Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Dunia Aburizeg"'
Autor:
Bilal Azab, Dunia Aburizeg, Sherin T. Shaaban, Weizhen Ji, Lina Mustafa, Nooredeen Jamal Isbeih, Amal Saleh Al-Akily, Hashim Mohammad, Lauren Jeffries, Mustafa Khokha, Saquib A. Lakhani, Iyad Al-Ammouri
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-14 (2024)
Abstract Pediatric cardiomyopathies are mostly attributed to variants in sarcomere-related genes. Unfortunately, the genetic architecture of pediatric cardiomyopathies has never been previously studied in Jordan. We sought to uncover the genetic land
Externí odkaz:
https://doaj.org/article/5f67b5f0f24440549110a09f99d7af09
Publikováno v:
Acta Dermato-Venereologica, Vol 104 (2024)
Abstract is missing (Short communication)
Externí odkaz:
https://doaj.org/article/8e009e16936747faa1b6fcb6c9dedd1c
Autor:
Eyad Altamimi, Omar Rabab’h, Dunia Aburizeg, Lynn Akasheh, Zain Dardas, Luma Srour, Heyam Awad, Bilal Azab
Publikováno v:
Journal of Applied Genetics. 64:71-80
Biliary atresia (BA) is a progressive inflammatory process of the biliary tree resulting in biliary obstruction. No single known genetic or environmental factor has been established to cause BA. Cystic fibrosis (CF) is a rare cause of neonatal choles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d211c0f2980bbc1f25b29691eee64ae5
https://doi.org/10.1007/s13353-022-00729-5
https://doi.org/10.1007/s13353-022-00729-5
Autor:
Mohamed Tawalbeh, Dunia Aburizeg, Bayan O. Abu Alragheb, Wala Sami Alaqrabawi, Zain Dardas, Luma Srour, Baraah Hatem Altarayra, Ayman A. Zayed, Zaid El Omari, Bilal Azab
Publikováno v:
Genes; Volume 13; Issue 12; Pages: 2192
SLC26A4 is one of the most common genes causing autosomal recessive non-syndromic sensorineural hearing loss (SNHL). It has been reported to cause Pendred Syndrome (PDS) and DFNB4 which is deafness with enlarged vestibular aqueduct (EVA). However, mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::048ef3a43e68b65e99a23143bfe56930
Autor:
Bilal, Azab, Omar, Rabab'h, Dunia, Aburizeg, Hashim, Mohammad, Zain, Dardas, Lina, Mustafa, Ruba A, Khasawneh, Heyam, Awad, Ma'mon M, Hatmal, Eyad, Altamimi
Publikováno v:
Genes. 13(6)
Niemann-Pick disease type C (NPC) is an autosomal recessive neurovisceral disease characterized by progressive neurodegeneration with variable involvement of multisystemic abnormalities. Crohn's disease (CD) is an inflammatory bowel disease (IBD) wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::ff8baa69acba828c32d59310be2e8a45
https://pubmed.ncbi.nlm.nih.gov/35741735
https://pubmed.ncbi.nlm.nih.gov/35741735
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87b8c313e9ffc9eb96661fbbf1320d9b
https://www.mdpi.com/2073-4425/12/4/593
https://www.mdpi.com/2073-4425/12/4/593