Surgery, Pediatrics, Obstetrics and Gynecology
Departamento
Erasmus University Medical Center
Róterdam, HolandaPublications in collaboration with researchers from Erasmus University Medical Center (13)
2024
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Particulate Matter Exposure during Pregnancy and Childhood Leukemia Incidence
Atmosphere, Vol. 15, Núm. 7
2023
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Durability of bioprosthetic aortic valve replacement in patients under the age of 60 years - 1-year follow-up from the prospective INDURE registry
Interdisciplinary cardiovascular and thoracic surgery, Vol. 37, Núm. 4
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Novel Benchmark Values for Open Major Anatomic Liver Resection in Non-cirrhotic Patients: A Multicentric Study of 44 International Expert Centers
Annals of Surgery, Vol. 278, Núm. 5, pp. 748-755
2021
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Impact of Bacillus Calmette-Gue´rin (BCG) vaccination on postoperative mortality in patients with perioperative SARS-CoV-2 infection
BJS Open
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Machine learning risk prediction of mortality for patients undergoing surgery with perioperative SARS-CoV-2: The COVIDSurg mortality score
British Journal of Surgery, Vol. 19, Núm. 4
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Perihilar Cholangiocarcinoma – Novel Benchmark Values for Surgical and Oncological Outcomes From 24 Expert Centers
Annals of Surgery, Vol. 274, Núm. 5, pp. 780-788
2020
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COVID-19 in children with underlying chronic respiratory diseases: Survey results from 174 centres
ERJ Open Research, Vol. 6, Núm. 4, pp. 1-8
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Durability of bioprosthetic aortic valves in patients under the age of 60 years - Rationale and design of the international INDURE registry
Journal of Cardiothoracic Surgery, Vol. 15, Núm. 1
2017
2016
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Development Refractoriness of MLL-Rearranged Human B Cell Acute Leukemias to Reprogramming into Pluripotency
Stem Cell Reports, Vol. 7, Núm. 4, pp. 602-618
2013
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Predictive factors, management, and clinical outcomes of coronary obstruction following transcatheter aortic valve implantation: Insights from a large multicenter registry
Journal of the American College of Cardiology, Vol. 62, Núm. 17, pp. 1552-1562
2011
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Mucopolysaccharidosis type II: European recommendations for the diagnosis and multidisciplinary management of a rare disease
Orphanet Journal of Rare Diseases, Vol. 6, Núm. 1
2010
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Deletions of the RUNX2 gene are present in about 10% of individuals with cleidocranial dysplasia
Human Mutation, Vol. 31, Núm. 8