Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Muhammad Waryah A"'
Autor:
Yar Muhammad Waryah, Feriha Fatima Khidri, Amir Ansari, Samia Mehmood, Sumera Abbasi, Shabahat Memon
Publikováno v:
JLUMHS, Vol 23, Iss 3, Pp 249-253 (2024)
OBJECTIVE: To identify the disease-causing allele of retinitis pigmentosa, a heterogeneous genetic disorder in a single affected family. METHODOLOGY: A cross-sectional descriptive study was conducted at the Sindh Institute of Ophthalmology & Visual
Externí odkaz:
https://doaj.org/article/32d7c8ba52a449b9aa6230cb677e4396
Autor:
Waqas Ali Surhio, Feriha Fatima Khidri, Mohsin Iqbal Haroon, Samia Mehmood, Yar Muhammad Waryah
Publikováno v:
JLUMHS, Vol 23, Iss 2, Pp 140-145 (2024)
OBJECTIVE: To identify the pathogenic alleles in primary congenital glaucoma patients for early cure of the disease METHODOLOGY: A cross-sectional descriptive study was carried out after approval from the ethical committee of SIOVS from December 2022
Externí odkaz:
https://doaj.org/article/1dc1090a74b7470a8b2b2234a74cc355
Autor:
Tarachand Devrajani, Shariq Abid, Hina Shaikh, Iram Shaikh, Durshana Bai Devrajani, Sikander Munir Memon, Ali Muhammad Waryah, Ikram Din Ujjan, Binafsha Manzoor Syed
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-8 (2023)
Abstract Aging is considered one of the major risk factors for several human disorders. The telomere plays a crucial role in regulating cellular responsiveness to stress and growth stimuli as well as maintaining the integrity of the Deoxyribonucleic
Externí odkaz:
https://doaj.org/article/5b4464b0d78147dcafe5b59eb96c6200
Publikováno v:
JLUMHS, Vol 22, Iss 3, Pp 197-200 (2023)
OBJECTIVE: To investigate the role of the first line and additional confirmatory assay to detect coronavirus based on Ct RT-PCR values. METHODOLOGY: A collaborative cross-sectional study was conducted using a systematic sampling type at Hyderabad's d
Externí odkaz:
https://doaj.org/article/28b8182db99a469ea81721c42a95a2cd
Publikováno v:
Journal of the Pakistan Medical Association, Vol 74, Iss 1 (2023)
The objectives of this study were to determine the association of methylenetetrahydrofolate reductase (MTHFR) gene variant C677T with non-syndromic cleft lip/palate (NSCLP) in Pakistani population and compare the maternal serum folic acid levels in N
Externí odkaz:
https://doaj.org/article/03c8ce61f7f944f49a80105001c3d0bd
Publikováno v:
Journal of the Pakistan Medical Association, Vol 73, Iss 10 (2023)
Objectives: To determine the molecular characterisation of beta-thalassemia major patients, pattern of major endocrine complications and its association with haemoglobin subunit beta gene variants. Method: The cross-sectional study was conducted fr
Externí odkaz:
https://doaj.org/article/05cf4ba9a2884613b0967212e497424d
Publikováno v:
JLUMHS, Vol 20, Iss 1, Pp 07-11 (2021)
OBJECTIVE: This study was aimed to access the capability of total dose infusion iron therapy for maintaining the hemoglobin level in local pregnant women METHODOLOGY: A descriptive study was carried out by using non probability consecutive sampling
Externí odkaz:
https://doaj.org/article/55bc089af25949dc94cf4c105bffc472
Autor:
Feriha Fatima Khidri, Yar Muhammad Waryah, Faiza Kamran Ali, Hina Shaikh, Ikram Din Ujjan, Ali Muhammad Waryah
Publikováno v:
BMC Medical Genetics, Vol 20, Iss 1, Pp 1-12 (2019)
Abstract Background To study the role of single nucleotide variants (SNVs) of genes related to preeclampsia in Pakistani pregnant women. Methods After ethical approval and getting informed consent; 250 pregnant women were enrolled and equally divided
Externí odkaz:
https://doaj.org/article/2d389aaba3e547a6a0f7bdd5954cd483
Autor:
Yar Muhammad Waryah, Muhammad Iqbal, Shakeel Ahmed Sheikh, Muhammad Azhar Baig, Ashok Kumar Narsani, Muhammad Atif, Munir Ahmad Bhinder, Attiq Ur Rahman, Azam Iqbal Memon, Muhammad Suleman Pirzado, Ali Muhammad Waryah
Publikováno v:
International Journal of Ophthalmology, Vol 12, Iss 1, Pp 8-15 (2019)
AIM: To find the CYP1B1 mutations associated with primary congenital glaucoma (PCG) in Pakistani consanguineous pedigrees. METHODS: After getting informed consent, 11 consanguineous pedigrees belonging to different ethnic groups were enrolled. Detai
Externí odkaz:
https://doaj.org/article/b39b89094ce34229a4350776d51ce7d0
Autor:
Anosha Ali Khan, Yar Muhammad Waryah, Muhammad Iqbal, Hafiz Muhammad Azhar Baig, Muhammad Rafique, Ali Muhammad Waryah
Publikováno v:
Journal of the Pakistan Medical Association, Vol 71, Iss 3 (2020)
Aim: To explore the genetic cause of autosomal recessive retinitis pigmentosa in consanguineous families. Methods: The multi-centre study was conducted from July 2015 to June 2018 at Liaquat University of Medical and health Sciences, Jamshoro, the
Externí odkaz:
https://doaj.org/article/dd4e74d67bab45ffab42e5aa746b8c5e