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of 6
pro vyhledávání: '"Muhammad Akram Shahzad"'
Autor:
Farzana Majeed, Atteaya Zaman, Saadia Moazzam, Muhammad Zeeshan Anwar, Muhammad Akram Shahzad, Momin Iqbal, Syed Irfan Raza
Publikováno v:
Journal of University Medical & Dental College, Vol 13, Iss 2 (2022)
BACKGROUND & OBJECTIVE: Leukocyte adhesion deficiency (LAD1) is an autosomal recessive type of inherited disorder caused by total or partial deficiency of CD18 expression. LAD1 is characterized by recurrent bacterial and fungal infections, in some ca
Externí odkaz:
https://doaj.org/article/66b04164b7e04046bb0b31f98b1595cf
Autor:
Rizwan Masud, Aiman Farogh Anjum, Muhammad Zeeshan Anwar, Wajahat Ullah Khan, Muhammad Akram Shahzad, Ghazala Jawwad
Publikováno v:
Chinese Journal of Physiology, Vol 64, Iss 6, Pp 298-305 (2021)
Cardiovascular disease (CVD) have multifactorial nature, and owing to their disparate etiological roots, it is difficult to ascertain exact determinants of CVD. In the current study, primary objective was to determine association of single nucleotide
Externí odkaz:
https://doaj.org/article/1d6caff5848e478ca924c4afb7dfaf57
Autor:
Muhammad Akram Shahzad, Madiha Riaz
The research is conducted on five regions and will have a significant contribution by proving the evidence that green finance has a considerable impact on environmental sustainability. Green finance is evaluated by variables including; GDP, investmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13ad8d4598ae37d6a0da90454f8ac1dd
Autor:
Syed Irfan Raza, Muhammad Zeeshan Anwar, Wasim Ahmad, Thashi Bharadwaj, Michael J. Bamshad, Abdul Nasir, Deborah A. Nickerson, Jenna L. Everard, Khurram Liaqat, Suzanne M. Leal, Muhammad Ansar, Isabelle Schrauwen, Anushree Acharya, Muhammad Akram Shahzad Khokhar
Publikováno v:
Journal of Human Genetics
J Hum Genet
J Hum Genet
Background Wolfram syndrome (WFS) is characterized by deafness, diabetes mellitus, and diabetes insipidus along with optic atrophy. WFS has an autosomal recessive mode of inheritance and is due to variants in WFS1 and CISD2. Methods We evaluated the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7f743556d951fb1805c7b3944e42f8b
http://europepmc.org/articles/PMC8472924
http://europepmc.org/articles/PMC8472924
Akademický článek
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Autor:
Acharya, Anushree, Raza, Syed Irfan, Anwar, Muhammad Zeeshan, Bharadwaj, Thashi, Liaqat, Khurram, Khokhar, Muhammad Akram Shahzad, Everard, Jenna L., Nasir, Abdul, Nickerson, Deborah A., Bamshad, Michael J., Ansar, Muhammad, Schrauwen, Isabelle, Ahmad, Wasim, Leal, Suzanne M.
Publikováno v:
Journal of Human Genetics; October 2021, Vol. 66 Issue: 10 p1019-1019, 1p