Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Kantipuly A"'
Autor:
Kantipuly, Aditi, Pillai, Manju R., Shroff, Sujani, Khatiwala, Rakhee, Raman, Ganesh V., Krishnadas, S.R., Lee Robin, Alan, Ehrlich, Joshua R.
Publikováno v:
In American Journal of Ophthalmology September 2019 205:106-114
Autor:
Sakkubai Naidu, Siddharth Gupta, Joel I. Brenner, Genila Bibat, Gayane Yenokyan, Constance Smith-Hicks, Scott M. Myers, Jane E. Crosson, Abanti Sanyal, Aditi Kantipuly, Siddharth Srivastava
Publikováno v:
American Journal of Medical Genetics Part A. 173:1495-1501
Rett syndrome (RTT) is caused by MECP2 mutations, resulting in various neurological symptoms. Prolonged corrected QT interval (QTc) is also reported and is a speculated cause of sudden death in RTT. The purpose of this study was to correlate QTc in R
Autor:
Sujani Shroff, Aditi Kantipuly, Ganesh Raman, Manju R Pillai, Joshua R. Ehrlich, Subbiah. R. Krishnadas, Alan L. Robin, Rakhee Khatiwala
Publikováno v:
Am J Ophthalmol
PURPOSE To evaluate the demographic, clinical, and socioeconomic factors associated with variation in the quality of life (QOL) in caregivers of children with primary congenital glaucoma (PCG) in south India. DESIGN Cross-sectional survey. METHODS Ca
Publikováno v:
Sleep in Children with Neurodevelopmental Disabilities ISBN: 9783319984124
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95df24a73020cdf291cf11af3136eac2
https://doi.org/10.1007/978-3-319-98414-8_24
https://doi.org/10.1007/978-3-319-98414-8_24
Autor:
Pamela Melvin, Mia S. Terkowitz, Aditi Kantipuly, Diana Stern, Feng Shu Brennen, Jay R. Shapiro, Emily L. Germain-Lee
Publikováno v:
Pediatric Research. 79:489-495
There is strikingly limited information on linear growth and weight in the different types of osteogenesis imperfecta (OI). Here, we define growth patterns further with the intent of implementing appropriate adaptations proactively.We report cross-se
Autor:
Crosson, Jane, Srivastava, Siddharth, Bibat, Genila M., Gupta, Siddharth, Kantipuly, Aditi, Smith-Hicks, Constance, Myers, Scott M., Sanyal, Abanti, Yenokyan, Gayane, Brenner, Joel, Naidu, Sakkubai R.
Rett syndrome (RTT) is caused by MECP2 mutations, resulting in various neurological symptoms. Prolonged corrected QT interval (QTc) is also reported and is a speculated cause of sudden death in RTT. The purpose of this study was to correlate QTc in R
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0076e0e0b061688ad03ec6cb6dcbbb82
https://europepmc.org/articles/PMC5444992/
https://europepmc.org/articles/PMC5444992/
Akademický článek
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Autor:
Girish Hiremath, Aditi Kantipuly, Shilpa Hundalani, Jay R. Shapiro, Sakkubai Naidu, Charles A. Rohde, Theodore Yablonski, Genila Bibat, Michael V. Johnston, Mary E. Blue
Rett Syndrome (RTT) is an X-linked neurodevelopmental disorder caused by mutations in the MECP2 gene. In 49 female RTT children, ages 1.9–17 years, bone mass was assessed and correlated with clinical parameters and mutations involving the MECP2 gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f659335d4b92d455a197ad3d4a636cbf
https://europepmc.org/articles/PMC3074246/
https://europepmc.org/articles/PMC3074246/
Publikováno v:
Talanta. 37:491-517
This review is concerned mainly with the applications of chelating polymeric resins for the separation and concentration of trace metals from oceans, rivers, streams and other natural systems. Commercially available resins, specially prepared polymer