Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Khadim, Shah"'
Autor:
Muhammad Mushtaq, Khadim Shah, Yasir Rahman Khattak, Nouman Khattak, Hooria Farheen, Sabiha Akhtar
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 4 (2024)
Objectives: To evaluate patient satisfaction and its associated factors in teaching hospitals. Method: The cross-sectional, analytical study was conducted from September to December 2022 at three public-sector medical teaching hospitals in Peshawar
Externí odkaz:
https://doaj.org/article/8d0900673fb24bb489bce103a5c9b6c8
Autor:
Muhammad Suleman, Tanveer Ahmad, Khadim shah, Norah A. Albekairi, Abdulrahman Alshammari, Abbas Khan, Dong-Qing Wei, Hadi M. Yassine, Sergio Crovella
Publikováno v:
Frontiers in Pharmacology, Vol 14 (2024)
Amid the ongoing monkeypox outbreak, there is an urgent need for the rapid development of effective therapeutic interventions capable of countering the immune evasion mechanisms employed by the monkeypox virus (MPXV). The evasion strategy involves th
Externí odkaz:
https://doaj.org/article/9fc2a6ea185e47b5b825b7c3ef46099a
Autor:
Nobia Aziz, Mukhtar Ullah, Abdur Rashid, Zubair Hussain, Khadim Shah, Azeem Awan, Muhammad Khan, Inam Ullah, Atta Ur Rehman
Publikováno v:
BMC Ophthalmology, Vol 23, Iss 1, Pp 1-8 (2023)
Abstract Background Retinitis pigmentosa (RP) is one of the most frequent hereditary retinal diseases that often starts with night blindness and eventually leads to legal blindness. Our study aimed to identify the underlying genetic cause of autosoma
Externí odkaz:
https://doaj.org/article/41977b789d00439aa61bc62bf1401d23
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-7 (2022)
Abstract Background Pyruvate kinase deficiency is an exceptionally rare autosomal recessive Mendelian disorder caused by bi-allelic pathogenic variants in the PKLR gene. It is mainly characterized by chronic nonspherocytic hemolytic anemia though oth
Externí odkaz:
https://doaj.org/article/dfdc65dc8ba94f759ebc2f7638305139
Autor:
Ambreen Ijaz, Khadim Shah, Abdul Aziz, Fazal U Rehman, Yasir Ali, Abdul M Tareen, Kafaitullah Khan, Muhammad Ayub, Abdul Wali
Publikováno v:
Indian Journal of Dermatology, Vol 66, Iss 2, Pp 220-222 (2021)
Externí odkaz:
https://doaj.org/article/3113ae84996d41a79c0830042fc8a376
Autor:
Niamatullah Khan, Khadim Shah, Fozia Fozia, Sher A. Khan, Nazif Muhammad, Abdul Nasir, Ijaz Ahmad, Zia U. Rehman, Abid Jan, Noor Muhammad, Saadullah Khan
Publikováno v:
International Journal of Dermatology. 62:672-680
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21050aa90eb1a7f932b722dc68324468
https://doi.org/10.1111/ijd.16614
https://doi.org/10.1111/ijd.16614
Autor:
Isabelle Schrauwen, Imen Chakchouk, Anushree Acharya, Khurram Liaqat, Irfanullah, University of Washington Center for Mendelian Genomics, Deborah A. Nickerson, Michael J. Bamshad, Khadim Shah, Wasim Ahmad, Suzanne M. Leal
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-6 (2018)
Abstract Background Digenic inheritance is the simplest model of oligenic disease. It can be observed when there is a strong epistatic interaction between two loci. For both syndromic and non-syndromic hearing impairment, several forms of digenic inh
Externí odkaz:
https://doaj.org/article/52e6e3121d234ce98f2a04c42420beb7
Autor:
Anwar Kamal Khan, Noor Muhammad, Abdul Aziz, Sher Alam Khan, Khadim Shah, Abdul Nasir, Muzammil Ahmad Khan, Saadullah Khan
Publikováno v:
BMC Medical Genetics, Vol 18, Iss 1, Pp 1-5 (2017)
Abstract Background Pure hair and nail ectodermal dysplasia (PHNED) is a congenital disorder of hair abnormalities and nail dysplasia. Both autosomal recessive and dominant inheritance fashion of PHNED occurs. In literature, to date, five different f
Externí odkaz:
https://doaj.org/article/4fc45552136043dfaf8e2134b6e2f8e5
Autor:
Devin Seli, Katharine T. Ellis, Mohamad Goldust, Khadim Shah, Ronghua Hu, Jing Zhou, Jennifer M. McNiff, Keith A. Choate
Publikováno v:
JAMA Dermatology.
ImportanceGrover disease (GD), a truncal eruption that typically occurs in older individuals, is exacerbated by sweating, irradiation, cancers, medications, kidney failure, and organ transplantation. The pathobiology of GD remains unknown.ObjectiveTo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d374fd1543e5d4744f2ebd755d7bc7d
https://doi.org/10.1001/jamadermatol.2023.1139
https://doi.org/10.1001/jamadermatol.2023.1139
Publikováno v:
Water, Air, & Soil Pollution. 234
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2cd189b559edfe74e31ca20f5d8eb3bd
https://doi.org/10.1007/s11270-023-06134-w
https://doi.org/10.1007/s11270-023-06134-w