Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Varuni, Pragya"'
Publikováno v:
JK Science, Vol 26, Iss 3 (2024)
Mevalonate kinase deficiency (MKD) is an exceedingly rare autosomal recessive inborn metabolism error characterized by mutations in the MVK gene, leading to impaired synthesis of cholesterol and isoprenoids. Two case reports of MKD in South India, sh
Externí odkaz:
https://doaj.org/article/a18e14ff7bc44d42880c5f6662ad093c
Publikováno v:
JK Science, Vol 26, Iss 2 (2024)
Autoimmune inner ear disease (AIED) is a rare rheumatological cause of sensorineural hearing loss, accounting for less than 1% of worldwide hearing loss. It presents with rapidly progressive, unilateral or bilateral SNHL, often fluctuating. The progr
Externí odkaz:
https://doaj.org/article/9b73418cb96243ebb4a9be8a11ac108e
Autor:
Varuni, Pragya1 pragya05varuni@gmail.com, Mahabaleshwar, Mamadapur2, Neethu, Priya3, Subramanian, R.2
Publikováno v:
Romanian Journal of Rheumatology / Revista Romana de Reumatologie. 2024, Vol. 33 Issue 1, p59-62. 4p.
Autor:
Varuni Pragya, M Kishor
Publikováno v:
Digital Journal of Clinical Medicine. 4:78-85
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::de74ee2695e19c91ae8ba8add8a75c5f
https://doi.org/10.55691/2582-3868.1112
https://doi.org/10.55691/2582-3868.1112