Overview
Ali Korulmaz practices practicing medicine in Kosekoy, Turkey.
Korulmaz is highly rated in 5 conditions, according to our data. Their clinical expertise encompasses Camptodactyly Taurinuria, Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia, Camptodactyly Syndrome Guadalajara Type 2, and Camptodactyly Syndrome Guadalajara Type 1.
They are actively involved in clinical research, co-authoring 9 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 Ali Korulmaz
Is Ali Korulmaz a top-rated expert for Camptodactyly Taurinuria?
MediFind is an objective health platform that identifies experts based on real-world data. Ali Korulmaz is classified as an Advanced expert for Camptodactyly Taurinuria, 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 Ali Korulmaz participate in research or clinical trials?
Yes. Ali Korulmaz has published 9 articles and abstracts on conditions like Camptodactyly Taurinuria. You can view a list of Ali Korulmaz'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
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaKorulmaz isAdvanced. Learn about Camptodactyly Taurinuria.
- Genital DwarfismKorulmaz isAdvanced. Learn about Genital Dwarfism.
- Experienced
- Achalasia Microcephaly SyndromeKorulmaz isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Biotinidase DeficiencyKorulmaz isExperienced. Learn about Biotinidase Deficiency.
- Congenital CataractKorulmaz isExperienced. Learn about Congenital Cataract.
- Congenital HypothyroidismKorulmaz isExperienced. Learn about Congenital Hypothyroidism.
- Cortical DysplasiaKorulmaz isExperienced. Learn about Cortical Dysplasia.
- CraniosynostosisKorulmaz isExperienced. Learn about Craniosynostosis.
- Crouzon SyndromeKorulmaz isExperienced. Learn about Crouzon Syndrome.
- HypospadiasKorulmaz isExperienced. Learn about Hypospadias.
- HypothyroidismKorulmaz isExperienced. Learn about Hypothyroidism.
- HypotoniaKorulmaz isExperienced. Learn about Hypotonia.
- Infantile PneumothoraxKorulmaz isExperienced. Learn about Infantile Pneumothorax.
- IntersexKorulmaz isExperienced. Learn about Intersex.
- Low Blood PressureKorulmaz isExperienced. Learn about Low Blood Pressure.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyKorulmaz isExperienced. Learn about Microcephaly.
- MicrognathiaKorulmaz isExperienced. Learn about Micrognathia.
- MicrophthalmiaKorulmaz isExperienced. Learn about Microphthalmia.
- Multiple Carboxylase DeficiencyKorulmaz isExperienced. Learn about Multiple Carboxylase Deficiency.
- Pediatric MyocarditisKorulmaz isExperienced. Learn about Pediatric Myocarditis.
- Undescended TesticleKorulmaz isExperienced. Learn about Undescended Testicle.