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237 related items for PubMed ID: 11080925
1. [A case of symptomatic cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)]. Nakamizo A, Koga H, Uyama E, Yamabe K. Fukuoka Igaku Zasshi; 2000 Sep; 91(9):239-42. PubMed ID: 11080925 [Abstract] [Full Text] [Related]
2. Mutation of the Notch 3 gene in a Thai cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy family. Suwanwela N, Srikiatkhachorn A, Tangwongchai S, Phanthumchina K, Suwanwela N. J Med Assoc Thai; 2003 Feb; 86(2):178-82. PubMed ID: 12678157 [Abstract] [Full Text] [Related]
3. [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 Feb; 41(2-3):144-6. PubMed ID: 11481859 [Abstract] [Full Text] [Related]
4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J. Nat Genet; 1993 Mar; 3(3):256-9. PubMed ID: 8485581 [Abstract] [Full Text] [Related]
5. 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]
6. [Hereditary CADASIL cerebral arteriopathy. Report of a family]. Mayer M, Dichgans M, Gasser T, Büttner U, Uttner I, Straube A. Nervenarzt; 1995 Dec; 66(12):927-32. PubMed ID: 8584078 [Abstract] [Full Text] [Related]
7. [From gene to disease; from Notch3 to cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy]. Oberstein SA, Bakker E, Ferrari MD, Haan J. Ned Tijdschr Geneeskd; 2001 Feb 24; 145(8):359-60. PubMed ID: 11257815 [Abstract] [Full Text] [Related]
8. CADASIL: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Ruchoux MM, Maurage CA. J Neuropathol Exp Neurol; 1997 Sep 24; 56(9):947-64. PubMed ID: 9291937 [Abstract] [Full Text] [Related]
9. [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 24; 57(5):415-8. PubMed ID: 15981641 [Abstract] [Full Text] [Related]
10. [Cerebral arteriopathy with subcortical infarctions and leukoencephalopathy with dominant autosomal inheritance (CADASIL). Clinical and morphological study]. Marrero Falcón C, Díez Tejedor E, Arpa Gutiérrez J, Barreiro Tella P. Neurologia; 1999 May 24; 14(6):275-82. PubMed ID: 10439621 [Abstract] [Full Text] [Related]
11. Role of subvoxel free fluid on diffusion parameters in brain tissue with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy and its correlation with physical disability: histogram analysis of standard and fluid-attenuated MR diffusion. Dichgans M, Pütz B, Boos D, Auer DP. AJNR Am J Neuroradiol; 2003 May 24; 24(6):1083-9. PubMed ID: 12812930 [Abstract] [Full Text] [Related]
16. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) presenting with sudden sensorineural hearing loss. Phillips JS, King JA, Chandran S, Prinsley PR, Dick D. J Laryngol Otol; 2005 Feb 24; 119(2):148-51. PubMed ID: 15829071 [Abstract] [Full Text] [Related]
17. Familial hemiplegic migraine and autosomal dominant arteriopathy with leukoencephalopathy (CADASIL). Hutchinson M, O'Riordan J, Javed M, Quin E, Macerlaine D, Wilcox T, Parfrey N, Nagy TG, Tournier-Lasserve E. Ann Neurol; 1995 Nov 24; 38(5):817-24. PubMed ID: 7486874 [Abstract] [Full Text] [Related]
18. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL): a case report with review of literature. Gurumukhani JK, Ursekar M, Singhal BS. Neurol India; 2004 Mar 24; 52(1):99-101. PubMed ID: 15069251 [Abstract] [Full Text] [Related]
19. Gene symbol: NOTCH3. Disease: cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Soong BW, Lee YC, Lu YC. Hum Genet; 2005 Feb 24; 116(3):242. PubMed ID: 15818833 [No Abstract] [Full Text] [Related]
20. [A case of CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and lekoencephalopathy) with Notch 3 (Arg169Cys) mutation and typical granular osmiophilic materials in peripheral small arteries]. Kotani N, Hara H, Fujimura H, Miyashita T, Miyaguchi K, Tabira T. Rinsho Shinkeigaku; 2004 Feb 24; 44(4-5):274-9. PubMed ID: 15287509 [Abstract] [Full Text] [Related] Page: [Next] [New Search]