Ricardo Cruciani, MD, PhD

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

• Systemic primary carnitine deficiency→
• Hereditary persistence of fetal hemoglobin-sickle cell disease syndrome→

Clinical trials (2)

• NCT00079599
• NCT00091169

Verify independently

• ClinicalTrials.gov PI search for Ricardo Cruciani, MD, PhD

Other specialists for Systemic primary carnitine deficiency

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

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• Kathleen Giacomini, PhD
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• Aurore CURIE, MD,PhD
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• Chris McIntyre, IDC
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See all specialists for Systemic primary carnitine deficiency →