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The American Journal of Pathology
|
January 6, 2001
Biochemical characterization of a neuroserpin variant associated with hereditary dementia
M Yazaki, J J Liepnieks, J R Murrell, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)
P Piccardo, C Seiler, S R Dlouhy, et al.
Cell
|
November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
F Tagliavini, F Prelli, M Porro, et al.
Obstetrics and Gynecology
|
July 2, 2008
Two-year outcomes after sacrocolpopexy with and without burch to prevent stress urinary incontinence
Linda Brubaker, Ingrid Nygaard, Holly E Richter, et al.
Journal of Diabetes and Metabolic Disorders
|
November 21, 2022
Parental marital relationship satisfaction is associated with glycemic outcomes in children with type 1 diabetes
Lindsey A Loomba, Amy Hughes Lansing, Justine N Cortez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 13, 2026
Classification of tauopathies from human brain homogenates through salt-modulated tau amplification
Alessia Santambrogio, Michael A Metrick, Peifeng Xu, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 27, 2019
Understanding Hippocampal Development in Young Children With Autism Spectrum Disorder
Vanessa P Reinhardt, Ana-Maria Iosif, Lauren Libero, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1995
Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165
P Piccardo, B Ghetti, D W Dickson, et al.
Brain : a Journal of Neurology
|
September 9, 2010
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
Piero Parchi, Maura Cescatti, Silvio Notari, et al.
Clinical and Experimental Immunology
|
June 1, 1992
Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy
E Mariani, A Facchini, M C Honorati, et al.
Page
of 98
Search research articles
Search
Showing results (551-560 of 974) with videos related to
Sort By:
Page
of 98
The American Journal of Pathology
|
January 6, 2001
Biochemical characterization of a neuroserpin variant associated with hereditary dementia
M Yazaki, J J Liepnieks, J R Murrell, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1996
Proteinase-K-resistant prion protein isoforms in Gerstmann-Sträussler-Scheinker disease (Indiana kindred)
P Piccardo, C Seiler, S R Dlouhy, et al.
Cell
|
November 18, 1994
Amyloid fibrils in Gerstmann-Sträussler-Scheinker disease (Indiana and Swedish kindreds) express only PrP peptides encoded by the mutant allele
F Tagliavini, F Prelli, M Porro, et al.
Obstetrics and Gynecology
|
July 2, 2008
Two-year outcomes after sacrocolpopexy with and without burch to prevent stress urinary incontinence
Linda Brubaker, Ingrid Nygaard, Holly E Richter, et al.
Journal of Diabetes and Metabolic Disorders
|
November 21, 2022
Parental marital relationship satisfaction is associated with glycemic outcomes in children with type 1 diabetes
Lindsey A Loomba, Amy Hughes Lansing, Justine N Cortez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
February 13, 2026
Classification of tauopathies from human brain homogenates through salt-modulated tau amplification
Alessia Santambrogio, Michael A Metrick, Peifeng Xu, et al.
Journal of the American Academy of Child and Adolescent Psychiatry
|
August 27, 2019
Understanding Hippocampal Development in Young Children With Autism Spectrum Disorder
Vanessa P Reinhardt, Ana-Maria Iosif, Lauren Libero, et al.
Journal of Neuropathology and Experimental Neurology
|
November 1, 1995
Gerstmann-Sträussler-Scheinker disease (PRNP P102L): amyloid deposits are best recognized by antibodies directed to epitopes in PrP region 90-165
P Piccardo, B Ghetti, D W Dickson, et al.
Brain : a Journal of Neurology
|
September 9, 2010
Agent strain variation in human prion disease: insights from a molecular and pathological review of the National Institutes of Health series of experimentally transmitted disease
Piero Parchi, Maura Cescatti, Silvio Notari, et al.
Clinical and Experimental Immunology
|
June 1, 1992
Immune defects in families and patients with xeroderma pigmentosum and trichothiodystrophy
E Mariani, A Facchini, M C Honorati, et al.
Page
of 98