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Haematologica|July 22, 2008
Clinical and hematologic features of 300 patients affected by hereditary spherocytosis grouped according to the type of the membrane protein defectMariagabriella Mariani, Wilma Barcellini, Cristina Vercellati, et al.
ERJ Open Research|August 6, 2024
Early serum biomarkers to characterise different phenotypes of primary graft dysfunction after lung transplantation: a systematic scoping reviewVittorio Scaravilli, Gloria Turconi, Sebastiano Maria Colombo, et al.
Trials|June 3, 2014
Variable versus conventional lung protective mechanical ventilation during open abdominal surgery: study protocol for a randomized controlled trialPeter M Spieth, Andreas Güldner, Christopher Uhlig, et al.
Blood Cells, Molecules & Diseases|March 18, 2008
Recessive hereditary methemoglobinemia: two novel mutations in the NADH-cytochrome b5 reductase geneElisa Fermo, Paola Bianchi, Cristina Vercellati, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|December 22, 2018
Benefits of Impella and Peripheral Veno-Arterial Extra Corporeal Life Support AllianceSébastien Colombier, Astrid Quessard, Ciro Mastroianni, et al.
Journal of Critical Care|May 14, 2024
Point of care guided coagulation management in adult patients on ECMO: A systematic review and meta-analysisAyten Saracoglu, Ibrahim Fawzy, Kemal Tolga Saracoglu, et al.
ASAIO Journal (American Society for Artificial Internal Organs : 1992)|March 29, 2022
Extracorporeal Life Support Organization Guidelines for Fluid Overload, Acute Kidney Injury, and Electrolyte ManagementBrian C Bridges, Archana Dhar, Kollengode Ramanathan, et al.
The Journal of Infection|March 1, 2011
A lethal case of meningitis due to Lactobacillus rhamnosus as a late complication of anterior cervical spine surgeryMatthieu Schmidt, Virginie Maxime, Francois Pareire, et al.
Journal of Artificial Organs : the Official Journal of the Japanese Society for Artificial Organs|December 10, 2016
ECMO for intractable status asthmaticus following atracuriumVittorio Scaravilli, Giacomo Grasselli, Annalisa Benini, et al.
Haematologica|September 8, 2006
Two new mutations of the P5'N-1 gene found in Italian patients with hereditary hemolytic anemia: the molecular basis of the red cell enzyme disorderLaurent R Chiarelli, Elisa Fermo, Patrizia Abrusci, et al.
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