Marcelo M Serra
Marcelo M Serra, PhD is an expert in Hematology at Hospital Italiano de Buenos Aires (Argentina). As of October 2026, ScienceLeadR ranks Marcelo M Serra in the top 1% of experts worldwide for Telangiectasis, and in the top 1% of experts in Argentina for Cardiovascular Abnormalities and Hemostatic Disorders. Marcelo M Serra has authored 38 publications, the most recent in 2025, and is an investigator in 3 clinical trials, 1 of them ongoing. SLR score: 175 (community average: 125). How the SLR is computed.
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Hematology
Subspecialties: Cardiology - Neurology - Pediatrics
Main Topics
Publications and Clinical Studies
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Short Biography
Internal Medicine specialist, head of Rare Diseases Program at Hospital Italiano de Buenos Aires, Argentina. I am passionate in vascular anomalies mainly in Hereditary Hemorrhagic Telangiectasia. I created and managing the HHT Referral Center at the same hospital. Also, I am the co-director of von Hippel Lindau Unit. I am a clinical-traslational researcher and PhD. As Rare Diseases Program director push up the best managing of complex and difficult clinical cases. I was designed Assistant Professor in the Hospital Italiano University and Associated Profesor int the Universidad de Buenos Aires, I am good at working on collaborative and multidisciplinary teams.
Organizations
Career arc: 1999 - 2025
Number : 38
Citations
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Latest Publications
5 most recent indexed articles
Source: Pubmed
| Title | Journal | Year | Citations |
|---|---|---|---|
| Standardization of Terminology, Definitions, and Outcome Criteria for Bleeding in Hereditary Hemorrhagic Telangiectasia: International Consensus Report. PMID 40662351 — epistaxis, hematology, hemorrhage, anemia, telangiectasia, hereditary hemorrhagic, telangiectasis, therapeutics, iron deficiencies, angiogenesis | Am J Hematol | 2025 | 0 |
| [Frequently asked questions about rare or uncommon diseases]. PMID 40793905 | Medicina (B Aires) | 2025 | 0 |
| Hereditary hemorrhagic telangiectasia in pediatrics: descriptive study in a specialized unit. PMID 40762448 — epistaxis, telangiectasia, hereditary hemorrhagic, arteriovenous malformations, telangiectasis, diagnosis, therapeutics, pediatrics, child | Arch Argent Pediatr | 2025 | 0 |
| Management of hereditary hemorrhagic telangiectasia-like symptoms induced by trastuzumab emtansine in a breast cancer patient: case report. PMID 39028266 — anti-infective agents, epistaxis, vascular malformations, propranolol, breast neoplasms, neoplasms, telangiectasia, hereditary hemorrhagic, drug therapy, telangiectasis, liver, maytansine, signs and symptoms, ado-trastuzumab emtansine, pharmacology, breast, therapeutics, trastuzumab | J Chemother | 2024 | 0 |
| Acute aortic dissection in a patient with Hereditary Hemorrhagic Telangiectasia associated with Juvenile Polyposis due to SMAD4 mutation: case report and literature review. PMID 40314862 — aortic aneurysm, aneurysm, telangiectasia, hereditary hemorrhagic, telangiectasis, aortic dissection, mutation, dissection | Angiogenesis | 2025 | 1 |
Clinical Studies 3
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Ongoing Clinical Trials
Ongoing trial started since 2021, where this expert is an investigator
Source: ClinicalTrials
| Study | Phase | Status | Start |
|---|---|---|---|
| Institutional Registry of Rare Diseases NCT06573723 — registries, vascular malformations, hypertension, paraganglioma, esophagitis, eosinophilic esophagitis, hypertension, pulmonary, sarcoidosis, von hippel-lindau disease, rare diseases, pheochromocytoma, immunoglobulin g4-related disease, neoplasms, angioedemas, hereditary, telangiectasia, hereditary hemorrhagic, multiple endocrine neoplasia, immunoglobulins, telangiectasis, metabolism, inborn errors, cardiomyopathy, hypertrophic, adrenal hyperplasia, congenital, amyloidosis, inflammatory bowel diseases, demyelinating diseases, mastocytosis, hepatolenticular degeneration, hyperplasia, gastrointestinal diseases, hirschsprung disease, gaucher disease, prader-willi syndrome, neurocutaneous syndromes, angioedema, cardiomyopathies, cushing syndrome | N/A | Recruiting | 2024 |
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