Surgery, Pediatrics, Obstetrics and Gynecology
Departamento


Universitat Pompeu Fabra
Barcelona, España
Publications in collaboration with researchers from Universitat Pompeu Fabra (12)
2025
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Complete hepatic caudate lobe resection: is robotic approach safe? Report from experienced centers
Journal of Robotic Surgery, Vol. 19, Núm. 1
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Correction to: Complete hepatic caudate lobe resection: is robotic approach safe? Report from experienced centers (Journal of Robotic Surgery, (2024), 19, 1, (23), 10.1007/s11701-024-02162-8)
Journal of Robotic Surgery
2024
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Abdominal Wall Surgery Units accreditation. The Spanish model
Cirugia Espanola, Vol. 102, Núm. 5, pp. 283-290
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Correction to: The role of resection in hepatocellular carcinoma BCLC stage B: A multi-institutional patient-level meta-analysis and systematic review (Langenbeck's Archives of Surgery, (2024), 409, 1, (277), 10.1007/s00423-024-03466-x)
Langenbeck's Archives of Surgery
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Integrative single-cell expression and functional studies unravels a sensitization to cytarabine-based chemotherapy through HIF pathway inhibition in AML leukemia stem cells
HemaSphere, Vol. 8, Núm. 2
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Particulate Matter Exposure during Pregnancy and Childhood Leukemia Incidence
Atmosphere, Vol. 15, Núm. 7
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The role of resection in hepatocellular carcinoma BCLC stage B: A multi-institutional patient-level meta-analysis and systematic review
Langenbeck's Archives of Surgery, Vol. 409, Núm. 1
2023
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First Spanish Consensus on the Use of Intraoperative Radiotherapy in Breast Cancer. Conclusions of the expert panel
Revista de Senologia y Patologia Mamaria, Vol. 36, Núm. 3
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Just medical oncology guidelines…
Clinical and Translational Oncology
2022
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Variability in Phelan-McDermid Syndrome in a Cohort of 210 Individuals
Frontiers in Genetics, Vol. 13
2019
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Unexpected relevant role of gene mosaicism in patients with primary immunodeficiency diseases
Journal of Allergy and Clinical Immunology, Vol. 143, Núm. 1, pp. 359-368
2014
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Human Molecular Genetics, Vol. 23, Núm. 11, pp. 2888-2900