Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Mohammed Abu-Ameerh"'
Publikováno v:
Journal of Ophthalmology, Vol 2023 (2023)
Purpose. To assess the relationship between diabetes mellitus (DM) and the presence of pinguecula and to identify other risk factors associated with pinguecula in patients attending the eye clinic at two tertiary university hospitals in Jordan. Metho
Externí odkaz:
https://doaj.org/article/ab90a6b6eb4b42499ef3290caf1522d5
Autor:
Saif Aldeen AlRyalat, Duha Atieh, Ayed AlHabashneh, Mariam Hassouneh, Rama Toukan, Renad Alawamleh, Taher Alshammari, Mohammed Abu-Ameerh
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
PurposeThis study aimed to assess preoperative predictors of visual outcome after phacoemulsification cataract surgery in Jordan, a Middle Eastern country.MethodsThis was a retrospective longitudinal study of adult patients who underwent phacoemulsif
Externí odkaz:
https://doaj.org/article/2bbb9ba745d1448fa598f7804aa69584
Autor:
Mohammed Abu‐Ameerh, Hashim Mohammad, Zain Dardas, Raghda Barham, Dema Ali, Maysa Bijawi, Mohamed Tawalbeh, Sami Amr, Ma'mon M. Hatmal, Muawyah Al‐Bdour, Abdalla Awidi, Belal Azab
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Abstract Background Inherited retinal dystrophies (IRDs) are characterized by extreme genetic and clinical heterogeneity. There are many genes that are known to cause IRD which makes the identification of the underlying genetic causes quite challengi
Externí odkaz:
https://doaj.org/article/52aa1d76770348c28ddef0fcb4d7fab1
Autor:
Saif Aldeen Alryalat, Mohammad Al-Antary, Yasmine Arafa, Babak Azad, Cornelia Boldyreff, Tasneem Ghnaimat, Nada Al-Antary, Safa Alfegi, Mutasem Elfalah, Mohammed Abu-Ameerh
Publikováno v:
Diagnostics, Vol 12, Iss 2, p 312 (2022)
Diabetic macular edema (DME) is the most common cause of visual impairment among patients with diabetes mellitus. Anti-vascular endothelial growth factors (Anti-VEGFs) are considered the first line in its management. The aim of this research has been
Externí odkaz:
https://doaj.org/article/db40b217d92141b0991423d9fe501500
Publikováno v:
Clinical Ophthalmology (Auckland, N.Z.)
Mohammed Abu-Ameerh, Ayat Alni’mat, Mo’ath AlShawabkeh, Saif Aldeen AlRyalat Ophthalmology Department, Jordan University Hospital, University of Jordan, Amman, JordanCorrespondence: Mo’ath AlShawabkehOphthalmology Department, Jordan University
Autor:
Mohammad Alsalem, Tareq Saleh, Sami S. Amr, Raghda Barham, Nidaa A. Ababneh, Mohammed Abu-Ameerh, Zain Dardas, Dunia Aburizeg, Abdalla Awidi, Hana Zouk, Bilal Azab, Ranad Maswadi, Muawyah D. Al-Bdour
Publikováno v:
Genes, Vol 12, Iss 593, p 593 (2021)
Genes
Volume 12
Issue 4
Genes
Volume 12
Issue 4
Whole Exome Sequencing (WES) is a powerful approach for detecting sequence variations in the human genome. The aim of this study was to investigate the genetic defects in Jordanian patients with inherited retinal dystrophies (IRDs) using WES. WES was
Autor:
Robert Rejdak, Yacoub A. Yousef, Mutasem Elfalah, Mo'ath AlShawabkeh, Sandrine Zweifel, Jehad Meqbil, Saif Aldeen AlRyalat, Amal Alwreikat, Muawyah D Al Bdour, Mario Damiano Toro, Maysa Al-Hussaini, Mohammed Abu-Ameerh, Osama H. Ababneh, Rashed Mustafa Nazzal, Almutez M. Gharaibeh, Zuhair Sharif
Publikováno v:
Clinical Ophthalmology, Vol Volume 15, Pp 661-669 (2021)
Clinical Ophthalmology (Auckland, N.Z.)
Clinical Ophthalmology (Auckland, N.Z.)
Mutasem Elfalah,1 Saif Aldeen AlRyalat,1 Mario Damiano Toro,2– 4 Robert Rejdak,4 Sandrine Zweifel,3 Rashed Nazzal,5 Mohammed Abu-Ameerh,1 Osama Ababneh,1 Almutez Gharaibeh,1 Zuhair Sharif,1 Jehad Meqbil,1 Mo’ath AlShawabkeh,1 Amal Alwreikat,6 Mua
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b6c947c94616f0fb5dbaf68044b367af
https://doi.org/10.5167/uzh-209866
https://doi.org/10.5167/uzh-209866
Autor:
Raghda Barham, Hashim Mohammad, Sami S. Amr, Abdalla Awidi, Dema Ali, Belal Azab, Mohammed Abu-Ameerh, Zain Dardas, Ma'mon M. Hatmal, Muawyah D. Al-Bdour, Mohamed Tawalbeh, Maysa Bijawi
Publikováno v:
Molecular Genetics & Genomic Medicine
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Molecular Genetics & Genomic Medicine, Vol 8, Iss 3, Pp n/a-n/a (2020)
Background Inherited retinal dystrophies (IRDs) are characterized by extreme genetic and clinical heterogeneity. There are many genes that are known to cause IRD which makes the identification of the underlying genetic causes quite challenging. And i
Autor:
Muawyah, Al-Bdour, Svenja, Pauleck, Zain, Dardas, Raghda, Barham, Dema, Ali, Sami, Amr, Lina, Mustafa, Mohammed, Abu-Ameerh, Ranad, Maswadi, Belal, Azab, Abdalla, Awidi
Publikováno v:
Molecular Vision
Purpose The aim of this study is to identify disease-causing variants in five consanguineous Jordanian families with a history of autosomal recessive retinitis pigmentosa (RP), and to investigate the clinical variability across the affected individua
Autor:
Muawyah D Al Bdour, Mohammed Abu-Ameerh, Ban Al-Kurdi, Mohammed M. Msallam, Abdelhalim Awidi, Hanan Jafar, Osama H. Ababneh, Abdalla Awidi, Dana Alhattab, Maram Hasan
Publikováno v:
International ophthalmology. 39(7)
To study the use of autologous platelet lysate prepared in a standardized method for the healing of persistent corneal epithelial defects (PED). Clinical and experimental investigation. In this prospective pilot study (ClinicalTrials.gov identifier N