyretin gene (TTR-FAP) is a
life-threatening disease transmitted as an autosomal dominant trait. Val30Met mutation …
life-threatening disease transmitted as an autosomal dominant trait. Val30Met mutation …