-Bernardino Ghetti Researcher Activity Profile

Research Author Detailed Information 

Bernardino Ghetti Publication Rate By Year

Bernardino Ghetti has published 4 paper(s) in 2005, 1 paper(s) in 2006, 18 paper(s) in 2007, 5 paper(s) in 2008, for a total of 28 research publications in total.

Bernardino B Ghetti Author Information

LAST NAME: ghetti

FIRST NAME: bernardino

INITIALS: B

AFFILIATION:

Papers

Bernardino Ghetti's Publication Record

1. Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene. Year Published: 2005
Department of Pathology and Laboratory Medicine, Division of Neuropathology, Indiana University School of Medicine, Indianapolis, IN 46202-5120, USA. bghetti@iupui.edu
2. Redox metals and oxidative abnormalities in human prion diseases. Year Published: 2005
Institute of Pathology, Case Western Reserve University, 2085 Adelbert Road, Cleveland, OH 44106, USA.
3. The A431E mutation in PSEN1 causing familial Alzheimer's disease originating in Jalisco State, Mexico: an additional fifteen families. Year Published: 2006
Department of Pathology and Laboratory Medicine, University of Indiana Medical School, 635 Barnhill Drive, MS A128, Indianapolis, IN 46202-5126, USA.
4. Year Published: 2007
Department of Neuropathology and Neurology, Istituto Nazionale Neurologico Carlo Besta, Milan, Italy.
5. Accumulation of prion protein in the brain that is not associated with transmissible disease. Year Published: 2007
Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, MD 20852, USA.
6. Corticobasal syndrome associated with the A9D Progranulin mutation. Year Published: 2007
Indiana Alzheimer Disease Center, Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
7. Association of a presenilin 1 S170F mutation with a novel Alzheimer disease molecular phenotype. Year Published: 2007
Department of Neurosciences, University of Genoa, Genoa, Italy.
8. Prion protein with an octapeptide insertion has impaired neuroprotective activity in transgenic mice. Year Published: 2007
Department of Cell Biology and Physiology, Washington University School of Medicine, St Louis, MO 63110, USA.
9. Performance on MMSE sub-items and education level in presenilin-1 mutation carriers without dementia. Year Published: 2007
Alzheimer's Disease Center, UCLA Department of Neurology, Los Angeles, CA, USA. jringman@mednet.ucla.edu
10. Generation and survival of midbrain dopaminergic neurons in weaver mice. Year Published: 2007
11. The genetics of very early onset Alzheimer disease. Year Published: 2007
Department of Neurology, University of Colorado School of Medicine, Denver, CO, USA. christopher.filley@uchsc.edu
12. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Year Published: 2007
Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA. rademakers.rosa@mayo.edu
13. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains. Year Published: 2007
Harvard Medical School, Massachusetts General Hospital, 114 16th Street, Charlestown, MA, 02129, USA.
14. Corticobasal syndrome associated with the A9D Progranulin mutation. Year Published: 2007
Indiana Alzheimer Disease Center, Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
15. Abundant neuritic inclusions and microvacuolar changes in a case of diffuse Lewy body disease with the A53T mutation in the alpha-synuclein gene. Year Published: 2005
Department of Pathology and Laboratory Medicine, Division of Neuropathology, Indiana University School of Medicine, Indianapolis, IN 46202-5120, USA. bghetti@iupui.edu
16. Redox metals and oxidative abnormalities in human prion diseases. Year Published: 2005
Institute of Pathology, Case Western Reserve University, 2085 Adelbert Road, Cleveland, OH 44106, USA.
17. Phenotypic variability associated with progranulin haploinsufficiency in patients with the common 1477C-->T (Arg493X) mutation: an international initiative. Year Published: 2007
Department of Neuroscience, Mayo Clinic College of Medicine, Jacksonville, FL 32224, USA. rademakers.rosa@mayo.edu
18. The tauopathy associated with mutation +3 in intron 10 of Tau: characterization of the MSTD family. Year Published: 2007
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
19. Corticobasal syndrome associated with the A9D Progranulin mutation. Year Published: 2007
Indiana Alzheimer Disease Center, Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
20. Purkinje cell age-distribution in fissures and in foliar crowns: a comparative study in the weaver cerebellum. Year Published: 2007
21. Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. Year Published: 2008
Pathology and Laboratory Medicine, Indiana Alzheimer Disease Center, Indianapolis, Indiana 46202, USA. rvidal@iupui.edu
22. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains. Year Published: 2007
Harvard Medical School, Massachusetts General Hospital, 114 16th Street, Charlestown, MA 02129, USA. martin.ingelsson@pubcare.uu.se
23. Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy. Year Published: 2008
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 OQH, UK. mg@mrc-lmb.cam.ac.uk.
24. Corticobasal syndrome associated with the A9D Progranulin mutation. Year Published: 2007
Indiana Alzheimer Disease Center, Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
25. Expression of a mutant form of the ferritin light chain gene induces neurodegeneration and iron overload in transgenic mice. Year Published: 2008
Pathology and Laboratory Medicine, Indiana Alzheimer Disease Center, Indianapolis, Indiana 46202, USA. rvidal@iupui.edu
26. Increase in the relative expression of tau with four microtubule binding repeat regions in frontotemporal lobar degeneration and progressive supranuclear palsy brains. Year Published: 2007
Harvard Medical School, Massachusetts General Hospital, 114 16th Street, Charlestown, MA 02129, USA. martin.ingelsson@pubcare.uu.se
27. Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy. Year Published: 2008
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 OQH, UK.
28. Analysis of tau phosphorylation and truncation in a mouse model of human tauopathy. Year Published: 2008
Medical Research Council Laboratory of Molecular Biology, Hills Road, Cambridge CB2 OQH, UK.