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Ashish Marwaha

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American Journal of Medical Genetics. Part A|February 28, 2022
Expansion of the neurodevelopmental phenotypic spectrum of CKAP2L-related Filippi syndrome to include an adolescent male with normal intellectXiao-Ru Yang, Ashish Marwaha
Journal of Obstetrics and Gynaecology of India|June 19, 2015
HELLP or Help: A Real ChallengeSushil Chawla, Ashish Marwaha, Raju Agarwal
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
Best Practices in Demographic Data Collection for Equity, Diversity, and Inclusion in Rare Disease Research: A Systematic ReviewIsraa Sinan, Molly Johnston, Ashish Marwaha
The Journal of Rheumatology|June 15, 2024
Autoinflammatory Diseases: A ReviewJason An, Ashish Marwaha, Ronald M Laxer
JCI Insight|February 28, 2017
Profiling of circulating microRNAs in children with recent onset of type 1 diabetesSuheda Erener, Ashish Marwaha, Rusung Tan, et al.
American Journal of Medical Genetics. Part A|February 8, 2021
The point-of-care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learningAshish Marwaha, David Chitayat, M Stephen Meyn, et al.
American Journal of Medical Genetics. Part A|March 25, 2020
Congenital hypothyroidism, cardiac defects, and pancreatic agenesis in an infant with GATA6 mutationNikhil Raghuram, Ashish Marwaha, Mary-Louise C Greer, et al.
The Journal of Dermatology|July 1, 2020
Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancyBrian R Earl, Marta Szybowska, Ashish Marwaha, et al.
Canadian Journal of Diabetes|November 10, 2025
General Population Screening for Type 1 Diabetes in Canada---CanScreenT1DPeter A Senior, Ashish Marwaha, Holly O Witteman, et al.
JIMD Reports|January 21, 2021
Two cases of carbonic anhydrase VA deficiency-An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcomeAshish Marwaha, Judy Ibrahim, Taylor Rice, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
American Journal of Medical Genetics. Part A|February 28, 2022
Expansion of the neurodevelopmental phenotypic spectrum of CKAP2L-related Filippi syndrome to include an adolescent male with normal intellectXiao-Ru Yang, Ashish Marwaha
Journal of Obstetrics and Gynaecology of India|June 19, 2015
HELLP or Help: A Real ChallengeSushil Chawla, Ashish Marwaha, Raju Agarwal
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 3, 2026
Best Practices in Demographic Data Collection for Equity, Diversity, and Inclusion in Rare Disease Research: A Systematic ReviewIsraa Sinan, Molly Johnston, Ashish Marwaha
The Journal of Rheumatology|June 15, 2024
Autoinflammatory Diseases: A ReviewJason An, Ashish Marwaha, Ronald M Laxer
JCI Insight|February 28, 2017
Profiling of circulating microRNAs in children with recent onset of type 1 diabetesSuheda Erener, Ashish Marwaha, Rusung Tan, et al.
American Journal of Medical Genetics. Part A|February 8, 2021
The point-of-care use of a facial phenotyping tool in the genetics clinic: Enhancing diagnosis and education with machine learningAshish Marwaha, David Chitayat, M Stephen Meyn, et al.
American Journal of Medical Genetics. Part A|March 25, 2020
Congenital hypothyroidism, cardiac defects, and pancreatic agenesis in an infant with GATA6 mutationNikhil Raghuram, Ashish Marwaha, Mary-Louise C Greer, et al.
The Journal of Dermatology|July 1, 2020
Epidermal growth factor receptor deficiency: Expanding the phenotype beyond infancyBrian R Earl, Marta Szybowska, Ashish Marwaha, et al.
Canadian Journal of Diabetes|November 10, 2025
General Population Screening for Type 1 Diabetes in Canada---CanScreenT1DPeter A Senior, Ashish Marwaha, Holly O Witteman, et al.
JIMD Reports|January 21, 2021
Two cases of carbonic anhydrase VA deficiency-An ultrarare metabolic decompensation syndrome presenting with hyperammonemia, lactic acidosis, ketonuria, and good clinical outcomeAshish Marwaha, Judy Ibrahim, Taylor Rice, et al.
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