Ghetti BF - Search Results

1

The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study.

Cash DM, Ridgway GR, Liang Y, Ryan NS, Kinnunen KM, Yeatman T, Malone IB, Benzinger TL, Jack CR Jr, Thompson PM, Ghetti BF, Saykin AJ, Masters CL, Ringman JM, Salloway SP, Schofield PR, Sperling RA, Cairns NJ, Marcus DS, Xiong C, Bateman RJ, Morris JC, Rossor MN, Ourselin S, Fox NC; Dominantly Inherited Alzheimer Network (DIAN). Cash DM, et al. Among authors: ghetti bf. Neurology. 2013 Oct 15;81(16):1425-33. doi: 10.1212/WNL.0b013e3182a841c6. Epub 2013 Sep 18. Neurology. 2013. PMID: 24049139 Free PMC article.

2

Gerstmann-Sträussler-Scheinker disease. II. Neurofibrillary tangles and plaques with PrP-amyloid coexist in an affected family.

Ghetti B, Tagliavini F, Masters CL, Beyreuther K, Giaccone G, Verga L, Farlow MR, Conneally PM, Dlouhy SR, Azzarelli B, et al. Ghetti B, et al. Neurology. 1989 Nov;39(11):1453-61. doi: 10.1212/wnl.39.11.1453. Neurology. 1989. PMID: 2573006

3

Gerstmann-Sträussler-Scheinker disease. I. Extending the clinical spectrum.

Farlow MR, Yee RD, Dlouhy SR, Conneally PM, Azzarelli B, Ghetti B. Farlow MR, et al. Neurology. 1989 Nov;39(11):1446-52. doi: 10.1212/wnl.39.11.1446. Neurology. 1989. PMID: 2812321

4

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

5

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. Neurology. 1996 Feb;46(2):406-12. doi: 10.1212/wnl.46.2.406. Neurology. 1996. PMID: 8614503

6

Familial Alzheimer's disease: site of mutation influences clinical phenotype.

Lippa CF, Swearer JM, Kane KJ, Nochlin D, Bird TD, Ghetti B, Nee LE, St George-Hyslop P, Pollen DA, Drachman DA. Lippa CF, et al. Ann Neurol. 2000 Sep;48(3):376-9. Ann Neurol. 2000. PMID: 10976645

7

Ectopic white matter neurons, a developmental abnormality that may be caused by the PSEN1 S169L mutation in a case of familial AD with myoclonus and seizures.

Takao M, Ghetti B, Murrell JR, Unverzagt FW, Giaccone G, Tagliavini F, Bugiani O, Piccardo P, Hulette CM, Crain BJ, Farlow MR, Heyman A. Takao M, et al. J Neuropathol Exp Neurol. 2001 Dec;60(12):1137-52. doi: 10.1093/jnen/60.12.1137. J Neuropathol Exp Neurol. 2001. PMID: 11764087

8

Neuropsychological function in nondemented carriers of presenilin-1 mutations.

Ringman JM, Diaz-Olavarrieta C, Rodriguez Y, Chavez M, Fairbanks L, Paz F, Varpetian A, Maldonado HC, Macias-Islas MA, Murrell J, Ghetti B, Kawas C. Ringman JM, et al. Neurology. 2005 Aug 23;65(4):552-8. doi: 10.1212/01.wnl.0000172919.50001.d6. Neurology. 2005. PMID: 16116115 Free PMC article.

9

Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia.

Ringman JM, Rodriguez Y, Diaz-Olavarrieta C, Chavez M, Thompson M, Fairbanks L, Paz F, Varpetian A, Chaparro H, Macias-Islas MA, Murrell J, Ghetti B, Kawas C. Ringman JM, et al. Int Psychogeriatr. 2007 Apr;19(2):323-32. doi: 10.1017/S1041610206003772. Int Psychogeriatr. 2007. PMID: 16805926 Free PMC article.

10

The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families.

Murrell J, Ghetti B, Cochran E, Macias-Islas MA, Medina L, Varpetian A, Cummings JL, Mendez MF, Kawas C, Chui H, Ringman JM. Murrell J, et al. Neurogenetics. 2006 Nov;7(4):277-9. doi: 10.1007/s10048-006-0053-1. Epub 2006 Aug 5. Neurogenetics. 2006. PMID: 16897084 Free PMC article.

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