Overview
Guilhem Sole practices practicing medicine in Bordeaux, France.
Sole is highly rated in 14 conditions, according to our data. Their clinical expertise encompasses Cramp-Fasciculation Syndrome, Charcot-Marie-Tooth Disease, Primary Lateral Sclerosis, and Pompe Disease.
They are actively involved in clinical research, co-authoring 126 peer reviewed articles and participating in 4 clinical trials.
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.
4 Clinical Trials
Frequently Asked Questions about Guilhem Sole
Is Guilhem Sole a top-rated expert for Cramp-Fasciculation Syndrome?
MediFind is an objective health platform that identifies experts based on real-world data. Guilhem Sole is classified as an Distinguished expert for Cramp-Fasciculation Syndrome, 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 Guilhem Sole participate in research or clinical trials?
Yes. Guilhem Sole has published 125 articles and abstracts on conditions like Cramp-Fasciculation Syndrome. You can view a list of Guilhem Sole'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
- Cramp-Fasciculation SyndromeSole isDistinguished. Learn about Cramp-Fasciculation Syndrome.
- Advanced
- CamptocormismSole isAdvanced. Learn about Camptocormism.
- Charcot-Marie-Tooth Disease
- Chronic Inflammatory Demyelinating Polyneuropathy
- Facioscapulohumeral Muscular Dystrophy (FSHD)
- Frontometaphyseal Dysplasia
- Limb-Girdle Muscular Dystrophy
- Myasthenia GravisSole isAdvanced. Learn about Myasthenia Gravis.
- ParaplegiaSole isAdvanced. Learn about Paraplegia.
- Pompe DiseaseSole isAdvanced. Learn about Pompe Disease.
- Primary Lateral Sclerosis
- Spastic Paraplegia Type 7
- SpasticitySole isAdvanced. Learn about Spasticity.
- Spinal Muscular Atrophy (SMA)
- Experienced
- Acromicric DysplasiaSole isExperienced. Learn about Acromicric Dysplasia.
- Acute Cerebellar AtaxiaSole isExperienced. Learn about Acute Cerebellar Ataxia.
- ADULT SyndromeSole isExperienced. Learn about ADULT Syndrome.
- Amyotrophic Lateral Sclerosis (ALS or Lou Gehrig's Disease)
- Andersen-Tawil SyndromeSole isExperienced. Learn about Andersen-Tawil Syndrome.
- Arthrogryposis Multiplex Congenita
- Autonomic NeuropathySole isExperienced. Learn about Autonomic Neuropathy.
- Becker Muscular DystrophySole isExperienced. Learn about Becker Muscular Dystrophy.
- Brachial PlexopathySole isExperienced. Learn about Brachial Plexopathy.
- Brachydactyly Mononen TypeSole isExperienced. Learn about Brachydactyly Mononen Type.
- Brown SyndromeSole isExperienced. Learn about Brown Syndrome.
- Cardiac AmyloidosisSole isExperienced. Learn about Cardiac Amyloidosis.
- CardiomyopathySole isExperienced. Learn about Cardiomyopathy.
- Carnitine Palmitoyltransferase 1 Deficiency
- Carnitine Palmitoyltransferase 2 Deficiency
- ChondrodystrophySole isExperienced. Learn about Chondrodystrophy.
- Chronic Polyradiculoneuritis
- Collagen VI-Related Myopathy
- Congenital ContracturesSole isExperienced. Learn about Congenital Contractures.
- Congenital Myasthenic Syndrome
- COVID-19Sole isExperienced. Learn about COVID-19.
- Drug Induced DyskinesiaSole isExperienced. Learn about Drug Induced Dyskinesia.
- Duchenne Muscular DystrophySole isExperienced. Learn about Duchenne Muscular Dystrophy.
- DysarthriaSole isExperienced. Learn about Dysarthria.
- DysferlinopathySole isExperienced. Learn about Dysferlinopathy.
- Familial Hemiplegic Migraine
- Familial Transthyretin Amyloidosis
- Fetal Enterovirus SyndromeSole isExperienced. Learn about Fetal Enterovirus Syndrome.
- Frontotemporal DementiaSole isExperienced. Learn about Frontotemporal Dementia.
- Giant Cell Arteritis (GCA)Sole isExperienced. Learn about Giant Cell Arteritis (GCA).
- Guillain-Barre SyndromeSole isExperienced. Learn about Guillain-Barre Syndrome.
- Hereditary AtaxiaSole isExperienced. Learn about Hereditary Ataxia.
- Juvenile Temporal ArteritisSole isExperienced. Learn about Juvenile Temporal Arteritis.
- Livedo ReticularisSole isExperienced. Learn about Livedo Reticularis.
- MacroglossiaSole isExperienced. Learn about Macroglossia.
- MigraineSole isExperienced. Learn about Migraine.
- Migraine with Brainstem Aura
- Miller-Fisher SyndromeSole isExperienced. Learn about Miller-Fisher Syndrome.
- Movement DisordersSole isExperienced. Learn about Movement Disorders.
- Multifocal Motor NeuropathySole isExperienced. Learn about Multifocal Motor Neuropathy.
- MyositisSole isExperienced. Learn about Myositis.
- Necrotizing Myopathy (NM)Sole isExperienced. Learn about Necrotizing Myopathy (NM).
- Olivopontocerebellar Atrophy
- PapilledemaSole isExperienced. Learn about Papilledema.
- Papular MucinosisSole isExperienced. Learn about Papular Mucinosis.
- Peripheral NeuropathySole isExperienced. Learn about Peripheral Neuropathy.
- PneumoniaSole isExperienced. Learn about Pneumonia.
- Primary AmyloidosisSole isExperienced. Learn about Primary Amyloidosis.
- RhabdomyolysisSole isExperienced. Learn about Rhabdomyolysis.
- Schwartz-Jampel SyndromeSole isExperienced. Learn about Schwartz-Jampel Syndrome.
- ScleromyxedemaSole isExperienced. Learn about Scleromyxedema.
- Severe Acute Respiratory Syndrome (SARS)
- Spastic Paraplegia Type 2Sole isExperienced. Learn about Spastic Paraplegia Type 2.
- Spinal Muscular Atrophy Type 2
- Spinal Muscular Atrophy Type 3
- Spinocerebellar AtaxiaSole isExperienced. Learn about Spinocerebellar Ataxia.
- Temporal ArteritisSole isExperienced. Learn about Temporal Arteritis.
- Transthyretin AmyloidosisSole isExperienced. Learn about Transthyretin Amyloidosis.
- Usher SyndromeSole isExperienced. Learn about Usher Syndrome.
- VasculitisSole isExperienced. Learn about Vasculitis.
- X-Linked Spondyloepiphyseal Dysplasia Tarda