Sevin, Caroline
Lucile Packard Children's Hospital · NewYork–Presbyterian Hospital · Emma Kinderziekenhuis · Amsterdam University Medical Centers · Weill Cornell Medicine · University of Amsterdam · Stanford University
7 papers on CoChatORCID 0000-0002-5856-068X
Most cited papers
- Verified
Hematopoietic stem-cell gene therapy for cerebral adrenoleukodystrophy
Eichler, F., Duncan, C., Musolino, P. L., Orchard, P. J., De Oliveira, S., Thrasher, A. J., Armant, M., Dansereau, C., Lund, T. C., Miller, W. P., et al. (2017) · New England Journal of Medicine
Virus-based gene therapy researchLysosomal Storage Disorders Research
Cited by 604
- Verified
Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
Menni, F., de Lonlay, P., Sevin, C., Touati, G., Peigné, C., Barbier, V., Nihoul-Fékété, C., Saudubray, J.-M., & Robert, J.-J. (2001) · PEDIATRICS
Pancreatic function and diabetesMetabolism and Genetic Disorders
Cited by 347
- Verified
International Recommendations for the Diagnosis and Management of Patients With Adrenoleukodystrophy
Engelen, M., van Ballegoij, W. J. C., Mallack, E. J., Van Haren, K. P., Köhler, W., Salsano, E., van Trotsenburg, A. S. P., Mochel, F., Sevin, C., Regelmann, M. O., et al. (2022) · Neurology
Metabolism and Genetic DisordersLysosomal Storage Disorders Research
Cited by 156
- Verified
Correction of Brain Oligodendrocytes by AAVrh.10 Intracerebral Gene Therapy in Metachromatic Leukodystrophy Mice
Piguet, F., Sondhi, D., Piraud, M., Fouquet, F., Hackett, N. R., Ahouansou, O., Vanier, M.-T., Bieche, I., Aubourg, P., Crystal, R. G., et al. (2012) · Human Gene Therapy
Lysosomal Storage Disorders ResearchVirus-based gene therapy research
Cited by 91
- Verified
Enzyme, cell and gene‐based therapies for metachromatic leukodystrophy
Sevin, C., Aubourg, P., & Cartier, N. (2007) · Journal of Inherited Metabolic Disease
Lysosomal Storage Disorders ResearchMetabolism and Genetic Disorders
Cited by 88
- Verified
Autosomal recessive cerebellar ataxia caused by mutations in the PEX2 gene
Sevin, C., Ferdinandusse, S., Waterham, H. R., Wanders, R. J., & Aubourg, P. (2011) · Orphanet Journal of Rare Diseases
Metabolism and Genetic DisordersGenetic Neurodegenerative Diseases
Cited by 66
- Verified
Comparative Efficacy and Safety of Multiple Routes of Direct CNS Administration of Adeno-Associated Virus Gene Transfer Vector Serotype rh.10 Expressing the Human Arylsulfatase A cDNA to Nonhuman Primates
Rosenberg, J. B., Sondhi, D., Rubin, D. G., Monette, S., Chen, A., Cram, S., De, B. P., Kaminsky, S. M., Sevin, C., Aubourg, P., et al. (2014) · Human Gene Therapy Clinical Development
Virus-based gene therapy researchLysosomal Storage Disorders Research
Cited by 58
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