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Luca Brunelli

Showing results (21-30 of 55) with videos related to

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Circulation Journal : Official Journal of the Japanese Circulation Society|June 16, 2016
Micro-Computed Tomography for the Quantitative 3-Dimensional Assessment of the Compact Myocardium in the Mouse EmbryoSamer S Merchant, Yasuhiro Kosaka, H Joseph Yost, et al.
Studies in Health Technology and Informatics|May 20, 2022
Impact Analysis of De-Identification in Clinical Notes ClassificationMartin Baumgartner, Günter Schreier, Dieter Hayn, et al.
Journal of Cardiothoracic and Vascular Anesthesia|June 21, 2025
Anticoagulation Monitoring During Extracorporeal Membrane Oxygenation: A Narrative ReviewSasa Rajsic, Christian Irsara, Andrea Griesmacher, et al.
American Journal of Medical Genetics. Part A|November 24, 2022
Variants in AQP11 may result in autosomal recessive bilateral cystic renal dysgenesisMichael E Price, Kristen P Fishler, Melissa Muff-Luett, et al.
Nature Methods|July 17, 2014
Isolation of rare recombinants without using selectable markers for one-step seamless BAC mutagenesisGeorge T Lyozin, Paul C Bressloff, Amit Kumar, et al.
Pediatric Research|May 13, 2006
Perfluorochemical liquids enhance delivery of superoxide dismutase to the lungs of juvenile rabbitsLuca Brunelli, Eric Hamilton, Jonathan M Davis, et al.
Studies in Health Technology and Informatics|May 19, 2023
Classification of Clinical Notes from a Heart Failure Telehealth NetworkFabian Wiesmüller, Aaron Lauschenski, Martin Baumgartner, et al.
Birth Defects Research|August 4, 2020
Congenital diaphragmatic hernia and maternal dietary nutrient pathways and diet qualitySuzan L Carmichael, Chen Ma, John S Witte, et al.
Children (Basel, Switzerland)|June 28, 2023
Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill InfantsJoseph Reiley, Pablo Botas, Christine E Miller, et al.
Case Reports in Genetics|July 15, 2025
A Rare Case of Neonatal Cholestasis Linked to FOCAD Gene Variants: Exploring the Variable Phenotypic Presentation and Its ImplicationsAriel Tarrell, Jessika Weber, Reem Shawar, et al.
Pageof 6

Showing results (21-30 of 55) with videos related to

Sort By:
Pageof 6
Circulation Journal : Official Journal of the Japanese Circulation Society|June 16, 2016
Micro-Computed Tomography for the Quantitative 3-Dimensional Assessment of the Compact Myocardium in the Mouse EmbryoSamer S Merchant, Yasuhiro Kosaka, H Joseph Yost, et al.
Studies in Health Technology and Informatics|May 20, 2022
Impact Analysis of De-Identification in Clinical Notes ClassificationMartin Baumgartner, Günter Schreier, Dieter Hayn, et al.
Journal of Cardiothoracic and Vascular Anesthesia|June 21, 2025
Anticoagulation Monitoring During Extracorporeal Membrane Oxygenation: A Narrative ReviewSasa Rajsic, Christian Irsara, Andrea Griesmacher, et al.
American Journal of Medical Genetics. Part A|November 24, 2022
Variants in AQP11 may result in autosomal recessive bilateral cystic renal dysgenesisMichael E Price, Kristen P Fishler, Melissa Muff-Luett, et al.
Nature Methods|July 17, 2014
Isolation of rare recombinants without using selectable markers for one-step seamless BAC mutagenesisGeorge T Lyozin, Paul C Bressloff, Amit Kumar, et al.
Pediatric Research|May 13, 2006
Perfluorochemical liquids enhance delivery of superoxide dismutase to the lungs of juvenile rabbitsLuca Brunelli, Eric Hamilton, Jonathan M Davis, et al.
Studies in Health Technology and Informatics|May 19, 2023
Classification of Clinical Notes from a Heart Failure Telehealth NetworkFabian Wiesmüller, Aaron Lauschenski, Martin Baumgartner, et al.
Birth Defects Research|August 4, 2020
Congenital diaphragmatic hernia and maternal dietary nutrient pathways and diet qualitySuzan L Carmichael, Chen Ma, John S Witte, et al.
Children (Basel, Switzerland)|June 28, 2023
Open-Source Artificial Intelligence System Supports Diagnosis of Mendelian Diseases in Acutely Ill InfantsJoseph Reiley, Pablo Botas, Christine E Miller, et al.
Case Reports in Genetics|July 15, 2025
A Rare Case of Neonatal Cholestasis Linked to FOCAD Gene Variants: Exploring the Variable Phenotypic Presentation and Its ImplicationsAriel Tarrell, Jessika Weber, Reem Shawar, et al.
Pageof 6