Overview
Arnaud Wiedemann practices practicing medicine in Nancy, France.
Mr. Wiedemann is highly rated in 5 conditions, according to our data. His clinical expertise encompasses Phenylketonuria (PKU), Vitamin B12 Deficiency Anemia, Multisystem Inflammatory Syndrome in Children (MIS-C), Aicardi-Goutieres Syndrome, and Rhizotomy.
He 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 Arnaud Wiedemann
Is Arnaud Wiedemann a top-rated expert for Phenylketonuria (PKU)?
MediFind is an objective health platform that identifies experts based on real-world data. Arnaud Wiedemann is classified as an Advanced expert for Phenylketonuria (PKU), 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 Arnaud Wiedemann participate in research or clinical trials?
Yes. Arnaud Wiedemann has published 49 articles and abstracts on conditions like Phenylketonuria (PKU). You can view a list of Arnaud Wiedemann'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
- Aicardi-Goutieres SyndromeMr. Wiedemann isAdvanced. Learn about Aicardi-Goutieres Syndrome.
- Cardiomyopathy Hypogonadism Metabolic Anomalies
- Multisystem Inflammatory Syndrome in Children (MIS-C)
- Phenylketonuria (PKU)Mr. Wiedemann isAdvanced. Learn about Phenylketonuria (PKU).
- Vitamin B12 Deficiency AnemiaMr. Wiedemann isAdvanced. Learn about Vitamin B12 Deficiency Anemia.
- Experienced
- AlkaptonuriaMr. Wiedemann isExperienced. Learn about Alkaptonuria.
- Brachydactyly Mononen TypeMr. Wiedemann isExperienced. Learn about Brachydactyly Mononen Type.
- Brain HerniationMr. Wiedemann isExperienced. Learn about Brain Herniation.
- Carbamoyl Phosphate Synthetase 1 DeficiencyMr. Wiedemann isExperienced. Learn about Carbamoyl Phosphate Synthetase 1 Deficiency.
- Cerebral PalsyMr. Wiedemann isExperienced. Learn about Cerebral Palsy.
- Congenital CataractMr. Wiedemann isExperienced. Learn about Congenital Cataract.
- Cyclic Vomiting SyndromeMr. Wiedemann isExperienced. Learn about Cyclic Vomiting Syndrome.
- Epilepsy in ChildrenMr. Wiedemann isExperienced. Learn about Epilepsy in Children.
- Hereditary Spastic ParaparesisMr. Wiedemann isExperienced. Learn about Hereditary Spastic Paraparesis.
- HypophosphatemiaMr. Wiedemann isExperienced. Learn about Hypophosphatemia.
- HypotoniaMr. Wiedemann isExperienced. Learn about Hypotonia.
- KwashiorkorMr. Wiedemann isExperienced. Learn about Kwashiorkor.
- Liver FailureMr. Wiedemann isExperienced. Learn about Liver Failure.
- MalnutritionMr. Wiedemann isExperienced. Learn about Malnutrition.
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- OchronosisMr. Wiedemann isExperienced. Learn about Ochronosis.
- Patent Foramen OvaleMr. Wiedemann isExperienced. Learn about Patent Foramen Ovale.
- Pectus CarinatumMr. Wiedemann isExperienced. Learn about Pectus Carinatum.
- PMM2-Congenital Disorder of GlycosylationMr. Wiedemann isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Primary HyperoxaluriaMr. Wiedemann isExperienced. Learn about Primary Hyperoxaluria.
- Primary Hyperoxaluria Type 1Mr. Wiedemann isExperienced. Learn about Primary Hyperoxaluria Type 1.
- Rett SyndromeMr. Wiedemann isExperienced. Learn about Rett Syndrome.
- RhabdomyolysisMr. Wiedemann isExperienced. Learn about Rhabdomyolysis.
- RhizotomyMr. Wiedemann isExperienced. Learn about Rhizotomy.
- RicketsMr. Wiedemann isExperienced. Learn about Rickets.
- Salmonella EnterocolitisMr. Wiedemann isExperienced. Learn about Salmonella Enterocolitis.
- Singleton-Merten SyndromeMr. Wiedemann isExperienced. Learn about Singleton-Merten Syndrome.
- Spastic Diplegia Infantile TypeMr. Wiedemann isExperienced. Learn about Spastic Diplegia Infantile Type.
- Spastic ParaparesisMr. Wiedemann isExperienced. Learn about Spastic Paraparesis.
- Spastic Paraplegia Type 2Mr. Wiedemann isExperienced. Learn about Spastic Paraplegia Type 2.
- Spastic Paraplegia Type 7Mr. Wiedemann isExperienced. Learn about Spastic Paraplegia Type 7.
- SpasticityMr. Wiedemann isExperienced. Learn about Spasticity.
- Sudden Infant Death Syndrome (SIDS)Mr. Wiedemann isExperienced. Learn about Sudden Infant Death Syndrome (SIDS).
- Urea Cycle Disorders (UCD)Mr. Wiedemann isExperienced. Learn about Urea Cycle Disorders (UCD).
- Vitamin D DeficiencyMr. Wiedemann isExperienced. Learn about Vitamin D Deficiency.
- X-Linked HypophosphatemiaMr. Wiedemann isExperienced. Learn about X-Linked Hypophosphatemia.