Case report of two presenilin (PS-1) mutations in a family with early-onset familial Alzheimer's disease (EOFAD)

被引：0
|
作者：
Ananth, UA
Seltzer, WK
St George-Hyslop, PH
Walsh, A
Abuelo, DN
机构：
来源：
NEUROLOGY | 1998年 / 50卷 / 04期
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
P04111
引用
收藏
页码：A234 / A234
页数：1
相关论文
共 50 条
  • [1] Clinical diagnostic testing for Presenilin-1 (PS-1) gene mutations and diagnosis of early-onset familiar Alzheimer's disease (EOFAD).
    Fafel, KC
    Ananth, UA
    Jones, JG
    Elles, J
    Allen, SK
    Liang, Y
    Song, YQ
    St George-Hyslop, P
    Seltzer, WK
    Boss, MA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (04) : A214 - A214
  • [2] Early-Onset Familial Alzheimer's Disease (EOFAD)
    Wu, Liyong
    Rosa-Neto, Pedro
    Hsiung, Ging-Yuek R.
    Sadovnick, A. Dessa
    Masellis, Mario
    Black, Sandra E.
    Jia, Jianping
    Gauthier, Serge
    [J]. CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 2012, 39 (04) : 436 - 445
  • [3] The development of Presenilin-1 (PS-1) as a clinical diagnostic test for early-onset familial Alzheimer's disease.
    Ananth, UA
    Jones, JG
    Fafel, KC
    Seltzer, WK
    St George-Hyslop, PH
    Boss, MA
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A217 - A217
  • [4] A variety of Presenilin 1 mutations in Japanese familial early-onset Alzheimer's disease
    Kamino, K
    Nishiwaki, Y
    Yoshiiwa, A
    Takeda, M
    Sato, S
    Sakaki, Y
    Ii, K
    Miki, T
    Ogihara, T
    [J]. ALZHEIMER'S DISEASE: BIOLOGY, DIAGNOSIS AND THERAPEUTICS, 1997, : 79 - 84
  • [5] Familial early-onset Alzheimer disease associated with mutations in presenilin-1.
    Abuelo, DN
    Walsh, A
    Kosik, KS
    Seltzer, WK
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A408 - A408
  • [6] Novel Presenilin 1 and Presenilin 2 mutations in early-onset Alzheimer's disease families
    Nacmias, B
    Tedde, A
    Ciantelli, M
    Cellini, E
    Bagnoli, S
    Forleo, P
    Caffarra, P
    Ghidoni, E
    Piccini, C
    Bracco, L
    Sorbi, S
    [J]. NEUROLOGY, 2002, 58 (07) : A37 - A37
  • [7] Identification of new presenilin gene mutations in early-onset familial Alzheimer disease
    Tedde, A
    Nacmias, B
    Ciantelli, M
    Forleo, P
    Cellini, E
    Bagnoli, S
    Piccini, C
    Caffarra, P
    Ghidoni, E
    Paganini, M
    Bracco, L
    Sorbi, S
    [J]. ARCHIVES OF NEUROLOGY, 2003, 60 (11) : 1541 - 1544
  • [8] Novel presenilin 1 and presenilin 2 mutations in early-onset Alzheimer's disease families
    Sorbi, S
    Tedde, A
    Nacmias, B
    Ciantelli, M
    Bracco, L
    Piccini, C
    Caffarra, P
    Ghidoni, E
    Emilia, R
    [J]. NEUROBIOLOGY OF AGING, 2002, 23 (01) : S312 - S313
  • [9] Presenilin 1 mutations in Polish families with early-onset Alzheimer's disease
    Kowalska, A
    Pruchnik-Wolinska, D
    Florczak, J
    Szczech, J
    Kozubski, W
    Rossa, G
    Wender, M
    [J]. FOLIA NEUROPATHOLOGICA, 2004, 42 (01) : 9 - 14
  • [10] Missense mutations of the PS-1/S182 gene in German early-onset Alzheimer's disease patients
    Sandbrink, R
    Zhang, D
    Schaeffer, S
    Masters, CL
    Bauer, J
    Forstl, H
    Beyreuther, K
    [J]. ANNALS OF NEUROLOGY, 1996, 40 (02) : 265 - 266
12345