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P Piccardo

Showing results (41-50 of 58) with videos related to

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Annals of Neurology|January 1, 1988
The role of HTLV-I in tropical spastic paraparesis in JamaicaP Rodgers-Johnson, O S Morgan, C Mora, et al.
Annals of Internal Medicine|February 1, 1989
T-cell lymphoma, tropical spastic paraparesis, and malignant fibrous histiocytoma in a patient with human T-cell lymphotropic virus, type 1J W Lee, E P Fox, P Rodgers-Johnson, et al.
Ultrastructural Pathology|September 1, 1994
Ultrastructural pathology of human T-cell lymphotropic virus type I encephalomyelopathy in a white patient with adult T-cell leukemia/lymphomaP P Liberski, P Rodgers-Johnson, R Yanagihara, et al.
Experimental Neurology|June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.
Neurology|June 1, 1995
Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patientsK Young, C K Jones, P Piccardo, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
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 seizuresM Takao, B Ghetti, J R Murrell, et al.
The American Journal of Pathology|June 17, 1998
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 encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 1999
Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's diseaseK R Bales, T Verina, D J Cummins, et al.
Journal of Neuropathology and Experimental Neurology|January 4, 2001
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsyM Takao, M D Benson, J R Murrell, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Annals of Neurology|January 1, 1988
The role of HTLV-I in tropical spastic paraparesis in JamaicaP Rodgers-Johnson, O S Morgan, C Mora, et al.
Annals of Internal Medicine|February 1, 1989
T-cell lymphoma, tropical spastic paraparesis, and malignant fibrous histiocytoma in a patient with human T-cell lymphotropic virus, type 1J W Lee, E P Fox, P Rodgers-Johnson, et al.
Ultrastructural Pathology|September 1, 1994
Ultrastructural pathology of human T-cell lymphotropic virus type I encephalomyelopathy in a white patient with adult T-cell leukemia/lymphomaP P Liberski, P Rodgers-Johnson, R Yanagihara, et al.
Experimental Neurology|June 1, 1990
Creutzfeldt-Jakob disease and kuru patients lack a mutation consistently found in the Gerstmann-Sträussler-Scheinker syndromeL G Goldfarb, P Brown, D Goldgaber, et al.
Neurology|March 1, 1991
Clinical and molecular genetic study of a large German kindred with Gerstmann-Sträussler-Scheinker syndromeP Brown, L G Goldfarb, W T Brown, et al.
Neurology|June 1, 1995
Gerstmann-Sträussler-Scheinker disease with mutation at codon 102 and methionine at codon 129 of PRNP in previously unreported patientsK Young, C K Jones, P Piccardo, et al.
Journal of Neuropathology and Experimental Neurology|January 5, 2002
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 seizuresM Takao, B Ghetti, J R Murrell, et al.
The American Journal of Pathology|June 17, 1998
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 encephalopathyP Piccardo, J P Langeveld, A F Hill, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 1999
Apolipoprotein E is essential for amyloid deposition in the APP(V717F) transgenic mouse model of Alzheimer's diseaseK R Bales, T Verina, D J Cummins, et al.
Journal of Neuropathology and Experimental Neurology|January 4, 2001
Neuroserpin mutation S52R causes neuroserpin accumulation in neurons and is associated with progressive myoclonus epilepsyM Takao, M D Benson, J R Murrell, et al.
Pageof 6