Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Alya Alkaff"'
Autor:
Bandr Hafidh, Saeed Baradwan, Hassan M. Latifah, Abdulrahim Gari, Hussein Sabban, Hanin Hassan Abduljabbar, Afaf Tawfiq, Ghaidaa Farouk Hakeem, Alya Alkaff, Nabigah Alzawawi, Radiah Iskandarani, Kausar Khurshid, Kausar Aisha Syed, Ammar Y. Alkhiary, Ibtihal Abdulaziz Bukhari, Maha Al Baalharith, Ahmed Abu-Zaid
Publikováno v:
Therapeutic Advances in Urology, Vol 15 (2023)
Background: Carbon dioxide (CO 2 ) laser therapy is an emerging treatment for women with stress urinary incontinence (SUI). Objectives: To examine the efficacy of CO 2 laser therapy for management of SUI-related symptoms in women. Design: A systemati
Externí odkaz:
https://doaj.org/article/72d9f2bd78ad413b88753518f19b056a
Autor:
Elaf MohammedHameed Aljifri, Rawan Fahad Bazuhayr, Ruqiah Abdulwahab Alqurashi, Ahdab Hashim Alharbi, Osama A. Bawazir, Alya Alkaff, Hadeel H. Alwadie
Publikováno v:
Journal of Pediatric Surgery Case Reports, Vol 73, Iss , Pp 101994- (2021)
Introduction: Cystic hygroma are macrocystic benign lymphatic manifestations, developing around 6th gestational week. Treatment options include surgery with associatedcomplications, sclerotherapyusing bleomycin injections. Herein, the case presented
Externí odkaz:
https://doaj.org/article/e02e1836fca44d3089b7db50208c064f
Autor:
Saeed Baradwan, Bandr Hafidh, Hassan M. Latifah, Abdulrahim Gari, Hussein Sabban, Hanin Hassan Abduljabbar, Afaf Tawfiq, Ghaidaa Farouk Hakeem, Alya Alkaff, Rayan AlSghan, Majed Saeed Alshahrani, Ehab Badghish, Ahmed Abu-Zaid
Publikováno v:
European Journal of Obstetrics & Gynecology and Reproductive Biology. 276:82-91
To conduct a systematic review and meta-analysis of randomized controlled trials on the clinical efficacy and safety of prophylactic tranexamic acid (TXA) versus control (normal saline/no treatment) during myomectomy.Six databases were screened from
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9acd6afa355df2323b47d1571d3f96b5
https://doi.org/10.1016/j.ejogrb.2022.07.004
https://doi.org/10.1016/j.ejogrb.2022.07.004
Autor:
Alya Alkaff, Wafaa Eyaid, Nada Alsahan, Rubina Khan, Niema Meriki, Yasser Alsaber, Saeed Al Tala, Mohamed Zain Seidahmed, Fatima Almusafri, Firdous Abdulwahab, Fowzan S. Alkuraya, Tawfeg Ben-Omran, Mariam Al Mulla, Hanan E. Shamseldin, Zeneb A. Babay, Eissa Faqeih, Ahmed Kurdi, Elham Al Mardawi, Karen El-Akouri, Ola Khalifa, Ranad Shaheen, Wesam Kurdi, Nour Ewida, Sebahattin Cirak, Eman Alobeid, Alya Qari, Zuhair Rahbeeni, Matthias Pergande, Maha Alnemer, Maha Tulbah, Bahauddin Sallout, Tarfa Alshidi, Amal Alhashem, Niema Ibrahim, Mais Hashem
Publikováno v:
Genetics in Medicine. 20:420-427
PurposeThe application of genomic sequencing to investigate unexplained death during early human development, a form of lethality likely enriched for severe Mendelian disorders, has been limited.MethodsIn this study, we employed exome sequencing as a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82ac4675b661434f7cd7e50ac6fca273
https://doi.org/10.1038/gim.2017.111
https://doi.org/10.1038/gim.2017.111
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