Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Shakeel Ahmed Sheikh"'
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:
Muhammad Yaqoob Shahani, Samreen Memon, Shakeel Ahmed Sheikh, Umbreen Bano, Pashmina Shaikh, Samina Gul Memon, Shazia Begum Shahani, Ikram din Ujjan, Ashok Kumar Narsani, Ali Muhammad Waryah
Publikováno v:
Saudi journal of biological sciences. 30(1)
Glaucoma is a neurodegenerative ophthalmic disorder and is considered among the leading causes of irreversible blindness. Primary open-angle glaucoma (POAG) is the most common type of glaucoma that affects after 30 years of life, progressing slowly,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20ad14f8b1b9c4c7f59f4b5433ce6e3c
https://pubmed.ncbi.nlm.nih.gov/36387029
https://pubmed.ncbi.nlm.nih.gov/36387029
Autor:
Priya, Jarwar, Shakeel Ahmed, Sheikh, Yar Muhammad, Waryah, Ikram Uddin, Ujjan, Saima, Riazuddin, Ali Muhammad, Waryah, Zubair M, Ahmed
Publikováno v:
International Journal of Molecular Sciences
Hereditary congenital cataract (HCC) is clinically and genetically heterogeneous. We investigated HCC that segregates in three inbred families (LUCC03, LUCC16, and LUCC24). Ophthalmological examinations revealed cataracts with variability related to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::04ed2a75c7e3ed72da216e8f771e9b4b
https://pubmed.ncbi.nlm.nih.gov/34638995
https://pubmed.ncbi.nlm.nih.gov/34638995
Autor:
Shakeel Ahmed Sheikh, Ali Muhammad Waryah, Saima Riazuddin, Priya Jarwar, Zubair M. Ahmed, Ikram Uddin Ujjan, Yar M. Waryah
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 10655, p 10655 (2021)
Hereditary congenital cataract (HCC) is clinically and genetically heterogeneous. We investigated HCC that segregates in three inbred families (LUCC03, LUCC16, and LUCC24). Ophthalmological examinations revealed cataracts with variability related to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd24e28168fe6a2a1e12eb76098c3383
https://www.mdpi.com/1422-0067/22/19/10655
https://www.mdpi.com/1422-0067/22/19/10655
Autor:
Attiq Ur Rahman, Muhammad Iqbal, Yar M. Waryah, Ashok Kumar Narsani, Shakeel Ahmed Sheikh, Ali Muhammad Waryah, Muhammad Azhar Baig, Munir Ahmad Bhinder, Muhammad Suleman Pirzado, Azam Iqbal Memon, Muhammad Atif
Publikováno v:
International Journal of Ophthalmology, Vol 12, Iss 1, Pp 8-15 (2019)
International Journal of Ophthalmology, Vol 1, Iss 12, Pp 8-15 (2019)
International Journal of Ophthalmology, Vol 1, Iss 12, 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. Detailed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f72e2f55b9592672fefac3db646653d9
http://www.ijo.cn/en_publish/2019/1/20190102.pdf
http://www.ijo.cn/en_publish/2019/1/20190102.pdf
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. 12(1)
To find theAfter getting informed consent, 11 consanguineous pedigrees belonging to different ethnic groups were enrolled. Detailed medical history was recorded and pedigrees were drawn. The standard ophthalmological examination was done to character
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f861f1b7976b2183334e9209d3b916c4
https://pubmed.ncbi.nlm.nih.gov/30662834
https://pubmed.ncbi.nlm.nih.gov/30662834
Autor:
Shakeel Ahmed Sheikh, Robert A. Sisk, Saima Riazuddin, David H. W. Steel, Robert B. Hufnagel, Zubair M. Ahmed, Cara R. Schiavon, John A. Sayer, Ali Muhammad Waryah, Muhammad A. Usmani, Richard A. Kahn, Ashok Kumar Narsani, Yar M. Waryah
Publikováno v:
Investigative Ophthalmology & Visual Science
Purpose Cone rod dystrophy (CRD) is a group of inherited retinopathies characterized by the loss of cone and rod photoreceptor cells, which results in poor vision. This study aims to clinically and genetically characterize the segregating CRD phenoty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a426528caaba6753bc691b858bff3569
https://doi.org/10.1167/iovs.19-27263
https://doi.org/10.1167/iovs.19-27263