Eva Rombout, MD

Rare Disease / Clinical Research

Sanquin Research and Blood Bank Divisions

QC-verified· March 2026 PI on 2 trials

ℹ

Specialists are identified from ClinicalTrials.gov principal investigators, PubMed publications, and the NPI registry, then ranked through an automated scoring pipeline.

Report missing data

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

Hereditary Hemochromatosis
Neonatal hemochromatosis

Clinical trials (2)

NCT00202436
NCT01398644

Verify independently

ClinicalTrials.gov PI search for Eva Rombout, MD

Other specialists for Hereditary Hemochromatosis

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

Curtis Scribner, MD, LCSW
Biojiva LLC
ME
Carina Levin, MD
Pediatric Hematology Unit, Ha'Emek Medical Center, Afula, Israel
Florian LEMAITRE
Rennes University Hospital
Rune J Ulvik
Dept. of Clinical Science and Lab. of Clinical Biochemistry, Univ. of Bergen and Haukeland University Hospital, Bergen, N5021, Norway
G Koek, Dr
Maastricht University Medical Center
Francesco Equitani
San Filippo Neri General Hospital
Tatjana Sundic
Department of Immunology and Transfusion Medicine, Haugesund Hospital
Scott Reeder, MD PhD
University of Wisconsin, Madison
WI

See all specialists for Hereditary Hemochromatosis →

← Back to specialists directory