Robert Yves Carlier

Prof. Robert Yves Carlier

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 July 2020 in Radiology Case Reports
Verified
Journal Article
Open access
OBOlivier de Barry
Olivier de Barry
AMAhmed Mekki
Ahmed Mekki
CDCaroline Diffre
Caroline Diffre
MSMartin Seror
Martin Seror
Mostafa El-HajjamMostafa El-Hajjam
Mostafa El-Hajjam
RCRobert Yves Carlier
Robert Yves Carlier
As coronavirus pandemic continue to spread over the world, we have to be aware of potential complications on hospitalized patients. We report a case of a 79-year-old woman with COVID-19 pneumonia complicated by combined arterial and venous thrombosis of upper mesenteric vessels. As unenhanced chest CT scan plays a key role in managing the COVID-19 pandemic, we should pay attention to indirect signs of thrombosis.

1 November 2019 in Neuromuscular Disorders
Verified
Journal Article
Closed access
JCJodi Warman Chardon
Jodi Warman Chardon
JDJordi Díaz-Manera
Jordi Díaz-Manera
Giorgio TascaGiorgio Tasca
Giorgio Tasca
CBCarsten G. Bönnemann
Carsten G. Bönnemann
DGDavid Gómez-Andrés
David Gómez-Andrés
RCRobert Yves Carlier
Robert Yves Carlier

18 December 2019 in Nature Communications
Verified
Journal Article
Open access
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AMAndreas Marg
Andreas Marg
HEHelena Escobar
Helena Escobar
NKNikos Karaiskos
Nikos Karaiskos
SGStefanie Grunwald
Stefanie Grunwald
Eric MetzlerEric Metzler
Eric Metzler
SSSimone Spuler
Simone Spuler
Skeletal muscle stem cells, called satellite cells and defined by the transcription factor PAX7, are responsible for postnatal muscle growth, homeostasis and regeneration. Attempts to utilize the regenerative potential of muscle stem cells for therapeutic purposes so far failed. We previously established the existence of human PAX7-positive cell colonies with high regenerative potential. We now identified PAX7-negative human muscle-derived cell colonies also positive for the myogenic markers desmin and MYF5. These include cells from a patient with a homozygous PAX7 c.86-1G > A mutation (PAX7null). Single cell and bulk transcriptome analysis show high intra- and inter-donor heterogeneity and reveal the endothelial cell marker CLEC14A to be highly expressed in PAX7null cells. All PAX7-negative cell populations, including PAX7null, form myofibers after transplantation into mice, and regenerate muscle after reinjury. Transplanted PAX7neg cells repopulate the satellite cell niche where they re-express PAX7, or, strikingly, CLEC14A. In conclusion, transplanted human cells do not depend on PAX7 for muscle regeneration.

1 April 2019 in Seminars in Pediatric Neurology
Verified
Journal Article
Closed access
RCRobert Yves Carlier
Robert Yves Carlier
SQSusana Quijano-Roy
Susana Quijano-Roy

18 October 2016 in BMC Musculoskeletal Disorders
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Journal Article
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BLBruno Law-Ye
Bruno Law-Ye
CHChloé Hangard
Chloé Hangard
AFAdrien Felter
Adrien Felter
DSDominique Safa
Dominique Safa
PDPhilippe Denormandie
Philippe Denormandie
RCRobert Yves Carlier
Robert Yves Carlier
Neurogenic Myositis Ossificans (NMO) is a rare disabling pathology characterized by peri-articular heterotopic ossifications following severe peripheral or central nervous system injuries. It results in ankylosis and vessels or nerves compressions. Our study aimed to describe the pre-operative findings of patients with NMO of the hip using biphasic computerized tomography (CT). Between 2006 and 2012, we retrospectively analyzed 101 consecutive patients with hip NMO. We analyzed all CTs and surgical reports following a standardized grid depicting the osteoma and its relations with joint capsule, vessels and nerves and bone mineralization. We studied surgical complications and recurrence during follow-up. Chi2-test and Fischer’s test were performed to compare qualitative values with respectively normal and non-normal distribution. Quantitative values were analyzed with a one factor analysis of variance (ANOVA) test. Agreement between pre-surgical CT and surgical observations was evaluated with Cohen’s kappa test. Correlation between pre-operative CT and surgical findings was excellent regarding relationships with vessels (0,82) and was good concerning relationships with sciatic nerves (0.62) and with joint capsule (0.68). Close contact or disruption of joint capsule (p = 0.005), joint space narrowing (p = 0.007) and bone demineralization (p < 0.001) were correlated with NMO recurrence. Biphasic enhanced-CT allows pre-operative assessment of NMO with good correlation to surgical observations and helps prevent surgical complications.

Verified
Journal Article
Open access
PDF file
SUSophie Urtado
Sophie Urtado
HHHélène Hergault
Hélène Hergault
SBStephen Binsse
Stephen Binsse
VAVincent Aidan
Vincent Aidan
MOMounir Ouadahi
Mounir Ouadahi
NMNicolas Mansencal
Nicolas Mansencal
Background. We assessed the usefulness of a longitudinal strain adjusted to regional thickness in hypertrophic cardiomyopathy (HCM). Indeed, with conventional software, the width of the region of interest (ROI) is the same over the entire myocardial wall, wherein the software analyzes only partially the left ventricular (LV) hypertrophic segments. Methods. We included 110 patients: 55 patients with HCM (HCM group) and 55 healthy subjects (age- and sex-matched control group). The global longitudinal strain (GLS) and regional strain for each of the 17 segments was calculated with standard software (for two groups) and with software adjusted to the myocardial wall thickness (for the HCM group). Results. GLS was significantly decreased in the HCM group compared to the control group (−15.1 ± 4.8% versus −20.5 ± 4.3%, p < 0.0001). In the HCM group, GLS (standard method versus adjusted to thickness) measurements were not significantly different (p = 0.34). Interestingly, the regional strain adjusted to thickness was significantly lower than the standard strain in the hypertrophic segments, especially in the basal inferoseptal segment (p = 0.0002), median inferoseptal segment (p < 0.001) and median anteroseptal segment (p = 0.02). The strain adjusted to thickness was still significantly lower in the most hypertrophic segments (≥20 mm) (−3.7 ± 3%, versus −5.9 ± 4.4%, p = 0.049 in the basal inferoseptal segment and −5.7 ± 3.5% versus −8.3 ± 4.5%, p = 0.0007 in the median inferoseptal segment). In the segments with significant myocardial fibrosis, the longitudinal strain adjusted to thickness was significantly lower than the conventional strain (−8.3 ± 3.3% versus −11.4 ± 4.5%, p = 0.002). The analysis of the strain adjusted to thickness had a better feasibility (97.5% versus 99%, p = 0.01). Conclusions. The analysis of a longitudinal strain adjusted to regional thickness is feasible in HCM and allows a better evaluation of myocardial deformation, especially in the most LV hypertrophic segments.