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Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort

European journal of neurology, 2023-08, Vol.30 (8), p.2506-2517

2023

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Macroglossia: A potentially severe complication of late‐onset Pompe disease

European journal of neurology, 2022-07, Vol.29 (7), p.2121-2128

2022

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Whole‐Body Muscle Magnetic Resonance Imaging in Glycogen‐Storage Disease Type III

Muscle & nerve, 2019-07, Vol.60 (1), p.72-79

2019

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Hyperckemia and myalgia are common presentations of anoctamin‐5‐related myopathy in French patients

Muscle & nerve, 2017-12, Vol.56 (6), p.1096-1100

2017

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Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients

Journal of inherited metabolic disease, 2015-05, Vol.38 (3), p.565-572

2015

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Arterial and venous abdominal thrombosis in a 79-year-old woman with COVID-19 pneumonia

Radiology case reports, 2020-07, Vol.15 (7), p.1054-1057

2020

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Pre-test probability for SARS-Cov-2-related infection score: The PARIS score

PloS one, 2020-12, Vol.15 (12), p.e0243342-e0243342

2020

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MRI in sarcoglycanopathies: a large international cohort study

Journal of neurology, neurosurgery and psychiatry, 2018-01, Vol.89 (1), p.72

2018

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Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity

European radiology, 2018-12, Vol.28 (12), p.5293-5303

2018

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Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

American journal of human genetics, 2012-02, Vol.90 (2), p.201-216

2012

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Recessive MYPN mutations cause cap myopathy with occasional nemaline rods

Annals of neurology, 2017-03, Vol.81 (3), p.467-473

2017

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WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codon

Neurogenetics, 2018-05, Vol.19 (2), p.67-76

2018

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Predictive factors for positive disco-vertebral biopsy culture in pyogenic vertebral osteomyelitis, and impact of fluoroscopic versus scanographic guidance

BMC infectious diseases, 2020-07, Vol.20 (1), p.1-512, Article 512

2020

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Severity Classification in Cases of Collagen Vi-Related Myopathy with Convolutional Neural Networks and Handcrafted Texture Features

2022 IEEE International Conference on Image Processing (ICIP), 2022, p.3596-3600

2022

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Comparison of magnetic resonance imaging and computed tomography for bone assessment of neurogenic heterotopic ossification of the hip: a preliminary study

Journal of orthopaedic surgery and research, 2021-12, Vol.16 (1), p.725-725, Article 725

2021

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Contribution of Interventional Radiologist in the Management of Pseudoaneurysm and Neck Hemorrhages in COVID-19 patients

Ear, nose, & throat journal, 2021-04, Vol.100 (2_suppl), p.148S-151S

2021

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SHOULD patients with asymptomatic pompe disease be treated? A nationwide study in france

Muscle & nerve, 2015-06, Vol.51 (6), p.884-889

2015

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Understanding a mass in the paraspinal region: an anatomical approach

Insights into imaging, 2023-07, Vol.14 (1), p.128-128, Article 128

2023

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Pre-surgical CT-assessment of neurogenic myositis ossificans of the hip and risk factors of recurrence: a series of 101 consecutive patients

BMC musculoskeletal disorders, 2016-10, Vol.17 (1), p.433-433, Article 433

2016

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The FLNC Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability

Biomedicines, 2024-01, Vol.12 (2), p.322

2024

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A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency

Annals of clinical and translational neurology, 2020-05, Vol.7 (5), p.846-854

2020

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Myoimaging in Congenital Myopathies

Seminars in pediatric neurology, 2019-04, Vol.29, p.30-43

2019

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Elevation of brain ADC (apparent diffusion coefficient) in HIV-associated neurocognitive disorders and evolution after treatment: A pilot study

Journal of the neurological sciences, 2022-11, Vol.442, p.120446-120446, Article 120446

2022

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Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations

Journal of neuromuscular diseases, 2020-01, Vol.7 (4), p.443-451

2020

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Caveolinopathy: Clinical, histological, and muscle imaging features and follow‐up in a multicenter retrospective cohort

Macroglossia: A potentially severe complication of late‐onset Pompe disease

Whole‐Body Muscle Magnetic Resonance Imaging in Glycogen‐Storage Disease Type III

Hyperckemia and myalgia are common presentations of anoctamin‐5‐related myopathy in French patients

Skeletal muscle quantitative nuclear magnetic resonance imaging follow-up of adult Pompe patients

Arterial and venous abdominal thrombosis in a 79-year-old woman with COVID-19 pneumonia

Pre-test probability for SARS-Cov-2-related infection score: The PARIS score

MRI in sarcoglycanopathies: a large international cohort study

Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity

Mutations in FKBP14 Cause a Variant of Ehlers-Danlos Syndrome with Progressive Kyphoscoliosis, Myopathy, and Hearing Loss

Recessive MYPN mutations cause cap myopathy with occasional nemaline rods

WES homozygosity mapping in a recessive form of Charcot-Marie-Tooth neuropathy reveals intronic GDAP1 variant leading to a premature stop codon

Predictive factors for positive disco-vertebral biopsy culture in pyogenic vertebral osteomyelitis, and impact of fluoroscopic versus scanographic guidance

Severity Classification in Cases of Collagen Vi-Related Myopathy with Convolutional Neural Networks and Handcrafted Texture Features

Comparison of magnetic resonance imaging and computed tomography for bone assessment of neurogenic heterotopic ossification of the hip: a preliminary study

Contribution of Interventional Radiologist in the Management of Pseudoaneurysm and Neck Hemorrhages in COVID-19 patients

SHOULD patients with asymptomatic pompe disease be treated? A nationwide study in france

Understanding a mass in the paraspinal region: an anatomical approach

Pre-surgical CT-assessment of neurogenic myositis ossificans of the hip and risk factors of recurrence: a series of 101 consecutive patients

The FLNC Ala1186Val Variant Linked to Cytoplasmic Body Myopathy and Cardiomyopathy Causes Protein Instability

A new congenital multicore titinopathy associated with fast myosin heavy chain deficiency

Myoimaging in Congenital Myopathies

AI-driven quantification, staging and outcome prediction of COVID-19 pneumonia

Elevation of brain ADC (apparent diffusion coefficient) in HIV-associated neurocognitive disorders and evolution after treatment: A pilot study

Phenotypic Spectrum of Myopathies with Recessive Anoctamin-5 Mutations

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