Osteogenesis imperfecta

Autor: Justin Easow Sam, Mala Dharmalingam

Publikováno v: Indian Journal of Endocrinology and Metabolism, Vol 21, Iss 6, Pp 903-908 (2017)

Osteogenesis imperfecta is a common heritable connective tissue disorder. Nearly ninety percent are due to Type I collagen mutations. Type I-IV are autosomal dominant, and Type VI–XIII are autosomal recessive. They are Graded 1-5 based on severity.

Externí odkaz: https://doaj.org/article/17bcdcbc8c05423ebe9f3ee5d32b0c28

Serum CCL 18 levels in women with polycystic ovarian syndrome

Autor: Mala Dharmalingam, K M Suryanarayana, Chitra Selvan, Pramila Kalra, Justin Easow Sam

Publikováno v: Indian Journal of Endocrinology and Metabolism
Indian Journal of Endocrinology and Metabolism, Vol 24, Iss 3, Pp 280-285 (2020)

Background: Polycystic ovarian syndrome (PCOS) is one of the most common metabolic disorders seen in women of the reproductive age group, with the majority of them having insulin resistance. There is a need to identify sensitive markers of insulin re

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9e8a0328a076ec78d7ac55616f7df4d
https://doi.org/10.4103/ijem.ijem_650_19