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201. The selective NLRP3-inflammasome inhibitor MCC950 reduces infarct size and preserves cardiac function in a pig model of myocardial infarction

202. Proteomics reveals reduced expression of transketolase in pyrimidine 5'-nucleotidase deficient patients

205. Translational failure of anti-inflammatory compounds for myocardial infarction : a meta-analysis of large animal models

206. Validity of diagnostic codes and laboratory measurements to identify patients with idiopathic acute liver injury in a hospital database

207. Patient monitoring: the hidden costs of antipsychotic treatment

209. Routinely analyzed leukocyte characteristics improve prediction of mortality after coronary angiography

210. Impaired bone healing in multitrauma patients is associated with altered leukocyte kinetics after major trauma

211. Proteomics reveals reduced expression of transketolase in pyrimidine 5'-nucleotidase deficient patients

212. New mAb therapies in multiple myeloma: interference with blood transfusion compatibility testing

213. Patient monitoring: the hidden costs of treatment with antipsychotics

214. Overestimation of hypoglycemia in infants with a high hematocrit

215. Routinely analyzed leukocyte characteristics improve prediction of mortality after coronary angiography

216. Display of GPI-anchored anti-EGFR nanobodies on extracellular vesicles promotes tumour cell targeting

217. Translational failure of anti-inflammatory compounds for myocardial infarction: a meta-analysis of large animal models

218. Validity of diagnostic codes and laboratory measurements to identify patients with idiopathic acute liver injury in a hospital database

221. The selective NLRP3-inflammasome inhibitor MCC950 reduces infarct size and preserves cardiac function in a pig model of myocardial infarction

222. One-Year Mortality, Causes of Death, and Cardiac Interventions in Patients with Postoperative Myocardial Injury

227. Reducing Test Utilization in Hospital Settings: A Narrative Review.

229. Contributors

232. Influence of a strict glucose protocol on serum potassium and glucose concentrations and their association with mortality in intensive care patients

233. Invasive surgery reduces infarct size and preserves cardiac function in a porcine model of myocardial infarction

234. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis

235. Hematological Parameters Improve Prediction of Mortality and Secondary Adverse Events in Coronary Angiography Patients : A Longitudinal Cohort Study

236. Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis : Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms

239. Influence of a strict glucose protocol on serum potassium and glucose concentrations and their association with mortality in intensive care patients

240. Adherence with Dosing Guideline in Patients with Impaired Renal Function at Hospital Discharge

241. Influence of a strict glucose protocol on serum potassium and glucose concentrations and their association with mortality in intensive care patients

242. Partial pyruvate kinase deficiency aggravates the phenotypic expression of band 3 deficiency in a family with hereditary spherocytosis

243. Invasive surgery reduces infarct size and preserves cardiac function in a porcine model of myocardial infarction

244. Hematological Parameters Improve Prediction of Mortality and Secondary Adverse Events in Coronary Angiography Patients: A Longitudinal Cohort Study

245. Novel Homozygous Mutation of the Internal Translation Initiation Start Site of VHL is Exclusively Associated with Erythrocytosis: Indications for Distinct Functional Roles of von Hippel-Lindau Tumor Suppressor Isoforms

246. Adherence with dosing guideline in patients with impaired renal function at hospital discharge

247. When blood transfusion medicine becomes complicated due to interference by monoclonal antibody therapy

250. Pyruvate kinase deficiency and severe congenital hemolytic anemia in a double heterozygous patient with paternal transmission of an early germ-linede novomutation

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