Génétique et cerveau: CADASIL, une nouvelle artériopathie cérébrale autosomale dominante - Genetics and cerebrovascular diseaeses: CADASIL, a new autosomal dominant cerebrovascular disease
Tournierlasserve,; Joutel, A.; Ibazizen, M.T.; Werissenbach, J.; Lathrop, M.; Bousser, M.G.; Chabriat, H.; Vahedi, K.; Nibbio, A.; Nagy, T.; Melki, J.; Mas, J.L.; Baudrimont, M.; Cabanis, E.A.
Stv. Sang Thrombose Vaisseaux 6(5): 23-28
1994
ISSN/ISBN: 0999-7385 Document Number: 234247
Document emailed within 1 workday
Related Documents
Iwamoto, T.; Umahara, T. 2004: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Nihon Rinsho. Japanese Journal of Clinical Medicine 62(Suppl 4): 174-179Nycz, E. 2017: Microangiopathy CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy) - a chalange for general practitioner Przeglad Lekarski 74(1): 37-40
Wesołowski, W.; Dziewulska, D.; Koziarska, M.; Iżycka-Świeszewska, E. 2015: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) - literature review apropos an autopsy case Polish Journal of Pathology: Official Journal of the Polish Society of Pathologists 66(3): 323-329
Kato, T.; Nishizawa, M.; Onodera, M. 2011: CADASIL (Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) and CARASIL (Cerebral Autosomal Recessive Arteriopathy with Subcortical Infarcts and Leukoencephalopathy) Nihon Rinsho. Japanese Journal of Clinical Medicine 69 Suppl 10 Pt 2: 320-324
Mendel, T.; Członkowska, A. 1999: Clinical autosomal dominating arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) Neurologia i Neurochirurgia Polska 33(5): 1117-1128
Reeders, S.T.; Germino, G.G. 1989: The molecular genetics of autosomal dominant polycystic kidney disease Seminars in Nephrology 9(2): 122-134
Brice, A.; Dubois, B.; Agid, Y.; Campion, D.; Martinez, M.; Clerger-Darpoux, F.; Bellis, M.; Mallet, J.; Frebourg, T.; Hannequin, D.; Puel, M.; Ledoze, F.; Pasquier, F.; Zimmerman, M.A.; Thomas-Anterion, C.; Moreaud, O.; Goas, J.Y. 1996: Genetics of dominant autosomal forms of Alzheimer disease: 3 genes and one phenotype. Groupe de Recherche Francais sur la Maladie d'Alzheimer Revue Neurologique (Paris) 152(12): 725-726
Kramer, P.L.; Ozelius, L.; Brin, M.F.; Fahn, S.; Kidd, K.K.; Gusella, J.; Breakefield, X.O. 1988: Molecular genetics of an autosomal dominant form of torsion dystonia Advances in Neurology 50: 57-66
Vahedi, K.; Bousser, M.G. 2000: Unusual disorder: CADASIL L'Encephale 26(Special Issue 3): 3-6
Davous, P.; Bequet, D. 1995: Cadasil--a new model for subcortical dementia Revue Neurologique (Paris) 151(11): 634-639
Kimper-Karl, A.C.; Jensen, H.B.; Kristensen, O. 2006: CADASIL versus multiple sclerosis Ugeskrift for Laeger 168(7): 702-703
Aurich, H. 1975: Physical therapy in cerebrovascular disorders (with special regard to physico-therapeutic measures after cerebrovascular insult) Zeitschrift für Arztliche Fortbildung 69(23): 1223-1225
Li, J.-c.; Jin, D.-x.; Yang, Y.-j.; Chen, X.-y.; Li, J.-l.; Wang, M.-h.; Wu, E.-f. 2007: Study of intracerebral focus changes on CADASIL by using MR imaging Zhonghua Yi Xue Za Zhi 87(26): 1854-1856
Fukutake, T. 2001: CADASIL associated with alopecia and lumbar herniated disk Rinsho Shinkeigaku 41(9): 639; Author Reply 640
Sempere, A.P.; Pérez-Tur, J.; García-Barragán, N.; Sellés, J.; Medrano, V.; Mola, S. 2004: Clinical and neuroimaging findings in a family with CADASIL associated to C475T mutation Revista de Neurologia 38(1): 37-41
Skowrońska, M.; Lewandowska, E.; Członkowska, A. 2006: Co-existing spinal canal tumours and CADASIL - a diagnostic challenge Neurologia i Neurochirurgia Polska 40(6): 526-529
Lewandowska, E.; Leszczyńska, A.; Wierzba-Bobrowicz, T.; Skowrońska, M.; Mierzewska, H.; Pasennik, E.; Członkowska, A. 2006: Ultrastructural picture of blood vessels in muscle and skin biopsy in CADASIL Folia Neuropathologica 44(4): 265-273
Chauveau, D.; Ferrandiz, I.ès.; Huart, A. 2014: Autosomal dominant polycystic kidney disease La Revue du Praticien 64(9): 1313-1321
Gunda, B.; Chabriat, H.; Bereczki, D.án. 2011: Cadasil and other hereditary small vessel diseases of the brain--increasingly diagnosed conditions underlying familial ischaemic stroke and dementia Ideggyogyaszati Szemle 64(3-4): 88-100
Devuyst, O. 2003: Variable renal disease progression in autosomal dominant polycystic kidney disease: a role for nitric oxide? Journal of Nephrology 16(3): 449-452