Overview
Muddathir Hamad practices practicing medicine in Riyadh, Saudi Arabia.
Hamad is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Mitochondrial Complex 3 Deficiency, Coenzyme Q Cytochrome C Reductase Deficiency, Osteopetrosis Autosomal Recessive Type 3, West Syndrome, and Gastrostomy.
They are actively involved in clinical research, co-authoring 49 peer reviewed articles.
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.
Frequently Asked Questions about Muddathir H. Hamad
Is Muddathir H. Hamad a top-rated expert for Mitochondrial Complex 3 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Muddathir H. Hamad is classified as an Distinguished expert for Mitochondrial Complex 3 Deficiency, meaning they are among the top experts in the country for this condition. This ranking is based on their volume of patients, published research, and peer connections.
Does Muddathir H. Hamad participate in research or clinical trials?
Yes. Muddathir H. Hamad has published 49 articles and abstracts on conditions like Mitochondrial Complex 3 Deficiency. You can view a list of Muddathir H. Hamad's latest peer-reviewed publications and clinical trial participation on their profile to see if they are active in new treatments.
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
- Distinguished
- Mitochondrial Complex 3 Deficiency
- Advanced
- Coenzyme Q Cytochrome C Reductase Deficiency
- Empty Sella SyndromeHamad isAdvanced. Learn about Empty Sella Syndrome.
- Osteopetrosis Autosomal Recessive Type 3
- West SyndromeHamad isAdvanced. Learn about West Syndrome.
- Experienced
- Absence SeizureHamad isExperienced. Learn about Absence Seizure.
- Achalasia Microcephaly Syndrome
- Aromatic L-Amino Acid Decarboxylase (AADC) Deficiency
- Attention Deficit Hyperactivity Disorder (ADHD)
- ChoreaHamad isExperienced. Learn about Chorea.
- Cortical DysplasiaHamad isExperienced. Learn about Cortical Dysplasia.
- Drug Induced DyskinesiaHamad isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaHamad isExperienced. Learn about Dysarthria.
- EpilepsyHamad isExperienced. Learn about Epilepsy.
- Epilepsy in ChildrenHamad isExperienced. Learn about Epilepsy in Children.
- Epilepsy Juvenile AbsenceHamad isExperienced. Learn about Epilepsy Juvenile Absence.
- Epilepsy with Myoclonic-Atonic Seizures
- GastrostomyHamad isExperienced. Learn about Gastrostomy.
- Generalized Tonic-Clonic Seizure
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hallervorden-Spatz DiseaseHamad isExperienced. Learn about Hallervorden-Spatz Disease.
- Head LiceHamad isExperienced. Learn about Head Lice.
- HeadacheHamad isExperienced. Learn about Headache.
- HyperventilationHamad isExperienced. Learn about Hyperventilation.
- Increased Intracranial Pressure
- Infantile Axonal NeuropathyHamad isExperienced. Learn about Infantile Axonal Neuropathy.
- Juvenile Myoclonic EpilepsyHamad isExperienced. Learn about Juvenile Myoclonic Epilepsy.
- Limb-Girdle Muscular Dystrophy
- MalnutritionHamad isExperienced. Learn about Malnutrition.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyHamad isExperienced. Learn about Microcephaly.
- Movement DisordersHamad isExperienced. Learn about Movement Disorders.
- Myoclonic EpilepsyHamad isExperienced. Learn about Myoclonic Epilepsy.
- Myoclonus-DystoniaHamad isExperienced. Learn about Myoclonus-Dystonia.
- Nephrotic SyndromeHamad isExperienced. Learn about Nephrotic Syndrome.
- Olivopontocerebellar AtrophyHamad isExperienced. Learn about Olivopontocerebellar Atrophy.
- OsteopetrosisHamad isExperienced. Learn about Osteopetrosis.
- Osteosclerosis Autosomal Dominant
- PapilledemaHamad isExperienced. Learn about Papilledema.
- Primary Lateral SclerosisHamad isExperienced. Learn about Primary Lateral Sclerosis.
- Pseudotumor Cerebri SyndromeHamad isExperienced. Learn about Pseudotumor Cerebri Syndrome.
- Renal Tubular AcidosisHamad isExperienced. Learn about Renal Tubular Acidosis.
- Riboflavin Transporter Deficiency Neuronopathy
- SeizuresHamad isExperienced. Learn about Seizures.
- Spasmus NutansHamad isExperienced. Learn about Spasmus Nutans.
- Spinocerebellar AtaxiaHamad isExperienced. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 4Hamad isExperienced. Learn about Spinocerebellar Ataxia Type 4.
- Spinocerebellar Ataxia Type 5Hamad isExperienced. Learn about Spinocerebellar Ataxia Type 5.
- Spinocerebellar Ataxia Type 8Hamad isExperienced. Learn about Spinocerebellar Ataxia Type 8.
- Vitamin D DeficiencyHamad isExperienced. Learn about Vitamin D Deficiency.