Zobrazeno 1 - 10
of 55
pro vyhledávání: '"Engy A Ashaat"'
Autor:
Ammal M Metwally, Maysa S Nassar, Ebtissam M Salah El-Din, Ali M Abdallah, Zeinab Khadr, Marwa W Abouelnaga, Engy A Ashaat, Mostafa M El-Saied, Ahmed M Elwan, Randa I Bassiouni, Zeinab M Monir, Hala Y Badawy, Eman M Dewdar, Hazem M El-Hariri, Ahmed Aboulghate, Carine Hanna, Thanaa M Rabah, Amira Mohsen, Mona A Elabd
Publikováno v:
PLoS ONE, Vol 18, Iss 9, p e0287315 (2023)
AimThis study aimed to estimate the national prevalence of developmental delays (DDs) and their determinants among Egyptian children aged 6 to 12 years. Such estimation is a prerequisite step toward the application of Life Skill Education (LSE) progr
Externí odkaz:
https://doaj.org/article/4ebb322a098c4df1bc511650dc7bd474
Autor:
Samira Ismail, Manal M Thomas, Laila A Hosny, Engy A Ashaat, Neveen A Ashaat, Moushira E Zaki
Publikováno v:
Journal of Clinical and Diagnostic Research, Vol 13, Iss 5, Pp GC01-GC05 (2019)
Introduction: Achondroplasia (ACH) is a dominant autosomal genetic disorder. The patients present with disproportionate short stature with short limbs and normal size torso due to abnormal bone growth. Growth charts are important tools that reflect p
Externí odkaz:
https://doaj.org/article/73c5cdf14d16447296c15a921cdd8d2f
Autor:
Alaaeldin G. Fayez, Nora N. Esmaiel, Sohair M. Salem, Engy A. Ashaat, Sonia A. El-Saiedi, Mona O. El Ruby
Publikováno v:
The Egyptian Heart Journal, Vol 74, Iss 1, Pp 1-10 (2022)
Abstract Background Childhood dilated cardiomyopathy (CDCM) is the most common cardiomyopathy in children and it is risk factor to heart failure and sudden death. Most of the different etiologic factors which have been postulated to DCM are idiopathi
Externí odkaz:
https://doaj.org/article/78294392449e440f9e65ee669d4e1b76
Autor:
Alaaeldin G. Fayez, Nora N. Esmaiel, Engy A. Ashaat, Miral M. Refeat, Randa S. Lotfy, Haiam Abdel Raouf, Mona O. El Ruby
Publikováno v:
Journal of Taibah University Medical Sciences. 18:1244-1253
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5a5b5d4209566f53cac2dc79f0a9a9c0
https://doi.org/10.1016/j.jtumed.2023.04.006
https://doi.org/10.1016/j.jtumed.2023.04.006
Autor:
Amal M. Mohamed, Alaa K. Kamel, Maha M. Eid, Ola M. Eid, Mona Mekkawy, Shymaa H. Hussein, Maha S. Zaki, Samira Esmail, Hanan H. Afifi, Ghada Y. El‐Kamah, Ghada A. Otaify, Heba Ahmed El‐Awady, Aya Elaidy, Mahmoud Y. Essa, Mona El‐Ruby, Engy A. Ashaat, Saida A. Hammad, Inas Mazen, Ghada M. H. Abdel‐Salam, Mona Aglan, Samia Temtamy
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 11, Pp n/a-n/a (2021)
Abstract Background This study aimed to delineate the clinical phenotype of patients with 9p deletions, pinpoint the chromosomal breakpoints, and identify the critical region for trigonocephaly, which is a frequent finding in 9p terminal deletion. Me
Externí odkaz:
https://doaj.org/article/2bfe665e28c74ca3b3ab3b493e122b7b
Autor:
Azza K. Abdel Megeid, Miral M. Refeat, Engy A. Ashaat, Ghada El-Kamah, Sonia A. El-Saiedi, Mona M. Elfalaki, Mona O. El Ruby, Khalda S. Amr
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-1 (2022)
Externí odkaz:
https://doaj.org/article/bf19b7f959e24bafaa102528c90762f5
Autor:
Inas H. Mazen, Mona A. El-Gammal, Aya A. Elaidy, Ghada M. Anwar, Engy A. Ashaat, Sherif F. Abdel-Ghafar, Mohamed S. Abdel-Hamid
Publikováno v:
Molecular Genetics and Genomics. 298:919-929
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::73939af2e0b1fb7187bd3d56f404cee1
https://doi.org/10.1007/s00438-023-02025-1
https://doi.org/10.1007/s00438-023-02025-1
Autor:
Mona K. Mekkawy, Alaa K. Kamel, Manal M. Thomas, Engy A. Ashaat, Maha S. Zaki, Ola M. Eid, Samira Ismail, Saida A. Hammad, Hisham Megahed, Heba ElAwady, Khaled M. Refaat, Shymaa Hussien, Nivine Helmy, Sally G. Abd Allah, Amal M. Mohamed, Mona O. El Ruby
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Wolf–Hirschhorn syndrome (WHS) (OMIM 194190) is a multiple congenital anomalies/intellectual disability syndrome. It is caused by partial loss of genetic material from the distal portion of the short arm of chromosome. Methods W
Externí odkaz:
https://doaj.org/article/cfd0db8f10ef41f3ad524533549fc2ed
Autor:
Nesma M. Elaraby, Hoda A. Ahmed, Neveen A. Ashaat, Sameh Tawfik, Mahmoud K. H. Ahmed, Nehal F. Hassib, Engy A. Ashaat
Publikováno v:
Journal of Molecular Neuroscience. 72:2242-2251
Alopecia intellectual disability syndromes 4 (APMR4) is a very rare autosomal recessive condition caused by a mutation in the LSS gene present on chromosome 21. This syndrome has a clinical heterogeneity mainly exhibited with variable degrees of inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::819803bda1a4c6700f57ca9ca54c2e85
https://doi.org/10.1007/s12031-022-02074-y
https://doi.org/10.1007/s12031-022-02074-y
Autor:
Ammal M. Metwally, Ehab R. Abdel Raouf, Amal Elsaied, Engy A. Ashaat, Mostafa M. El-Saied, Ghada A. Abdel-Latif, Ebtissam M. Salah El-Din, Marwa M. El-Sonbaty, Adel F. Hashish, Nayra Sh. Mehanna, Saleh M. Al Swailem, Hanaa R. M. Attia, Walaa S. Mahmoud, Maie M. Naga, Asmaa M. Fathy, Nihad A. Ibrahim, Mohamed M. El-Sonbaty
Aim To investigate the effectiveness of a 90-day regular consumption of Dates fruit on alleviating autism severity symptoms in 131 Egyptian children aged 3–12 years with confirmed Autism spectrum disorder (ASD). The influence of the baseline and im
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22f1cfc6e2af8dbc49f5c11ab46e3254
https://doi.org/10.21203/rs.3.rs-2909141/v1
https://doi.org/10.21203/rs.3.rs-2909141/v1
