Overview
Camille Wicker practices practicing medicine in Strasbourg, France.
Ms. Wicker is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Phosphomannoisomerase Deficiency, PMM2-Congenital Disorder of Glycosylation, Propionic Acidemia, Glycogen Storage Disease Type 3, and Gastrostomy.
She is actively involved in clinical research, co-authoring 14 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 Camille Wicker
Is Camille Wicker a top-rated expert for Phosphomannoisomerase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Camille Wicker is classified as an Advanced expert for Phosphomannoisomerase 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 Camille Wicker participate in research or clinical trials?
Yes. Camille Wicker has published 14 articles and abstracts on conditions like Phosphomannoisomerase Deficiency. You can view a list of Camille Wicker'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
- Phosphomannoisomerase DeficiencyMs. Wicker isAdvanced. Learn about Phosphomannoisomerase Deficiency.
- Experienced
- AgranulocytosisMs. Wicker isExperienced. Learn about Agranulocytosis.
- Cholesteryl Ester Storage DiseaseMs. Wicker isExperienced. Learn about Cholesteryl Ester Storage Disease.
- GastrostomyMs. Wicker isExperienced. Learn about Gastrostomy.
- Glutaric Acidemia Type 2Ms. Wicker isExperienced. Learn about Glutaric Acidemia Type 2.
- Glycogen Storage Disease Type 3Ms. Wicker isExperienced. Learn about Glycogen Storage Disease Type 3.
- Hepatocerebral DegenerationMs. Wicker isExperienced. Learn about Hepatocerebral Degeneration.
- Inborn Amino Acid Metabolism DisorderMs. Wicker isExperienced. Learn about Inborn Amino Acid Metabolism Disorder.
- Lactic AcidosisMs. Wicker isExperienced. Learn about Lactic Acidosis.
- Lipidosis with Triglycerid Storage Disease
- Low Blood SugarMs. Wicker isExperienced. Learn about Low Blood Sugar.
- Lysosomal Acid Lipase DeficiencyMs. Wicker isExperienced. Learn about Lysosomal Acid Lipase Deficiency.
- Maple Syrup Urine DiseaseMs. Wicker isExperienced. Learn about Maple Syrup Urine Disease.
- Metabolic AcidosisMs. Wicker isExperienced. Learn about Metabolic Acidosis.
- MPI-CDGMs. Wicker isExperienced. Learn about MPI-CDG.
- PMM2-Congenital Disorder of Glycosylation
- Propionic AcidemiaMs. Wicker isExperienced. Learn about Propionic Acidemia.
- RhabdomyolysisMs. Wicker isExperienced. Learn about Rhabdomyolysis.
- Urea Cycle Disorders (UCD)Ms. Wicker isExperienced. Learn about Urea Cycle Disorders (UCD).
- Von Gierke DiseaseMs. Wicker isExperienced. Learn about Von Gierke Disease.
- Wolman DiseaseMs. Wicker isExperienced. Learn about Wolman Disease.