Clinical, neuroradiological and genetic findings in a cohort of patients with multiple Cerebral Cavernous Malformations
Author:
Funder
Ministero della Salute
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Neurology (clinical),Biochemistry
Link
https://link.springer.com/content/pdf/10.1007/s11011-021-00809-1.pdf
Reference38 articles.
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2. Apra C, Dumot C, Bourdillon P, Pelissou-Guyotat I (2019) Could propranolol be beneficial in adult cerebral cavernous malformations? Neurosurg Rev 42:403–408. https://doi.org/10.1007/s10143-018-01074-0
3. Bergametti F, Denier C, Labauge P, Arnoult M, Boetto S, Clanet M, Coubes P, Echenne B, Ibrahim R, Irthum B, Jacquet G, Lonjon M, Moreau JJ, Neau JP, Parker F, Tremoulet M, Tournier-Lasserve E, Société Française de Neurochirurgie (2005) Mutations within the programmed cell death 10 gene cause cerebral cavernous malformations. Am J Hum Genet 76:42–51. https://doi.org/10.1086/426952
4. Chen JM, Férec C, Cooper DN (2013) Patterns and mutational signatures of tandem base substitutions causing human inherited disease. Hum Mutat 34:1119–1130. https://doi.org/10.1002/humu.22341
5. Choquet H, Pawlikowska L, Lawton MT, Kim H (2015) Genetics of cerebral cavernous malformations: current status and future prospects. J Neurosurg Sci 59:211–220
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