Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) characteristics in Japan: Variety of clinical features

被引:4
作者
Adachi, Y [1 ]
Nakashima, K [1 ]
机构
[1] Tottori Univ, Fac Med, Inst Neurol Sci, Div Neurol, Yonago, Tottori 6830826, Japan
关键词
CADASIL; leukoencephalopathy; Notch3;
D O I
10.2169/internalmedicine.39.681
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
[No abstract available]
引用
收藏
页码:681 / 682
页数:2
相关论文
共 11 条
[1]
ADACHI Y, IN PRESS CLIN NEUROL
[2]
The phenotypic spectrum of CADASIL:: Clinical findings in 102 cases [J].
Dichgans, M ;
Mayer, M ;
Uttner, I ;
Brüning, R ;
Müller-Höcker, J ;
Rungger, G ;
Ebke, M ;
Klockgether, T ;
Gasser, T .
ANNALS OF NEUROLOGY, 1998, 44 (05) :731-739
[3]
CADASIL: Skin biopsy allows diagnosis in early stages [J].
Ebke, M ;
Dichgans, M ;
Bergmann, M ;
Voelter, HU ;
Rieger, P ;
Gasser, T ;
Schwendemann, G .
ACTA NEUROLOGICA SCANDINAVICA, 1997, 95 (06) :351-357
[4]
Strong clustering and stereotyped nature of Notch3 mutations in CADASIL patients [J].
Joutel, A ;
Vahedi, K ;
Corpechot, C ;
Troesch, A ;
Chabriat, H ;
Vayssiere, C ;
Cruaud, C ;
Maciazek, J ;
Weissenbach, J ;
Bousser, MG ;
Bach, JF ;
TournierLasserve, E .
LANCET, 1997, 350 (9090) :1511-1515
[5]
Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia [J].
Joutel, A ;
Corpechot, C ;
Ducros, A ;
Vahedi, K ;
Chabriat, H ;
Mouton, P ;
Alamowitch, S ;
Domenga, V ;
Cecillion, M ;
Marechal, E ;
Maciazek, J ;
Vayssiere, C ;
Cruaud, C ;
Cabanis, EA ;
Ruchoux, MM ;
Weissenbach, J ;
Bach, JF ;
Bousser, MG ;
TournierLasserve, E .
NATURE, 1996, 383 (6602) :707-710
[6]
SPECT study of a German CADASIL family -: A phenotype with migraine and progressive dementia only [J].
Mellies, JK ;
Bäumer, T ;
Müller, JA ;
Tournier-Lasserve, E ;
Chabriat, H ;
Knobloch, O ;
Hackelöer, HJ ;
Goebel, HH ;
Wetzig, L ;
Haller, P .
NEUROLOGY, 1998, 50 (06) :1715-1721
[7]
Nishio T, 1997, Rinsho Shinkeigaku, V37, P910
[8]
RUCHOUX MM, 1995, ACTA NEUROPATHOL, V89, P500
[9]
CEREBRAL AUTOSOMAL DOMINANT ARTERIOPATHY WITH SUBCORTICAL INFARCTS AND LEUKOENCEPHALOPATHY MAPS TO CHROMOSOME-19Q12 [J].
TOURNIERLASSERVE, E ;
JOUTEL, A ;
MELKI, J ;
WEISSENBACH, J ;
LATHROP, GM ;
CHABRIAT, H ;
MAS, JL ;
CABANIS, EA ;
BAUDRIMONT, M ;
MACIAZEK, J ;
BACH, MA ;
BOUSSER, MG .
NATURE GENETICS, 1993, 3 (03) :256-259
[10]
Autosomal dominant early onset dementia and leukoencephalopathy in a Japanese family: Clinical, neuroimaging and genetic studies [J].
Utatsu, Y ;
Takashima, H ;
Michizono, K ;
Kanda, N ;
Endou, K ;
Mitsuyama, Y ;
Fujimoto, T ;
Nagai, M ;
Umehara, F ;
Higuchi, I ;
Arimura, K ;
Nakagawa, M ;
Osame, M .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 147 (01) :55-62