Overview
Ana Quilez-Marin practices practicing medicine in Murcia, Spain.
Ms. Quilez-Marin is highly rated in 4 conditions, according to our data. Her clinical expertise encompasses RUNX1 Familial Platelet Disorder, Thrombocytopenia, Glanzmann Thrombasthenia, and Platelet Storage Pool Deficiency.
She is actively involved in clinical research, co-authoring 23 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 Ana Quilez-Marin
Is Ana Quilez-Marin a top-rated expert for RUNX1 Familial Platelet Disorder?
MediFind is an objective health platform that identifies experts based on real-world data. Ana Quilez-Marin 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 Ana Quilez-Marin participate in research or clinical trials?
Yes. Ana Quilez-Marin has published 23 articles and abstracts on conditions like RUNX1 Familial Platelet Disorder. You can view a list of Ana Quilez-Marin'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 DisorderMs. Quilez-Marin isDistinguished. Learn about RUNX1 Familial Platelet Disorder.
- ThrombocytopeniaMs. Quilez-Marin isDistinguished. Learn about Thrombocytopenia.
- Advanced
- Glanzmann ThrombastheniaMs. Quilez-Marin isAdvanced. Learn about Glanzmann Thrombasthenia.
- Platelet Storage Pool DeficiencyMs. Quilez-Marin isAdvanced. Learn about Platelet Storage Pool Deficiency.
- Experienced
- Acute Myeloid Leukemia (AML)Ms. Quilez-Marin isExperienced. Learn about Acute Myeloid Leukemia (AML).
- AlbinismMs. Quilez-Marin isExperienced. Learn about Albinism.
- Blood ClotsMs. Quilez-Marin isExperienced. Learn about Blood Clots.
- Classic GalactosemiaMs. Quilez-Marin isExperienced. Learn about Classic Galactosemia.
- Galactokinase DeficiencyMs. Quilez-Marin isExperienced. Learn about Galactokinase Deficiency.
- Galactose Epimerase DeficiencyMs. Quilez-Marin isExperienced. Learn about Galactose Epimerase Deficiency.
- GalactosemiaMs. Quilez-Marin isExperienced. Learn about Galactosemia.
- Hermansky-Pudlak SyndromeMs. Quilez-Marin isExperienced. Learn about Hermansky-Pudlak Syndrome.
- Hypomelanotic DisorderMs. Quilez-Marin isExperienced. Learn about Hypomelanotic Disorder.
- LeukemiaMs. Quilez-Marin isExperienced. Learn about Leukemia.
- MenorrhagiaMs. Quilez-Marin isExperienced. Learn about Menorrhagia.
- MYH9 Related ThrombocytopeniaMs. Quilez-Marin isExperienced. Learn about MYH9 Related Thrombocytopenia.
- Oculocutaneous AlbinismMs. Quilez-Marin isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1Ms. Quilez-Marin isExperienced. Learn about Oculocutaneous Albinism Type 1.
- Oculocutaneous Albinism Type 2Ms. Quilez-Marin isExperienced. Learn about Oculocutaneous Albinism Type 2.