C. Bellesme

发表

Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy

Manfred Schmidt, Philippe Leboulch, Cynthia C. Bartholomae, 2009, Science.

Epidemiology, Clinical Features, and Outcome in a Cohort of Adolescents With Cerebral Venous Thrombosis

Y. Béjot, D. Germanaud, P. Tuppin, 2021, Neurology.

Regional Pediatric Acute Stroke Protocol: Initial Experience During 3 Years and 13 Recanalization Treatments in Children

O. Naggara, A. Ozanne, I. Desguerre, 2017, Stroke.

De novo mutations in CBL causing early-onset paediatric moyamoya angiopathy

F. Brunelle, S. Lyonnet, D. Hervé, 2017, Journal of Medical Genetics.

Functional classification of ATM variants in ataxia‐telangiectasia patients

T. Dörk, M. Stern, P. Calvas, 2019, Human mutation.

Extracranial vertebral artery dissection in children: natural history and management

D. Ducreux, M. Tardieu, K. Deiva, 2015, Neuroradiology.

Recanalization Treatments for Pediatric Acute Ischemic Stroke in France

O. Naggara, G. Boulouis, A. Ozanne, 2022, JAMA network open.

Liver transplantation as a rescue therapy for severe neurologic forms of Wilson disease

V. de Lédinghen, W. Meissner, E. Broussolle, 2020, Neurology.

Adult-onset genetic leukoencephalopathies: a MRI pattern-based approach in a comprehensive study of 154 patients.

P. Vermersch, M. Giroud, M. Clanet, 2015, Brain : a journal of neurology.

Early and Aggressive Treatment May Modify Anti-Hu Associated Encephalitis Prognosis

H. Maurey, K. Deiva, C. Bellesme, 2021, Neuropediatrics.

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

A. Munnich, C. Fallet-Bianco, I. Gut, 2021, Journal of Medical Genetics.

Functional characterization of RELN missense mutations involved in recessive and dominant forms of Neuronal Migration Disorders

A. Pierani, R. Guerrini, F. Causeret, 2021, bioRxiv.

Cerebral venous thrombosis after embolization of pediatric AVM with jugular bulb stenosis or occlusion: management and prevention.

D. Ducreux, K. Deiva, C. Bellesme, 2014, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Adult-onset cerebral X-linked adrenoleukodystrophy with major contrast-enhancement mimicking acquired disease

C. Verny, C. Scherer, P. Labauge, 2013, Clinical Neurology and Neurosurgery.

Acute ischemic stroke in adolescents

Y. Béjot, S. Crozier, D. Smadja, 2019, Journal of the Neurological Sciences.

Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects.

I. Gut, M. Bayés, J. Melki, 2014, Human molecular genetics.

Long-term follow-up of Hematopoietic Stem-Cell Gene Therapy for Cerebral Adrenoleukodystrophy.

C. Adamsbaum, P. Bougnères, Manfred Schmidt, 2021, Human gene therapy.

Toward a Better Understanding of Brain Lesions during Metachromatic Leukodystrophy Evolution

C. Adamsbaum, C. Lazarus, P. Aubourg, 2012, American Journal of Neuroradiology.

Fatigue, depression, and quality of life in children with multiple sclerosis: a comparative study with other demyelinating diseases

H. Maurey, K. Deiva, C. Bellesme, 2020, Developmental medicine and child neurology.

Mild Encephalitis/Encephalopathy with reversible splenial lesion syndrome: An unusual presentation of anti-GFAP astrocytopathy.

C. Adamsbaum, J. Honnorat, H. Maurey, 2020, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Intracerebral gene therapy in children with metachromatic leukodystrophy: Results of a phase I/II trial

M. Souweidane, R. Crystal, C. Adamsbaum, 2018 .