Zobrazeno 1 - 10
of 157
pro vyhledávání: '"Kulvinder Kochar Kaur"'
Autor:
Kulvinder Kochar Kaur
Publikováno v:
Frontiers in Reproductive Health, Vol 5 (2023)
Externí odkaz:
https://doaj.org/article/c6f11d3aaaeb40cba865d2549a4ad2e0
Publikováno v:
Iberoamerican Journal of Medicine, Vol 2, Iss 2, Pp 110-123 (2020)
Since the outbreak of the novel Coronavirus in December 2019 in Wuhan China, this novel Coronavirus disease(COVID-19) has spread worldwide taking not only epidemic proportions but with its rapid spread world health organization(WHO) was forced to dec
Externí odkaz:
https://doaj.org/article/6346ef6206db4441a779e055416d1409
Publikováno v:
Acta Scientifci Nutritional Health. 7:17-20
Publikováno v:
Acta Scientific Women's Health. 5:24-30
Autor:
Kulvinder Kochar Kaur
Publikováno v:
Acta Scientific Cancer Biology. :07-14
Autor:
Kulvinder Kochar Kaur
Publikováno v:
Journal of Internal Medicine and Health Affairs. 1:01-06
Earlier we have reviewed regarding how patients of AN who present with primary/secondary hypothalamic amenorrhoea were markedly recalcitrant to any forms oftreatment besides deficiency in reward appreciation .Furthermore we concentrated on the pathop
Publikováno v:
Journal of Pharmacy and Nutrition Sciences. 12:35-53
Bile Acids (BAs) possess a considerably significant part in the form of emulsifiers in digestion besides absorption of dietary lipids. BAs represent amphiphilic molecules, that are primary metabolites formed from cholesterol by the aid of enzymes act
Autor:
Kulvinder Kochar Kaur
Publikováno v:
Endocrine System and Diabetes. 1:01-03
Objective- Premature ovarian insufficiency (POI) comprises of enhanced gonadotropins, specifically follicle stimulating hormone (FSH) and irregularity/ lack of menstruation inwomen< 40yrs of age.Having reviewed literatureearlier with a case report on
Autor:
Kulvinder Kochar Kaur
Publikováno v:
International Journal of Reproductive Research. 1:01-03
Congenital adrenal hyperplasia (CAH) represents a disorder that takes place secondary to the deficiency of the adrenal enzymes, most commonly 21 hydroxylases (21OH) along with the commonest autosomal recessive condition in humans. In case of milder n
Publikováno v:
Acta Scientifci Nutritional Health. :38-41