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Biochimica Et Biophysica Acta|June 4, 1999
Identification of a novel substitution in the constant region of a gene coding for an amyloidogenic kappa1 light chainJ Wally, G Kica, Y Zhang, et al.The Journal of Clinical Investigation|December 1, 1990
A point mutation in transthyretin increases affinity for thyroxine and produces euthyroid hyperthyroxinemiaA C Moses, H N Rosen, D E Moller, et al.Journal of the Neurological Sciences|July 12, 2014
Retrospective study of a TTR FAP cohort to modify NIS+7 for therapeutic trialsN Suanprasert, J L Berk, M D Benson, et al.Lancet (London, England)|September 18, 1993
Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseasesA M Saunders, K Schmader, J C Breitner, et al.Surgical Neurology|December 14, 1999
Cerebrovascular biomodelling: a technical noteP S D'Urso, R G Thompson, R L Atkinson, et al.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.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.Pageof 21