Overview
Anas Alyazidi practices in Jeddah, Saudi Arabia. Mr. Alyazidi is rated as an Advanced expert by MediFind in the treatment of Guanidinoacetate Methyltransferase Deficiency. His top areas of expertise are Guanidinoacetate Methyltransferase Deficiency, Myoclonic Epilepsy, Seizures, and Dravet Syndrome.
His clinical research consists of co-authoring 39 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, he has co-authored 2 articles in the study of Guanidinoacetate Methyltransferase Deficiency.
Locations
Clinical Research
Clinical research consists of overseeing clinical studies of patients undergoing new treatments and therapies, and publishing articles in peer reviewed medical journals. Experts who actively participate in clinical research are generally at the forefront of the fields and aware of the most up-to-date advances in treatments for their patients.
Areas of Expertise
MediFind evaluates expertise by pulling from factors such as number of articles a doctor has published in medical journals, participation in clinical trials, speaking at industry conferences, prescribing and referral patterns, and strength of connections with other experts in their field.
Learn more about MediFind’s expert tiers
- Advanced
- Dravet SyndromeMr. Alyazidi isAdvanced. Learn about Dravet Syndrome.
- Guanidinoacetate Methyltransferase Deficiency
- Myoclonic EpilepsyMr. Alyazidi isAdvanced. Learn about Myoclonic Epilepsy.
- SeizuresMr. Alyazidi isAdvanced. Learn about Seizures.
- Experienced
- ApraxiaMr. Alyazidi isExperienced. Learn about Apraxia.
- Autism Spectrum DisorderMr. Alyazidi isExperienced. Learn about Autism Spectrum Disorder.
- Cerebral Ventricle CancerMr. Alyazidi isExperienced. Learn about Cerebral Ventricle Cancer.
- Choroid Plexus CarcinomaMr. Alyazidi isExperienced. Learn about Choroid Plexus Carcinoma.
- Choroid Plexus PapillomaMr. Alyazidi isExperienced. Learn about Choroid Plexus Papilloma.
- Chromosome 13q DuplicationMr. Alyazidi isExperienced. Learn about Chromosome 13q Duplication.