Overview
Fatma Bulut practices practicing medicine in Adana, Turkey.
Ms. Bulut is highly rated in 14 conditions, according to our data. Her clinical expertise encompasses Enlarged Liver, Visceromegaly, Mucolipidosis Type 4, Mucolipidosis 3, and Hormone Replacement Therapy (HRT).
She is actively involved in clinical research, co-authoring 49 peer reviewed articles.
Gender
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 Fatma D. Bulut
Is Fatma D. Bulut a top-rated expert for Enlarged Liver?
MediFind is an objective health platform that identifies experts based on real-world data. Fatma D. Bulut is classified as an Distinguished expert for Enlarged Liver, 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 Fatma D. Bulut participate in research or clinical trials?
Yes. Fatma D. Bulut has published 49 articles and abstracts on conditions like Enlarged Liver. You can view a list of Fatma D. Bulut'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
- Enlarged LiverMs. Bulut isDistinguished. Learn about Enlarged Liver.
- Advanced
- Cerebrotendinous XanthomatosisMs. Bulut isAdvanced. Learn about Cerebrotendinous Xanthomatosis.
- Familial HypopituitarismMs. Bulut isAdvanced. Learn about Familial Hypopituitarism.
- Farber LipogranulomatosisMs. Bulut isAdvanced. Learn about Farber Lipogranulomatosis.
- Gaucher DiseaseMs. Bulut isAdvanced. Learn about Gaucher Disease.
- Glycogen Storage Disease Type 0Ms. Bulut isAdvanced. Learn about Glycogen Storage Disease Type 0.
- Mitochondrial Neurogastrointestinal Encephalopathy Disease
- Mucolipidosis 3Ms. Bulut isAdvanced. Learn about Mucolipidosis 3.
- Mucolipidosis Type 4Ms. Bulut isAdvanced. Learn about Mucolipidosis Type 4.
- Phenylketonuria (PKU)Ms. Bulut isAdvanced. Learn about Phenylketonuria (PKU).
- Short-Chain Acyl-CoA Dehydrogenase Deficiency
- SialidosisMs. Bulut isAdvanced. Learn about Sialidosis.
- VisceromegalyMs. Bulut isAdvanced. Learn about Visceromegaly.
- XanthomaMs. Bulut isAdvanced. Learn about Xanthoma.
- Experienced
- Adrenoleukodystrophy (ALD)Ms. Bulut isExperienced. Learn about Adrenoleukodystrophy (ALD).
- Bile Duct ObstructionMs. Bulut isExperienced. Learn about Bile Duct Obstruction.
- Biotinidase DeficiencyMs. Bulut isExperienced. Learn about Biotinidase Deficiency.
- Brachydactyly Mononen TypeMs. Bulut isExperienced. Learn about Brachydactyly Mononen Type.
- CACH SyndromeMs. Bulut isExperienced. Learn about CACH Syndrome.
- Camptodactyly Fibrous Tissue Hyperplasia Skeletal Dysplasia
- Camptodactyly Syndrome Guadalajara Type 1
- Camptodactyly Syndrome Guadalajara Type 2
- Camptodactyly TaurinuriaMs. Bulut isExperienced. Learn about Camptodactyly Taurinuria.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- Childhood PancreatitisMs. Bulut isExperienced. Learn about Childhood Pancreatitis.
- CholestasisMs. Bulut isExperienced. Learn about Cholestasis.
- Cholesteryl Ester Storage DiseaseMs. Bulut isExperienced. Learn about Cholesteryl Ester Storage Disease.
- Congenital Erythropoietic PorphyriaMs. Bulut isExperienced. Learn about Congenital Erythropoietic Porphyria.
- CystinosisMs. Bulut isExperienced. Learn about Cystinosis.
- Dubin-Johnson SyndromeMs. Bulut isExperienced. Learn about Dubin-Johnson Syndrome.
- EpilepsyMs. Bulut isExperienced. Learn about Epilepsy.
- Familial HypertriglyceridemiaMs. Bulut isExperienced. Learn about Familial Hypertriglyceridemia.
- Fanconi Bickel SyndromeMs. Bulut isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMs. Bulut isExperienced. Learn about Fanconi Syndrome.
- Growth Hormone Deficiency (GHD)Ms. Bulut isExperienced. Learn about Growth Hormone Deficiency (GHD).
- Hearing LossMs. Bulut isExperienced. Learn about Hearing Loss.
- Hemolytic AnemiaMs. Bulut isExperienced. Learn about Hemolytic Anemia.
- HistiocytosisMs. Bulut isExperienced. Learn about Histiocytosis.
- Hormone Replacement Therapy (HRT)Ms. Bulut isExperienced. Learn about Hormone Replacement Therapy (HRT).
- Hypogonadotropic HypogonadismMs. Bulut isExperienced. Learn about Hypogonadotropic Hypogonadism.
- HypopituitarismMs. Bulut isExperienced. Learn about Hypopituitarism.
- Interstitial NephritisMs. Bulut isExperienced. Learn about Interstitial Nephritis.
- Intestinal Pseudo-ObstructionMs. Bulut isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Isolated ACTH DeficiencyMs. Bulut isExperienced. Learn about Isolated ACTH Deficiency.
- Juvenile Idiopathic Arthritis (JIA)Ms. Bulut isExperienced. Learn about Juvenile Idiopathic Arthritis (JIA).
- LeukodystrophyMs. Bulut isExperienced. Learn about Leukodystrophy.
- LymphadenitisMs. Bulut isExperienced. Learn about Lymphadenitis.
- Lysosomal Acid Lipase DeficiencyMs. Bulut isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- Maternal HyperphenylalaninemiaMs. Bulut isExperienced. Learn about Maternal Hyperphenylalaninemia.
- Methylmalonic AcidemiaMs. Bulut isExperienced. Learn about Methylmalonic Acidemia.
- Mucopolysaccharidoses (MPS)Ms. Bulut isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 2 (MPS II, Hunter Syndrome)
- Mucopolysaccharidosis Type 3 (MPS III, Sanfilippo Syndrome)
- Mucopolysaccharidosis Type 3B (MPS IIIB, Sanfilippo Syndrome B)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Multicentric Carpotarsal Osteolysis Syndrome
- Multiple Carboxylase DeficiencyMs. Bulut isExperienced. Learn about Multiple Carboxylase Deficiency.
- Myoglobinuria RecurrentMs. Bulut isExperienced. Learn about Myoglobinuria Recurrent.
- Niemann-Pick DiseaseMs. Bulut isExperienced. Learn about Niemann-Pick Disease.
- Non-Langerhans-Cell HistiocytosisMs. Bulut isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Oculopharyngeal Muscular DystrophyMs. Bulut isExperienced. Learn about Oculopharyngeal Muscular Dystrophy.
- PanhypopituitarismMs. Bulut isExperienced. Learn about Panhypopituitarism.
- Pediatric Growth Hormone DeficiencyMs. Bulut isExperienced. Learn about Pediatric Growth Hormone Deficiency.
- Perrault SyndromeMs. Bulut isExperienced. Learn about Perrault Syndrome.
- Pompe DiseaseMs. Bulut isExperienced. Learn about Pompe Disease.
- PorphyriaMs. Bulut isExperienced. Learn about Porphyria.
- Premature Ovarian FailureMs. Bulut isExperienced. Learn about Premature Ovarian Failure.
- Propionic AcidemiaMs. Bulut isExperienced. Learn about Propionic Acidemia.
- PurpuraMs. Bulut isExperienced. Learn about Purpura.
- Renal Tubular AcidosisMs. Bulut isExperienced. Learn about Renal Tubular Acidosis.
- ReticulohistiocytomaMs. Bulut isExperienced. Learn about Reticulohistiocytoma.
- RhabdomyolysisMs. Bulut isExperienced. Learn about Rhabdomyolysis.
- Rotor SyndromeMs. Bulut isExperienced. Learn about Rotor Syndrome.
- Sensorimotor PolyneuropathyMs. Bulut isExperienced. Learn about Sensorimotor Polyneuropathy.
- Sheehan SyndromeMs. Bulut isExperienced. Learn about Sheehan Syndrome.
- Short Bowel SyndromeMs. Bulut isExperienced. Learn about Short Bowel Syndrome.
- SplenomegalyMs. Bulut isExperienced. Learn about Splenomegaly.
- Turner SyndromeMs. Bulut isExperienced. Learn about Turner Syndrome.
- Von Gierke DiseaseMs. Bulut isExperienced. Learn about Von Gierke Disease.
- Wolman DiseaseMs. Bulut isExperienced. Learn about Wolman Disease.
- X-Linked Creatine DeficiencyMs. Bulut isExperienced. Learn about X-Linked Creatine Deficiency.