Publications by authors named "Fahad A Bashiri"

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Emotional coping strategies in children with and without special educational needs during the COVID-19 pandemic in Saudi Arabia.
Shuliweeh Alenezi, Mohammed Alarabi, Ahmed S Alyahya, Ahmad H Almadani, Afnan Almarshedi, Fahad A Bashiri

Front Public Health· September 2025

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Pioneering SMA therapies for all types: survival gains, cost dynamics, and performance-based agreements.
Ahmed Al-Jedai, Hajer Al-Mudaiheem, AlJohara AlSakran, Fahad A Bashiri, Fouad Ghamdi

Cost Eff Resour Alloc· August 2025

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A copy number variant overlapping the 3'UTR of PLP1 causes spastic paraplegia.
Malak Alghamdi, Essa Alharbi, Salman Aljarallah, Ghaida Alghamdi, Reham M Balahmar, Fahad A Bashiri

J Hum Genet· July 2025

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Sodium Oxybate-Treated Familial Myoclonus-Dystonia Syndrome Due to Novel SGCE Variant.
Malak Ali Alghamdi, Muddathir H Hamad, Isra Alghamdi, Ghiada Alghamdi, Muneera Al-Jelaify, Fahad A Bashiri

Am J Med Genet A· May 2025

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Risk factors, clinical characteristics, and outcomes of perinatal stroke in a Tertiary University Hospital.
Shaden S Alfayez, Muddathir H Hamad, Amal Y Kentab, Ahmad A Alanezi, Daniah M Kurdi, Fahad A Bashiri

Neurosciences (Riyadh)· April 2025

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The correlation of intracranial parenchymal calcium score and the severity of neurological clinical presentation in carbonic anhydrase deficiency type 2.
Basma AlFaris, Fahad B AlBader, Rawan AlSheikh, Fahad A Bashiri, Muddathir H Hamad

Brain Dev· February 2025

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Neurological Sequelae in Children Born After Assisted Conception Techniques in a Tertiary University Hospital in Riyadh, Saudi Arabia: A Retrospective Cohort Study.
Fadi Busaleh, Fahad A Bashiri, Ahmed A Almasabi, Aljoharah A Almaziad, Alhanouf Alhaluli

Cureus· January 2025

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Corrigendum: Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendations.
Fahad A Bashiri, Khaled Hundallah, Musaad Abukhaled, Mossaed Mohammed Alyahya, Amna Al Futaisi

Front Oncol· October 2024

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Vitamin D Supplementation for Children with Epilepsy on Antiseizure Medications: A Randomized Controlled Trial.
Fahad A Bashiri, Abrar Hudairi, Muddathir H Hamad, Lujain K Al-Sulimani, Doua Al Homyani

Children (Basel)· September 2024

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Diagnosis and management of neurofibromatosis type 1 in Arabian Gulf Cooperation Council Region: challenges and recommendations.
Fahad A Bashiri, Khaled Hundallah, Musaad Abukhaled, Mossaed Mohammed Alyahya, Amna Al Futaisi

Front Oncol· August 2024

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Clinical and Molecular Characteristics of Neuronal Ceroid Lipofuscinosis in Saudi Arabia.
Mohammed M Saleh, Abdulrahim M Hamhom, Ali Al-Otaibi, Malak AlGhamdi, Yousef Housawi, Fahad A Bashiri

Pediatr Neurol· June 2024

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Virtual Objective Structured Clinical Examination (OSCE) Training in the Pandemic Era: Feasibility, Satisfaction, and the Road Ahead.
Elshazaly Saeed, Muddathir H Hamad, Abdullah N Alhuzaimi, Fadi Aljamaan, Hossameldin Elsenterisi, Fahad A Bashiri

Cureus· June 2024

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Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement.
Fahad A Bashiri, Khalid Hundallah, Raidah Al-Baradie, Ali Al-Otaibi, Omar Ismayl

Seizure· April 2024

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Case Report: A rare treatable metabolic syndrome (Brown-Vialetto-Van Laere syndrome) masquerading as chronic inflammatory demyelinating polyneuropathy from Saudi Arabia.
Amal Y Kentab, Yara Alsalloum, Mai Labani, Abrar Hudairi, Muddathir H Hamad, Fahad A Bashiri

Front Pediatr· April 2024

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Social Anxiety, Social Support, and Quality of Life in Patients With Epilepsy at a Tertiary Care Hospital in Saudi Arabia.
Faisal I Alkoblan, Musaeb M Alsoadan, Abdulrahman A Alhajri, Mohammed M Almousa, Faisal S Alsalamah, Fahad A Bashiri

Cureus· September 2023

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Corrigendum to: Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, Malak Ali Alghamdi, Yair Anikster, Fahad A Bashiri

Mol Genet Metab· August 2023

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Genotype-Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital.
Fahad A Bashiri, Rawan AlSheikh, Muddathir H Hamad, Hamad Alsheikh, Rana Abdullah Alsheikh

Children (Basel)· August 2023

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Prevalence of DDC genotypes in patients with aromatic L-amino acid decarboxylase (AADC) deficiency and in silico prediction of structural protein changes.
Nastassja Himmelreich, Mariarita Bertoldi, Majid Alfadhel, Malak Ali Alghamdi, Yair Anikster, Fahad A Bashiri

Mol Genet Metab· July 2023

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Prevalence and Related Risk Factors of Vitamin D Deficiency in Saudi Children with Epilepsy.
Reem Al Khalifah, Muddathir H Hamad, Abrar Hudairi, Lujain K Al-Sulimani, Doua Al Homyani, Fahad A Bashiri

Children (Basel)· November 2022

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Mental health impact of COVID-19 on Saudi families and children with special educational needs and disabilities in Saudi Arabia: A national perspective.
Shuliweeh Alenezi, Mohamad-Hani Temsah, Ahmed S Alyahya, Ahmad H Almadani, Afnan Almarshedi, Fahad A Bashiri

Front Public Health· October 2022

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Pattern and etiology of early childhood epilepsy: An Experience at a tertiary care University Center.
Amal Y Kentab, Shumukh Al Bulayhi, Muddathir H Hamad, Ali Al Wadei, Fahad A Bashiri

Neurosciences (Riyadh)· October 2022

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Hypermanganesemia with Dystonia Type 2: A Potentially Treatable Neurodegenerative Disorder: A Case Series in a Tertiary University Hospital.
Khalid A Alhasan, Walaa Alshuaibi, Muddathir H Hamad, Suha Salim, Dima Z Jamjoom, Fahad A Bashiri

Children (Basel)· September 2022

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Patient demographics and characteristics from an ambispective, observational study of patients with duchenne muscular dystrophy in Saudi Arabia.
Abdulaziz S AlSaman, Fouad Al Ghamdi, Ahmed K Bamaga, Nahla AlShaikh, Mohammed Al Muqbil, Fahad A Bashiri

Front Pediatr· September 2022

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AGREEing on Clinical Practice Guidelines for Autism Spectrum Disorders in Children: A Systematic Review and Quality Assessment.
Yasser S Amer, Shuliweeh Alenezi, Fahad A Bashiri, Amel Hussain Alawami, Ayman Shawqi Alhazmi

Children (Basel)· July 2022

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Genomic, Proteomic, and Phenotypic Spectrum of Novel O-Sialoglycoprotein Endopeptidase Variant in Four Affected Individuals With Galloway-Mowat Syndrome.
Malak Ali Alghamdi, Hicham Benabdelkamel, Afshan Masood, Narjes Saheb Sharif-Askari, Mahmood Y Hachim, Fahad A Bashiri

Front Genet· June 2022

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