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M D Benson

Showing results (221-230 of 227) with videos related to

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Blood|January 7, 1998
Renal amyloidosis with a frame shift mutation in fibrinogen aalpha-chain gene producing a novel amyloid proteinL Hamidi Asl, J J Liepnieks, T Uemichi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 22, 1999
Nomenclature of amyloid fibril proteins. Report from the meeting of the International Nomenclature Committee on Amyloidosis, August 8-9, 1998. Part 1P Westermark, S Araki, M D Benson, et al.
Journal of Neuropathology and Experimental Neurology|April 22, 2004
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide geneR Vidal, B Ghetti, M Takao, 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.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
European Journal of Neurology|April 29, 2020
Early data on long-term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2-year update from the open-label extension of the NEURO-TTR trialT H Brannagan, A K Wang, T Coelho, et al.
Neurology|February 1, 1996
Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathwayC F Lippa, A M Saunders, T W Smith, et al.
Pageof 23

Showing results (221-230 of 227) with videos related to

Sort By:
Pageof 23
You have reached the last page of results.This site can display upto 227 results.
Blood|January 7, 1998
Renal amyloidosis with a frame shift mutation in fibrinogen aalpha-chain gene producing a novel amyloid proteinL Hamidi Asl, J J Liepnieks, T Uemichi, et al.
Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis|April 22, 1999
Nomenclature of amyloid fibril proteins. Report from the meeting of the International Nomenclature Committee on Amyloidosis, August 8-9, 1998. Part 1P Westermark, S Araki, M D Benson, et al.
Journal of Neuropathology and Experimental Neurology|April 22, 2004
Intracellular ferritin accumulation in neural and extraneural tissue characterizes a neurodegenerative disease associated with a mutation in the ferritin light polypeptide geneR Vidal, B Ghetti, M Takao, 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.
The American Journal of Pathology|June 8, 2001
Prion proteins with different conformations accumulate in Gerstmann-Sträussler-Scheinker disease caused by A117V and F198S mutationsP Piccardo, J J Liepnieks, A William, et al.
European Journal of Neurology|April 29, 2020
Early data on long-term efficacy and safety of inotersen in patients with hereditary transthyretin amyloidosis: a 2-year update from the open-label extension of the NEURO-TTR trialT H Brannagan, A K Wang, T Coelho, et al.
Neurology|February 1, 1996
Familial and sporadic Alzheimer's disease: neuropathology cannot exclude a final common pathwayC F Lippa, A M Saunders, T W Smith, et al.
Pageof 23