Benson MD - Search Results

1

Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathway.

Lippa CF, Saunders AM, Smith TW, Swearer JM, Drachman DA, Ghetti B, Nee L, Pulaski-Salo D, Dickson D, Robitaille Y, Bergeron C, Crain B, Benson MD, Farlow M, Hyman BT, George-Hyslop SP, Roses AD, Pollen DA. Lippa CF, et al. Among authors: benson md. Neurology. 1996 Feb;46(2):406-12. doi: 10.1212/wnl.46.2.406. Neurology. 1996. PMID: 8614503

2

Clinical characteristics in a kindred with early-onset Alzheimer's disease and their linkage to a G-->T change at position 2149 of the amyloid precursor protein gene.

Farlow M, Murrell J, Ghetti B, Unverzagt F, Zeldenrust S, Benson M. Farlow M, et al. Neurology. 1994 Jan;44(1):105-11. doi: 10.1212/wnl.44.1.105. Neurology. 1994. PMID: 8290042

3

A mutation in the amyloid precursor protein associated with hereditary Alzheimer's disease.

Murrell J, Farlow M, Ghetti B, Benson MD. Murrell J, et al. Among authors: benson md. Science. 1991 Oct 4;254(5028):97-9. doi: 10.1126/science.1925564. Science. 1991. PMID: 1925564

4

Characterization of amyloid fibril beta-peptide in familial Alzheimer's disease with APP717 mutations.

Liepnieks JJ, Ghetti B, Farlow M, Roses AD, Benson MD. Liepnieks JJ, et al. Among authors: benson md. Biochem Biophys Res Commun. 1993 Dec 15;197(2):386-92. doi: 10.1006/bbrc.1993.2491. Biochem Biophys Res Commun. 1993. PMID: 8267572

5

RFLP analysis for APP 717 mutations associated with Alzheimer's disease.

Zeldenrust SR, Murrell J, Farlow M, Ghetti B, Roses AD, Benson MD. Zeldenrust SR, et al. Among authors: benson md. J Med Genet. 1993 Jun;30(6):476-8. doi: 10.1136/jmg.30.6.476. J Med Genet. 1993. PMID: 7686976 Free PMC article.

6

Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsy.

Takao M, Benson MD, Murrell JR, Yazaki M, Piccardo P, Unverzagt FW, Davis RL, Holohan PD, Lawrence DA, Richardson R, Farlow MR, Ghetti B. Takao M, et al. Among authors: benson md. J Neuropathol Exp Neurol. 2000 Dec;59(12):1070-86. doi: 10.1093/jnen/59.12.1070. J Neuropathol Exp Neurol. 2000. PMID: 11138927

7

A new transthyretin mutation associated with leptomeningeal amyloidosis.

Liepnieks JJ, Dickson DW, Benson MD. Liepnieks JJ, et al. Among authors: benson md. Amyloid. 2011 Jun;18 Suppl 1:160-2. doi: 10.3109/13506129.2011.574354060. Amyloid. 2011. PMID: 21838472 No abstract available.

8

Diagnosis of Maryland/German familial amyloidotic polyneuropathy using allele-specific, enzymatically amplified, genomic DNA.

Mendell JR, Jiang XS, Warmolts JR, Nichols WC, Benson MD. Mendell JR, et al. Among authors: benson md. Ann Neurol. 1990 May;27(5):553-7. doi: 10.1002/ana.410270516. Ann Neurol. 1990. PMID: 2360796

9

Biochemical characterization of a neuroserpin variant associated with hereditary dementia.

Yazaki M, Liepnieks JJ, Murrell JR, Takao M, Guenther B, Piccardo P, Farlow MR, Ghetti B, Benson MD. Yazaki M, et al. Among authors: benson md. Am J Pathol. 2001 Jan;158(1):227-33. doi: 10.1016/S0002-9440(10)63961-2. Am J Pathol. 2001. PMID: 11141496 Free PMC article.

10

Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutations.

Piccardo P, Liepnieks JJ, William A, Dlouhy SR, Farlow MR, Young K, Nochlin D, Bird TD, Nixon RR, Ball MJ, DeCarli C, Bugiani O, Tagliavini F, Benson MD, Ghetti B. Piccardo P, et al. Among authors: benson md. Am J Pathol. 2001 Jun;158(6):2201-7. doi: 10.1016/S0002-9440(10)64692-5. Am J Pathol. 2001. PMID: 11395398 Free PMC article.

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