Laurent Servais
Rare Disease / Clinical Research
Centre Hospitalier Universitaire de Liege
PI on 1 trial 28 publications
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Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.
Report missing dataRare diseases treated or studied
Based on trial PI assignments and publication topics.
- Mitochondrial disease with epilepsy
- Citrullinemia type II
- Dopa-responsive dystonia
- Timothy syndrome type 2
- Citrin deficiency
- Fanconi-Bickel syndrome
- Episodic ataxia type 6
- Ataxia with vitamin E deficiency
- Carnitine palmitoyl transferase 1A deficiency
- Glycogen storage disease due to phosphoglucomutase deficiency
- Congenital nephrotic syndrome, Finnish type
- Pulmonary agenesis
- Late-onset citrullinemia type I
- Charcot-Marie-Tooth disease type 1
- Central nervous system cystic malformation
- Glutaryl-CoA dehydrogenase deficiency
- Isolated dystonia
- Primary congenital hypothyroidism
- Maple syrup urine disease
- Mucopolysaccharidosis type 6
- X-linked alpha-thalassemia-intellectual disability syndrome
- Neuronal tumor
- Congenital hypothyroidism
- Central congenital hypothyroidism
- Gordon syndrome
- Carbamoyl-phosphate synthetase 1 deficiency
- Medium chain acyl-CoA dehydrogenase deficiency
- Hereditary progressive cardiac conduction defect
- X-linked recessive ocular albinism
- Multiple symmetric lipomatosis
Clinical trials (1)
Verify independently
Other specialists for Mitochondrial disease with epilepsy
Peers ranked by clinical-trial PI role, publications, and verification quality.
- Michio Hirano, MD, M.DColumbia UniversityNY
- Elizabeth M McCormick, MSChildren's Hospital of Philadelphia
- Vinay Penematsa, MDPTC Therapeutics
- Robert Fischer, MDOmeicos Therapeutics GmbH
See all specialists for Mitochondrial disease with epilepsy →