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Majid Alfadhel

Showing results (1-10 of 222) with videos related to

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Journal of Central Nervous System Disease|November 11, 2017
Early Infantile Leigh-like <i>SLC19A3</i> Gene Defects Have a Poor Prognosis: Report and ReviewMajid Alfadhel
International Journal of Health Sciences|December 12, 2018
Prevention genetics program is an efficient model for precision medicineMajid Alfadhel
Child Neurology Open|May 21, 2019
Multiple Mitochondrial Dysfunctions Syndrome 4 Due to <i>ISCA2</i> Gene Defects: A ReviewMajid Alfadhel
Neuropediatrics|September 30, 2017
SLC19A3 Gene Defects Sorting the Phenotype and Acronyms: ReviewMajid Alfadhel, Brahim Tabarki
Child Neurology Open|March 1, 2019
Glycine Transporter 1 Encephalopathy From Biochemical Pathway to Clinical Disease: ReviewRayan Alfallaj, Majid Alfadhel
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|May 1, 2008
Senior-Loken syndrome in a Saudi childMajid AlFadhel, Abdulrahman AlAmir
Cells|December 15, 2019
Genetic Disorders Associated with Metal MetabolismMuhammad Umair, Majid Alfadhel
BMC Medical Genomics|March 22, 2024
First successful outcomes of pegvaliase (PALYNZIQ) in childrenMajid Alfadhel, Rayyan Albarakati
Therapeutics and Clinical Risk Management|March 30, 2011
Enzyme replacement therapy for Fabry disease: some answers but more questionsMajid Alfadhel, Sandra Sirrs
Journal of Central Nervous System Disease|January 24, 2014
Aromatic amino Acid decarboxylase deficiency not responding to pyridoxine and bromocriptine therapy: case report and review of response to treatmentMajid Alfadhel, Rana Kattan
Pageof 23

Showing results (1-10 of 222) with videos related to

Sort By:
Pageof 23
Journal of Central Nervous System Disease|November 11, 2017
Early Infantile Leigh-like <i>SLC19A3</i> Gene Defects Have a Poor Prognosis: Report and ReviewMajid Alfadhel
International Journal of Health Sciences|December 12, 2018
Prevention genetics program is an efficient model for precision medicineMajid Alfadhel
Child Neurology Open|May 21, 2019
Multiple Mitochondrial Dysfunctions Syndrome 4 Due to <i>ISCA2</i> Gene Defects: A ReviewMajid Alfadhel
Neuropediatrics|September 30, 2017
SLC19A3 Gene Defects Sorting the Phenotype and Acronyms: ReviewMajid Alfadhel, Brahim Tabarki
Child Neurology Open|March 1, 2019
Glycine Transporter 1 Encephalopathy From Biochemical Pathway to Clinical Disease: ReviewRayan Alfallaj, Majid Alfadhel
Saudi Journal of Kidney Diseases and Transplantation : an Official Publication of the Saudi Center for Organ Transplantation, Saudi Arabia|May 1, 2008
Senior-Loken syndrome in a Saudi childMajid AlFadhel, Abdulrahman AlAmir
Cells|December 15, 2019
Genetic Disorders Associated with Metal MetabolismMuhammad Umair, Majid Alfadhel
BMC Medical Genomics|March 22, 2024
First successful outcomes of pegvaliase (PALYNZIQ) in childrenMajid Alfadhel, Rayyan Albarakati
Therapeutics and Clinical Risk Management|March 30, 2011
Enzyme replacement therapy for Fabry disease: some answers but more questionsMajid Alfadhel, Sandra Sirrs
Journal of Central Nervous System Disease|January 24, 2014
Aromatic amino Acid decarboxylase deficiency not responding to pyridoxine and bromocriptine therapy: case report and review of response to treatmentMajid Alfadhel, Rana Kattan
Pageof 23