Overview
Sebile Kılavuz practices practicing medicine in Ihlas Marmara Evleri - I. Kisim, Turkey.
Kılavuz is highly rated in 6 conditions, according to our data. Their clinical expertise encompasses Gaucher Disease, Tyrosinemia Type 3, Gaucher Disease Type 2, and Von Gierke Disease.
They are actively involved in clinical research, co-authoring 34 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 Sebile Kılavuz
Is Sebile Kılavuz a top-rated expert for Gaucher Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Sebile Kılavuz is classified as an Advanced expert for Gaucher Disease, 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 Sebile Kılavuz participate in research or clinical trials?
Yes. Sebile Kılavuz has published 34 articles and abstracts on conditions like Gaucher Disease. You can view a list of Sebile Kılavuz'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
- Farber LipogranulomatosisKılavuz isAdvanced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseKılavuz isAdvanced. Learn about Gaucher Disease.
- Gaucher Disease Type 2Kılavuz isAdvanced. Learn about Gaucher Disease Type 2.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Tyrosinemia Type 3Kılavuz isAdvanced. Learn about Tyrosinemia Type 3.
- Von Gierke DiseaseKılavuz isAdvanced. Learn about Von Gierke Disease.
- Experienced
- Adrenal Insufficiency PediatricKılavuz isExperienced. Learn about Adrenal Insufficiency Pediatric.
- Adrenoleukodystrophy (ALD)Kılavuz isExperienced. Learn about Adrenoleukodystrophy (ALD).
- AgranulocytosisKılavuz isExperienced. Learn about Agranulocytosis.
- Alpha ThalassemiaKılavuz isExperienced. Learn about Alpha Thalassemia.
- Biotinidase DeficiencyKılavuz isExperienced. Learn about Biotinidase Deficiency.
- Brachydactyly Mononen TypeKılavuz isExperienced. Learn about Brachydactyly Mononen Type.
- Carnitine Palmitoyltransferase 1 Deficiency
- Childhood PancreatitisKılavuz isExperienced. Learn about Childhood Pancreatitis.
- Congenital Erythropoietic Porphyria
- CystinosisKılavuz isExperienced. Learn about Cystinosis.
- Fanconi Bickel SyndromeKılavuz isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeKılavuz isExperienced. Learn about Fanconi Syndrome.
- Fetal EdemaKılavuz isExperienced. Learn about Fetal Edema.
- GangliosidosisKılavuz isExperienced. Learn about Gangliosidosis.
- Glutaric Acidemia Type 1Kılavuz isExperienced. Learn about Glutaric Acidemia Type 1.
- GM1 GangliosidosisKılavuz isExperienced. Learn about GM1 Gangliosidosis.
- Hallervorden-Spatz DiseaseKılavuz isExperienced. Learn about Hallervorden-Spatz Disease.
- Hemolytic Disease of the NewbornKılavuz isExperienced. Learn about Hemolytic Disease of the Newborn.
- Hydrops FetalisKılavuz isExperienced. Learn about Hydrops Fetalis.
- Infantile NeutropeniaKılavuz isExperienced. Learn about Infantile Neutropenia.
- Interstitial NephritisKılavuz isExperienced. Learn about Interstitial Nephritis.
- Low Blood SugarKılavuz isExperienced. Learn about Low Blood Sugar.
- Low Sodium LevelKılavuz isExperienced. Learn about Low Sodium Level.
- MelanomaKılavuz isExperienced. Learn about Melanoma.
- Methylmalonic AcidemiaKılavuz isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidoses (MPS)Kılavuz isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Mucopolysaccharidosis Type 6 (MPS VI, Maroteaux-Lamy Syndrome)
- Multiple Carboxylase DeficiencyKılavuz isExperienced. Learn about Multiple Carboxylase Deficiency.
- Pantothenate Kinase-Associated Neurodegeneration
- Phenylketonuria (PKU)Kılavuz isExperienced. Learn about Phenylketonuria (PKU).
- Pompe DiseaseKılavuz isExperienced. Learn about Pompe Disease.
- PorphyriaKılavuz isExperienced. Learn about Porphyria.
- Precocious PubertyKılavuz isExperienced. Learn about Precocious Puberty.
- Propionic AcidemiaKılavuz isExperienced. Learn about Propionic Acidemia.
- PurpuraKılavuz isExperienced. Learn about Purpura.
- RhabdomyolysisKılavuz isExperienced. Learn about Rhabdomyolysis.
- Sandhoff DiseaseKılavuz isExperienced. Learn about Sandhoff Disease.
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- Tay-Sachs DiseaseKılavuz isExperienced. Learn about Tay-Sachs Disease.
- ThalassemiaKılavuz isExperienced. Learn about Thalassemia.
- Wolff-Parkinson-White SyndromeKılavuz isExperienced. Learn about Wolff-Parkinson-White Syndrome.