Overview
Qamre Alam practices practicing medicine in Riyadh, Saudi Arabia.
Alam is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses Polydactyly, Phosphoglycerate Mutase Deficiency, Bardet-Biedl Syndrome, and Cerebral Hypoxia.
They are actively involved in clinical research, co-authoring 57 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 Qamre Alam
Is Qamre Alam a top-rated expert for Polydactyly?
MediFind is an objective health platform that identifies experts based on real-world data. Qamre Alam is classified as an Advanced expert for Polydactyly, 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 Qamre Alam participate in research or clinical trials?
Yes. Qamre Alam has published 57 articles and abstracts on conditions like Polydactyly. You can view a list of Qamre Alam'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
- Advanced
- Phosphoglycerate Mutase Deficiency
- PolydactylyAlam isAdvanced. Learn about Polydactyly.
- Experienced
- 47 XYY SyndromeAlam isExperienced. Learn about 47 XYY Syndrome.
- Alzheimer's DiseaseAlam isExperienced. Learn about Alzheimer's Disease.
- Autosomal Recessive Primary Microcephaly
- Bardet-Biedl SyndromeAlam isExperienced. Learn about Bardet-Biedl Syndrome.
- Brachydactyly Mononen TypeAlam isExperienced. Learn about Brachydactyly Mononen Type.
- Castleman DiseaseAlam isExperienced. Learn about Castleman Disease.
- Cerebral HypoxiaAlam isExperienced. Learn about Cerebral Hypoxia.
- Chromosome 13q DuplicationAlam isExperienced. Learn about Chromosome 13q Duplication.
- DementiaAlam isExperienced. Learn about Dementia.
- Kaposi SarcomaAlam isExperienced. Learn about Kaposi Sarcoma.
- Klinefelter SyndromeAlam isExperienced. Learn about Klinefelter Syndrome.
- Maturity Onset Diabetes of the Young
- Movement DisordersAlam isExperienced. Learn about Movement Disorders.
- Parkinson's DiseaseAlam isExperienced. Learn about Parkinson's Disease.
- Partial Deletion of YAlam isExperienced. Learn about Partial Deletion of Y.
- Trisomy 13Alam isExperienced. Learn about Trisomy 13.
- Trisomy 18Alam isExperienced. Learn about Trisomy 18.
- Type 2 Diabetes (T2D)Alam isExperienced. Learn about Type 2 Diabetes (T2D).
- Y Chromosome InfertilityAlam isExperienced. Learn about Y Chromosome Infertility.