Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Monu Rani"'
Publikováno v:
Indian Journal of Endocrinology and Metabolism, Vol 25, Iss 3, Pp 247-251 (2021)
Context: The delayed growth of a child is a major cause of concern for the parents. There is a multitude of etiological factors which must be considered in relation to this common aspect of healthcare. Aim: The study was done to evaluate the etiologi
Externí odkaz:
https://doaj.org/article/71d28332db4c40c2bed29e0b3d6fcd0d
Publikováno v:
Diabetes & Metabolic Syndrome: Clinical Research & Reviews. 15:823-827
Background and aims Previous studies suggest that body composition and handgrip strength are significantly altered in individuals with type 2 diabetes mellitus. Only few studies are available in prediabetic individuals. The aim is to study the change
Publikováno v:
Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism, Vol 25, Iss 3, Pp 247-251 (2021)
Indian Journal of Endocrinology and Metabolism, Vol 25, Iss 3, Pp 247-251 (2021)
Context: The delayed growth of a child is a major cause of concern for the parents. There is a multitude of etiological factors which must be considered in relation to this common aspect of healthcare. Aim: The study was done to evaluate the etiologi
Publikováno v:
BMJ Case Rep
A 44-year-old woman, known case of type 2 diabetes mellitus with poor glycaemic control (glycated haemoglobin 10.8%), was hospitalised for continuous glucose monitoring (CGM). On enquiring retrospectively during her hospital stay, she also reported a
Publikováno v:
BMJ Case Rep
A 41-year-old man presented with vomiting and loose stools. He had a history of long-term intermittent fever, generalised skin hyperpigmentation, dragging sensation in the left hypochondrium and unintentional weight loss. He was receiving combination
Publikováno v:
BMJ Case Rep
Non-compaction of ventricular myocardium is a rare cardiomyopathy involving an early arrest of normal compaction of myocardium during fetal ontogenesis. Autosomal dominant polycystic kidney disease (ADPKD) is a hereditary nephropathy characterised by
Publikováno v:
International Journal of Engineering Trends and Technology. 12:265-267