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F Tagliavini

Showing results (41-50 of 133) with videos related to

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Neuroscience Letters|July 8, 1991
Alzheimer patients: preamyloid deposits are immunoreactive with antibodies to extracellular domains of the amyloid precursor proteinF Tagliavini, G Giaccone, L Verga, et al.
Biochemical and Biophysical Research Communications|May 15, 1992
A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathiesF Tagliavini, F Prelli, M Porro, et al.
Acta Neuropathologica|January 1, 1982
Anderson-Fabry's disease: neuropathological and neurochemical investigationF Tagliavini, V Pietrini, F Gemignani, et al.
Neurology|December 22, 1999
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brainG Puoti, G Giaccone, G Rossi, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Meningiomas. A light and electron microscopy studyF Tedeschi, R Brizzi, A Lechi, et al.
Biochemical and Biophysical Research Communications|June 25, 1996
PrP27-30 is a normal soluble prion protein fragment released by human plateletsF Perini, R Vidal, B Ghetti, et al.
Neuroscience Letters|November 6, 1989
Alzheimer patients and Down patients: cerebral preamyloid deposits differ ultrastructurally and histochemically from the amyloid of senile plaquesL Verga, B Frangione, F Tagliavini, et al.
Minerva Medica|October 13, 1980
[Fabry's disease and familial lymphedema. Description of 2 cases]M Savi, T M Neri, G Asinari, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 1, 1990
Coexistence of Alzheimer's amyloid precursor protein and amyloid protein in cerebral vessel wallsF Tagliavini, J Ghiso, W F Timmers, et al.
European Journal of Biochemistry|December 3, 1999
Determination of solution conformations of PrP106-126, a neurotoxic fragment of prion protein, by 1H NMR and restrained molecular dynamicsE Ragg, F Tagliavini, P Malesani, et al.
Pageof 14

Showing results (41-50 of 133) with videos related to

Sort By:
Pageof 14
Neuroscience Letters|July 8, 1991
Alzheimer patients: preamyloid deposits are immunoreactive with antibodies to extracellular domains of the amyloid precursor proteinF Tagliavini, G Giaccone, L Verga, et al.
Biochemical and Biophysical Research Communications|May 15, 1992
A soluble form of prion protein in human cerebrospinal fluid: implications for prion-related encephalopathiesF Tagliavini, F Prelli, M Porro, et al.
Acta Neuropathologica|January 1, 1982
Anderson-Fabry's disease: neuropathological and neurochemical investigationF Tagliavini, V Pietrini, F Gemignani, et al.
Neurology|December 22, 1999
Sporadic Creutzfeldt-Jakob disease: co-occurrence of different types of PrP(Sc) in the same brainG Puoti, G Giaccone, G Rossi, et al.
Acta Neuropathologica. Supplementum|January 1, 1981
Meningiomas. A light and electron microscopy studyF Tedeschi, R Brizzi, A Lechi, et al.
Biochemical and Biophysical Research Communications|June 25, 1996
PrP27-30 is a normal soluble prion protein fragment released by human plateletsF Perini, R Vidal, B Ghetti, et al.
Neuroscience Letters|November 6, 1989
Alzheimer patients and Down patients: cerebral preamyloid deposits differ ultrastructurally and histochemically from the amyloid of senile plaquesL Verga, B Frangione, F Tagliavini, et al.
Minerva Medica|October 13, 1980
[Fabry's disease and familial lymphedema. Description of 2 cases]M Savi, T M Neri, G Asinari, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|June 1, 1990
Coexistence of Alzheimer's amyloid precursor protein and amyloid protein in cerebral vessel wallsF Tagliavini, J Ghiso, W F Timmers, et al.
European Journal of Biochemistry|December 3, 1999
Determination of solution conformations of PrP106-126, a neurotoxic fragment of prion protein, by 1H NMR and restrained molecular dynamicsE Ragg, F Tagliavini, P Malesani, et al.
Pageof 14