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David Adams

Showing results (241-250 of 370) with videos related to

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Orphanet Journal of Rare Diseases|September 5, 2015
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose studyOle B Suhr, Teresa Coelho, Juan Buades, et al.
Journal of Medical Case Reports|August 14, 2017
Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case reportBenjamin Terrier, Magali Colombat, Caroline Beugnet, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|March 11, 2023
The Use of Artificial Intelligence Guidance for Rheumatic Heart Disease Screening by NovicesDaniel Peck, Joselyn Rwebembera, Doreen Nakagaayi, et al.
American Journal of Medical Genetics. Part A|December 10, 2015
MRI/MRS as a surrogate marker for clinical progression in GM1 gangliosidosisDebra S Regier, Hyuk Joon Kwon, Jean Johnston, et al.
European Journal of Neurology|September 4, 2024
Nonamyloidogenic TTR gene variants c.76G>A and c.337-18G>C are not associated with idiopathic small-fiber neuropathyCéline Konecki, Bruno Francou, Kenneth Chappell, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|January 7, 2005
Patient concerns about medical errors in emergency departmentsThomas E Burroughs, Amy D Waterman, Thomas H Gallagher, et al.
Research Square|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik Ganapathy, Sandra Donkervoort, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 22, 2017
A Novel <i>Pkhd1</i> Mutation Interacts with the Nonobese Diabetic Genetic Background To Cause Autoimmune CholangitisWenting Huang, Daniel B Rainbow, Yuehong Wu, et al.
Journal of Pathology Informatics|September 11, 2023
The Comparative Pathology Workbench: Interactive visual analytics for biomedical dataMichael N Wicks, Michael Glinka, Bill Hill, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 16, 2023
Pathological spectrum of hereditary transthyretin renal amyloidosis and clinicopathologic correlation: a French observational studyJulien Dang, Sophie Ferlicot, Micheline Misrahi, et al.
Pageof 37

Showing results (241-250 of 370) with videos related to

Sort By:
Pageof 37
Orphanet Journal of Rare Diseases|September 5, 2015
Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose studyOle B Suhr, Teresa Coelho, Juan Buades, et al.
Journal of Medical Case Reports|August 14, 2017
Vitreous amyloidosis with autonomic neuropathy of the digestive tract associated with a novel transthyretin p.Gly87Arg variant in a Bangladeshi patient: a case reportBenjamin Terrier, Magali Colombat, Caroline Beugnet, et al.
Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography|March 11, 2023
The Use of Artificial Intelligence Guidance for Rheumatic Heart Disease Screening by NovicesDaniel Peck, Joselyn Rwebembera, Doreen Nakagaayi, et al.
American Journal of Medical Genetics. Part A|December 10, 2015
MRI/MRS as a surrogate marker for clinical progression in GM1 gangliosidosisDebra S Regier, Hyuk Joon Kwon, Jean Johnston, et al.
European Journal of Neurology|September 4, 2024
Nonamyloidogenic TTR gene variants c.76G>A and c.337-18G>C are not associated with idiopathic small-fiber neuropathyCéline Konecki, Bruno Francou, Kenneth Chappell, et al.
Academic Emergency Medicine : Official Journal of the Society for Academic Emergency Medicine|January 7, 2005
Patient concerns about medical errors in emergency departmentsThomas E Burroughs, Amy D Waterman, Thomas H Gallagher, et al.
Research Square|February 6, 2026
Benchmarking RNA-seq Tools for Real-World Diagnostic ApplicationsSarah Silverstein, Kaushik Ganapathy, Sandra Donkervoort, et al.
Journal of Immunology (Baltimore, Md. : 1950)|November 22, 2017
A Novel <i>Pkhd1</i> Mutation Interacts with the Nonobese Diabetic Genetic Background To Cause Autoimmune CholangitisWenting Huang, Daniel B Rainbow, Yuehong Wu, et al.
Journal of Pathology Informatics|September 11, 2023
The Comparative Pathology Workbench: Interactive visual analytics for biomedical dataMichael N Wicks, Michael Glinka, Bill Hill, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 16, 2023
Pathological spectrum of hereditary transthyretin renal amyloidosis and clinicopathologic correlation: a French observational studyJulien Dang, Sophie Ferlicot, Micheline Misrahi, et al.
Pageof 37