Overview
Yasemin Akin practices practicing medicine in Kartal, Turkey.
Ms. Akin is highly rated in 3 conditions, according to our data. Her clinical expertise encompasses Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency, Hyperprolinemia, Frank Ter Haar Syndrome, and Bilirubin Encephalopathy.
She is actively involved in clinical research, co-authoring 15 peer reviewed articles.
Gender
Locations
Istanbul, Turkey
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 Yasemin Akin
Is Yasemin Akin a top-rated expert for Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Yasemin Akin is classified as an Advanced expert for Delta-1-Pyrroline-5-Carboxylate Dehydrogenase 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 Yasemin Akin participate in research or clinical trials?
Yes. Yasemin Akin has published 15 articles and abstracts on conditions like Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency. You can view a list of Yasemin Akin'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
- Delta-1-Pyrroline-5-Carboxylate Dehydrogenase Deficiency
- Frank Ter Haar SyndromeMs. Akin isAdvanced. Learn about Frank Ter Haar Syndrome.
- HyperprolinemiaMs. Akin isAdvanced. Learn about Hyperprolinemia.
- Experienced
- ABO IncompatibilityMs. Akin isExperienced. Learn about ABO Incompatibility.
- Bilirubin EncephalopathyMs. Akin isExperienced. Learn about Bilirubin Encephalopathy.
- Brachydactyly Mononen TypeMs. Akin isExperienced. Learn about Brachydactyly Mononen Type.
- ChondrodystrophyMs. Akin isExperienced. Learn about Chondrodystrophy.
- EpilepsyMs. Akin isExperienced. Learn about Epilepsy.
- Epilepsy Juvenile AbsenceMs. Akin isExperienced. Learn about Epilepsy Juvenile Absence.
- Generalized Tonic-Clonic SeizureMs. Akin isExperienced. Learn about Generalized Tonic-Clonic Seizure.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hemolytic Disease of the NewbornMs. Akin isExperienced. Learn about Hemolytic Disease of the Newborn.
- HyperventilationMs. Akin isExperienced. Learn about Hyperventilation.
- JaundiceMs. Akin isExperienced. Learn about Jaundice.
- Juvenile Myoclonic EpilepsyMs. Akin isExperienced. Learn about Juvenile Myoclonic Epilepsy.
- Newborn JaundiceMs. Akin isExperienced. Learn about Newborn Jaundice.
- Schwartz-Jampel SyndromeMs. Akin isExperienced. Learn about Schwartz-Jampel Syndrome.
- SeizuresMs. Akin isExperienced. Learn about Seizures.
- Spastic Paraplegia Type 2Ms. Akin isExperienced. Learn about Spastic Paraplegia Type 2.
- Transient Familial Hyperbilirubinemia
- X-Linked Spondyloepiphyseal Dysplasia Tarda