Cazeneuve, Cécile

Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology

Teyssou, E., Takeda, T., Lebon, V., Boillée, S., Doukouré, B., Bataillon, G., Sazdovitch, V., Cazeneuve, C., Meininger, V., LeGuern, E., et al. (2013) · Acta Neuropathologica

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 241

TBK1 mutation frequencies in French frontotemporal dementia and amyotrophic lateral sclerosis cohorts

Le Ber, I., De Septenville, A., Millecamps, S., Camuzat, A., Caroppo, P., Couratier, P., Blanc, F., Lacomblez, L., Sellal, F., Fleury, M.-C., et al. (2015) · Neurobiology of Aging

Amyotrophic Lateral Sclerosis ResearchAlzheimer's disease research and treatments

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Accumulation of TDP-43 and α-actin in an amyotrophic lateral sclerosis patient with the K17I ANG mutation

Seilhean, D., Cazeneuve, C., Thuriès, V., Russaouen, O., Millecamps, S., Salachas, F., Meininger, V., LeGuern, E., & Duyckaerts, C. (2009) · Acta Neuropathologica

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 71

Mutations in UBQLN2 are rare in French amyotrophic lateral sclerosis

Millecamps, S., Corcia, P., Cazeneuve, C., Boillée, S., Seilhean, D., Danel-Brunaud, V., Vandenberghe, N., Pradat, P.-F., Le Forestier, N., Lacomblez, L., et al. (2012) · Neurobiology of Aging

Amyotrophic Lateral Sclerosis ResearchHereditary Neurological Disorders

Cited by 40

Cystic fibrosis patients with the 3272-26A>G splicing mutation have milder disease than F508del homozygotes: a large European study

Amaral, M. D., Pacheco, P., Beck, S., Farinha, C. M., Penque, D., Nogueira, P., Barreto, C., Lopes, B., Casals, T., Dapena, J., et al. (2001) · Journal of Medical Genetics

Cystic Fibrosis Research AdvancesGenetic and Kidney Cyst Diseases

Cited by 37