Overview
Stojan Peric practices practicing medicine in Belgrade, Serbia.
Peric is highly rated in 24 conditions, according to our data. Their clinical expertise encompasses Paramyotonia Congenita, Myotonic Dystrophy, Myotonic Dystrophy Type 2, and Multifocal Motor Neuropathy.
They are actively involved in clinical research, co-authoring 167 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 Stojan Z. Peric
Is Stojan Z. Peric a top-rated expert for Paramyotonia Congenita?
MediFind is an objective health platform that identifies experts based on real-world data. Stojan Z. Peric is classified as an Elite expert for Paramyotonia Congenita, 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 Stojan Z. Peric participate in research or clinical trials?
Yes. Stojan Z. Peric has published 167 articles and abstracts on conditions like Paramyotonia Congenita. You can view a list of Stojan Z. Peric'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
- Elite
- Chronic Inflammatory Demyelinating Polyneuropathy
- Chronic Polyradiculoneuritis
- Guillain-Barre Syndrome
- Multifocal Motor Neuropathy
- Myasthenia GravisPeric isElite. Learn about Myasthenia Gravis.
- Myotonic Dystrophy
- Myotonic Dystrophy Type 2
- Paramyotonia Congenita
- Distinguished
- Spinal Muscular Atrophy with Arthrogryposis
- Tomaculous NeuropathyPeric isDistinguished. Learn about Tomaculous Neuropathy.
- Advanced
- Arthrogryposis Multiplex Congenita
- Charcot-Marie-Tooth Disease
- Congenital ContracturesPeric isAdvanced. Learn about Congenital Contractures.
- Congenital Myasthenic Syndrome
- Excessive Daytime Sleepiness
- HemangioblastomaPeric isAdvanced. Learn about Hemangioblastoma.
- Limb-Girdle Muscular Dystrophy
- Limb-Girdle Muscular Dystrophy Type 2A
- Metabolic SyndromePeric isAdvanced. Learn about Metabolic Syndrome.
- NeuralgiaPeric isAdvanced. Learn about Neuralgia.
- Primary Lateral Sclerosis
- Spinal Muscular Atrophy (SMA)
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Experienced
- Abdominal Obesity Metabolic Syndrome
- Acute PainPeric isExperienced. Learn about Acute Pain.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- AnhidrosisPeric isExperienced. Learn about Anhidrosis.
- CACH SyndromePeric isExperienced. Learn about CACH Syndrome.
- CataractPeric isExperienced. Learn about Cataract.
- Central Sleep ApneaPeric isExperienced. Learn about Central Sleep Apnea.
- COVID-19Peric isExperienced. Learn about COVID-19.
- Cramp-Fasciculation SyndromePeric isExperienced. Learn about Cramp-Fasciculation Syndrome.
- DrowsinessPeric isExperienced. Learn about Drowsiness.
- Drug Induced DyskinesiaPeric isExperienced. Learn about Drug Induced Dyskinesia.
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Familial DysautonomiaPeric isExperienced. Learn about Familial Dysautonomia.
- Familial HypertriglyceridemiaPeric isExperienced. Learn about Familial Hypertriglyceridemia.
- Genetic Epilepsy with Febrile Seizures Plus (GEFS+)
- Hajdu-Cheney SyndromePeric isExperienced. Learn about Hajdu-Cheney Syndrome.
- Hashimoto ThyroiditisPeric isExperienced. Learn about Hashimoto Thyroiditis.
- HeadachePeric isExperienced. Learn about Headache.
- HemangiomaPeric isExperienced. Learn about Hemangioma.
- Hereditary Sensory and Autonomic Neuropathy Type 2
- Hereditary Sensory Neuropathy Type 1 (HSN1)
- Lambert-Eaton SyndromePeric isExperienced. Learn about Lambert-Eaton Syndrome.
- LeukocytosisPeric isExperienced. Learn about Leukocytosis.
- Localized SclerodermaPeric isExperienced. Learn about Localized Scleroderma.
- Mitral Valve ProlapsePeric isExperienced. Learn about Mitral Valve Prolapse.
- Monoclonal Gammopathy of Undetermined Significance (MGUS)
- MosaicismPeric isExperienced. Learn about Mosaicism.
- Movement DisordersPeric isExperienced. Learn about Movement Disorders.
- Muscle AtrophyPeric isExperienced. Learn about Muscle Atrophy.
- MyositisPeric isExperienced. Learn about Myositis.
- Neuromyelitis OpticaPeric isExperienced. Learn about Neuromyelitis Optica.
- Oculopharyngeal Muscular Dystrophy
- Optic NeuritisPeric isExperienced. Learn about Optic Neuritis.
- Paget's Disease of BonePeric isExperienced. Learn about Paget's Disease of Bone.
- ParaplegiaPeric isExperienced. Learn about Paraplegia.
- Pompe DiseasePeric isExperienced. Learn about Pompe Disease.
- Restless Legs SyndromePeric isExperienced. Learn about Restless Legs Syndrome.
- RhabdomyolysisPeric isExperienced. Learn about Rhabdomyolysis.
- Spastic Paraplegia Type 2Peric isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Peric isExperienced. Learn about Spastic Paraplegia Type 7.
- StrokePeric isExperienced. Learn about Stroke.
- Transverse MyelitisPeric isExperienced. Learn about Transverse Myelitis.
- Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency