Overview
Agnes Guet practices practicing medicine in Colombes, France.
Ms. Guet is highly rated in 1 condition, according to our data. Her clinical expertise encompasses Pyruvate Carboxylase Deficiency, Schizencephaly, Corpus Callosum Agenesis, and Porencephaly.
She is actively involved in clinical research, co-authoring 14 peer reviewed articles.
Gender
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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 Agnes Guet
Is Agnes Guet a top-rated expert for Pyruvate Carboxylase Deficiency?
MediFind is an objective health platform that identifies experts based on real-world data. Agnes Guet is classified as an Advanced expert for Pyruvate Carboxylase Deficiency, 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 Agnes Guet participate in research or clinical trials?
Yes. Agnes Guet has published 14 articles and abstracts on conditions like Pyruvate Carboxylase Deficiency. You can view a list of Agnes Guet'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
- Advanced
- Pyruvate Carboxylase Deficiency
- Experienced
- Achalasia Microcephaly SyndromeMs. Guet isExperienced. Learn about Achalasia Microcephaly Syndrome.
- Corpus Callosum AgenesisMs. Guet isExperienced. Learn about Corpus Callosum Agenesis.
- Cortical DysplasiaMs. Guet isExperienced. Learn about Cortical Dysplasia.
- Familial PorencephalyMs. Guet isExperienced. Learn about Familial Porencephaly.
- Joubert SyndromeMs. Guet isExperienced. Learn about Joubert Syndrome.
- Microcephalic Osteodysplastic Primordial Dwarfism Type 1 (MOPD1)
- Microcephalic Osteodysplastic Primordial Dwarfism Type 2 (MOPD2)
- MicrocephalyMs. Guet isExperienced. Learn about Microcephaly.
- PolymicrogyriaMs. Guet isExperienced. Learn about Polymicrogyria.
- PorencephalyMs. Guet isExperienced. Learn about Porencephaly.
- Pyruvate Decarboxylase DeficiencyMs. Guet isExperienced. Learn about Pyruvate Decarboxylase Deficiency.
- Pyruvate Dehydrogenase DeficiencyMs. Guet isExperienced. Learn about Pyruvate Dehydrogenase Deficiency.
- SchizencephalyMs. Guet isExperienced. Learn about Schizencephaly.
- Septo-Optic DysplasiaMs. Guet isExperienced. Learn about Septo-Optic Dysplasia.
- Spastic ParaparesisMs. Guet isExperienced. Learn about Spastic Paraparesis.