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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
Mitochondria
Kidney
Newborn
OPA1
Gene Expression Regulation
Mitochondrial dynamics
Pain
France
Infant
Prognosis
Adult
North Africa
Mitochondrial diseases
Acute kidney injury
Retrospective Studies
Amyotrophic lateral sclerosis
Cultured
Intellectual disability
Cerebellum
Middle Aged
Exercise
Follow-Up Studies
Pulmonary embolism
Metabolomics
Case-Control Studies
Treatment Outcome
Child
Cancer
Fibroblasts
Shock
Biomarkers
Humans
Cohort Studies
Cell Line
Septic shock
Pregnancy
Intermittent claudication
GTP Phosphohydrolases
Mortality
Preschool
Myocardial infarction
Remodeling
Microcirculation
Blood flow
Blood pressure
Male
80 and over
Intellectual Disability
Ankle brachial index
Venous thromboembolism
Optic Atrophy
Mitochondrial Proteins
Mitochondrial DNA
Critical care
Antiphospholipid syndrome
Retina
Pseudoxanthoma elasticum
Ischemia
Hypertension
Animals
Cells
Blood Pressure
Peripheral arterial disease
Mitochondrial
SARS-CoV-2
Endothelium
Estrogens
Signal Transduction
Time Factors
Peripheral artery disease
Prevalence
Genotype
Lipidomics
Diagnosis
Predictive Value of Tests
Brain
Prospective Studies
Claudication
Female
Aged
Mutation
Age
Muscle
Adolescent
Skeletal
Young Adult
Exercise Test
Angiogenesis
Angiotensin II
Oxidative stress
DNA
Fetal programming
Shear stress
Exercise oximetry
Mice
Phenotype
Aging
COVID-19
Inflammation
Optic neuropathy
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⟩