Overview
Sylvie Daliphard practices in Rouen, France. Ms. Daliphard is rated as an Experienced expert by MediFind in the treatment of Glucose-6-Phosphate Dehydrogenase Deficiency. Her top areas of expertise are Hereditary Ovalocytosis, Hereditary Elliptocytosis, Hemolytic Anemia, Hereditary Pyropoikilocytosis, and Splenectomy.
Her clinical research consists of co-authoring 25 peer reviewed articles. MediFind looks at clinical research from the past 15 years. In particular, she has co-authored 2 articles in the study of Glucose-6-Phosphate Dehydrogenase Deficiency.
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.
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
- Hereditary ElliptocytosisMs. Daliphard isAdvanced. Learn about Hereditary Elliptocytosis.
- Hereditary OvalocytosisMs. Daliphard isAdvanced. Learn about Hereditary Ovalocytosis.
- Experienced
- Acute Myeloid Leukemia (AML)Ms. Daliphard isExperienced. Learn about Acute Myeloid Leukemia (AML).
- Anaplastic Large Cell LymphomaMs. Daliphard isExperienced. Learn about Anaplastic Large Cell Lymphoma.
- AnemiaMs. Daliphard isExperienced. Learn about Anemia.
- Congenital Hemolytic AnemiaMs. Daliphard isExperienced. Learn about Congenital Hemolytic Anemia.
- Folate DeficiencyMs. Daliphard isExperienced. Learn about Folate Deficiency.
- Glucose-6-Phosphate Dehydrogenase DeficiencyMs. Daliphard isExperienced. Learn about Glucose-6-Phosphate Dehydrogenase Deficiency.