186 related articles for article (PubMed ID: 11100036)
21. 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
[TBL] [Abstract][Full Text] [Related]
22. CADASIL: underdiagnosed in psychiatric patients?
Leyhe T; Wiendl H; Buchkremer G; Wormstall H
Acta Psychiatr Scand; 2005 May; 111(5):392-6; discussion 396-7. PubMed ID: 15819734
[TBL] [Abstract][Full Text] [Related]
23. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL): a morphological study of a German family.
Bergmann M; Ebke M; Yuan Y; Brück W; Mugler M; Schwendemann G
Acta Neuropathol; 1996 Oct; 92(4):341-50. PubMed ID: 8891065
[TBL] [Abstract][Full Text] [Related]
24. Histopathological abnormalities in ocular blood vessels of CADASIL patients.
Haritoglou C; Hoops JP; Stefani FH; Mehraein P; Kampik A; Dichgans M
Am J Ophthalmol; 2004 Aug; 138(2):302-5. PubMed ID: 15289148
[TBL] [Abstract][Full Text] [Related]
25. [A study of subcortical infarcts and leukoencephalopathy (CADASIL) in a family with autosomal cerebral dominant arteriopathy].
Jin DX; Chen XY; Zhang X
Zhonghua Nei Ke Za Zhi; 2004 Dec; 43(12):924-7. PubMed ID: 15730739
[TBL] [Abstract][Full Text] [Related]
26. [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]
27. 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]
28. Retinal findings in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (cadasil).
Robinson W; Galetta SL; McCluskey L; Forman MS; Balcer LJ
Surv Ophthalmol; 2001; 45(5):445-8. PubMed ID: 11274696
[TBL] [Abstract][Full Text] [Related]
29. Vasculopathic changes of CADASIL can be focal in skin biopsies.
Schultz A; Santoianni R; Hewan-Lowe K
Ultrastruct Pathol; 1999; 23(4):241-7. PubMed ID: 10503743
[TBL] [Abstract][Full Text] [Related]
30. ["CADASIL"--a newly discovered hereditary cerebrovascular disease].
Søndergaard H; Jørgensen HS; Olsen TS
Ugeskr Laeger; 1998 Mar; 160(11):1617-20. PubMed ID: 9522653
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Extensive loss of arterial medial smooth muscle cells and mural extracellular matrix in cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy (CARASIL).
Oide T; Nakayama H; Yanagawa S; Ito N; Ikeda S; Arima K
Neuropathology; 2008 Apr; 28(2):132-42. PubMed ID: 18021191
[TBL] [Abstract][Full Text] [Related]
33. [Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)].
Iwamoto T; Umahara T
Nihon Rinsho; 2004 Apr; 62 Suppl 4():174-9. PubMed ID: 15174666
[No Abstract] [Full Text] [Related]
34. [Cadasil: a case with molecular diagnosis].
Zurrú MC; Casas Parera I; Moya G; Giovanelli C; Genovese O; Gatto E
Medicina (B Aires); 2002; 62(1):48-52. PubMed ID: 11965850
[TBL] [Abstract][Full Text] [Related]
35. [Clinical characteristics of hereditary cerebrovascular disease in a large family from Colombia].
Lopera F; Arboleda J; Moreno S; Almeida N; Cuartas M; Arcos-Burgos M
Rev Neurol; 2000 Nov 16-30; 31(10):901-7. PubMed ID: 11244680
[TBL] [Abstract][Full Text] [Related]
36. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)--confirmation by cerebral biopsy in 2 cases.
Lammie GA; Rakshi J; Rossor MN; Harding AE; Scaravilli F
Clin Neuropathol; 1995; 14(4):201-6. PubMed ID: 8521622
[TBL] [Abstract][Full Text] [Related]
37. Migraine and cerebral white matter lesions: when to suspect cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).
Gladstone JP; Dodick DW
Neurologist; 2005 Jan; 11(1):19-29. PubMed ID: 15631641
[TBL] [Abstract][Full Text] [Related]
38. [Hereditary cerebral arteriopathy].
Gustavsen WR; Eiklid K
Tidsskr Nor Laegeforen; 2003 Nov; 123(21):3045-6. PubMed ID: 14618173
[TBL] [Abstract][Full Text] [Related]
39. [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
[TBL] [Abstract][Full Text] [Related]
40. CADASIL-an unusual manifestation with prominent cutaneous involvement.
Ratzinger G; Ransmayr G; Romani N; Zelger B
Br J Dermatol; 2005 Feb; 152(2):346-9. PubMed ID: 15727650
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
