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P Shankar

Showing results (131-140 of 144) with videos related to

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American Journal of Medical Genetics. Part A|June 22, 2019
Costello syndrome: Clinical phenotype, genotype, and management guidelinesKaren W Gripp, Lindsey A Morse, Marni Axelrad, et al.
Molecular Genetics and Metabolism|June 23, 2015
Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatmentElsa G Shapiro, Igor Nestrasil, Kyle Rudser, et al.
Molecular Genetics and Metabolism|January 11, 2022
Quantitative brain MRI morphology in severe and attenuated forms of mucopolysaccharidosis type IVictor Kovac, Elsa G Shapiro, Kyle D Rudser, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 1, 2002
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS MEDICAL GUIDELINES FOR CLINICAL PRACTICE FOR THE EVALUATION AND TREATMENT OF HYPERTHYROIDISM AND HYPOTHYROIDISMH Jack Baskin, Rhoda H Cobin, Daniel S Duick, et al.
Microbial Pathogenesis|May 27, 2026
Surveillance of Equine Glanders in India (2019-2023): Prevalence Estimate, Risk Analysis and Future StrategyHarisankar Singha, K Shanmugasundaram, Punit Jhandai, et al.
Pediatric Neurology|November 5, 2021
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability SyndromeJacqueline L Steele, Michelle M Morrow, Harvey B Sarnat, et al.
American Journal of Human Genetics|June 5, 2021
Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of careDavid Dimmock, Sara Caylor, Bryce Waldman, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
First International Conference on RASopathies and Neurofibromatoses in Asia: Identification and advances of new therapeuticsKatherine A Rauen, Abeer Alsaegh, Shay Ben-Shachar, et al.
The New England Journal of Medicine|August 11, 2016
Treatment of Fabry's Disease with the Pharmacologic Chaperone MigalastatDominique P Germain, Derralynn A Hughes, Kathleen Nicholls, et al.
Journal of Medical Genetics|November 12, 2016
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT studyDerralynn A Hughes, Kathleen Nicholls, Suma P Shankar, et al.
Pageof 15

Showing results (131-140 of 144) with videos related to

Sort By:
Pageof 15
American Journal of Medical Genetics. Part A|June 22, 2019
Costello syndrome: Clinical phenotype, genotype, and management guidelinesKaren W Gripp, Lindsey A Morse, Marni Axelrad, et al.
Molecular Genetics and Metabolism|June 23, 2015
Neurocognition across the spectrum of mucopolysaccharidosis type I: Age, severity, and treatmentElsa G Shapiro, Igor Nestrasil, Kyle Rudser, et al.
Molecular Genetics and Metabolism|January 11, 2022
Quantitative brain MRI morphology in severe and attenuated forms of mucopolysaccharidosis type IVictor Kovac, Elsa G Shapiro, Kyle D Rudser, et al.
Endocrine Practice : Official Journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists|November 1, 2002
AMERICAN ASSOCIATION OF CLINICAL ENDOCRINOLOGISTS MEDICAL GUIDELINES FOR CLINICAL PRACTICE FOR THE EVALUATION AND TREATMENT OF HYPERTHYROIDISM AND HYPOTHYROIDISMH Jack Baskin, Rhoda H Cobin, Daniel S Duick, et al.
Microbial Pathogenesis|May 27, 2026
Surveillance of Equine Glanders in India (2019-2023): Prevalence Estimate, Risk Analysis and Future StrategyHarisankar Singha, K Shanmugasundaram, Punit Jhandai, et al.
Pediatric Neurology|November 5, 2021
Semaphorin-Plexin Signaling: From Axonal Guidance to a New X-Linked Intellectual Disability SyndromeJacqueline L Steele, Michelle M Morrow, Harvey B Sarnat, et al.
American Journal of Human Genetics|June 5, 2021
Project Baby Bear: Rapid precision care incorporating rWGS in 5 California children's hospitals demonstrates improved clinical outcomes and reduced costs of careDavid Dimmock, Sara Caylor, Bryce Waldman, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
First International Conference on RASopathies and Neurofibromatoses in Asia: Identification and advances of new therapeuticsKatherine A Rauen, Abeer Alsaegh, Shay Ben-Shachar, et al.
The New England Journal of Medicine|August 11, 2016
Treatment of Fabry's Disease with the Pharmacologic Chaperone MigalastatDominique P Germain, Derralynn A Hughes, Kathleen Nicholls, et al.
Journal of Medical Genetics|November 12, 2016
Oral pharmacological chaperone migalastat compared with enzyme replacement therapy in Fabry disease: 18-month results from the randomised phase III ATTRACT studyDerralynn A Hughes, Kathleen Nicholls, Suma P Shankar, et al.
Pageof 15