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Nisha Patel

Showing results (161-170 of 200) with videos related to

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American Journal of Human Genetics|June 3, 2017
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and HypomyelinationViorica Chelban, Nisha Patel, Jana Vandrovcova, et al.
HIV Medicine|January 12, 2024
Clinical epidemiology of COVID-19 in people of black ethnicity living with HIV in the UKZoe Ottaway, Lucy Campbell, Laura R Cechin, et al.
The Journal of Allergy and Clinical Immunology. in Practice|June 12, 2025
Incidence and Mortality Indicate Sex Differences in Chronic Rhinosinusitis with Nasal PolyposisMichael D'Netto, Alex iAkushev, Phillip Link, et al.
Dermatitis : Contact, Atopic, Occupational, Drug|May 19, 2023
Patch Testing With Cobalt in Adults: A North American Contact Dermatitis Group Experience, 2001-2018Jonathan Ian Silverberg, Nisha Patel, Erin M Warshaw, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|April 8, 2021
Returning to Growth: One Academic Medical Center's Successful Five-Step Approach to Change ManagementSelwyn M Vickers, Anupam Agarwal, Nisha Patel, et al.
Journal of the American Academy of Dermatology|August 8, 2022
Hand and foot dermatitis in patients referred for patch testing: Analysis of North American Contact Dermatitis Group Data, 2001-2018Jonathan I Silverberg, Nisha Patel, Erin M Warshaw, et al.
Contact Dermatitis|July 8, 2022
Patch testing with cobalt in children and adolescents: North American contact dermatitis group experience, 2001-2018Jonathan I Silverberg, Nisha Patel, Erin M Warshaw, et al.
Hepatology (Baltimore, Md.)|October 10, 2019
Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in HumansRanad Shaheen, Saud Alsahli, Nour Ewida, et al.
American Journal of Medical Genetics. Part A|March 30, 2021
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndromeClara C Hildebrandt, Nisha Patel, John M Graham, et al.
Human Genetics|November 24, 2016
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataractNisha Patel, Deepti Anand, Dorota Monies, et al.
Pageof 20

Showing results (161-170 of 200) with videos related to

Sort By:
Pageof 20
American Journal of Human Genetics|June 3, 2017
Mutations in NKX6-2 Cause Progressive Spastic Ataxia and HypomyelinationViorica Chelban, Nisha Patel, Jana Vandrovcova, et al.
HIV Medicine|January 12, 2024
Clinical epidemiology of COVID-19 in people of black ethnicity living with HIV in the UKZoe Ottaway, Lucy Campbell, Laura R Cechin, et al.
The Journal of Allergy and Clinical Immunology. in Practice|June 12, 2025
Incidence and Mortality Indicate Sex Differences in Chronic Rhinosinusitis with Nasal PolyposisMichael D'Netto, Alex iAkushev, Phillip Link, et al.
Dermatitis : Contact, Atopic, Occupational, Drug|May 19, 2023
Patch Testing With Cobalt in Adults: A North American Contact Dermatitis Group Experience, 2001-2018Jonathan Ian Silverberg, Nisha Patel, Erin M Warshaw, et al.
Academic Medicine : Journal of the Association of American Medical Colleges|April 8, 2021
Returning to Growth: One Academic Medical Center's Successful Five-Step Approach to Change ManagementSelwyn M Vickers, Anupam Agarwal, Nisha Patel, et al.
Journal of the American Academy of Dermatology|August 8, 2022
Hand and foot dermatitis in patients referred for patch testing: Analysis of North American Contact Dermatitis Group Data, 2001-2018Jonathan I Silverberg, Nisha Patel, Erin M Warshaw, et al.
Contact Dermatitis|July 8, 2022
Patch testing with cobalt in children and adolescents: North American contact dermatitis group experience, 2001-2018Jonathan I Silverberg, Nisha Patel, Erin M Warshaw, et al.
Hepatology (Baltimore, Md.)|October 10, 2019
Biallelic Mutations in Tetratricopeptide Repeat Domain 26 (Intraflagellar Transport 56) Cause Severe Biliary Ciliopathy in HumansRanad Shaheen, Saud Alsahli, Nour Ewida, et al.
American Journal of Medical Genetics. Part A|March 30, 2021
Further delineation of van den Ende-Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndromeClara C Hildebrandt, Nisha Patel, John M Graham, et al.
Human Genetics|November 24, 2016
Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataractNisha Patel, Deepti Anand, Dorota Monies, et al.
Pageof 20