Overview
Nur Arslan practices in Dokuz Eylul, Turkey. Arslan is rated as an Experienced expert by MediFind in the treatment of Vitamin B12 Deficiency Anemia. Their top areas of expertise are Lipogranulomatosis, Farber Lipogranulomatosis, Maternal Hyperphenylalaninemia, and Xanthoma.
Their clinical research consists of co-authoring 79 peer reviewed articles and participating in 1 clinical trial. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 2 articles in the study of Vitamin B12 Deficiency Anemia.
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.
1 Clinical Trials
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
- Elite
- LipogranulomatosisArslan isElite. Learn about Lipogranulomatosis.
- Distinguished
- Farber LipogranulomatosisArslan isDistinguished. Learn about Farber Lipogranulomatosis.
- Advanced
- AlkaptonuriaArslan isAdvanced. Learn about Alkaptonuria.
- Cerebrotendinous Xanthomatosis
- Dyggve-Melchior-Clausen Syndrome
- Fabry DiseaseArslan isAdvanced. Learn about Fabry Disease.
- Maternal Hyperphenylalaninemia
- OchronosisArslan isAdvanced. Learn about Ochronosis.
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)
- Apolipoprotein C2 DeficiencyArslan isExperienced. Learn about Apolipoprotein C2 Deficiency.
- Biotinidase DeficiencyArslan isExperienced. Learn about Biotinidase Deficiency.
- Brachydactyly Mononen TypeArslan isExperienced. Learn about Brachydactyly Mononen Type.
- Carbamoyl Phosphate Synthetase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency