Lendon CL - Search Results

1

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

Wragg MA, Talbot CJ, Morris JC, Lendon CL, Goate AM. Wragg MA, et al. Among authors: lendon cl. Neurosci Lett. 1995 Dec 8;201(2):107-10. doi: 10.1016/0304-3940(95)12146-3. Neurosci Lett. 1995. PMID: 8848229

2

Exploring the etiology of Alzheimer disease using molecular genetics.

Lendon CL, Ashall F, Goate AM. Lendon CL, et al. JAMA. 1997 Mar 12;277(10):825-31. JAMA. 1997. PMID: 9052714 Review.

3

Genetic association studies between dementia of the Alzheimer's type and three receptors for apolipoprotein E in a Caucasian population.

Lendon CL, Talbot CJ, Craddock NJ, Han SW, Wragg M, Morris JC, Goate AM. Lendon CL, et al. Neurosci Lett. 1997 Feb 7;222(3):187-90. doi: 10.1016/s0304-3940(97)13381-x. Neurosci Lett. 1997. PMID: 9148246

4

A polymorphism in the presenilin 1 gene does not modify risk for Alzheimer's disease in a cohort with sporadic early onset.

Lendon CL, Myers A, Cumming A, Goate AM, St Clair D. Lendon CL, et al. Neurosci Lett. 1997 Jun 13;228(3):212-4. doi: 10.1016/s0304-3940(97)00393-5. Neurosci Lett. 1997. PMID: 9218645 Clinical Trial.

5

E280A PS-1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles.

Lendon CL, Martinez A, Behrens IM, Kosik KS, Madrigal L, Norton J, Neuman R, Myers A, Busfield F, Wragg M, Arcos M, Arango Viana JC, Ossa J, Ruiz A, Goate AM, Lopera F. Lendon CL, et al. Hum Mutat. 1997;10(3):186-95. doi: 10.1002/(SICI)1098-1004(1997)10:3<186::AID-HUMU2>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9298817

6

Polymorphism in AACT gene may lower age of onset of Alzheimer's disease.

Talbot C, Houlden H, Craddock N, Crook R, Hutton M, Lendon C, Prihar G, Morris JC, Hardy J, Goate A. Talbot C, et al. Neuroreport. 1996 Jan 31;7(2):534-6. doi: 10.1097/00001756-199601310-00038. Neuroreport. 1996. PMID: 8730823 Clinical Trial.

7

The role of presenilin 1 in the genetics of Alzheimer's disease.

Clark RF, Hutton M, Talbot C, Wragg M, Lendon C, Busfield F, Han SW, Perez-Tur J, Adams M, Fuldner R, Roberts G, Karran E, Hardy J, Goate A. Clark RF, et al. Cold Spring Harb Symp Quant Biol. 1996;61:551-8. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246481

8

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. Among authors: lendon cl. Arch Neurol. 2005 Dec;62(12):1821-30. doi: 10.1001/archneur.62.12.1821. Arch Neurol. 2005. PMID: 16344340

9

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

Lendon CL, Lynch T, Norton J, McKeel DW Jr, Busfield F, Craddock N, Chakraverty S, Gopalakrishnan G, Shears SD, Grimmett W, Wilhelmsen KC, Hansen L, Morris JC, Goate AM. Lendon CL, et al. Neurology. 1998 Jun;50(6):1546-55. doi: 10.1212/wnl.50.6.1546. Neurology. 1998. PMID: 9633693

10

Protection against Alzheimer's disease with apoE epsilon 2.

Talbot C, Lendon C, Craddock N, Shears S, Morris JC, Goate A. Talbot C, et al. Lancet. 1994 Jun 4;343(8910):1432-3. doi: 10.1016/s0140-6736(94)92557-7. Lancet. 1994. PMID: 7910910 No abstract available.

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