Similar articles for PMID: 16033913

Year	Number of Results
1987	2
1989	1
1991	1
1993	2
1995	6
1996	15
1997	5
1998	15
1999	17
2000	10
2001	10
2002	9
2003	13
2004	19
2005	17
2006	22
2007	12
2008	19
2009	14
2010	13
2011	10
2012	15
2013	12
2014	22
2015	10
2016	20
2017	13
2018	14
2019	17
2020	16
2021	11
2022	10
2023	3
2024	0

1

Molecular diagnosis of autosomal dominant early onset Alzheimer's disease: an update.

Raux G, Guyant-Maréchal L, Martin C, Bou J, Penet C, Brice A, Hannequin D, Frebourg T, Campion D. Raux G, et al. J Med Genet. 2005 Oct;42(10):793-5. doi: 10.1136/jmg.2005.033456. Epub 2005 Jul 20. J Med Genet. 2005. PMID: 16033913 Free PMC article.

2

A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.

Ezquerra M, Lleó A, Castellví M, Queralt R, Santacruz P, Pastor P, Molinuevo JL, Blesa R, Oliva R. Ezquerra M, et al. Arch Neurol. 2003 Aug;60(8):1149-51. doi: 10.1001/archneur.60.8.1149. Arch Neurol. 2003. PMID: 12925374

3

Mutations in presenilin 1, presenilin 2 and amyloid precursor protein genes in patients with early-onset Alzheimer's disease in Poland.

Zekanowski C, Styczyńska M, Pepłońska B, Gabryelewicz T, Religa D, Ilkowski J, Kijanowska-Haładyna B, Kotapka-Minc S, Mikkelsen S, Pfeffer A, Barczak A, Łuczywek E, Wasiak B, Chodakowska-Zebrowska M, Gustaw K, Łaczkowski J, Sobów T, Kuźnicki J, Barcikowska M. Zekanowski C, et al. Exp Neurol. 2003 Dec;184(2):991-6. doi: 10.1016/S0014-4886(03)00384-4. Exp Neurol. 2003. PMID: 14769392

4

[Alzheimer's disease. Present and future role of genetics].

Roks G. Roks G. Tijdschr Gerontol Geriatr. 2003 Feb;34(1):13-20. Tijdschr Gerontol Geriatr. 2003. PMID: 12629906 Dutch.

5

A novel presenilin-1 mutation (Leu85Pro) in early-onset Alzheimer disease with spastic paraparesis.

Ataka S, Tomiyama T, Takuma H, Yamashita T, Shimada H, Tsutada T, Kawabata K, Mori H, Miki T. Ataka S, et al. Arch Neurol. 2004 Nov;61(11):1773-6. doi: 10.1001/archneur.61.11.1773. Arch Neurol. 2004. PMID: 15534188

6

[Genes in Alzheimer's disease].

Hoenicka J. Hoenicka J. Rev Neurol. 2006 Mar 1-15;42(5):302-5. Rev Neurol. 2006. PMID: 16538594 Free article. Review. Spanish.

7

Early-onset autosomal dominant Alzheimer disease: prevalence, genetic heterogeneity, and mutation spectrum.

Campion D, Dumanchin C, Hannequin D, Dubois B, Belliard S, Puel M, Thomas-Anterion C, Michon A, Martin C, Charbonnier F, Raux G, Camuzat A, Penet C, Mesnage V, Martinez M, Clerget-Darpoux F, Brice A, Frebourg T. Campion D, et al. Am J Hum Genet. 1999 Sep;65(3):664-70. doi: 10.1086/302553. Am J Hum Genet. 1999. PMID: 10441572 Free PMC article.

8

Evidence that Abeta42 plasma levels in presenilin-1 mutation carriers do not allow for prediction of their clinical phenotype.

De Jonghe C, Cras P, Vanderstichele H, Cruts M, Vanderhoeven I, Smouts I, Vanmechelen E, Martin JJ, Hendriks L, Van Broeckhoven C. De Jonghe C, et al. Neurobiol Dis. 1999 Aug;6(4):280-7. doi: 10.1006/nbdi.1999.0247. Neurobiol Dis. 1999. PMID: 10448055

9

Novel presenilin 1 mutation (S170F) causing Alzheimer disease with Lewy bodies in the third decade of life.

Snider BJ, Norton J, Coats MA, Chakraverty S, Hou CE, Jervis R, Lendon CL, Goate AM, McKeel DW Jr, Morris JC. Snider BJ, et al. Arch Neurol. 2005 Dec;62(12):1821-30. doi: 10.1001/archneur.62.12.1821. Arch Neurol. 2005. PMID: 16344340

10

Clinical and genetic analysis of a Chilean family with early-onset autosomal dominant Alzheimer's disease.

Sinning M, van Rooyen JP, Venegas-Francke P, Vásquez C, Behrens MI, Ramírez A. Sinning M, et al. J Alzheimers Dis. 2010;21(3):757-61. doi: 10.3233/JAD-2010-100135. J Alzheimers Dis. 2010. PMID: 20571222

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

360 results

Results by year