Overview
Aslıhan Tolun practices practicing medicine in Istanbul, Turkey.
Tolun is highly rated in 13 conditions, according to our data. Their clinical expertise encompasses Multiple Synostoses Syndrome 1, Brachydactyly, Camptodactyly Taurinuria, and Camptodactyly Syndrome Guadalajara Type 1.
They are actively involved in clinical research, co-authoring 38 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 Aslıhan Tolun
Is Aslıhan Tolun a top-rated expert for Multiple Synostoses Syndrome 1?
MediFind is an objective health platform that identifies experts based on real-world data. Aslıhan Tolun is classified as an Distinguished expert for Multiple Synostoses Syndrome 1, 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 Aslıhan Tolun participate in research or clinical trials?
Yes. Aslıhan Tolun has published 38 articles and abstracts on conditions like Multiple Synostoses Syndrome 1. You can view a list of Aslıhan Tolun'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
- Distinguished
- Multiple Synostoses Syndrome 1Tolun isDistinguished. Learn about Multiple Synostoses Syndrome 1.
- Advanced
- Acromicric DysplasiaTolun isAdvanced. Learn about Acromicric Dysplasia.
- Autosomal Recessive Cutis Laxa Type 1
- BrachydactylyTolun isAdvanced. Learn about Brachydactyly.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly Taurinuria
- Cutis LaxaTolun isAdvanced. Learn about Cutis Laxa.
- Learman SyndromeTolun isAdvanced. Learn about Learman Syndrome.
- Short Stature (Growth Disorders)
- Steatocystoma MultiplexTolun isAdvanced. Learn about Steatocystoma Multiplex.
- SyndactylyTolun isAdvanced. Learn about Syndactyly.
- Experienced
- 2q37 Deletion SyndromeTolun isExperienced. Learn about 2q37 Deletion Syndrome.
- Acanthosis NigricansTolun isExperienced. Learn about Acanthosis Nigricans.
- Achalasia Microcephaly Syndrome
- AcheiropodyTolun isExperienced. Learn about Acheiropody.
- AchondrogenesisTolun isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaTolun isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Aplasia Cutis CongenitaTolun isExperienced. Learn about Aplasia Cutis Congenita.
- Autosomal Recessive Primary Microcephaly
- Bardet-Biedl SyndromeTolun isExperienced. Learn about Bardet-Biedl Syndrome.
- Brachydactyly Mononen TypeTolun isExperienced. Learn about Brachydactyly Mononen Type.
- Chondrodysplasia Punctata Syndrome
- ChondrodystrophyTolun isExperienced. Learn about Chondrodystrophy.
- Clouston SyndromeTolun isExperienced. Learn about Clouston Syndrome.
- Congenital HypothyroidismTolun isExperienced. Learn about Congenital Hypothyroidism.
- Cortical DysplasiaTolun isExperienced. Learn about Cortical Dysplasia.
- Drug Induced DyskinesiaTolun isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaTolun isExperienced. Learn about Dysarthria.
- Ectodermal DysplasiasTolun isExperienced. Learn about Ectodermal Dysplasias.
- EncopresisTolun isExperienced. Learn about Encopresis.
- FolliculitisTolun isExperienced. Learn about Folliculitis.
- Fraser SyndromeTolun isExperienced. Learn about Fraser Syndrome.
- Genital DwarfismTolun isExperienced. Learn about Genital Dwarfism.
- HyperhidrosisTolun isExperienced. Learn about Hyperhidrosis.
- HypospadiasTolun isExperienced. Learn about Hypospadias.
- HypotoniaTolun isExperienced. Learn about Hypotonia.
- Keratosis PilarisTolun isExperienced. Learn about Keratosis Pilaris.
- Laron SyndromeTolun isExperienced. Learn about Laron Syndrome.
- LeukodystrophyTolun isExperienced. Learn about Leukodystrophy.
- LissencephalyTolun isExperienced. Learn about Lissencephaly.
- LordosisTolun isExperienced. Learn about Lordosis.
- Mevalonate Kinase DeficiencyTolun isExperienced. Learn about Mevalonate Kinase Deficiency.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyTolun isExperienced. Learn about Microcephaly.
- Microcephaly Deafness Syndrome
- Olivopontocerebellar AtrophyTolun isExperienced. Learn about Olivopontocerebellar Atrophy.
- Pachyonychia CongenitaTolun isExperienced. Learn about Pachyonychia Congenita.
- Pectus ExcavatumTolun isExperienced. Learn about Pectus Excavatum.
- PolydactylyTolun isExperienced. Learn about Polydactyly.
- Robinow SyndromeTolun isExperienced. Learn about Robinow Syndrome.
- Schwartz-Jampel SyndromeTolun isExperienced. Learn about Schwartz-Jampel Syndrome.
- Spinocerebellar AtaxiaTolun isExperienced. Learn about Spinocerebellar Ataxia.
- Spinocerebellar Ataxia Type 4Tolun isExperienced. Learn about Spinocerebellar Ataxia Type 4.
- Spinocerebellar Ataxia Type 5Tolun isExperienced. Learn about Spinocerebellar Ataxia Type 5.
- Syndactyly Type 1Tolun isExperienced. Learn about Syndactyly Type 1.
- Syndactyly Type 2Tolun isExperienced. Learn about Syndactyly Type 2.
- TNF Receptor-Associated Periodic Syndrome
- X-Linked Chondrodysplasia Punctata 2
- X-Linked Spondyloepiphyseal Dysplasia Tarda