Vidaud, Michel
Inserm · Sorbonne Paris Cité · Université Paris Descartes
6 papers on CoChat
Most cited papers
- Verified
Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy
Cartier, N., Hacein-Bey-Abina, S., Bartholomae, C. C., Veres, G., Schmidt, M., Kutschera, I., Vidaud, M., Abel, U., Dal-Cortivo, L., Caccavelli, L., et al. (2009) · Science
Virus-based gene therapy researchLysosomal Storage Disorders Research
Cited by 1,508
- Verified
CYP46A1 inhibition, brain cholesterol accumulation and neurodegeneration pave the way for Alzheimer’s disease
Djelti, F., Braudeau, J., Hudry, E., Dhenain, M., Varin, J., Bièche, I., Marquer, C., Chali, F., Ayciriex, S., Auzeil, N., et al. (2015) · Brain
Alzheimer's disease research and treatmentsCholesterol and Lipid Metabolism
Cited by 223
- Verified
Decreased expression of ABCD4 and BG1 genes early in the pathogenesis of X-linked adrenoleukodystrophy
Asheuer, M., Bieche, I., Laurendeau, I., Moser, A., Hainque, B., Vidaud, M., & Aubourg, P. (2005) · Human Molecular Genetics
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 86
- Verified
Microarray-Based Identification of Tenascin C and Tenascin XB , Genes Possibly Involved in Tumorigenesis Associated with Neurofibromatosis Type 1
Lévy, P., Ripoche, H., Laurendeau, I., Lazar, V., Ortonne, N., Parfait, B., Leroy, K., Wechsler, J., Salmon, I., Wolkenstein, P., et al. (2007) · Clinical Cancer Research
Neurofibromatosis and Schwannoma CasesNeuroblastoma Research and Treatments
Cited by 53
- Verified
CYP4F2 affects phenotypic outcome in adrenoleukodystrophy by modulating the clearance of very long-chain fatty acids
van Engen, C. E., Ofman, R., Dijkstra, I. M. E., van Goethem, T. J., Verheij, E., Varin, J., Vidaud, M., Wanders, R. J. A., Aubourg, P., Kemp, S., et al. (2016) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 26
- Verified
CD1 Gene Polymorphisms and Phenotypic Variability in X-Linked Adrenoleukodystrophy
Barbier, M., Sabbagh, A., Kasper, E., Asheuer, M., Ahouansou, O., Pribill, I., Forss-Petter, S., Vidaud, M., Berger, J., & Aubourg, P. (2012) · PLoS ONE
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 18
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