Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Midhat, Salman"'
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Hearing loss affects around 5% of the global population. Two preliminary studies have described genetic variants in sporadic individuals with hearing loss from Pakistan. Here we extend these studies to determine the spectrum of variants in a
Externí odkaz:
https://doaj.org/article/499c4c6f5b40489a89432874fd06b5a1
Autor:
Marc Irqsusi, Azza Labene Mansouri, Anette Ramaswamy, Peter Rexin, Midhat Salman, Saqib Mahmood, Nikolas Mirow, Tamer Ghazi, Rabia Ramzan, Ardawan J. Rastan, Sebastian Vogt
Publikováno v:
Journal of Cardiac Surgery. 37:1613-1622
The pathogenesis of mitral valve insufficiency is not yet fully understood. Several studies stressed the role of matrix metalloproteinases (MMPs) in the emergence of valvular pathologies. The primary objective of the present study is to analyze the r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13f2612f79054d20df643df16ff97334
https://doi.org/10.1111/jocs.16449
https://doi.org/10.1111/jocs.16449
Autor:
Rizwan Yousaf, Botond Banfi, Christophe Philippe, Azeddine Ibrahimi, Zunaira Munir, Oumaima Zarrik, Sophie Nambot, Inna A. Belyantseva, Nara Sobreria, Rasheeda Basheer, Souad Kartti, Cristina Fenollar-Ferrer, Yoko Nakano, Ayesha Imtiaz, Hafiza Idrees, Antonio Vitobello, Sebastien Moutton, Midhat Salman, P. Dane Witmer, Risa Tona, Sadaf Naz, Rabia Faridi, Thomas B. Friedman, Memoona Ramzan
Publikováno v:
Hum Mutat
Hereditary deafness is clinically and genetically heterogeneous. We investigated deafness segregating as a recessive trait in two families. Audiological examinations revealed an asymmetric mild to profound hearing loss with childhood or adolescent on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f68564ce171b0955324ddf9020a429
https://doi.org/10.1002/humu.24260
https://doi.org/10.1002/humu.24260
Autor:
Naveed Akhtar Shad, Anam Munawar, Yasir Javed, Allah Rakha, Ahsan Riaz, Salah Ud Din, Iqra Zareef, Muhammad Munir Sajid, Muahmmad Farhan Khan, Sareen Akhtar, Midhat Salman
Publikováno v:
Analytica Chimica Acta. 1259:341204
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b197f14611611689cdedeb4c05eaf02e
https://doi.org/10.1016/j.aca.2023.341204
https://doi.org/10.1016/j.aca.2023.341204
Publikováno v:
Pakistan journal of pharmaceutical sciences. 35(1)
Coronavirus disease (COVID-19) pandemic has recently become a global health crisis. On the basis of this study the data reported from ten different countries on confirmed daily deaths caused by COVID-19. By fitting the linear regression models based
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::e74eb60d269c34f8ba03996132b43a0b
https://pubmed.ncbi.nlm.nih.gov/35221283
https://pubmed.ncbi.nlm.nih.gov/35221283
Autor:
Sadaf Naz, P. Dane Witmer, Midhat Salman, Memoona Ramzan, Ghulam Mujtaba, Nara Sobreira, Rasheeda Bashir
Publikováno v:
Scientific Reports
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Scientific Reports, Vol 10, Iss 1, Pp 1-7 (2020)
Hearing loss affects 380 million people worldwide due to environmental or genetic causes. Determining the cause of deafness in individuals without previous family history of hearing loss is challenging and has been relatively unexplored in Pakistan.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4b17a1435802bd4e6b07f89ad47342a
https://doi.org/10.1038/s41598-020-68779-5
https://doi.org/10.1038/s41598-020-68779-5
Autor:
Ayesha Imtiaz, Rasheeda Bashir, Midhat Salman, Muddassar Iqbal, Ghulam Mujtaba, Azra Maqsood, Sadaf Naz
Publikováno v:
European Archives of Oto-Rhino-Laryngology. 272:2071-2075
Mutations of GJB2 which encodes connexin 26, contribute to 6–7% of profound deafness in Pakistan. We investigated the involvement of GJB2 mutations in a cohort of 84 pedigrees and 86 sporadic individuals with moderate or severe hearing loss. Indivi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e53575fb1ee8a43baac250f9f73d3802
https://doi.org/10.1007/s00405-015-3523-y
https://doi.org/10.1007/s00405-015-3523-y