Carina Levin, MD

Rare Disease / Clinical Research

Pediatric Hematology Unit, Ha'Emek Medical Center, Afula, Israel

PI on 5 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.

Hereditary Hemochromatosis
Thalassemia
Hemoglobinopathy
Sickle cell disease
Sickle cell-beta-thalassemia disease
Ataxia-telangiectasia variant
Beta-thalassemia
Beta-thalassemia major
Genetic hemoglobinopathy
Beta-thalassemia intermedia
Dietary iron overload disease

Clinical trials (5)

NCT00972231
NCT00736008
NCT00456690
NCT01935661
NCT00736060

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ClinicalTrials.gov PI search for Carina Levin, MD

Other specialists for Hereditary Hemochromatosis

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

Eva Rombout, MD
Sanquin Research and Blood Bank Divisions
Curtis Scribner, MD, LCSW
Biojiva LLC
ME
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

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