Zobrazeno 1 - 10
of 83
pro vyhledávání: '"Shibani, Kanungo"'
Publikováno v:
Physiologia, Vol 4, Iss 2, Pp 202-212 (2024)
Exercise physiology is the science that studies the processes of physical activity and their impact on the body. It usually requires a multidisciplinary approach with a team of experts because of the multiple physiological systems involved. At the ce
Externí odkaz:
https://doaj.org/article/881f51b60216496eb36005a7748a51ed
Autor:
Daniela V. Pinto Payares, Logan Spooner, Jennifer Vosters, Samantha Dominguez, Lauren Patrick, Ann Harris, Shibani Kanungo
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
IntroductionMitochondrial diseases are known inborn errors affecting energy metabolism and are as common as chronic diseases such as diabetes, affecting approximately 1 in 5,000 people. The role of mitochondrial diseases/dysfunction has been highligh
Externí odkaz:
https://doaj.org/article/bcc3ca16d5864e1dbbc5eb4398d16982
Publikováno v:
Kidney & Blood Pressure Research (2023)
Introduction: The use of race in estimation of glomerular filtration rate (eGFR) started a critical national conversation on numerous areas of medicine touched by racism; with a call for removal of race from calculation of eGFR. We scrutinized use of
Externí odkaz:
https://doaj.org/article/499a4f6ae20245c28464db4d37f68974
Publikováno v:
Endocrines, Vol 3, Iss 2, Pp 240-254 (2022)
Turner syndrome (TS) affects approximately 1 out of every 1500–2500 live female births, with clinical features including short stature, premature ovarian failure, dysmorphic features and other endocrine, skeletal, cardiovascular, renal, gastrointes
Externí odkaz:
https://doaj.org/article/c7bb0a9340af480a9f683a920b8976e1
Publikováno v:
Endocrines, Vol 3, Iss 1, Pp 107-114 (2022)
Two endocrine disorders, congenital hypothyroidism (CH) and congenital adrenal hyperplasia (CAH), when untreated, can have devastating, irreversible and fatal outcomes. Permanent cognitive impairment, growth failure and dysmorphic appearance are seen
Externí odkaz:
https://doaj.org/article/70f940d215314b6cb9f540d0e0a90c0a
Publikováno v:
Endocrines, Vol 3, Iss 1, Pp 115-126 (2022)
Congenital or monogenic hyperinsulinism (HI) is a group of rare genetic disorders characterized by dysregulated insulin secretion and is the most common cause of persistent hypoglycemia in children. Knowledge of normal glucose homeostasis allows for
Externí odkaz:
https://doaj.org/article/93ca5ae88a3943bd80627cd2285a2ed3
Publikováno v:
Kidney & Blood Pressure Research, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/3564809d7e354cc8bf63e8f41ca1c79a
Autor:
Martin B. Draznin, Shibani Kanungo
Publikováno v:
Endocrines, Vol 3, Iss 4, Pp 601-602 (2022)
The inception of pediatric endocrinology in the United States began little less than a century ago, but it has grown as a subspecialty field since the 1950s [...]
Externí odkaz:
https://doaj.org/article/e5400908b7b74434bb9ba65cb9fe2eca
A critical national conversation over the use of race in estimation of glomerular filtration rate (eGFR) was stimulated by medical students at the University of Washington over the past few years. They explored, with overdue scrutiny, the ways race i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e6d25297ed7410a6379a2721b3c69cfe
https://doi.org/10.1101/2022.05.25.22275472
https://doi.org/10.1101/2022.05.25.22275472
Publikováno v:
Appl Clin Inform
Background Advances in technology and access to expanded genetic testing have resulted in more children and adolescents receiving genetic testing for diagnostic and prognostic purposes. With increased adoption of the electronic health record (EHR), g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9bec5bb77b1291c55e814e575eb9d064
https://doi.org/10.1055/s-0040-1718753
https://doi.org/10.1055/s-0040-1718753