Overview
Annie Harroche practices practicing medicine in Paris, France.
Ms. Harroche is highly rated in 9 conditions, according to our data. Her clinical expertise encompasses Blood Clots, Hemophilia A, Von Willebrand Disease (VWD), and Phosphomannoisomerase Deficiency.
She is actively involved in clinical research, co-authoring 69 peer reviewed articles and participating in 2 clinical trials.
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.
2 Clinical Trials
Frequently Asked Questions about Annie Harroche
Is Annie Harroche a top-rated expert for Blood Clots?
MediFind is an objective health platform that identifies experts based on real-world data. Annie Harroche is classified as an Elite expert for Blood Clots, 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 Annie Harroche participate in research or clinical trials?
Yes. Annie Harroche has published 69 articles and abstracts on conditions like Blood Clots. You can view a list of Annie Harroche'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
- Elite
- Blood ClotsMs. Harroche isElite. Learn about Blood Clots.
- Hemophilia AMs. Harroche isElite. Learn about Hemophilia A.
- Distinguished
- Phosphomannoisomerase DeficiencyMs. Harroche isDistinguished. Learn about Phosphomannoisomerase Deficiency.
- Von Willebrand Disease (VWD)Ms. Harroche isDistinguished. Learn about Von Willebrand Disease (VWD).
- Advanced
- Factor 11 DeficiencyMs. Harroche isAdvanced. Learn about Factor 11 Deficiency.
- Factor 13 DeficiencyMs. Harroche isAdvanced. Learn about Factor 13 Deficiency.
- Hemophilia BMs. Harroche isAdvanced. Learn about Hemophilia B.
- MenorrhagiaMs. Harroche isAdvanced. Learn about Menorrhagia.
- MPI-CDGMs. Harroche isAdvanced. Learn about MPI-CDG.
- Experienced
- AlbinismMs. Harroche isExperienced. Learn about Albinism.
- Angiodysplasia of the ColonMs. Harroche isExperienced. Learn about Angiodysplasia of the Colon.
- Brain AbscessMs. Harroche isExperienced. Learn about Brain Abscess.
- C SyndromeMs. Harroche isExperienced. Learn about C Syndrome.
- CHARGE SyndromeMs. Harroche isExperienced. Learn about CHARGE Syndrome.
- Congenital AfibrinogenemiaMs. Harroche isExperienced. Learn about Congenital Afibrinogenemia.
- Corpus Callosum AgenesisMs. Harroche isExperienced. Learn about Corpus Callosum Agenesis.
- Cutis LaxaMs. Harroche isExperienced. Learn about Cutis Laxa.
- EmpyemaMs. Harroche isExperienced. Learn about Empyema.
- Familial HypofibrinogenemiaMs. Harroche isExperienced. Learn about Familial Hypofibrinogenemia.
- Gastrointestinal BleedingMs. Harroche isExperienced. Learn about Gastrointestinal Bleeding.
- Hemophilic ArthropathyMs. Harroche isExperienced. Learn about Hemophilic Arthropathy.
- Hermansky-Pudlak SyndromeMs. Harroche isExperienced. Learn about Hermansky-Pudlak Syndrome.
- MastoiditisMs. Harroche isExperienced. Learn about Mastoiditis.
- Membranoproliferative GlomerulonephritisMs. Harroche isExperienced. Learn about Membranoproliferative Glomerulonephritis.
- Noonan SyndromeMs. Harroche isExperienced. Learn about Noonan Syndrome.
- Oculocutaneous AlbinismMs. Harroche isExperienced. Learn about Oculocutaneous Albinism.
- Oculocutaneous Albinism Type 1Ms. Harroche isExperienced. Learn about Oculocutaneous Albinism Type 1.
- Oculocutaneous Albinism Type 2Ms. Harroche isExperienced. Learn about Oculocutaneous Albinism Type 2.
- Osteogenesis ImperfectaMs. Harroche isExperienced. Learn about Osteogenesis Imperfecta.
- Platelet Storage Pool DeficiencyMs. Harroche isExperienced. Learn about Platelet Storage Pool Deficiency.
- PMM2-Congenital Disorder of GlycosylationMs. Harroche isExperienced. Learn about PMM2-Congenital Disorder of Glycosylation.
- Prader-Willi SyndromeMs. Harroche isExperienced. Learn about Prader-Willi Syndrome.
- Protein S DeficiencyMs. Harroche isExperienced. Learn about Protein S Deficiency.
- RASopathiesMs. Harroche isExperienced. Learn about RASopathies.
- Von Gierke DiseaseMs. Harroche isExperienced. Learn about Von Gierke Disease.