Overview
Samia Pichard practices practicing medicine in Paris, France.
Ms. Pichard is highly rated in 11 conditions, according to our data. Her clinical expertise encompasses Gaucher Disease, Pompe Disease, Pyruvate Decarboxylase Deficiency, Pyruvate Dehydrogenase Deficiency, and Splenectomy.
She is actively involved in clinical research, co-authoring 52 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 Samia Pichard
Is Samia Pichard a top-rated expert for Gaucher Disease?
MediFind is an objective health platform that identifies experts based on real-world data. Samia Pichard is classified as an Advanced expert for Gaucher Disease, 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 Samia Pichard participate in research or clinical trials?
Yes. Samia Pichard has published 52 articles and abstracts on conditions like Gaucher Disease. You can view a list of Samia Pichard'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
- Beta-Ketothiolase DeficiencyMs. Pichard isAdvanced. Learn about Beta-Ketothiolase Deficiency.
- Carnitine-Acylcarnitine Translocase Deficiency
- Gaucher DiseaseMs. Pichard isAdvanced. Learn about Gaucher Disease.
- GM1 GangliosidosisMs. Pichard isAdvanced. Learn about GM1 Gangliosidosis.
- HypotoniaMs. Pichard isAdvanced. Learn about Hypotonia.
- Niemann-Pick DiseaseMs. Pichard isAdvanced. Learn about Niemann-Pick Disease.
- Pompe DiseaseMs. Pichard isAdvanced. Learn about Pompe Disease.
- Propionic AcidemiaMs. Pichard isAdvanced. Learn about Propionic Acidemia.
- Pyruvate Decarboxylase DeficiencyMs. Pichard isAdvanced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Pichard isAdvanced. Learn about Pyruvate Dehydrogenase Deficiency.
- Tyrosinemia Type 1Ms. Pichard isAdvanced. Learn about Tyrosinemia Type 1.
- Experienced
- Acid Sphingomyelinase Deficiency (ASMD)Ms. Pichard isExperienced. Learn about Acid Sphingomyelinase Deficiency (ASMD).
- Batten DiseaseMs. Pichard isExperienced. Learn about Batten Disease.
- Brachydactyly Mononen TypeMs. Pichard isExperienced. Learn about Brachydactyly Mononen Type.
- CLN1 DiseaseMs. Pichard isExperienced. Learn about CLN1 Disease.
- CLN2 DiseaseMs. Pichard isExperienced. Learn about CLN2 Disease.
- CLN3 DiseaseMs. Pichard isExperienced. Learn about CLN3 Disease.
- CLN4 DiseaseMs. Pichard isExperienced. Learn about CLN4 Disease.
- CLN5 DiseaseMs. Pichard isExperienced. Learn about CLN5 Disease.
- Dihydrolipoamide Dehydrogenase DeficiencyMs. Pichard isExperienced. Learn about Dihydrolipoamide Dehydrogenase Deficiency.
- Drug Induced DyskinesiaMs. Pichard isExperienced. Learn about Drug Induced Dyskinesia.
- Early Infantile Epileptic EncephalopathyMs. Pichard isExperienced. Learn about Early Infantile Epileptic Encephalopathy.
- Enlarged LiverMs. Pichard isExperienced. Learn about Enlarged Liver.
- Fanconi Bickel SyndromeMs. Pichard isExperienced. Learn about Fanconi Bickel Syndrome.
- Fanconi SyndromeMs. Pichard isExperienced. Learn about Fanconi Syndrome.
- Farber LipogranulomatosisMs. Pichard isExperienced. Learn about Farber Lipogranulomatosis.
- GangliosidosisMs. Pichard isExperienced. Learn about Gangliosidosis.
- Gaucher Disease Type 1Ms. Pichard isExperienced. Learn about Gaucher Disease Type 1.
- HistiocytosisMs. Pichard isExperienced. Learn about Histiocytosis.
- Intestinal Pseudo-ObstructionMs. Pichard isExperienced. Learn about Intestinal Pseudo-Obstruction.
- Maple Syrup Urine DiseaseMs. Pichard isExperienced. Learn about Maple Syrup Urine Disease.
- Methylmalonic AcidemiaMs. Pichard isExperienced. Learn about Methylmalonic Acidemia.
- Movement DisordersMs. Pichard isExperienced. Learn about Movement Disorders.
- Mucopolysaccharidoses (MPS)Ms. Pichard isExperienced. Learn about Mucopolysaccharidoses (MPS).
- Mucopolysaccharidosis Type 1 (MPS I, Hurler Syndrome)
- Mucopolysaccharidosis Type 4 (MPS IV, Morquio Syndrome)
- Non-Langerhans-Cell HistiocytosisMs. Pichard isExperienced. Learn about Non-Langerhans-Cell Histiocytosis.
- Pediatric MyocarditisMs. Pichard isExperienced. Learn about Pediatric Myocarditis.
- Phenylketonuria (PKU)Ms. Pichard isExperienced. Learn about Phenylketonuria (PKU).
- Prolidase DeficiencyMs. Pichard isExperienced. Learn about Prolidase Deficiency.
- Pyridoxine DeficiencyMs. Pichard isExperienced. Learn about Pyridoxine Deficiency.
- ReticulohistiocytomaMs. Pichard isExperienced. Learn about Reticulohistiocytoma.
- Sinus of Valsalva AneurysmMs. Pichard isExperienced. Learn about Sinus of Valsalva Aneurysm.
- Sjogren-Larsson SyndromeMs. Pichard isExperienced. Learn about Sjogren-Larsson Syndrome.
- Spinocerebellar Ataxia Type 7Ms. Pichard isExperienced. Learn about Spinocerebellar Ataxia Type 7.
- SplenectomyMs. Pichard isExperienced. Learn about Splenectomy.
- Vitamin B12 Deficiency AnemiaMs. Pichard isExperienced. Learn about Vitamin B12 Deficiency Anemia.