Overview
Marcus Deschauer practices practicing medicine in Munich, Germany.
Mr. Deschauer is highly rated in 13 conditions, according to our data. His clinical expertise encompasses Carnitine Palmitoyltransferase 2 Deficiency, Primary Lateral Sclerosis, Cramp-Fasciculation Syndrome, and Spinal Muscular Atrophy (SMA).
He is actively involved in clinical research, co-authoring 122 peer reviewed articles.
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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 Marcus Deschauer
Is Marcus Deschauer a top-rated expert for Carnitine Palmitoyltransferase 2 Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Marcus Deschauer is classified as an Distinguished expert for Carnitine Palmitoyltransferase 2 Deficiency, 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 Marcus Deschauer participate in research or clinical trials?
Yes. Marcus Deschauer has published 122 articles and abstracts on conditions like Carnitine Palmitoyltransferase 2 Deficiency. You can view a list of Marcus Deschauer'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
- Carnitine Palmitoyltransferase 2 DeficiencyMr. Deschauer isDistinguished. Learn about Carnitine Palmitoyltransferase 2 Deficiency.
- Cramp-Fasciculation SyndromeMr. Deschauer isDistinguished. Learn about Cramp-Fasciculation Syndrome.
- Primary Lateral SclerosisMr. Deschauer isDistinguished. Learn about Primary Lateral Sclerosis.
- Advanced
- Acute Cerebellar AtaxiaMr. Deschauer isAdvanced. Learn about Acute Cerebellar Ataxia.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Carnitine Palmitoyltransferase 1 Deficiency
- Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Chorea-AcanthocytosisMr. Deschauer isAdvanced. Learn about Chorea-Acanthocytosis.
- Limb-Girdle Muscular DystrophyMr. Deschauer isAdvanced. Learn about Limb-Girdle Muscular Dystrophy.
- Limb-Girdle Muscular Dystrophy Type 1AMr. Deschauer isAdvanced. Learn about Limb-Girdle Muscular Dystrophy Type 1A.
- Pompe DiseaseMr. Deschauer isAdvanced. Learn about Pompe Disease.
- Progressive External OphthalmoplegiaMr. Deschauer isAdvanced. Learn about Progressive External Ophthalmoplegia.
- Spinal Muscular Atrophy (SMA)Mr. Deschauer isAdvanced. Learn about Spinal Muscular Atrophy (SMA).
- Experienced
- Adult Polyglucosan Body DiseaseMr. Deschauer isExperienced. Learn about Adult Polyglucosan Body Disease.
- Arachnoid CystsMr. Deschauer isExperienced. Learn about Arachnoid Cysts.
- Brown SyndromeMr. Deschauer isExperienced. Learn about Brown Syndrome.
- CACH SyndromeMr. Deschauer isExperienced. Learn about CACH Syndrome.
- Cockayne SyndromeMr. Deschauer isExperienced. Learn about Cockayne Syndrome.
- Cockayne Syndrome Type 1Mr. Deschauer isExperienced. Learn about Cockayne Syndrome Type 1.
- Cockayne Syndrome Type 2Mr. Deschauer isExperienced. Learn about Cockayne Syndrome Type 2.
- Congenital Fiber-Type DisproportionMr. Deschauer isExperienced. Learn about Congenital Fiber-Type Disproportion.
- Congenital HypothyroidismMr. Deschauer isExperienced. Learn about Congenital Hypothyroidism.
- Congenital Myasthenic SyndromeMr. Deschauer isExperienced. Learn about Congenital Myasthenic Syndrome.
- Distal Myopathy 2Mr. Deschauer isExperienced. Learn about Distal Myopathy 2.
- Drug Induced DyskinesiaMr. Deschauer isExperienced. Learn about Drug Induced Dyskinesia.
- DysarthriaMr. Deschauer isExperienced. Learn about Dysarthria.
- Facioscapulohumeral Muscular Dystrophy (FSHD)Mr. Deschauer isExperienced. Learn about Facioscapulohumeral Muscular Dystrophy (FSHD).
- Glycogen Storage Disease Type 5Mr. Deschauer isExperienced. Learn about Glycogen Storage Disease Type 5.
- Hallervorden-Spatz DiseaseMr. Deschauer isExperienced. Learn about Hallervorden-Spatz Disease.
- HeadacheMr. Deschauer isExperienced. Learn about Headache.
- Hereditary AtaxiaMr. Deschauer isExperienced. Learn about Hereditary Ataxia.
- Hereditary Spastic ParaparesisMr. Deschauer isExperienced. Learn about Hereditary Spastic Paraparesis.
- LeukocytosisMr. Deschauer isExperienced. Learn about Leukocytosis.
- Macrophagic MyofasciitisMr. Deschauer isExperienced. Learn about Macrophagic Myofasciitis.
- Mcleod Neuroacanthocytosis SyndromeMr. Deschauer isExperienced. Learn about Mcleod Neuroacanthocytosis Syndrome.
- MELAS SyndromeMr. Deschauer isExperienced. Learn about MELAS Syndrome.
- Miyoshi MyopathyMr. Deschauer isExperienced. Learn about Miyoshi Myopathy.
- Movement DisordersMr. Deschauer isExperienced. Learn about Movement Disorders.
- Muscle AtrophyMr. Deschauer isExperienced. Learn about Muscle Atrophy.
- Myoclonic EpilepsyMr. Deschauer isExperienced. Learn about Myoclonic Epilepsy.
- MyositisMr. Deschauer isExperienced. Learn about Myositis.
- Myotonic DystrophyMr. Deschauer isExperienced. Learn about Myotonic Dystrophy.
- Myotonic Dystrophy Type 2Mr. Deschauer isExperienced. Learn about Myotonic Dystrophy Type 2.
- PapilledemaMr. Deschauer isExperienced. Learn about Papilledema.
- Paramyotonia CongenitaMr. Deschauer isExperienced. Learn about Paramyotonia Congenita.
- Progressive Multifocal LeukoencephalopathyMr. Deschauer isExperienced. Learn about Progressive Multifocal Leukoencephalopathy.
- RhabdomyolysisMr. Deschauer isExperienced. Learn about Rhabdomyolysis.
- Spastic Paraplegia Type 2Mr. Deschauer isExperienced. Learn about Spastic Paraplegia Type 2.
- SpasticityMr. Deschauer isExperienced. Learn about Spasticity.
- Spinal Muscular Atrophy Type 2Mr. Deschauer isExperienced. Learn about Spinal Muscular Atrophy Type 2.
- Spinal Muscular Atrophy Type 3Mr. Deschauer isExperienced. Learn about Spinal Muscular Atrophy Type 3.
- Spinocerebellar AtaxiaMr. Deschauer isExperienced. Learn about Spinocerebellar Ataxia.
- Tubular Aggregate MyopathyMr. Deschauer isExperienced. Learn about Tubular Aggregate Myopathy.
- X-Linked Myotubular MyopathyMr. Deschauer isExperienced. Learn about X-Linked Myotubular Myopathy.
- Xeroderma PigmentosumMr. Deschauer isExperienced. Learn about Xeroderma Pigmentosum.