Graff-Radford NR - Search Results

1

Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma.

Carrasquillo MM, Nicholson AM, Finch N, Gibbs JR, Baker M, Rutherford NJ, Hunter TA, DeJesus-Hernandez M, Bisceglio GD, Mackenzie IR, Singleton A, Cookson MR, Crook JE, Dillman A, Hernandez D, Petersen RC, Graff-Radford NR, Younkin SG, Rademakers R. Carrasquillo MM, et al. Am J Hum Genet. 2010 Dec 10;87(6):890-7. doi: 10.1016/j.ajhg.2010.11.002. Epub 2010 Nov 18. Am J Hum Genet. 2010. PMID: 21087763 Free PMC article.

2

Rapidly progressive aphasic dementia and motor neuron disease.

Caselli RJ, Windebank AJ, Petersen RC, Komori T, Parisi JE, Okazaki H, Kokmen E, Iverson R, Dinapoli RP, Graff-Radford NR, et al. Caselli RJ, et al. Ann Neurol. 1993 Feb;33(2):200-7. doi: 10.1002/ana.410330210. Ann Neurol. 1993. PMID: 8257465

3

A new pathogenic mutation in the APP gene (I716V) increases the relative proportion of A beta 42(43).

Eckman CB, Mehta ND, Crook R, Perez-tur J, Prihar G, Pfeiffer E, Graff-Radford N, Hinder P, Yager D, Zenk B, Refolo LM, Prada CM, Younkin SG, Hutton M, Hardy J. Eckman CB, et al. Hum Mol Genet. 1997 Nov;6(12):2087-9. doi: 10.1093/hmg/6.12.2087. Hum Mol Genet. 1997. PMID: 9328472

4

Pathologic heterogeneity in clinically diagnosed corticobasal degeneration.

Boeve BF, Maraganore DM, Parisi JE, Ahlskog JE, Graff-Radford N, Caselli RJ, Dickson DW, Kokmen E, Petersen RC. Boeve BF, et al. Neurology. 1999 Sep 11;53(4):795-800. doi: 10.1212/wnl.53.4.795. Neurology. 1999. PMID: 10489043

5

No association between TAU haplotype and Alzheimer's disease in population or clinic based series or in familial disease.

Baker M, Graff-Radford D, Wavrant DeVrièze F, Graff-Radford N, Petersen RC, Kokmen E, Boeve B, Myllykangas L, Polvikoski T, Sulkava R, Verkoniemmi A, Tienari P, Haltia M, Hardy J, Hutton M, Perez-Tur J. Baker M, et al. Neurosci Lett. 2000 May 12;285(2):147-9. doi: 10.1016/s0304-3940(00)01057-0. Neurosci Lett. 2000. PMID: 10793248

6

Linkage of plasma Abeta42 to a quantitative locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.

Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Baker M, Adamson J, Ronald J, Blangero J, Hutton M, Younkin SG. Ertekin-Taner N, et al. Science. 2000 Dec 22;290(5500):2303-4. doi: 10.1126/science.290.5500.2303. Science. 2000. PMID: 11125143

7

Heritability of plasma amyloid beta in typical late-onset Alzheimer's disease pedigrees.

Ertekin-Taner N, Graff-Radford N, Younkin LH, Eckman C, Adamson J, Schaid DJ, Blangero J, Hutton M, Younkin SG. Ertekin-Taner N, et al. Genet Epidemiol. 2001 Jul;21(1):19-30. doi: 10.1002/gepi.1015. Genet Epidemiol. 2001. PMID: 11443731

8

Differences in tau and apolipoprotein E polymorphism frequencies in sporadic frontotemporal lobar degeneration syndromes.

Short RA, Graff-Radford NR, Adamson J, Baker M, Hutton M. Short RA, et al. Arch Neurol. 2002 Apr;59(4):611-5. doi: 10.1001/archneur.59.4.611. Arch Neurol. 2002. PMID: 11939896

9

Serum creatinine levels correlate with plasma amyloid Beta protein.

Arvanitakis Z, Lucas JA, Younkin LH, Younkin SG, Graff-Radford NR. Arvanitakis Z, et al. Alzheimer Dis Assoc Disord. 2002 Jul-Sep;16(3):187-90. doi: 10.1097/00002093-200207000-00009. Alzheimer Dis Assoc Disord. 2002. PMID: 12218650

10

Dementia with Lewy bodies may present as dementia and REM sleep behavior disorder without parkinsonism or hallucinations.

Ferman TJ, Boeve BF, Smith GE, Silber MH, Lucas JA, Graff-Radford NR, Dickson DW, Parisi JE, Petersen RC, Ivnik RJ. Ferman TJ, et al. J Int Neuropsychol Soc. 2002 Nov;8(7):907-14. doi: 10.1017/s1355617702870047. J Int Neuropsychol Soc. 2002. PMID: 12405541

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