Publication | Year | ||||||||
---|---|---|---|---|---|---|---|---|---|
First successful outcomes of pegvaliase (PALYNZIQ) in children Authors : Majid Alfadhel , Rayyan AlbarakatiJournal : BMC Medical Genomics Journal Reference count : 25 Volume : 17 |
2024 | ||||||||
Artificial Intelligence in Genomic Analysis: Revolutionizing Healthcare Authors : Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Pages : 089-090 |
2023 | ||||||||
Variants of uncertain significance is a clinical dilemma Authors : Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Journal Reference count : 4 Pages : 68-69 |
2021 | ||||||||
Authors :
Muhammad Umair
, Majid Alfadhel
Journal : Journal of Biochemical and Clinical Genetics Journal Reference count : 1 Pages : 94-99 |
2020 | ||||||||
Genetic Disorders Associated with Metal Metabolism Authors : Muhammad Umair , Majid AlfadhelJournal : Cells Journal Reference count : 138 Volume : 8 Pages : 1598 |
2019 | ||||||||
Multiple Mitochondrial Dysfunctions Syndrome 4 Due to ISCA2 Gene Defects: A Review Authors : Majid AlfadhelJournal : Child Neurology Open Journal Reference count : 22 Volume : 6 |
2019 | ||||||||
A new case of BainbridgeRopers syndrome (BRPS): delineating the phenotype and review of literature Authors : Faroug Ababneh , Marwan Nashabat , Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Journal Reference count : 1 Pages : 65-69 |
2019 | ||||||||
Authors :
Abeer Al Tuwaijri
, Majid Alfadhel
Journal : Journal of Pediatric Endocrinology and Metabolism Journal Reference count : 46 Volume : 32 Pages : 409-413 |
2019 | ||||||||
Glycine Transporter 1 Encephalopathy From Biochemical Pathway to Clinical Disease: Review Authors : Rayan Alfallaj , Majid AlfadhelJournal : Child Neurology Open Journal Reference count : 16 Volume : 6 |
2019 | ||||||||
Epileptic encephalopathy caused by biallelic mutation in PPM1D: a case report Authors : Hind AlMaghthawi , Marwan Nashabat , Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Journal Reference count : 14 Pages : 47-50 |
2018 | ||||||||
Mitchell-Riley Syndrome Report of Novel Mutation and Review of the Literature Authors : Nourah Alruqaie , Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Journal Reference count : 1 Pages : 87-92 |
2018 | ||||||||
Journal of Biochemical and Clinical Genetics: A Great Step Forward in Genomic Research Authors : Majid AlfadhelJournal : Journal of Biochemical and Clinical Genetics Journal Reference count : 1 Pages : 1-1 |
2018 | ||||||||
Authors :
Saud Alsahli
, Majid Alfadhel
Journal : Neurology Volume : 88 |
2017 | ||||||||
SLC19A3 Gene Defects Sorting the Phenotype and Acronyms: Review Authors : Brahim Tabarki , Majid AlfadhelJournal : Neuropediatrics Volume : 49 Pages : 083-092 |
2017 | ||||||||
Psychological Assessment of Patients With Biotin-Thiamine-Responsive Basal Ganglia Disease Authors : Majid Alfadhel , Amal Al-BluwiJournal : Child Neurology Open Journal Reference count : 12 Volume : 4 |
2017 | ||||||||
Early Infantile Leigh-like SLC19A3 Gene Defects Have a Poor Prognosis: Report and Review Authors : Majid AlfadhelJournal : Journal of Central Nervous System Disease Journal Reference count : 15 Volume : 9 Pages : 117957351773752 |
2017 | ||||||||
Authors :
Muhammad Talal Alrifai
, Majid Alfadhel
Journal : Pediatric Neurology Journal Reference count : 10 Volume : 58 Pages : 98-100 |
2016 | ||||||||
Authors :
Majid Alfadhel
, Rana Kattan
Journal : Journal of Central Nervous System Disease Journal Reference count : 18 Volume : 6 Pages : JCNSD.S12938 |
2014 | ||||||||
Enzyme replacement therapy for Fabry disease: some answers but more questions Authors : Sandra Sirrs , Majid AlfadhelJournal : Therapeutics and Clinical Risk Management Pages : 69 |
2011 |