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Bienvenue sur la collection HAL du MITOVASC
Direction | Guy LENAERS
Référent·e·s HAL | Guy LENAERS, Cyril LE CORRE
Fichiers
330
Références
404
Proportion d'Open Access
70 %
Mots-Clés
Hypertension
Remodeling
Septic shock
Critical care
Intellectual disability
Adult
Cancer
Humans
Skeletal
Optic neuropathy
Optic Atrophy
Predictive Value of Tests
GTP Phosphohydrolases
Mitochondria
Blood pressure
Mortality
Estrogens
Adolescent
Pulmonary embolism
Cells
Amyotrophic lateral sclerosis
Infant
Aged
Mutation
Phenotype
Exercise
Shear stress
Shock
Mitochondrial
Retina
Newborn
Prognosis
Brain
Venous thromboembolism
OPA1
Child
Microcirculation
Claudication
Age
Gene Expression Regulation
Young Adult
Mice
Retrospective Studies
Angiotensin II
Blood flow
Oxidative stress
Preschool
Case-Control Studies
Ankle brachial index
Myocardial infarction
Cohort Studies
Signal Transduction
Inflammation
Peripheral arterial disease
Male
Fibroblasts
Aging
Time Factors
Exercise oximetry
Prospective Studies
Mitochondrial diseases
Muscle
DNA
Genotype
Antiphospholipid syndrome
Endothelium
Kidney
Mitochondrial dynamics
Treatment Outcome
Fetal programming
Cultured
Intermittent claudication
Acute kidney injury
Mitochondrial Proteins
Exercise Test
Ischemia
Middle Aged
80 and over
Follow-Up Studies
Mitochondrial DNA
France
Pain
COVID-19
Pregnancy
Diagnosis
Female
Animals
Pseudoxanthoma elasticum
Blood Pressure
Angiogenesis
Cerebellum
Prevalence
Intellectual Disability
North Africa
Cell Line
Lipidomics
Peripheral artery disease
Metabolomics
SARS-CoV-2
Biomarkers
Publications des équipes de recherche du MITOVASC
MitoLab | Mitochondrial Pathophysiology CarME | Cardiovascular PathophysiologyDernières parutions
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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⟩
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Marine Tessarech, Gaëlle Friocourt, Florent Marguet, Maryline Lecointre, Morgane Le Mao, et al.. De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity. Genetics in Medicine, 2024, 26 (5), pp.101087. ⟨10.1016/j.gim.2024.101087⟩. ⟨hal-04530295⟩