Bernardino Ghetti

  • 29265 Citations
  • 81 h-Index
1967 …2021
If you made any changes in Pure, your changes will be visible here soon.

Publications 1967 2019

Filter
Article
2000
122 Citations (Scopus)

Presenilin-1 mutations in Alzheimer's disease

Russo, C., Schettini, G., Saido, T. C., Hulette, C., Lippa, C., Lannfelt, L., Ghetti, B., Gambetti, P., Tabaton, M. & Teller, J. K., Jun 1 2000, In : Nature. 405, 6786, p. 531-532 2 p.

Research output: Contribution to journalArticle

Aspartic Acid Endopeptidases
Presenilin-1
Endopeptidases
Amyloid Precursor Protein Secretases
Amyloid beta-Protein Precursor
7 Citations (Scopus)

Presymptomatic genetic testing with an APP mutation in Early-onset Alzheimer disease: A descriptive study of sibship dynamics

Quaid, K. A., Murrell, J. R., Hake, A., Farlow, M. & Ghetti, B., 2000, In : Journal of Genetic Counseling. 9, 4, p. 327-341 15 p.

Research output: Contribution to journalArticle

Amyloid beta-Protein Precursor
Genetic Testing
Alzheimer Disease
Mutation
Presenilin-2
29 Citations (Scopus)

Progress in hereditary tauopathies: A mutation in the Tau gene (G389R) causes a pick disease-like syndrome

Ghetti, B., Murrell, J. R., Zolo, P., Spillantini, M. G. & Goedert, M., 2000, In : Annals of the New York Academy of Sciences. 920, p. 52-62 11 p.

Research output: Contribution to journalArticle

Pick Disease of the Brain
Tauopathies
tau Proteins
Rigidity
Magnetic resonance imaging
51 Citations (Scopus)

Senile dementia associated with amyloid β protein angiopathy and tau perivascular pathology but not neuritic plaques in patients homozygous for the APOE-ε4 allele

Vidal, R., Calero, M., Piccardo, P., Farlow, M., Unverzagt, F., Méndez, E., Jiménez-Huete, A., Beavis, R., Gallo, G., Gomez-Tortosa, E., Ghiso, J., Hyman, B. T., Frangione, B. & Ghetti, B., Jul 2000, In : Acta Neuropathologica. 100, 1, p. 1-12 12 p.

Research output: Contribution to journalArticle

Apolipoprotein E4
Amyloidogenic Proteins
Amyloid Plaques
Alzheimer Disease
Alleles
41 Citations (Scopus)
tau Proteins
Frontotemporal Dementia
Chromosomes, Human, Pair 17
Parkinsonian Disorders
Chromosomes
9 Citations (Scopus)

The weaver gene continues to target late-generated dopaminergic neurons in midbrain areas at P90

Martí, J., Wills, K. V., Ghetti, B. & Bayer, S. A., Aug 30 2000, In : Developmental Brain Research. 122, 2, p. 173-181 9 p.

Research output: Contribution to journalArticle

Dopaminergic Neurons
Mesencephalon
Thymidine
Neurologic Mutant Mice
Genes
7 Citations (Scopus)

The weaver gene has no effect on the generation patterns of mesencephalic dopaminergic neurons

Martí, J., Wills, K. V., Ghetti, B. & Bayer, S. A., Aug 30 2000, In : Developmental Brain Research. 122, 2, p. 165-172 8 p.

Research output: Contribution to journalArticle

Cohort Effect
Dopaminergic Neurons
Mesencephalon
Thymidine
Neurologic Mutant Mice
1999
48 Citations (Scopus)

A cell cycle alteration precedes apoptosis of granule cell precursors in the weaver mouse cerebellum

Migheli, A., Piva, R., Casolino, S., Atzori, C., Dlouhy, S. & Ghetti, B., Aug 1999, In : American Journal of Pathology. 155, 2, p. 365-373 9 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Cerebellum
Cell Cycle
Apoptosis
Cell Cycle Proteins
10 Citations (Scopus)

Alteration of IGF system gene expression during the postnatal development of pcd mice

Zhang, W., Ghetti, B., Yang, X. L. & Lee, W. H., 1999, In : Journal of Endocrinology. 163, 2, p. 191-198 8 p.

Research output: Contribution to journalArticle

Insulin-Like Growth Factor I
Gene Expression
Insulin-Like Growth Factor Binding Proteins
Messenger RNA
Insulin-Like Growth Factor II
139 Citations (Scopus)

A mutation at codon 279 (N279K) in exon 10 of the Tau gene causes a tauopathy with dementia and supranuclear palsy

Delisle, M. B., Murrell, J. R., Richardson, R., Trofatter, J. A., Rascol, O., Soulages, X., Mohr, M., Calvas, P. & Ghetti, B., Jul 1999, In : Acta Neuropathologica. 98, 1, p. 62-77 16 p.

Research output: Contribution to journalArticle

Tauopathies
Codon
Paralysis
Dementia
Exons
377 Citations (Scopus)

Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's disease

Bales, K. R., Verina, T., Cummins, D. J., Du, Y., Dodel, R. C., Saura, J., Fishman, C. E., Delong, C. A., Piccardo, P., Petegnief, V., Ghetti, B. & Paul, S. M., Dec 21 1999, In : Proceedings of the National Academy of Sciences of the United States of America. 96, 26, p. 15233-15238 6 p.

Research output: Contribution to journalArticle

Apolipoproteins E
Amyloid
Transgenic Mice
Alzheimer Disease
Amyloid Plaques
6 Citations (Scopus)

Chapter 5 Human Prion Diseases

Ghetti, B. & Gambetti, P., 1999, In : Advances in Cell Aging and Gerontology. 3, C, p. 135-187 53 p.

Research output: Contribution to journalArticle

Prion Diseases
1003 Citations (Scopus)

Classification of sporadic Creutzfeldt-Jakob disease based on molecular and phenotypic analysis of 300 subjects

Parchi, P., Giese, A., Capellari, S., Brown, P., Schulz-Schaeffer, W., Windl, O., Zerr, I., Budka, H., Kopp, N., Piccardo, P., Poser, S., Rojiani, A., Streichemberger, N., Julien, J., Vital, C., Ghetti, B., Gambetti, P. & Kretzschmar, H., 1999, In : Annals of Neurology. 46, 2, p. 224-233 10 p.

Research output: Contribution to journalArticle

Codon
Valine
Phenotype
Methionine
Dementia
291 Citations (Scopus)

Frontotemporal dementia and corticobasal degeneration in a family with a P301S mutation in tau

Bugiani, O., Murrell, J. R., Giaccone, G., Hasegawa, M., Ghigo, G., Tabaton, M., Morbin, M., Primavera, A., Carella, F., Solaro, C., Grisoli, M., Savoiardo, M., Spillantini, M. G., Tagliavini, F., Goedert, M. & Ghetti, B., 1999, In : Journal of Neuropathology and Experimental Neurology. 58, 6, p. 667-677 11 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
tau Proteins
Mutation
Genes
Chromosomes, Human, Pair 17
15 Citations (Scopus)

Glial cell line-derived neurotrophic factor protects midbrain dopamine neurons from the lethal action of the weaver gene: A quantitative immunocytochemical study

Broome, J. D., Wills, K. V., Lapchak, P. A., Ghetti, B., Camp, L. L. & Bayer, S. A., Aug 5 1999, In : Developmental Brain Research. 116, 1, p. 1-7 7 p.

Research output: Contribution to journalArticle

Glial Cell Line-Derived Neurotrophic Factor
Dopaminergic Neurons
Mesencephalon
Genes
Tyrosine
6 Citations (Scopus)

Mutations in the Tau gene cause frontotemporal dementia

Ghetti, B., Murrell, J. & Spillantini, M. G., Nov 1999, In : Brain Research Bulletin. 50, 5-6, p. 471-472 2 p.

Research output: Contribution to journalArticle

20th Century History
tau Proteins
Frontotemporal Dementia
Frontal Lobe
Temporal Lobe
181 Citations (Scopus)

Structure of tau exon 10 splicing regulatory element RNA and destabilization by mutations of frontotemporal dementia and parkinsonism linked to chromosome 17

Varani, L., Hasegawa, M., Spillantini, M. G., Smith, M. J., Murrell, J. R., Ghetti, B., Klug, A., Goedert, M. & Varani, G., Jul 6 1999, In : Proceedings of the National Academy of Sciences of the United States of America. 96, 14, p. 8229-8234 6 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
Chromosomes, Human, Pair 17
Parkinsonian Disorders
Exons
RNA
185 Citations (Scopus)

Tau gene mutation G389R causes a tauopathy with abundant pick body-like inclusions and axonal deposits

Murrell, J. R., Spillantini, M. G., Zolo, P., Guazzelli, M., Smith, M. J., Hasegawa, M., Redi, F., Crowther, R. A., Pietrini, P., Ghetti, B. & Goedert, M., Dec 1999, In : Journal of Neuropathology and Experimental Neurology. 58, 12, p. 1207-1226 20 p.

Research output: Contribution to journalArticle

Tauopathies
Inclusion Bodies
Mutation
Genes
Frontotemporal Dementia
146 Citations (Scopus)

Tau pathology in a family with dementia and a P301L mutation in tau

Mirra, S. S., Murrell, J. R., Gearing, M., Spillantini, M. G., Goedert, M., Crowther, R. A., Levey, A. I., Jones, R., Green, J., Shoffner, J. M., Wainer, B. H., Schmidt, M. L., Trojanowski, J. Q. & Ghetti, B., Apr 1999, In : Journal of Neuropathology and Experimental Neurology. 58, 4, p. 335-345 11 p.

Research output: Contribution to journalArticle

Tauopathies
Dementia
Siblings
Frontotemporal Dementia
Chromosomes, Human, Pair 17
1998
6 Citations (Scopus)

Altered responses to potassium in cerebellar neurons from weaver heterozygote mice

Fox, A. P., Dlouhy, S., Ghetti, B., Hurley, J., Nucifora, P. G. P., Nelson, D. J., Won, L. & Heller, A., 1998, In : Experimental Brain Research. 123, 3, p. 298-306 9 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Heterozygote
Potassium
Neurons
Dopaminergic Neurons
21 Citations (Scopus)

An antibody raised against a conserved sequence of the prion protein recognizes pathological isoforms in human and animal prion diseases, including Creutzfeldt-Jakob disease and bovine spongiform encephalopathy

Piccardo, P., Langeveld, J. P. M., Hill, A. F., Dlouhy, S., Young, K., Giaccone, G., Rossi, G., Bugiani, M., Bugiani, O., Meloen, R. H., Collinge, J., Tagliavini, F. & Ghetti, B., Jun 1998, In : American Journal of Pathology. 152, 6, p. 1415-1420 6 p.

Research output: Contribution to journalArticle

Bovine Spongiform Encephalopathy
Animal Diseases
Creutzfeldt-Jakob Syndrome
Prion Diseases
Conserved Sequence
40 Citations (Scopus)

Characterization of murine Girk2 transcript isoforms: Structure and differential expression

Wei, J., Hodes, M. E., Piva, R., Feng, Y., Wang, Y., Ghetti, B. & Dlouhy, S., Aug 1 1998, In : Genomics. 51, 3, p. 379-390 12 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Exons
Protein Isoforms
GTP-Binding Proteins
Testis
29 Citations (Scopus)

Creutzfeldt-Jakob disease in a husband and wife

Brown, P., Cervenáková, L., McShane, L., Goldfarb, L. G., Bishop, K., Bastian, F., Kirkpatrick, J., Piccardo, P., Ghetti, B. & Gajdusek, D. C., Mar 1998, In : Neurology. 50, 3, p. 684-688 5 p.

Research output: Contribution to journalArticle

Creutzfeldt-Jakob Syndrome
Spouses
Amyloidogenic Proteins
Widowhood
Nervous System Diseases
144 Citations (Scopus)

Endogenous proteolytic cleavage of normal and disease-associated isoforms of the human prion protein in neural and non-neural tissues

Jiménez-Huete, A., Lievens, P. M. J., Vidal, R., Piccardo, P., Ghetti, B., Tagliavini, F., Frangione, B. & Prelli, F., Nov 1998, In : American Journal of Pathology. 153, 5, p. 1561-1572 12 p.

Research output: Contribution to journalArticle

Protein Isoforms
Creutzfeldt-Jakob Syndrome
Prion Diseases
Prions
Brain
57 Citations (Scopus)

FDG-PET and MRI in temporal lobe epilepsy: Relationship to febrile seizures, hippocampal sclerosis and outcome

Salanova, V., Markand, O., Worth, R., Smith, R., Wellman, H., Hutchins, G., Park, H., Ghetti, B. & Azzarelli, B., 1998, In : Acta Neurologica Scandinavica. 97, 3, p. 146-153 8 p.

Research output: Contribution to journalArticle

Febrile Seizures
Temporal Lobe Epilepsy
Sclerosis
Positron-Emission Tomography
Magnetic Resonance Imaging
344 Citations (Scopus)

Frontotemporal dementia and Parkinsonism linked to chromosome 17: A new group of tauopathies

Spillantini, M. G., Bird, T. D. & Ghetti, B., 1998, In : Brain Pathology. 8, 2, p. 387-402 16 p.

Research output: Contribution to journalArticle

Tauopathies
Frontotemporal Dementia
Chromosomes, Human, Pair 17
Parkinsonian Disorders
Pick Disease of the Brain
13 Citations (Scopus)

Hypothalamic-pituitary-gonadal axis in the mutant weaver mouse

Schwartz, N. B., Szabo, M., Verina, T., Wei, J., Dlouhy, S., Won, L., Heller, A., Hodes, M. E. & Ghetti, B., 1998, In : Neuroendocrinology. 68, 6, p. 374-385 12 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Homozygote
Seminiferous Epithelium
Follicle Stimulating Hormone
Luteinizing Hormone
385 Citations (Scopus)

Lewy bodies contain altered α-synuclein in brains of many familial Alzheimer's disease patients with mutations in presenilin and amyloid precursor protein genes

Lippa, C. F., Fujiwara, H., Mann, D. M. A., Giasson, B., Baba, M., Schmidt, M. L., Nee, L. E., O'Connell, B., Pollen, D. A., St. George-Hyslop, P., Ghetti, B., Nochlin, D., Bird, T. D., Cairns, N. J., Lee, V. M. Y., Iwatsubo, T. & Trojanowski, J. Q., Nov 1998, In : American Journal of Pathology. 153, 5, p. 1365-1370 6 p.

Research output: Contribution to journalArticle

Synucleins
Presenilins
Lewy Bodies
Amyloid beta-Protein Precursor
Alzheimer Disease
1173 Citations (Scopus)

Mutation in the tau gene in familial multiple system tauopathy with presenile dementia

Spillantini, M. G., Murrell, J. R., Goedert, M., Farlow, M., Klug, A. & Ghetti, B., Jun 23 1998, In : Proceedings of the National Academy of Sciences of the United States of America. 95, 13, p. 7737-7741 5 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
tau Proteins
Mutation
Protein Isoforms
Genes
260 Citations (Scopus)

Neurological illness in transgenic mice expressing a prion protein with an insertional mutation

Chiesa, R., Piccardo, P., Ghetti, B. & Harris, D. A., Dec 1998, In : Neuron. 21, 6, p. 1339-1351 13 p.

Research output: Contribution to journalArticle

Transgenic Mice
Mutation
Endopeptidase K
Cerebellar Ataxia
Genetically Modified Animals
166 Citations (Scopus)

Phenotypic variability of Gerstmann-Straussler-Scheinker disease is associated with prion protein heterogeneity

Piccardo, P., Dlouhy, S., Lievens, P. M. J., Young, K., Bird, T. D., Nochlin, D., Dickson, D. W., Vinters, H. V., Zimmerman, T. R., Mackenzie, I. R. A., Kish, S. J., Ang, L. C., De Carli, C., Pocchiari, M., Brown, P., Gibbs, C. J., Gajdusek, D. C., Bugiani, O., Ironside, J., Tagliavini, F. & 1 others, Ghetti, B., Oct 1998, In : Journal of Neuropathology and Experimental Neurology. 57, 10, p. 979-988 10 p.

Research output: Contribution to journalArticle

Gerstmann-Straussler-Scheinker Disease
Protein Isoforms
Prion Proteins
Endopeptidase K
Creutzfeldt-Jakob Syndrome
1997
31 Citations (Scopus)

A possible role for tyrosine kinases in the regulation of the neuronal dopamine transporter in mouse striatum

Simon, J. R., Bare, D. J., Ghetti, B. & Richter, J. A., 1997, In : Neuroscience Letters. 224, 3, p. 201-205 5 p.

Research output: Contribution to journalArticle

Dopamine Plasma Membrane Transport Proteins
Genistein
Protein-Tyrosine Kinases
Dopamine
Corpus Striatum
14 Citations (Scopus)

Atrophy and loss of dopaminergic mesencephalic neurons in heterozygous weaver mice

Verina, T., Norton, J. A., Sorbel, J. J., Triarhou, L. C., Laferty, D., Richter, J. A., Simon, J. R. & Ghetti, B., Jan 1997, In : Experimental Brain Research. 113, 1, p. 5-12 8 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Dopaminergic Neurons
Substantia Nigra
Atrophy
Ventral Tegmental Area
31 Citations (Scopus)

Decreased IGF-I gene expression during the apoptosis of Purkinje cells in pcd mice

Zhang, W., Ghetti, B. & Lee, W. H., Feb 20 1997, In : Developmental Brain Research. 98, 2, p. 164-176 13 p.

Research output: Contribution to journalArticle

Purkinje Cells
Insulin-Like Growth Factor I
Apoptosis
Gene Expression
Cerebellum
38 Citations (Scopus)

Diverse cell death pathways result from a single missense mutation in weaver mouse

Migheli, A., Piva, R., Wei, J., Attanasio, A., Casolino, S., Hodes, M. E., Dlouhy, S., Bayer, S. A. & Ghetti, B., Dec 1997, In : American Journal of Pathology. 151, 6, p. 1629-1638 10 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Missense Mutation
Electron Microscopy
Cell Death
Cerebellum
267 Citations (Scopus)

Familial multiple system tauopathy with presenile dementia: A disease with abundant neuronal and glial tau filaments

Spillantini, M. G., Goedert, M., Crowther, R. A., Murrell, J. R., Farlow, M. & Ghetti, B., Apr 15 1997, In : Proceedings of the National Academy of Sciences of the United States of America. 94, 8, p. 4113-4118 6 p.

Research output: Contribution to journalArticle

tau Proteins
Frontotemporal Dementia
Neuroglia
Alzheimer Disease
Neurons
64 Citations (Scopus)

Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17

Murrell, J. R., Koller, D., Foroud, T., Goedert, M., Spillantini, M. G., Edenberg, H., Farlow, M. & Ghetti, B., Nov 1997, In : American Journal of Human Genetics. 61, 5, p. 1131-1138 8 p.

Research output: Contribution to journalArticle

Frontotemporal Dementia
Chromosomes, Human, Pair 17
Oligodendroglia
Memory Disorders
Pedigree
47 Citations (Scopus)

Gerstmann-Straussler-Scheinker disease with the PRNP P102L mutation and valine at codon 129

Young, K., Clark, H. B., Piccardo, P., Dlouhy, S. & Ghetti, B., Feb 1997, In : Molecular Brain Research. 44, 1, p. 147-150 4 p.

Research output: Contribution to journalArticle

Gerstmann-Straussler-Scheinker Disease
Valine
Codon
Mutation
Methionine
25 Citations (Scopus)

In situ hybridization analysis of Girk2 expression in the developing central nervous system in normal and weaver mice

Wei, J., Dlouhy, S., Bayer, S., Piva, R., Verina, T., Wang, Y., Feng, Y., Dupree, B., Hodes, M. E. & Ghetti, B., Jul 1997, In : Journal of Neuropathology and Experimental Neurology. 56, 7, p. 762-771 10 p.

Research output: Contribution to journalArticle

Neurologic Mutant Mice
Mesencephalon
Cerebellum
In Situ Hybridization
Central Nervous System
7 Citations (Scopus)
Dopaminergic Neurons
Heterozygote
Cell Communication
Corpus Striatum
Mesencephalon
627 Citations (Scopus)

Lack of apolipoprotein E dramatically reduces amyloid beta-peptide deposition.

Bales, K. R., Verina, T., Dodel, R. C., Du, Y., Altstiel, L., Bender, M., Hyslop, P., Johnstone, E. M., Little, S. P., Cummins, D. J., Piccardo, P., Ghetti, B. & Paul, S. M., Nov 1997, In : Nature Genetics. 17, 3, p. 263-264 2 p.

Research output: Contribution to journalArticle

15 Citations (Scopus)
Gerstmann-Straussler-Scheinker Disease
Motor Skills
Aptitude
Neuropsychological Tests
Memory Disorders
33 Citations (Scopus)

Subacute sclerosing panencephalitis manifesting as viral retinitis: Clinical and histopathologic findings

Park, D. W., Boldt, H. C., Massicotte, S. J., Akang, E. E. U., Roos, K., Bodnar, A., Pless, J., Ghetti, B. & Pascuzzi, R., 1997, In : American Journal of Ophthalmology. 123, 4, p. 533-542 10 p.

Research output: Contribution to journalArticle

Subacute Sclerosing Panencephalitis
Retinitis
Virus Diseases
Drug Users
Cerebrospinal Fluid
1996
18 Citations (Scopus)

Cloning a cDNA for carbonyl reductase (Cbr) from mouse cerebellum: Murine genes that express Cbr map to chromosomes 16 and 11

Jianjun, W., Dlouhy, S., Hara, A., Ghetti, B. & Hodes, M. E., May 15 1996, In : Genomics. 34, 1, p. 147-148 2 p.

Research output: Contribution to journalArticle

Alcohol Oxidoreductases
Chromosomes, Human, Pair 16
Chromosomes, Human, Pair 11
Cerebellum
Organism Cloning
8 Citations (Scopus)

Direct cDNA selection with DNA microdissected from mouse chromosome 16: Isolation of novel clones and construction of a partial transcription map of the C3-C4 region

Wei, J., Hodes, M. E., Wang, Y., Feng, Y., Ghetti, B. & Dlouhy, S., Aug 1996, In : Genome Research. 6, 8, p. 678-687 10 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Complementary DNA
Clone Cells
Microdissection
DNA
87 Citations (Scopus)

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

Lippa, C. F., Saunders, A. M., Smith, T. W., Swearer, J. M., Drachman, D. A., Ghetti, B., Nee, L., Pulaski-Salo, D., Dickson, D., Robitaille, Y., Bergeron, C., Crain, B., Benson, M., Farlow, M., Hyman, B. T., St. George-Hyslop, P., Roses, A. D. & Pollen, D. A., Feb 1996, In : Neurology. 46, 2, p. 406-412 7 p.

Research output: Contribution to journalArticle

Alzheimer Disease
Amyloid Plaques
Neurofibrillary Tangles
Chromosomes, Human, Pair 14
Chromosomes, Human, Pair 21
3 Citations (Scopus)

Linkage mapping of microdissected clones from distal mouse chromosome 16

Wei, J., Dlouhy, S., Wang, Y., Zhu, J., Fitzpatrick, L., Ghetti, B. & Hodes, M. E., May 1996, In : Somatic Cell and Molecular Genetics. 22, 3, p. 227-232 6 p.

Research output: Contribution to journalArticle

Chromosomes, Human, Pair 16
Chromosome Mapping
Clone Cells
Microdissection
Organism Cloning
642 Citations (Scopus)

Molecular basis of phenotypic variability in sporadic Creutzfeldt-Jakob disease

Parchi, P., Castellani, R., Capellari, S., Ghetti, B., Young, K., Chen, S. G., Farlow, M., Dickson, D. W., Sima, A. A. F., Trojanowski, J. Q., Petersen, R. B. & Gambetti, P., Jun 1996, In : Annals of Neurology. 39, 6, p. 767-778 12 p.

Research output: Contribution to journalArticle

Peptide Hydrolases
Codon
Methionine
Creutzfeldt-Jakob Syndrome
Valine
23 Citations (Scopus)

Phenotypic effects of the weaver gene are evident in the embryonic cerebellum but not in the ventral midbrain

Bayer, S. A., Wills, K. V., Wei, J., Feng, Y., Dlouhy, S., Hodes, M. E., Verina, T. & Ghetti, B., Oct 23 1996, In : Developmental Brain Research. 96, 1-2, p. 130-137 8 p.

Research output: Contribution to journalArticle

Mesencephalon
Cerebellum
Thymidine
Genes
Purkinje Cells
154 Citations (Scopus)

Prion protein amyloidosis

Ghetti, B., Piccardo, P., Frangione, B., Bugiani, O., Giaccone, G., Young, K., Prelli, F., Farlow, M., Dlouhy, S. & Tagliavini, F., Apr 1996, In : Brain Pathology. 6, 2, p. 127-145 19 p.

Research output: Contribution to journalArticle

Amyloidosis
Gerstmann-Straussler-Scheinker Disease
Prion Diseases
Amyloid
Spastic Paraparesis