Olivier Nardi
Overview
Explore the profile of Olivier Nardi including associated specialties, affiliations and a list of published articles.
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Articles
29
Citations
350
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Recent Articles
1.
Fayssoil A, Mansencal N, Nguyen L, Nardi O, Ben Yaou R, Leturcq F, et al.
J Am Heart Assoc
. 2023 Aug;
12(16):e027231.
PMID: 37581390
Background Chronic respiratory failure and heart involvement may occur in Duchenne muscular dystrophy. We aimed to assess the prognostic value of the right ventricular (RV) systolic dysfunction in patients with...
2.
Fayssoil A, Ogna A, Chaffaut C, Lamothe L, Ambrosi X, Nardi O, et al.
Medicine (Baltimore)
. 2018 Jul;
97(27):e11381.
PMID: 29979426
Heart impairment is classical in dystrophinopathies and its management relies on medical drugs. Mechanical ventilation is used to treat respiratory failure, but can affect cardiac function. We aimed to investigate...
3.
Fayssoil A, Nguyen L, Ogna A, Meng P, Nardi O, Laforet P, et al.
Am J Cardiol
. 2018 May;
122(2):353-355.
PMID: 29793889
Cardiac and respiratory function may be impaired in sarcoglycanopathies, a subgroup of muscular dystrophies due to sarcoglycan proteins (α, β, γ, and δ) genes mutations. Management of patients with restrictive...
4.
Nardi O, Zavala E, Martin C, Nanas S, Scheeren T, Polito A, et al.
BMJ Open
. 2018 Mar;
8(3):e017581.
PMID: 29555789
Objective: Evaluation of the ratio of oxyhaemoglobin to total haemoglobin in skeletal muscle (StO) using near-infrared spectroscopy may aid in the monitoring of patients with sepsis. This study assessed the...
5.
Fayssoil A, Ben Yaou R, Ogna A, Chaffaut C, Leturcq F, Nardi O, et al.
PLoS One
. 2018 Jan;
13(1):e0190518.
PMID: 29304097
Background: Duchenne muscular dystrophy (DMD) is an inherited myogenic disorder due to mutations in the dystrophin gene on chromosome Xp21.1. We designed this study to determine the prevalence of left...
6.
Fayssoil A, Ben Yaou R, Ogna A, Leturcq F, Nardi O, Clair B, et al.
ESC Heart Fail
. 2017 Nov;
4(4):527-534.
PMID: 29154419
Aims: Duchenne muscular dystrophy (DMD) is characterized by respiratory and heart involvements. In the context of permanently wheelchair bound and on mechanical ventilation (MV) patients, the clinical presentation of acute...
7.
Fayssoil A, Lazarus A, Wahbi K, Ogna A, Nardi O, Lofaso F, et al.
Int J Cardiol
. 2016 Aug;
222:975-977.
PMID: 27526372
Background/objectives: Muscular dystrophies are genetic muscle disorders, in which heart involvement and chronic respiratory impairment affect survival. Cardiac conduction disturbances require implantable cardiac pacemaker. Implantable defibrillators may also be necessary...
8.
Fayssoil A, Ogna A, Chaffaut C, Chevret S, Guimaraes-Costa R, Leturcq F, et al.
PLoS One
. 2016 Apr;
11(4):e0153095.
PMID: 27120200
Background: Type 2C and 2D limb girdle muscular dystrophies (LGMD) are a group of autosomal recessive limb girdle muscular dystrophies manifested by proximal myopathy, impaired respiratory muscle function and cardiomyopathy....
9.
Fayssoil A, Nardi O, Annane D, Orlikowski D
Neurol Int
. 2014 Apr;
6(1):5140.
PMID: 24744846
Myotonic dystrophy type 1 (MD) is the most common autosomal dominant muscular dystrophy in adults. Cardiac involvement is mainly characterized by conduction abnormalities and arrhythmias. We sought to assess diastolic...
10.
Fayssoil A, Nardi O, Annane D, Orlikowski D
Acta Neurol Belg
. 2014 Jan;
114(4):257-9.
PMID: 24464767
Sarcoglycanopathies are autosomic recessive muscular dystrophies, secondary to mutations of the sarcoglycan complex. Heart can be involved in sarcoglycanopathies. We sought to analyse left ventricular function in patients with alpha-sarcoglycanopathy...