Hélène Dollfus, MD

Rare Disease / Clinical Research

Fédération Génétique

PI on 3 trials

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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.

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Rare diseases treated or studied

Based on trial PI assignments and publication topics.

Bardet-Biedl syndrome
Retinal ciliopathy
Rare retinal disorder
Rare genetic retinal disorder
Alström syndrome
Rare genetic eye disease
Rare ophthalmic disorder
Developmental defect of the eye
Laurence-Moon syndrome

Clinical trials (3)

NCT00213811
NCT02890550
NCT02860520

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ClinicalTrials.gov PI search for Hélène Dollfus, MD

Other specialists for Bardet-Biedl syndrome

Peers ranked by clinical-trial PI role, publications, and verification quality.

Robert M Haws, M.D., MD
Marshfield Clinic Research Institute
WI
Leslie G Biesecker, M.D., MD
National Human Genome Research Institute (NHGRI)
MD
J-Louis Mandel, MD
IGBMC
Alain Verloes, MD
Unité de Génétique Robert Debré
Didier Lacombe, MD
Service de Génétique Médicale/Bordeaux
Christian Brandt, MD
CIC Strasbourg
Lisa Guay-Woodford, MD, MD
Children's Hospital of Philadelphia
DC
Todd Durham, PhD
Senior Vice President, Clinical and Outcomes Research

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