Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Ahmed Al-Maskari"'
Autor:
Ahmed Al-Maskari, MSc, Ghanima Al-Zaabi, BSc, Hafsa A. AL-Mamari, MD, Manar Al-mawali, MD, Sunil K. Nadar, MD
Publikováno v:
Journal of Taibah University Medical Sciences, Vol 19, Iss 1, Pp 28-34 (2024)
الملخص: أهداف البحث: ترتبط أمراض القلب والأوعية الدموية بتأثيرات نفسية كبيرة يمكن أن تكون لها تأثير سلبي على التوقعات طويلة الأجل. هدفت ه
Externí odkaz:
https://doaj.org/article/e3713ef3cc0742c1ab77b242fe77a1d3
Autor:
Vito Romano, Stephen Kaye, Gabriela Czanner, Luca Pagano, Esmaeil M Arbabi, Fadi Alfaqawi, Ahmed Al-Maskari
Publikováno v:
BMJ Open Ophthalmology, Vol 8, Iss Suppl 1 (2023)
Externí odkaz:
https://doaj.org/article/a568364015d24f8ca53073df3bcfd3d2
Autor:
Fadi Alfaqawi, Luca Pagano, Esmaeil M Arbabi, Vito Romano, Ahmed Al-Maskari, Gabriela Czanner, Stephen Kaye
Publikováno v:
Oral abstract presentation.
Publikováno v:
Journal of Hypertension. 41:e422
Autor:
Eamonn Sheridan, Graham R. Taylor, Joanne E. Morgan, Narcis Fernandez-Fuentes, Hussain Jafri, Ahmed Al-Maskari, Özlem Yenice, Colin A. Johnson, Clare V. Logan, Carmel Toomes, Nursel Elcioglu, Manir Ali, Yasmin Raashid, David A. Parry, Martin McKibbin, Chris F. Inglehearn, Kamron N. Khan, Moin Mohamed, Zakia Abdelhamed, James A. Poulter, Ian M. Carr
Publikováno v:
Human Molecular Genetics
The atonal homolog 7 (ATOH7) gene encodes a transcription factor involved in determining the fate of retinal progenitor cells and is particularly required for optic nerve and ganglion cell development. Using a combination of autozygosity mapping and
Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacity
Autor:
Chris F. Inglehearn, Martin McKibbin, Manir Ali, Eamonn Sheridan, Ahmed Al-Maskari, Carmel Toomes, Tehseen Sahi, Aine Rice, Clara V. Logan, Yasmin Raashid, James A. Poulter, Alex F. Markham, Salina Siddiqui, Colin A. Johnson, David A. Parry, Adam Booth, Moin Mohamed, Kamron N. Khan, Ian M. Carr, Hussain Jafri, Anwar Hashmi
Publikováno v:
Investigative ophthalmologyvisual science. 52(7)
To investigate whether three consanguineous families from the Punjab province of Pakistan, with affected members with recessively inherited congenital cataract microcornea with corneal opacity, are genetically homogeneous.An ophthalmic examination wa
Publikováno v:
Archives of Ophthalmology. 129:1506