Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Muawyah D Al-Bdour"'
Autor:
Diala Walid Abu-Hassan, Muawyah D Al-Bdour, Ibraheem Saleh, Mona Freihat, Mohammed El-Khateeb
Publikováno v:
Journal of Research in Medical Sciences, Vol 26, Iss 1, Pp 2-2 (2021)
Background: Hyperglycemia over-activates glucose reduction to sorbitol by aldose reductase (ALR) leading to osmoregulation disruption and cellular damage that cause diabetic complications. We investigated the association of C106T polymorphism of ALR2
Externí odkaz:
https://doaj.org/article/b56d8c3b5db24f388a80126c2d7bee15
Autor:
Hussam H. Alhawari, Yousef S. Khader, Hussein H. Alhawari, Amal F. Alomari, Hiba N. Abbasi, Muhannd S. El-Faouri, Muawyah D. Al Bdour
Publikováno v:
International Journal of Endocrinology, Vol 2018 (2018)
Purpose. The association between autoimmune diseases and keratoconus (KC) has been proposed based on previous retrospective studies and case reports. The aim of our study is to investigate whether KC is associated with autoimmune thyroid disease. Met
Externí odkaz:
https://doaj.org/article/2a4af0e4f0694554923ccd25bd9b2db2
Publikováno v:
Journal of Medical Biochemistry, Vol 40, Iss 3, Pp 302-309 (2021)
Journal of Medical Biochemistry
Journal of Medical Biochemistry
Angiotensin-converting enzyme (ACE) stimulates angiogenesis that leads to the development of diabetic retinopathy (DR). Alu repetitive elements in ACE gene increase the expression of this enzyme. We investigated the frequency of Alu repetitive elemen
Autor:
Hashem Al Hawamdeh, Khaled A Elubous, Aws Khanfar, Zuhair Sharif, Osama H. Ababneh, Muawyah D Al Bdour, Walid Sharif, Saif Aldeen AlRyalat, Mohammed A Abu-Rumaileh
Publikováno v:
Cureus
Introduction Few studies have highlighted the correlation between shoulder dislocation and keratoconus (KC). This study aimed to examine the association between KC and shoulder dislocation using patients with KC and matched controls. Methods This cro
Autor:
Muawyah D Al Bdour, Mohammed Abu Ameerha, Issa Jeris, Saif Aldeen AlRyalat, Taher Alshammari, Allaa Roto, Khaled A Elubous
Publikováno v:
Cureus
Purpose To identify environmental risk factors associated with the need for penetrating keratoplasty (PKP) (full-thickness corneal transplantation) in patients with keratoconus in a Middle Eastern country. Methods This is a retrospective case-control
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
Publikováno v:
Journal of Research in Medical Sciences : The Official Journal of Isfahan University of Medical Sciences
Journal of Research in Medical Sciences, Vol 26, Iss 1, Pp 2-2 (2021)
Journal of Research in Medical Sciences, Vol 26, Iss 1, Pp 2-2 (2021)
Background: Hyperglycemia over-activates glucose reduction to sorbitol by aldose reductase (ALR) leading to osmoregulation disruption and cellular damage that cause diabetic complications. We investigated the association of C106T polymorphism of ALR2
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
Publikováno v:
Madridge Journal of Ophthalmology. 2:17-21