Zobrazeno 1 - 10
of 21
pro vyhledávání: '"Mohamed El Kalioby"'
Publikováno v:
Health Professions Education, Vol 2, Iss 1, Pp 44-50 (2016)
There are currently 22 public and 2 private medical schools in Egypt, which graduate around 10,000 physicians annually. While Kasr Al-Eini (Cairo University) is the oldest one; established in 1827, the Suez Canal Faculty of Medicine (FOM/SCU) is the
Externí odkaz:
https://doaj.org/article/ab0e718fe853463087912351ad83908e
Knowledge Improvement of Blood Transfusion Safety Among Pediatricians: Post Educational Intervention
Publikováno v:
Transfusion medicine reviews. 35(2)
Human factors account for most reported errors in the serious hazards of blood transfusion report, thus staff training on safe blood transfusion is strongly recommended. This study aimed to assess knowledge of blood transfusion safety among pediatric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a9bd5f1b363bb1e56987781cdb882446
https://pubmed.ncbi.nlm.nih.gov/33849745
https://pubmed.ncbi.nlm.nih.gov/33849745
Autor:
Tariq Faquih, Dorota Monies, Mohamed El-Kalioby, Ewa Goljan, Nada Al-Tassan, Mohamed Abouelhoda, Basma S. AlAbdulaziz, Khalid Al Abdelrahman, Shazia Subhani, Mohammad Shagrani, Jessica Burkholder, Fowzan S. Alkuraya, Nejat Mazhar, Dieter C. Broering, Renad Albar
Publikováno v:
Clinical Genetics. 92:52-61
Advanced cholestatic liver disease is a leading referral to pediatric liver transplant centers. Recent advances in the genetic classification of this group of disorders promise a highly personalized management although the genetic heterogeneity also
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c9807f652d4a4654100a5e6fdb6235d0
https://doi.org/10.1111/cge.12959
https://doi.org/10.1111/cge.12959
Publikováno v:
Health Professions Education, Vol 2, Iss 1, Pp 44-50 (2016)
There are currently 22 public and 2 private medical schools in Egypt, which graduate around 10,000 physicians annually. While Kasr Al-Eini (Cairo University) is the oldest one; established in 1827, the Suez Canal Faculty of Medicine (FOM/SCU) is the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5dfa62527844de4432df5d1e9164a0c
https://doi.org/10.1016/j.hpe.2016.01.007
https://doi.org/10.1016/j.hpe.2016.01.007
Autor:
Mohamed Abouelhoda, John A. Sayer, Maha Alnemer, Dorota Monies, Maha Tulbah, Nada Al-Tassan, Salma Majid, Haya Al-Jurayb, Ahmed Alahmed, Mamdouh Albaqumi, Brian F. Meyer, Nada Alsahan, Dania S. Khalil, Mohamed H Al-Hamed, Basma Al Abdulaziz, Faisal S. BinHumaid, Rania Abudraz, Wesam Kurdi, Mohamed El-Kalioby, Noel Edwards, Asma I. Tahir, Zainab Alabdullah, Rubina Khan, Tariq Faquih
Publikováno v:
Journal of Medical Genetics
Background Inherited cystic kidney disorders are a common cause of end-stage renal disease. Over 50 ciliopathy genes, which encode proteins that influence the structure and function of the primary cilia, are implicated in cystic kidney disease. Metho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2f95f0d1dfcafd00aaf7b2bf67d7639
https://doi.org/10.1136/jmedgenet-2015-103469
https://doi.org/10.1136/jmedgenet-2015-103469
Autor:
Tariq Faquih, Shazia Subhani, Ashiq Anjum, Yasser Obaidallah Alnakhli, Mohamed Abouelhoda, Mohamed El-Kalioby, Moustafa Shokrof, Zeeshan Shah, Hussain Aljafar
Publikováno v:
Bioinformatics and Biomedical Engineering ISBN: 9783319787220
IWBBIO (1)
IWBBIO (1)
With the increasing adoption of next generation sequencing technology in the medical practice, there is an increasing demand for faster data processing to gain immediate insights from the patient’s genome. Due to the extensive amount of genomic inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::091a8b387803c18d9a0930b7ee67e54e
https://doi.org/10.1007/978-3-319-78723-7_35
https://doi.org/10.1007/978-3-319-78723-7_35
Autor:
Hesham Aldhalaan, Hana Akleh, Saeed Bohlega, Imaduddin Kanaan, Fathiya Al-Murshedi, Sarar Mohamed, Mohammed AlQuaiz, Mohammad Shagrani, Fahad A. Bashiri, Fowzan S. Alkuraya, Banan Al-Younes, Saif Alshahrani, Maha Alotaibi, Saeed Hassan, Amal Alqassmi, Farrukh Sheikh, Fahad I. Alsohaibani, Edward Cupler, Saad AlShahwan, Majid Alfadhel, Dalal K. Bubshait, Aziza Chedrawi, Hamad Al-Mojalli, Adila Al-Kindy, Amal Alhashem, Mohammad A. Al-Muhaizea, Shamshad Gulab, Khalid Alsaleem, Maisoon Almugbel, Dorota Monies, Faisal Abaalkhail, Ahmed S Alenizi, Suad Alyamani, Abeer Al-Saegh, Ayaz Shah, Dyala Jaroudi, Khalid S. Alqadi, Maha Alnemer, Tariq Faquih, Renad Albar, Khalid Al-Thihli, Heba Y. El Khashab, Sulaiman M. Al-Mayouf, Moayad El-Haj, Brian F. Meyer, Hasan Al-Dhekri, Ibraheem F. Abosoudah, Zuhair Rahbeeni, A. Al-Ghonaium, Alya Qari, Asma Akilan, Mohammed Al-Owain, Nabil Moghrabi, Hamoud Al-Mousa, Amira Oshi, Taghreed Shuaib, Maha Faden, M. Al-Sebayel, Maha Tulbah, Ali Al-Mehaidib, Shazia Subhani, Raashda A Sulaiman, Wesam Kurdi, Hisham Alkuraya, Abdulaziz Al-Saman, Abdullah Alshanbary, Saeed Al Tala, Mustafa A. Salih, Wajeeh Aldekhail, Mohamed El-Kalioby, Zeeshan Shah, Mohammed Zain Seidahmed, Zuhair N. Al-Hassnan, Yasser Sabr, Tahani Alqasim, Moeenaldeen Al-Sayed, Abdullah Alsonbul, Hussien Elsiesy, Rand Arnaout, Saad Alsaadoun, Muddathir H. Hamad, Brahim Tabarki, Sami Al-Hajjar, Randa Bassiouni, Maged H. Hussein, Dieter C. Broering, Soher Balkhy, Abdullah Tamim, Mohamed Abouelhoda, Talal Algoufi, Nawal Makhseed, Ewa Goljan, Turki M. Alkharfy, Talal A. Basha, Bandar K. Al Saud, Eissa Faqeih, Hamad Al-Zaidan, Laszlo Szonyi, Husam R. Kayyali, Habiba Sultana, Suzan Alhomadi, Hadeel Elbardisy, Omar Dabbagh, Wafa Eyaid, Fuad Al Mutairi, Sameena Khan, Mohamed Ibrahim Khalil
Publikováno v:
Human Genetics
In this study, we report the experience of the only reference clinical next-generation sequencing lab in Saudi Arabia with the first 1000 families who span a wide-range of suspected Mendelian phenotypes. A total of 1019 tests were performed in the pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78d7400f1ed91704112fd5669cc5c9c8
https://pubmed.ncbi.nlm.nih.gov/28600779
https://pubmed.ncbi.nlm.nih.gov/28600779
Autor:
Malak Alghamdi, Susan Alhumaidi, Saeed Altala, Mirna Assoum, Aziza Chedrawi, Moeen Al-Sayed, Hisham Aldhalaan, Suzan A AlKhater, M. Abouelhoda, Turki Alshareef, Maha Alotaibi, Khalid S. Alqadi, Alya Alkaff, Syed Ahmed, Musad Abu Khaled, Suad Al Yamani, Bassem Albeirouti, Ali Al-Mehaidib, Walaa Alshuaibi, Nawal Makhseed, Ghada M H Abdel-Salam, Ewa Goljan, Zuhair Rahbeeni, Maisoon Almugbel, Shaza Makki, Ranad Albar, Fuad Al Mutairi, Khalid Alsaleem, Hanaa Banjar, Fahad A. Bashiri, Abdulaziz Bin Manee, Mona Alsaleh, Marwan Shaheen, Mohammed Fawzy, Sami Wali, Fahad Almohareb, Hisham Alkuraya, Shakir Bahzad, Ayman Shawli, Wesam Kurdi, Wajeeh Aldekhail, Somaya Alzelaye, Rand Arnaout, Abdullah Alsonbul, Sami Al-Hajjar, Saeed Hassan, Sameena Khan, Mohammed AlBalwi, Khalid Awartani, Sulaiman M. Al-Mayouf, Amal Alhashem, Hamoud Al-Mousa, Abdulaziz Alsemari, Hadeel Elbardisy, Mohamed El-Kalioby, Edward Cupler, Bandar Al-Saud, Hadeel Alghamdi, Isam Salih, Saadeh Sermin, Fahad Alsohaibaini, Shapar Nahrir, Hibah Alruwaili, Hamad Al-Zaidan, Nada Alsahan, Abdullah Alfaifi, Dalal K. Bubshait, Mohammed Nasr, Ahmed Alnahari, Ameen Tajuddin, Maged H. Hussein, Muddathir H Hamad, Asma Akilan, Afaf Alsagheir, Dorota Monies, Shamsad Shahrukh, Emadia Alaki, Tariq Abalkhail, Ahmed Sahly, Hamsa T. Tayeb, Badi Alenazi, Fowzan S. Alkuraya, Mohammed Al-Owain, Mohammed Abanemai, Ali Al-Ahmari, Maha Faden, Neama Meriki, Amal Alqasmi, Talal A. Basha, Hatem Murad, Hanna Akleh, Nabil Moghrabi, Asma I. Tahir, Abdulhadi Altalhi, Amal Jaafar, Ola Jarrad, Salah Baz, Abdullah Tamim, Ibraheem F. Abosoudah, Shazia Subhani, Manal Badawi, Raashida Sulaiman, Essam Al-Sabban, Brian F. Meyer, Talal Algoufi, Alya Qari, Mohammed Mahnashi, Hasan Al-Dhekri, Saeed Bohlega, Rafiullah Rafiullah, Naif A.M. Almontashiri, Mustafa A. Salih, Shahrukh K. Hashmi, Ibrahim Ghemlas, Zeeshan Shah, Abdullah Alashwal, Ehab Tous
Publikováno v:
The American Journal of Human Genetics. 105:879
We report the results of clinical exome sequencing (CES) on >2,200 previously unpublished Saudi families as a first-tier test. The predominance of autosomal-recessive causes allowed us to make several key observations. We highlight 155 genes that we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0365855d2d5af752e8f99d9baffcda1e
https://doi.org/10.1016/j.ajhg.2019.09.019
https://doi.org/10.1016/j.ajhg.2019.09.019
Autor:
Samhaa R. El-Beltagy, Ahmed Gamal, Sourya Ezzat, Moustafa Ghanem, Heba Ezzat, Mohmmed Aboelhouda, Mohamed El-Kalioby, Shady Issa
Publikováno v:
International Journal of Computer Applications. 67:21-28
This paper describes an approach taken to analyze and categorize a sizable dataset of politically oriented posts that were submitted to a popular idea bank, Egypt 2.0, created following the Egyptian revolution. The aim of the analysis was to organize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3eac0b16bac839dc97b6cfdcb446d081
https://doi.org/10.5120/11399-6712
https://doi.org/10.5120/11399-6712
Publikováno v:
Genome Biology
Background The pathogenicity of many Mendelian variants has been challenged by large-scale sequencing efforts. However, many rare and benign “disease mutations” are difficult to analyze due to their rarity. The Saudi Arabian variome is enriched f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3dbbf9c4dc9b94806958e3d4e54545fc
http://europepmc.org/articles/PMC5123336
http://europepmc.org/articles/PMC5123336