108 related articles for article (PubMed ID: 10818517)
1. Skin biopsy value and leukoaraiosis.
Ruchoux MM; Brulin P; Leteurtre E; Maurage CA
Ann N Y Acad Sci; 2000 Apr; 903():285-92. PubMed ID: 10818517
[TBL] [Abstract][Full Text] [Related]
2. Lessons from CADASIL.
Ruchoux MM; Brulin P; Brillault J; Dehouck MP; Cecchelli R; Bataillard M
Ann N Y Acad Sci; 2002 Nov; 977():224-31. PubMed ID: 12480754
[TBL] [Abstract][Full Text] [Related]
3. Morphometric analysis of ultrastructural vascular changes in CADASIL: analysis of 50 skin biopsy specimens and pathogenic implications.
Brulin P; Godfraind C; Leteurtre E; Ruchoux MM
Acta Neuropathol; 2002 Sep; 104(3):241-8. PubMed ID: 12172909
[TBL] [Abstract][Full Text] [Related]
4. A CADASIL case with normal skin biopsy and without mutations in exons 3 and 4 of the Notch3 gene.
de Freitas GR; Miklossy J; Christen-Zäch S; Reichhart M; Bogousslavsky J
J Neurol Sci; 2001 Dec; 193(1):43-7. PubMed ID: 11718749
[TBL] [Abstract][Full Text] [Related]
5. Transgenic mice expressing mutant Notch3 develop vascular alterations characteristic of cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Ruchoux MM; Domenga V; Brulin P; Maciazek J; Limol S; Tournier-Lasserve E; Joutel A
Am J Pathol; 2003 Jan; 162(1):329-42. PubMed ID: 12507916
[TBL] [Abstract][Full Text] [Related]
6. [Atypical CADASIL phenotypes and pathological findings in two new French families].
Mikol J; Hénin D; Baudrimont M; Gaulier A; Bacri D; Tillier JN; Davous P
Rev Neurol (Paris); 2001 Jul; 157(6-7):655-67. PubMed ID: 11458185
[TBL] [Abstract][Full Text] [Related]
7. [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; 44(4-5):274-9. PubMed ID: 15287509
[TBL] [Abstract][Full Text] [Related]
8. Endothelial changes in muscle and skin biopsies in patients with CADASIL.
Ruchoux MM; Maurage CA
Neuropathol Appl Neurobiol; 1998 Feb; 24(1):60-5. PubMed ID: 9549730
[TBL] [Abstract][Full Text] [Related]
9. An Italian case of CADASIL with mutation CGC-TCG in codon 1006, exon 19 Notch3 gene.
Guidetti D; Casali B; Mazzei RL; Cenacchi G; De Berti G; Zuccoli G; Nicoli D; Conforti FL; Sprovieri T; Pasquinelli G; Brini M
Neurol Sci; 2004 Feb; 24(6):401-6. PubMed ID: 14767686
[TBL] [Abstract][Full Text] [Related]
10. Arg133Cys mutation of Notch3 in two unrelated Japanese families with CADASIL.
Uyama E; Tokunaga M; Suenaga A; Kotorii S; Kamimura K; Takahashi K; Tabira T; Uchino M
Intern Med; 2000 Sep; 39(9):732-7. PubMed ID: 10969905
[TBL] [Abstract][Full Text] [Related]
11. CADASIL (cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy): diagnostic skin biopsy changes determined by electron microscopy.
Walsh JS; Perniciaro C; Meschia JF
J Am Acad Dermatol; 2000 Dec; 43(6):1125-7. PubMed ID: 11100036
[TBL] [Abstract][Full Text] [Related]
12. CADASIL: skin biopsy allows diagnosis in early stages.
Ebke M; Dichgans M; Bergmann M; Voelter HU; Rieger P; Gasser T; Schwendemann G
Acta Neurol Scand; 1997 Jun; 95(6):351-7. PubMed ID: 9228269
[TBL] [Abstract][Full Text] [Related]
13. Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.
Ruchoux MM; Guerouaou D; Vandenhaute B; Pruvo JP; Vermersch P; Leys D
Acta Neuropathol; 1995; 89(6):500-12. PubMed ID: 7676806
[TBL] [Abstract][Full Text] [Related]
14. [A case of CADASIL in early stage].
Kotorii S; Sakae N; Yamada N; Yamanaka H; Fujii N; Nakashima Y
Rinsho Shinkeigaku; 2001 Jun; 41(6):306-9. PubMed ID: 11771160
[TBL] [Abstract][Full Text] [Related]
15. CADASIL: a monogenic condition causing stroke and subcortical vascular dementia.
Dichgans M
Cerebrovasc Dis; 2002; 13 Suppl 2():37-41. PubMed ID: 11901241
[TBL] [Abstract][Full Text] [Related]
16. A novel mutation (C67Y)in the NOTCH3 gene in a Korean CADASIL patient.
Moon SY; Kim HY; Seok JI; Kwon JC; Ki CS; Kim JW; Suh YL; Na DL
J Korean Med Sci; 2003 Feb; 18(1):141-4. PubMed ID: 12589106
[TBL] [Abstract][Full Text] [Related]
17. Notch3 ectodomain is a major component of granular osmiophilic material (GOM) in CADASIL.
Ishiko A; Shimizu A; Nagata E; Takahashi K; Tabira T; Suzuki N
Acta Neuropathol; 2006 Sep; 112(3):333-9. PubMed ID: 16871402
[TBL] [Abstract][Full Text] [Related]
18. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
Ueda M; Nakaguma R; Ando Y
Rinsho Byori; 2009 Mar; 57(3):242-51. PubMed ID: 19363995
[TBL] [Abstract][Full Text] [Related]
19. CADASIL: hereditary arteriopathy leading to multiple brain infarcts and dementia.
Viitanen M; Kalimo H
Ann N Y Acad Sci; 2000 Apr; 903():273-84. PubMed ID: 10818516
[TBL] [Abstract][Full Text] [Related]
20. CADASIL: new cases and new questions.
Rafalowska J; Fidziańska A; Dziewulska D; Podlecka A; Szpak GM; Kwieciński H
Acta Neuropathol; 2003 Dec; 106(6):569-74. PubMed ID: 14520480
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
