Overview
Neslihan Mungan-Onenli practices in Adana, Turkey. Mungan-Onenli is rated as an Experienced expert by MediFind in the treatment of Multiple Carboxylase Deficiency. Their top areas of expertise are Fanconi Bickel Syndrome, Fanconi Syndrome, Short-Chain Acyl-CoA Dehydrogenase Deficiency, and Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome).
Their clinical research consists of co-authoring 28 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, they have co-authored 1 article in the study of Multiple Carboxylase 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
- Fanconi Bickel SyndromeMungan-Onenli isAdvanced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMungan-Onenli isAdvanced. Learn about Fanconi Syndrome.
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Experienced
- Acromesomelic DysplasiaMungan-Onenli isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson TypeMungan-Onenli isExperienced. Learn about Acromesomelic Dysplasia Hunter Thompson Type.
- Acromesomelic Dysplasia Maroteaux TypeMungan-Onenli isExperienced. Learn about Acromesomelic Dysplasia Maroteaux Type.
- Adrenoleukodystrophy (ALD)Mungan-Onenli isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Biotinidase DeficiencyMungan-Onenli isExperienced. Learn about Biotinidase Deficiency.