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300 related items for PubMed ID: 9291937
21. [Japanese CADASIL case with limited dementia who had the Notch 3 R141C mutation]. Ishibashi K, Murata T, Miki Y, Hara M, Mori H. No To Shinkei; 2005 May; 57(5):415-8. PubMed ID: 15981641 [Abstract] [Full Text] [Related]
22. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) in a Greek family. Mandellos D, Limbitaki G, Papadimitriou A, Anastasopoulos D. Neurol Sci; 2005 Oct; 26(4):278-81. PubMed ID: 16193256 [Abstract] [Full Text] [Related]
23. [Report of a patient with CADASIL having a novel missense mutation of the Notch 3 gene--association with alopecia and lumbar herniated disk]. Yamada H, Yasuda T, Kotorii S, Takahashi K, Tabira T, Sunada Y. Rinsho Shinkeigaku; 2001 Oct; 41(2-3):144-6. PubMed ID: 11481859 [Abstract] [Full Text] [Related]
24. Autosomal dominant cerebral arteriopathy: neuropsychiatric syndrome in a family. Adair JC, Hart BL, Kornfeld M, Graham GD, Swanda RM, Ptacek LJ, Davis LE. Neuropsychiatry Neuropsychol Behav Neurol; 1998 Jan; 11(1):31-9. PubMed ID: 9560826 [Abstract] [Full Text] [Related]
26. [The clinical and genetic studies in a family of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]. Zhang LF, Yang XS, Wang YF, Pei LT. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):187-90. PubMed ID: 19350513 [Abstract] [Full Text] [Related]
27. Subcortical angiopathic encephalopathy in a German kindred suggests an autosomal dominant disorder distinct from CADASIL. Hagel C, Groden C, Niemeyer R, Stavrou D, Colmant HJ. Acta Neuropathol; 2004 Sep; 108(3):231-40. PubMed ID: 15221337 [Abstract] [Full Text] [Related]
33. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cécillion M, Marechal E, Maciazek J, Vayssiere C, Cruaud C, Cabanis EA, Ruchoux MM, Weissenbach J, Bach JF, Bousser MG, Tournier-Lasserve E. Nature; 1996 Oct 24; 383(6602):707-10. PubMed ID: 8878478 [Abstract] [Full Text] [Related]
34. Autosomal dominant migraine with MRI white-matter abnormalities mapping to the CADASIL locus. Chabriat H, Tournier-Lasserve E, Vahedi K, Leys D, Joutel A, Nibbio A, Escaillas JP, Iba-Zizen MT, Bracard S, Tehindrazanarivelo A. Neurology; 1995 Jun 24; 45(6):1086-91. PubMed ID: 7783868 [Abstract] [Full Text] [Related]
35. CADASIL: hereditary disease of arteries causing brain infarcts and dementia. Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Pöyhönen M, Rinne JO, Savontaus M, Tuisku S, Winblad B. Neuropathol Appl Neurobiol; 1999 Aug 24; 25(4):257-65. PubMed ID: 10476042 [Abstract] [Full Text] [Related]
36. Fibrosis and stenosis of the long penetrating cerebral arteries: the cause of the white matter pathology in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Miao Q, Paloneva T, Tuominen S, Pöyhönen M, Tuisku S, Viitanen M, Kalimo H. Brain Pathol; 2004 Oct 24; 14(4):358-64. PubMed ID: 15605982 [Abstract] [Full Text] [Related]
38. Identification of a key recombinant narrows the CADASIL gene region to 8 cM and argues against allelism of CADASIL and familial hemiplegic migraine. Dichgans M, Mayer M, Müller-Myhsok B, Straube A, Gasser T. Genomics; 1996 Feb 15; 32(1):151-4. PubMed ID: 8786108 [Abstract] [Full Text] [Related]
39. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) characteristics in Japan: variety of clinical features. Adachi Y, Nakashima K. Intern Med; 2000 Sep 15; 39(9):681-2. PubMed ID: 10969895 [No Abstract] [Full Text] [Related]
40. An Italian kindred with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Ragno M, Tournier-Lasserve E, Fiori MG, Manca A, Patrosso MC, Ferlini A, Sirocchi G, Trojano L, Chabriat H, Salvi F. Ann Neurol; 1995 Aug 15; 38(2):231-6. PubMed ID: 7654071 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]