Overview
Pascaline Letard practices practicing medicine in Poitiers, France.
Letard is highly rated in 8 conditions, according to our data. Their clinical expertise encompasses Cerebelloolivary Atrophy, Microcephaly, Achalasia Microcephaly Syndrome, and Autosomal Recessive Cutis Laxa Type 1.
They are actively involved in clinical research, co-authoring 14 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 Pascaline Letard
Is Pascaline Letard a top-rated expert for Cerebelloolivary Atrophy?
MediFind is an objective health platform that identifies experts based on real-world data. Pascaline Letard is classified as an Advanced expert for Cerebelloolivary Atrophy, 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 Pascaline Letard participate in research or clinical trials?
Yes. Pascaline Letard has published 14 articles and abstracts on conditions like Cerebelloolivary Atrophy. You can view a list of Pascaline Letard'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
- Achalasia Microcephaly Syndrome
- Achard SyndromeLetard isAdvanced. Learn about Achard Syndrome.
- ArachnodactylyLetard isAdvanced. Learn about Arachnodactyly.
- Autosomal Recessive Cutis Laxa Type 1
- Cerebelloolivary AtrophyLetard isAdvanced. Learn about Cerebelloolivary Atrophy.
- Chondrodysplasia Punctata Syndrome
- MicrocephalyLetard isAdvanced. Learn about Microcephaly.
- X-Linked Chondrodysplasia Punctata 2
- Experienced
- AchondrogenesisLetard isExperienced. Learn about Achondrogenesis.
- Acromesomelic DysplasiaLetard isExperienced. Learn about Acromesomelic Dysplasia.
- Acromesomelic Dysplasia Campailla Martinelli Type
- Acromesomelic Dysplasia Hunter Thompson Type
- Acromesomelic Dysplasia Maroteaux Type
- Arthrogryposis Multiplex Congenita
- Autosomal Recessive Primary Microcephaly
- Chromosome 13q DuplicationLetard isExperienced. Learn about Chromosome 13q Duplication.
- ClubfootLetard isExperienced. Learn about Clubfoot.
- Congenital Aplastic AnemiaLetard isExperienced. Learn about Congenital Aplastic Anemia.
- Congenital ContracturesLetard isExperienced. Learn about Congenital Contractures.
- Cortical DysplasiaLetard isExperienced. Learn about Cortical Dysplasia.
- Cutis LaxaLetard isExperienced. Learn about Cutis Laxa.
- Diaphragmatic HerniaLetard isExperienced. Learn about Diaphragmatic Hernia.
- Fanconi AnemiaLetard isExperienced. Learn about Fanconi Anemia.
- Hiatal HerniaLetard isExperienced. Learn about Hiatal Hernia.
- Microcephaly Deafness SyndromeLetard isExperienced. Learn about Microcephaly Deafness Syndrome.
- Pontocerebellar HypoplasiaLetard isExperienced. Learn about Pontocerebellar Hypoplasia.
- Trisomy 13Letard isExperienced. Learn about Trisomy 13.
- Williams SyndromeLetard isExperienced. Learn about Williams Syndrome.