Overview
Pascale Schneider practices in Rouen, France. Ms. Schneider is highly rated in 4 conditions, according to our data. Her top areas of expertise are Chronic Graft Versus Host Disease (cGvHD), Febrile Neutropenia, Acute Lymphoblastic Leukemia (ALL), Leukemia, and Bone Marrow Transplant.
Her clinical research consists of co-authoring 53 peer reviewed articles and participating in 2 clinical trials. MediFind looks at clinical research from the past 15 years.
Locations
Lille, France
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.
2 Clinical Trials
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
- Acute Lymphoblastic Leukemia (ALL)Ms. Schneider isAdvanced. Learn about Acute Lymphoblastic Leukemia (ALL).
- Chronic Graft Versus Host Disease (cGvHD)
- Febrile NeutropeniaMs. Schneider isAdvanced. Learn about Febrile Neutropenia.
- LeukemiaMs. Schneider isAdvanced. Learn about Leukemia.
- Experienced
- Acute Myeloid Leukemia (AML)Ms. Schneider isExperienced. Learn about Acute Myeloid Leukemia (AML).
- AgranulocytosisMs. Schneider isExperienced. Learn about Agranulocytosis.
- Blood ClotsMs. Schneider isExperienced. Learn about Blood Clots.
- Bone Marrow TransplantMs. Schneider isExperienced. Learn about Bone Marrow Transplant.
- Childhood Acute Myeloid LeukemiaMs. Schneider isExperienced. Learn about Childhood Acute Myeloid Leukemia.
- Congenital AfibrinogenemiaMs. Schneider isExperienced. Learn about Congenital Afibrinogenemia.