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Clinical recurrences of COVID-19 symptoms after recovery: Viral relapse, reinfection or inflammatory rebound?

The Journal of infection, 2020-11, Vol.81 (5), p.816-846

2020

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Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice

Journal of molecular and cellular cardiology, 2012-06, Vol.52 (6), p.1299-1307

2012

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French political bargaining over undocumented migrants’ health

The Lancet (British edition), 2024-01, Vol.403 (10422), p.140-141, Article 140-141

2024

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Are immigrants living in France more reluctant to receive vaccines than native-born French citizens? findings from the national health Barometer study

Vaccine, 2022-06, Vol.40 (28), p.3869-3883

2022

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Utility of the Tétanos Quick Stick® in the vaccine catch-up of adult migrants without proof of prior vaccination

Vaccine, 2020-11, Vol.38 (47), p.7517-7525

2020

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The French medical community united against cuts to State Medical Aid

Health policy (Amsterdam), 2024-05, Vol.143, p.105037-105037, Article 105037

2024

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Striated muscle laminopathies

Seminars in cell & developmental biology, 2014-05, Vol.29, p.107-115

2014

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Clinical Presentation of Dengue Among Patients Admitted to the Adult Emergency Department of a Tertiary Care Hospital in Martinique: Implications for Triage, Management, and Reporting

Annals of emergency medicine, 2012, Vol.59 (1), p.42-50

2012

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Structure, Genetic Localization, and Identification of the Cardiac and Skeletal Muscle Transcripts of the Human Integrin α7 Gene (ITGA7)

Biochemical and biophysical research communications, 1999-07, Vol.260 (2), p.357-364

1999

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Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

Neuromuscular disorders : NMD, 2003-03, Vol.13 (3), p.216-222

2003

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Targeted inactivation of the murine cardiac myosin-binding protein C gene leads to hypertrophic cardiomyopathy

Journal of molecular and cellular cardiology, 2002-06, Vol.34 (6), p.A15-A15

2002

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Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene

Neuromuscular disorders : NMD, 2003-03, Vol.13 (3), p.216-222

2003

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Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci

Neuromuscular disorders : NMD, 2000-12, Vol.10 (8), p.548-552

2000

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Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

Neuromuscular disorders : NMD, 1997, Vol.7 (3), p.180-186

1997

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Identification of homozygous and heterozygous dy 2J mice by PCR

Neuromuscular disorders : NMD, 2000-01, Vol.10 (1), p.59-62

2000

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Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings

Neuromuscular disorders : NMD, 1998-05, Vol.8 (3), p.169-174

1998

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Clinical recurrences of COVID-19 symptoms after recovery: Viral relapse, reinfection or inflammatory rebound?

Increased myofilament Ca2+ sensitivity and diastolic dysfunction as early consequences of Mybpc3 mutation in heterozygous knock-in mice

French political bargaining over undocumented migrants’ health

Are immigrants living in France more reluctant to receive vaccines than native-born French citizens? findings from the national health Barometer study

Utility of the Tétanos Quick Stick® in the vaccine catch-up of adult migrants without proof of prior vaccination

The French medical community united against cuts to State Medical Aid

Striated muscle laminopathies

Clinical Presentation of Dengue Among Patients Admitted to the Adult Emergency Department of a Tertiary Care Hospital in Martinique: Implications for Triage, Management, and Reporting

Structure, Genetic Localization, and Identification of the Cardiac and Skeletal Muscle Transcripts of the Human Integrin α7 Gene (ITGA7)

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin α2 chain gene

Targeted inactivation of the murine cardiac myosin-binding protein C gene leads to hypertrophic cardiomyopathy

Spontaneous muscular dystrophy caused by a retrotransposal insertion in the mouse laminin alpha2 chain gene

Merosin-deficient congenital muscular dystrophy with mental retardation and cerebellar cysts unlinked to the LAMA2, FCMD and MEB loci

Genetics of laminin α2 chain (or merosin) deficient congenital muscular dystrophy: from identification of mutations to prenatal diagnosis

Identification of homozygous and heterozygous dy 2J mice by PCR

Merosin-deficient congenital muscular dystrophy with severe mental retardation and normal cranial MRI: a report of two siblings

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