Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Sara H. El‐Dessouky"'
Autor:
Ola M. Eid, Maha M. Eid, Marwa Farid, Rania M. A. Abdel Kader, Rana Mahrous, Sara H. El-Dessouky
Publikováno v:
Journal of Genetic Engineering and Biotechnology, Vol 20, Iss 1, Pp 1-7 (2022)
Abstract Background The prenatal diagnosis of syndromes caused by chromosomal abnormality is a long-established part of obstetric care. Several DNA-based molecular approaches have provided rapid prenatal diagnosis of of cytogenomic abnormalities. MLP
Externí odkaz:
https://doaj.org/article/c83d0b82f769483691c477f6ced6b73c
Autor:
Manal M. Thomas, Heba Mostafa Ahmed, Sara H. El-Dessouky, Abeer Ramadan, Osama Ezzat Botrous, Mohamed S. Abdel-Hamid
Publikováno v:
Molecular Genetics and Genomics. 297:689-698
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::526170c157d4429ad343dacbc2c1b1c8
https://doi.org/10.1007/s00438-022-01877-3
https://doi.org/10.1007/s00438-022-01877-3
Autor:
Sahar Sabry, Sara H. El‐Dessouky, Sherif F. Abdel‐Ghafar, Ghada M H Abdel-Salam, Mohamed Abdelhamid
Publikováno v:
neurogenetics. 22:287-295
Fetal brain arrest is an extremely rare genetic disorder that was described in few patients and encompasses very unique findings of underdeveloped cerebral hemispheres in association with collapsed skull bones. Based on the recurrence among sibs, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ac05db8507db849d172a1dc1f0289b70
https://doi.org/10.1007/s10048-021-00665-2
https://doi.org/10.1007/s10048-021-00665-2
Autor:
Shaimaa Abdelshafi, Sherif Elsirgany, Nirvana AbdelHakim, Ahmed Khalil, Ahmad El-Sheikhah, Sherif Elanwary, Sara H. El‐Dessouky, Ahmed Okasha
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 258:437-442
Abstract objective To assess the accuracy of middle cerebral artery peak systolic velocity (MCA-PSV) in prediction of severe fetal anemia resulting from Red Cell Alloimmunization (Anti-D) in un-transfused and transfused fetuses. In addition to compar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f59b977991652528e0d924d07ee0b1f0
https://doi.org/10.1016/j.ejogrb.2021.01.046
https://doi.org/10.1016/j.ejogrb.2021.01.046
Publikováno v:
Donald School Journal of Ultrasound in Obstetrics and Gynecology. 14:231-236
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a16940ede6a791706cc332728d84962a
https://doi.org/10.5005/jp-journals-10009-1652
https://doi.org/10.5005/jp-journals-10009-1652
Autor:
Maha M. Eid, Samah M. Aboelsaud, Hassan M. Gaafar, Mona M. Aboulghar, Walaa H. Zidan, Rana Abdella, Mohamed I. Ateya, Rania M. Helal, Sara H. El‐Dessouky, Ghada M H Abdel-Salam, Marwa F. Sharaf, Ahmed Ezz Elarab
Publikováno v:
Prenatal Diagnosis. 40:565-576
Objective The objective of this study is to evaluate the prenatal diagnosis, postnatal characteristics, and the spectrum of associated findings in fetuses with holoprosencephaly (HPE). Methods Fetal neurosonograms, postnatal assessment, and chromosom
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eefdb82cc097156dabc66c69240ddcbe
https://doi.org/10.1002/pd.5649
https://doi.org/10.1002/pd.5649
Autor:
Manal M, Thomas, Heba Mostafa, Ahmed, Sara H, El-Dessouky, Abeer, Ramadan, Osama Ezzat, Botrous, Mohamed S, Abdel-Hamid
Publikováno v:
Molecular genetics and genomics : MGG. 297(3)
The aim of this study is to screen for variants in NPHS1 and NPHS2, in a cohort of Egyptian children with steroid-resistant nephrotic syndrome (SRNS)/focal segmental glomerulosclerosis (FSGS) and compare the prevalence of such variants among other et
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::5952b933d4b2987f599a6913683e89b8
https://pubmed.ncbi.nlm.nih.gov/35278126
https://pubmed.ncbi.nlm.nih.gov/35278126
Autor:
Mohamed Ehab, Hassan M. Gaafar, Mona M. Aboulghar, Mohamed Momtaz, Rasha Kamal, Sherif Elsirgany, Omaima Idris, Sahar S. Sheta, Ahmed El Sheikhah, Mohamed Abd-El-Kader, Alaa Ebrashy, Mohamed Elhodiby, Sara H. El‐Dessouky, S. Negm
Publikováno v:
Journal of Perinatal Medicine. 47:871-878
Objective To evaluate our ability in classifying the fetal heart as normal or abnormal during the 1st trimester scan through fetal cardiac examination and determining the best time for this examination. Methods This was a prospective study performed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f3079d6beeacb5e8c34bbd53dac4732d
https://doi.org/10.1515/jpm-2019-0222
https://doi.org/10.1515/jpm-2019-0222
Autor:
Mohamed S, Abdel-Hamid, Sahar, Sabry, Sherif F, Abdel-Ghafar, Sara H, El-Dessouky, Ghada M H, Abdel-Salam
Publikováno v:
Neurogenetics. 22(4)
Fetal brain arrest is an extremely rare genetic disorder that was described in few patients and encompasses very unique findings of underdeveloped cerebral hemispheres in association with collapsed skull bones. Based on the recurrence among sibs, an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::814b582ab53d444a38fc2892da063d45
https://pubmed.ncbi.nlm.nih.gov/34338917
https://pubmed.ncbi.nlm.nih.gov/34338917
Publikováno v:
Egyptian Journal of Medical Human Genetics. 21
Background Walker–Warburg syndrome (WWS) is a rare, lethal, genetically, and clinically heterogeneous congenital muscular dystrophy resulting from defective glycosylation of α-dystroglycan (α-DG) and is associated with both cranial and ocular mal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b212baae1d273e10311bc479378f3dcc
https://doi.org/10.1186/s43042-020-00093-1
https://doi.org/10.1186/s43042-020-00093-1