Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Maryam Wahid"'
Autor:
Umar Saeed, Rawal Alies Insaf, Zahra Zahid Piracha, Muhammad Nouman Tariq, Azka Sohail, Umer Ali Abbasi, Muhammad Shahmeer Fida Rana, Syed Shayan Gilani, Seneen Noor, Elyeen Noor, Yasir Waheed, Maryam Wahid, Muzammil Hasan Najmi, Imran Fazal
Publikováno v:
Frontiers in Microbiology, Vol 14 (2023)
The efficacy of antibiotics and other antimicrobial agents in combating bacterial infections faces a grave peril in the form of antimicrobial resistance (AMR), an exceedingly pressing global health issue. The emergence and dissemination of drug-resis
Externí odkaz:
https://doaj.org/article/f9952e8dab0b404c8a118290493b2abc
Publikováno v:
Digital Photographer; 2021, Issue 241, p74-81, 8p, 10 Color Photographs
Autor:
Maryam Wahid
Publikováno v:
Journal of Rawalpindi Medical College, Vol 13, Iss 1 (2009)
Background:. A3243G mutation in tRNA Leu (UUR) leads to a specific clinical syndrome characterized by diabetes and sensorineural hearing defect, hence called as “Maternally Inherited Diabetes and Deafness (MIDD)”.. Methods: The study was retrospe
Externí odkaz:
https://doaj.org/article/e28090aab7c342d9bdd85cea8ff5efa6
Publikováno v:
JPMA. The Journal of the Pakistan Medical Association. 67(7)
To determine the association of interferon alpha receptor-1 with success rate of interferon therapy in patients co-infected with hepatitis C virus and hepatitis B virus.The study was conducted at the Army Medical College, Rawalpindi, Pakistan, from D
Autor:
Maryam, Wahid, Mohammad, Kamran
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 28(3)
Mitochondrial DNA mutation and hormonal imbalance is involved in the pathogenesis of early onset diabetes but data is lacking in Pakistani population. The study was planned to delineate the clinical presentation of early onset diabetes with possible
Autor:
Maryam Wahid
Publikováno v:
Anatomy Physiology & Biochemistry International Journal. 1
Publikováno v:
International Journal of Diabetes Mellitus. 1(1):11-15
Background and objectives Maternally Inherited Diabetes Mellitus and Deafness (MIDD) occurs due to the mutations in mitochondrial DNA (mtDNA). The most common heteroplasmic point mutation reported, is in the tRNA Leu(UUR) gene, i.e., A 3243 G , accom
Autor:
Maryam, Wahid, Abdul Khaliq, Naveed
Publikováno v:
Journal of Ayub Medical College, Abbottabad : JAMC. 25(1-2)
Diabetes mellitus is accompanied with drastic hormonal and metabolic alterations. In uncontrolled diabetes, these disturbances worsen the condition leading to development of life threatening complications. Present study was planned to compare hormona
Publikováno v:
Journal of the College of Physicians and Surgeons--Pakistan : JCPSP. 16(1)
To assess the role of insulin / glucagon ratio in pathophysiology of diabetic ketoacidosis and hyperosmolar hyperglycemic non-ketotic diabetes.Case control, analytical study.Military Hospital, Rawalpindi from September 2003 to August 2004.The study i
Autor:
Ward, Saffron
Publikováno v:
Aesthetica; Jun/Jul2023, Issue 113, p124-125, 2p, 1 Color Photograph