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Bienvenue sur la collection HAL du MITOVASC
Direction | Guy LENAERS
Référent·e·s HAL | Guy LENAERS, Cyril LE CORRE
Fichiers
332
Références
404
Proportion d'Open Access
70 %
Mots-Clés
Diagnosis
Pseudoxanthoma elasticum
Genotype
Peripheral artery disease
Middle Aged
France
Exercise oximetry
Phenotype
Peripheral arterial disease
Cell Line
Preschool
Predictive Value of Tests
OPA1
Antiphospholipid syndrome
Treatment Outcome
Child
Angiotensin II
Pregnancy
Septic shock
Skeletal
Intellectual Disability
Intellectual disability
Ischemia
Optic Atrophy
Mitochondrial dynamics
Myocardial infarction
Cultured
GTP Phosphohydrolases
Endothelium
Mortality
Gene Expression Regulation
Muscle
Kidney
Blood pressure
DNA
Pulmonary embolism
Follow-Up Studies
Signal Transduction
Cohort Studies
Case-Control Studies
Mice
Mitochondrial DNA
Remodeling
Young Adult
COVID-19
Cancer
Shear stress
Metabolomics
Acute kidney injury
Male
SARS-CoV-2
Cells
Aged
Venous thromboembolism
Animals
Newborn
Blood flow
Prognosis
Mitochondria
Estrogens
Microcirculation
Prevalence
Retrospective Studies
Aging
Humans
Oxidative stress
Brain
Mitochondrial diseases
Mitochondrial Proteins
Exercise
Angiogenesis
Infant
Hypertension
Claudication
Intermittent claudication
Time Factors
Pain
Retina
Adolescent
Biomarkers
Optic neuropathy
Amyotrophic lateral sclerosis
Mitochondrial
Adult
Mutation
Inflammation
North Africa
Lipidomics
Prospective Studies
Shock
Age
80 and over
Female
Blood Pressure
Exercise Test
Cerebellum
Ankle brachial index
Critical care
Fetal programming
Fibroblasts
Publications des équipes de recherche du MITOVASC
MitoLab | Mitochondrial Pathophysiology CarME | Cardiovascular PathophysiologyDernières parutions
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Nicolas Peschanski, Florian Zores, Jacques Boddaert, Bénedicte Douay, Clément Delmas, et al.. 2023 SFMU/GICC-SFC/SFGG expert recommendations for the emergency management of older patients with acute heart failure. Part 1: Prehospital management and diagnosis. Archives of cardiovascular diseases, 2024, ⟨10.1016/j.acvd.2024.08.002⟩. ⟨hal-04695313⟩
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Rahma Mkaouar, Zied Riahi, Jihene Marrakchi, Nessrine Mezzi, Lilia Romdhane, et al.. Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health. Frontiers in Genetics, 2024, 15, pp.1437233. ⟨10.3389/fgene.2024.1437233⟩. ⟨pasteur-04691609⟩