Overview
Marc Raaijmakers practices practicing medicine in Rotterdam, Netherlands.
Raaijmakers is highly rated in 2 conditions, according to our data. Their clinical expertise encompasses RUNX1 Familial Platelet Disorder, Severe Congenital Neutropenia, Familial Multiple Lipomatosis, and Acute Myeloid Leukemia (AML).
They are actively involved in clinical research, co-authoring 49 peer reviewed articles.
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 Marc P. Raaijmakers
Is Marc P. Raaijmakers a top-rated expert for RUNX1 Familial Platelet Disorder?
MediFind is an objective health platform that identifies experts based on real-world data. Marc P. Raaijmakers is classified as an Distinguished expert for RUNX1 Familial Platelet Disorder, 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 Marc P. Raaijmakers participate in research or clinical trials?
Yes. Marc P. Raaijmakers has published 49 articles and abstracts on conditions like RUNX1 Familial Platelet Disorder. You can view a list of Marc P. Raaijmakers'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
- Distinguished
- RUNX1 Familial Platelet DisorderRaaijmakers isDistinguished. Learn about RUNX1 Familial Platelet Disorder.
- Advanced
- Severe Congenital NeutropeniaRaaijmakers isAdvanced. Learn about Severe Congenital Neutropenia.
- Experienced
- Acute Erythroid Leukemia (AEL)Raaijmakers isExperienced. Learn about Acute Erythroid Leukemia (AEL).
- Acute Myeloid Leukemia (AML)Raaijmakers isExperienced. Learn about Acute Myeloid Leukemia (AML).
- AgranulocytosisRaaijmakers isExperienced. Learn about Agranulocytosis.
- AnemiaRaaijmakers isExperienced. Learn about Anemia.
- Aplastic AnemiaRaaijmakers isExperienced. Learn about Aplastic Anemia.
- Chronic Familial NeutropeniaRaaijmakers isExperienced. Learn about Chronic Familial Neutropenia.
- Exocrine Pancreatic InsufficiencyRaaijmakers isExperienced. Learn about Exocrine Pancreatic Insufficiency.
- Familial Multiple LipomatosisRaaijmakers isExperienced. Learn about Familial Multiple Lipomatosis.
- Febrile NeutropeniaRaaijmakers isExperienced. Learn about Febrile Neutropenia.
- LeukemiaRaaijmakers isExperienced. Learn about Leukemia.
- Myelodysplastic Syndrome (MDS)Raaijmakers isExperienced. Learn about Myelodysplastic Syndrome (MDS).
- Shwachman-Diamond SyndromeRaaijmakers isExperienced. Learn about Shwachman-Diamond Syndrome.
- VEXAS SyndromeRaaijmakers isExperienced. Learn about VEXAS Syndrome.