Fahad A Bashiri

Fahad A Bashiri

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Fahad A Bashiri

Fahad A Bashiri

Publications by authors named "Fahad A Bashiri"

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23Publications

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Hypokalemic periodic paralysis due to CACNA1S gene mutation.

Neurosciences (Riyadh) 2019 Jul;24(3):225-230

Division of Pediatric Nephrology, Pediatric Department, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2018.3.20180005DOI Listing
July 2019

Satisfaction and perceived usefulness with newly-implemented Electronic Health Records System among pediatricians at a university hospital.

Comput Methods Programs Biomed 2019 Feb 26;169:51-57. Epub 2018 Dec 26.

Pediatrics Department, College of Medicine, King Saud University, Riyadh, Saudi Arabia; Clinical Practice Guidelines Unit, Quality Management Department, King Saud University Medical City, Riyadh, Saudi Arabia; Research Chair for Evidence-Based Health Care and Knowledge Translation, King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1016/j.cmpb.2018.12.026DOI Listing
February 2019

Effect of new modalities of treatment on physicians management plan for patients with spinal muscular atrophy.

Neurosciences (Riyadh) 2019 Jan;24(1):16-21

Division of Neurology, Department of Pediatrics, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2019.1.20180321DOI Listing
January 2019

Assessment of physicians knowledge and attitudes in the management of febrile seizures.

Neurosciences (Riyadh) 2018 Oct;23(4):314-319

Division of Neurology, Department of Pediatrics, College of Medicine, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://dx.doi.org/10.17712/nsj.2018.4.20180097DOI Listing
October 2018

Respiratory support attitudes among pediatric intensive care staff for spinal muscular atrophy patients in Saudi Arabia.

Neurosciences (Riyadh) 2018 Jan;23(1):62-65

Pediatric Intensive Care Unit, Pediatric Department, King Khalid University Hospital, King Saud University, Riyadh, Kingdom of Saudi Arabia.

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http://www.neurosciencesjournal.org/PDFFiles/Jan18/11Respira
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http://dx.doi.org/10.17712/nsj.2018.1.20170103DOI Listing
January 2018

The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes.

Authors:
Dorota Monies Mohamed Abouelhoda Moeenaldeen AlSayed Zuhair Alhassnan Maha Alotaibi Husam Kayyali Mohammed Al-Owain Ayaz Shah Zuhair Rahbeeni Mohammad A Al-Muhaizea Hamad I Alzaidan Edward Cupler Saeed Bohlega Eissa Faqeih Maha Faden Banan Alyounes Dyala Jaroudi Ewa Goljan Hadeel Elbardisy Asma Akilan Renad Albar Hesham Aldhalaan Shamshad Gulab Aziza Chedrawi Bandar K Al Saud Wesam Kurdi Nawal Makhseed Tahani Alqasim Heba Y El Khashab Hamoud Al-Mousa Amal Alhashem Imaduddin Kanaan Talal Algoufi Khalid Alsaleem Talal A Basha Fathiya Al-Murshedi Sameena Khan Adila Al-Kindy Maha Alnemer Sami Al-Hajjar Suad Alyamani Hasan Aldhekri Ali Al-Mehaidib Rand Arnaout Omar Dabbagh Mohammad Shagrani Dieter Broering Maha Tulbah Amal Alqassmi Maisoon Almugbel Mohammed AlQuaiz Abdulaziz Alsaman Khalid Al-Thihli Raashda A Sulaiman Wajeeh Al-Dekhail Abeer Alsaegh Fahad A Bashiri Alya Qari Suzan Alhomadi Hisham Alkuraya Mohammed Alsebayel Muddathir H Hamad Laszlo Szonyi Faisal Abaalkhail Sulaiman M Al-Mayouf Hamad Almojalli Khalid S Alqadi Hussien Elsiesy Taghreed M Shuaib Mohammed Zain Seidahmed Ibraheem Abosoudah Hana Akleh Abdulaziz AlGhonaium Turki M Alkharfy Fuad Al Mutairi Wafa Eyaid Abdullah Alshanbary Farrukh R Sheikh Fahad I Alsohaibani Abdullah Alsonbul Saeed Al Tala Soher Balkhy Randa Bassiouni Ahmed S Alenizi Maged H Hussein Saeed Hassan Mohamed Khalil Brahim Tabarki Saad Alshahwan Amira Oshi Yasser Sabr Saad Alsaadoun Mustafa A Salih Sarar Mohamed Habiba Sultana Abdullah Tamim Moayad El-Haj Saif Alshahrani Dalal K Bubshait Majid Alfadhel Tariq Faquih Mohamed El-Kalioby Shazia Subhani Zeeshan Shah Nabil Moghrabi Brian F Meyer Fowzan S Alkuraya

Hum Genet 2017 08 9;136(8):921-939. Epub 2017 Jun 9.

Deparment of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1007/s00439-017-1821-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5502059PMC
August 2017

Mutations in NKX6-2 Cause Progressive Spastic Ataxia and Hypomyelination.

Am J Hum Genet 2017 Jun;100(6):969-977

Department of Molecular Neuroscience, University College London, London WC1N 3BG, UK; Neurogenetics Laboratory, The National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.

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http://dx.doi.org/10.1016/j.ajhg.2017.05.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5473715PMC
June 2017

Childhood epilepsies: What should a pediatrician know?

Authors:
Fahad A Bashiri

Neurosciences (Riyadh) 2017 01;22(1):14-19

Department of Pediatrics, College of Medicine, King Saud University Medical City, King Saud University, Riyadh, Kingdom of Saudi Arabia. E-mail:

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5726831PMC
http://dx.doi.org/10.17712/nsj.2017.1.20160244DOI Listing
January 2017

Sturge-Weber syndrome: Continued vigilance is needed.

Sudan J Paediatr 2015 ;15(2):63-70

(1) Division of Pediatric Neurology, College of Medicine and King Saud University Medical City, King Saud University , Riyadh , Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4958665PMC
August 2016

Mycoplasma pneumoniae Infection: Risk Factor for Childhood Stroke.

Authors:
Fahad A Bashiri

Glob Pediatr Health 2015 23;2:2333794X15592764. Epub 2015 Jun 23.

Division of Neurology,Department of Pediatrics,College of Medicine & King Khalid University Hospital,King Saud University, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1177/2333794X15592764DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4784591PMC
June 2016

Idiopathic intracranial hypertension in children: Diagnostic and management approach.

Sudan J Paediatr 2016 ;16(2):67-76

Division of Neurology, Departments of Pediatrics, King Khalid University Hospital, College of Medicine, King Saud University , Riyadh , Saudi Arabia.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5237838PMC
January 2016

ARL6IP6, a susceptibility locus for ischemic stroke, is mutated in a patient with syndromic Cutis Marmorata Telangiectatica Congenita.

Hum Genet 2015 Aug 10;134(8):815-22. Epub 2015 May 10.

Developmental Genetics Unit, Department of Genetics, King Faisal Specialist Hospital and Research Center, MBC-03 PO BOX 3354, Riyadh, 11211, Saudi Arabia.

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http://link.springer.com/content/pdf/10.1007/s00439-015-1561
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http://link.springer.com/10.1007/s00439-015-1561-6
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http://dx.doi.org/10.1007/s00439-015-1561-6DOI Listing
August 2015

Accelerating novel candidate gene discovery in neurogenetic disorders via whole-exome sequencing of prescreened multiplex consanguineous families.

Cell Rep 2015 Jan 31;10(2):148-61. Epub 2014 Dec 31.

Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh 11211, Saudi Arabia; Department of Anatomy and Cell Biology, College of Medicine, Alfaisal University, Riyadh 11533, Saudi Arabia; Saudi Human Genome Program, King Abdulaziz City for Science and Technology, Riyadh 11442, Saudi Arabia. Electronic address:

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http://dx.doi.org/10.1016/j.celrep.2014.12.015DOI Listing
January 2015