Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Haiba Kaul"'
Autor:
Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Publikováno v:
PLoS ONE, Vol 18, Iss 10, p e0293769 (2023)
[This corrects the article DOI: 10.1371/journal.pone.0273685.].
Externí odkaz:
https://doaj.org/article/755c42dba4ee478580e1d2f0c801034a
Autor:
Afia Iqbal, Shagufta Naz, Haiba Kaul, Saima Sharif, Aysha Khushbakht, Muhammad Asif Naeem, Mehwish Iqtedar, Afshan Kaleem, Sabika Firasat, Farkhanda Manzoor
Publikováno v:
PLoS ONE, Vol 17, Iss 8, p e0273685 (2022)
AimTo identify the molecular basis of Congenital Hereditary Endothelial Dystrophy CHED caused by mutations in SLC4A11, in the consanguineous Pakistani families.MethodsA total of 7 consanguineous families affected with Congenital Hereditary Endothelia
Externí odkaz:
https://doaj.org/article/e23ee688634546e4914ab0c4e27edc9c
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 6 (2021)
Objective: Intrahepatic Cholestasis of Pregnancy (ICP) is a rare pregnancy specific disorder. Genetic variants of ABCB4 gene increase ICP risk. This study was conducted to determine frequency of ICP cases presented at a tertiary care hospital in Rawa
Externí odkaz:
https://doaj.org/article/02302817aa214fb5ae7b48cd3af6fce3
Autor:
Xiaodong Jiao, Shahid Y Khan, Haiba Kaul, Tariq Butt, Muhammad Asif Naeem, Sheikh Riazuddin, J Fielding Hejtmancik, S Amer Riazuddin
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0225010 (2019)
PurposeTo investigate the genetic basis of autosomal recessive congenital cataracts (arCC) in a large consanguineous Pakistani family.MethodsAll participating members of family, PKCC074 underwent an ophthalmic examination. Slit-lamp photographs were
Externí odkaz:
https://doaj.org/article/94816b39b6e244aabe4e691174a06824
Autor:
Muhammad Shakil, Muhammad Ikram Ullah, Shabbir Hussain, Sabika Firasat, Saqib Mahmood, Haiba Kaul
Publikováno v:
International Journal of Ophthalmology, Vol 9, Iss 5, Pp 794-796 (2016)
Letter to the editor
Externí odkaz:
https://doaj.org/article/ee9960113eef4b15ab6facd860a2d9b7
Autor:
Bushra Irum, Shahid Y Khan, Muhammad Ali, Haiba Kaul, Firoz Kabir, Bushra Rauf, Fareeha Fatima, Raheela Nadeem, Arif O Khan, Saif Al Obaisi, Muhammad Asif Naeem, Idrees A Nasir, Shaheen N Khan, Tayyab Husnain, Sheikh Riazuddin, Javed Akram, Allen O Eghrari, S Amer Riazuddin
Publikováno v:
PLoS ONE, Vol 11, Iss 11, p e0162620 (2016)
To identify the molecular basis of non-syndromic autosomal recessive congenital cataracts (arCC) in a consanguineous family.All family members participating in the study received a comprehensive ophthalmic examination to determine their ocular phenot
Externí odkaz:
https://doaj.org/article/22aedd3823ee4215ad62eaf53586fee8
Autor:
Saira Bano, Muhammad Sheraz, Haiba Kaul, Khuzeema Tanveer, Zeenat Zafar, Sheikh Muhammad Azam, Shumaila Arif, Shoaib Hassan, Mm Khan
Publikováno v:
Pakistan Journal of Medical and Health Sciences. 16:413-416
Aim: Cancer incidence are rising but its prevalence in District Dera Ghazi is not available on government or private level. Therefore, it is difficult to deal with cancer about its statistics and specific type prevalence. Our study was aimed to find
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d60026a396cbe5665a1e01d4fd13c245
https://doi.org/10.53350/pjmhs20221611413
https://doi.org/10.53350/pjmhs20221611413
Publikováno v:
Pakistan Journal of Medical Sciences. 39
Objectives: Insulin like growth factor-1(IGF-1), is a modulator of immunity and inflammation, it promotes the anabolic role of growth hormone (GH) on bone and skeletal tissue. Genetic polymorphism in IGF-1 gene is reported to affect the transcription
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8b31569c2a7b2d4da8715b31d0d64550
https://doi.org/10.12669/pjms.39.3.6561
https://doi.org/10.12669/pjms.39.3.6561
Autor:
Ayesha Khush Bakht, Shagufta Naz, Muhammad Asif Naeem, Saima Sharif, Muhammad Qasim, Haiba Kaul, Sabika Firasat, Khajista Jabeen, Afia Iqbal
Background: Granular Corneal Dystrophy Type 2 (GCD2) is an inherited condition characterized by snowflake-shaped opacities in the cornea. The disorder is caused by mutations in the TGFBI gene, which encodes keratoepithelin. The objective of this stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0efb9bd2af686d8b3a2080fb2b07581
https://doi.org/10.21203/rs.3.rs-2713586/v1
https://doi.org/10.21203/rs.3.rs-2713586/v1
Publikováno v:
Proceedings of the Pakistan Academy of Sciences: B. Life and Environmental Sciences. 59:49-56
Endothelial Corneal Dystrophy (ECD) is, by definition, an endogenous degeneration that progresses slowly in the corneal endothelium as a result of genetic predisposition. A transverse study was conducted from September 2018 to June 2019, and the subj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::499f6d8038a798a7a1fe7cef48ef8fc0
https://doi.org/10.53560/ppasb(59-1)670
https://doi.org/10.53560/ppasb(59-1)670