-Bernardino Ghetti Researcher Activity Profile

Research Author Detailed Information 

Bernardino Ghetti Publication Rate By Year

Bernardino Ghetti has published 1 paper(s) in 1987, 2 paper(s) in 1988, 2 paper(s) in 1989, 1 paper(s) in 1990, 1 paper(s) in 1991, 2 paper(s) in 1996, 2 paper(s) in 1997, 1 paper(s) in 1999, 4 paper(s) in 2005, 1 paper(s) in 2006, 20 paper(s) in 2007, 5 paper(s) in 2008, for a total of 42 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. Clinicopathologic features of frontotemporal dementia with progranulin sequence variation. Year Published: 2007
Indiana Alzheimer Disease Center, Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN 46202, USA.
6. 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.
7. 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.
8. 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.
9. 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.
10. 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
11. Clinical and genetic features of families with frontotemporal dementia and parkinsonism linked to chromosome 17 with a P301S tau mutation. Year Published: 2007
Department of Neurology, Mayo Clinic, Jacksonville, Florida, U.S.A..
12. Generation and survival of midbrain dopaminergic neurons in weaver mice. Year Published: 2007
13. 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
14. 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
15. 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.
16. 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.
17. 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
18. 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.
19. 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
20. 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.
21. 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.
22. Purkinje cell age-distribution in fissures and in foliar crowns: a comparative study in the weaver cerebellum. Year Published: 2007
23. 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
24. 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
25. 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.
26. 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.
27. 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
28. Anterograde transsynaptic degeneration in the deep cerebellar nuclei of Purkinje cell degeneration (pcd) mutant mice. Year Published: 1987
29. Neuroanatomical substrate of behavioural impairment in weaver mutant mice. Year Published: 1988
Department of Pathology, Indiana University School of Medicine, Indianapolis 46223.
30. Mesencephalic dopamine cell deficit involves areas A8, A9 and A10 in weaver mutant mice. Year Published: 1988
Department of Pathology, Indiana University School of Medicine, Indianapolis 46223.
31. Developmental expression of polypeptide PEP-19 in cerebellar cell suspensions transplanted into the cerebellum of pcd mutant mice. Year Published: 1989
Department of Pathology, Indiana University School of Medicine, Indianapolis 46223.
32. Degeneration and graft-induced restoration of dopamine innervation in the weaver mouse neostriatum: a quantitative radioautographic study of [3H]dopamine uptake. Year Published: 1989
Department of Medical Cell Research University of Lund, Sweden.
33. Intrastriatal implants of mesencephalic cell suspensions in weaver mutant mice: ultrastructural relationships of dopaminergic dendrites and axons issued from the graft. Year Published: 1990
Department of Pathology, Indiana University School of Medicine, Indianapolis 46223.
34. Age-related changes in striatal dopamine D2 receptor binding in weaver mice and effects of ventral mesencephalic grafts. Year Published: 1991
Department of Physiology and Biophysics, Indiana University School of Medicine, Indianapolis 46202-5120.
35. Time of neuron origin and gradients of neurogenesis in midbrain dopaminergic neurons in the mouse. Year Published: 1996
Department of Biology, Indiana Purdue University, Indianapolis 46202, USA.
36. Systematic differences in time of dopaminergic neuron origin between normal mice and homozygous weaver mutants. Year Published: 1996
Department of Biology, Indiana Purdue University, Indianapolis 46202, USA.
37. Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice. Year Published: 1997
Department of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis 46202-5120, USA.
38. In vitro evidence that the reduction in mesencephalic dopaminergic neurons in the weaver heterozygote is not due to a failure in target cell interaction. Year Published: 1997
Department of Pharmacological and Physiological Sciences, The University of Chicago, IL 60637, USA.
39. Altered responses to potassium in cerebellar neurons from weaver heterozygote mice. Year Published: 1999
The University of Chicago, Department of Pharmacological and Physiological Sciences, IL 60637, USA. Aaron@Drugs.bsd.uchicago.edu
40. 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
41. 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.
42. 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.