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Brain : a Journal of Neurology|June 16, 2001
Clinical, biochemical and molecular genetic characteristics of 19 patients with the Sjögren-Larsson syndromeM A Willemsen, L IJlst, P M Steijlen, et al.Genes, Chromosomes & Cancer|December 29, 1999
Somatic mutations of the APC, KRAS, and TP53 genes in nonpolypoid colorectal adenomasR van Wyk, P Slezak, V M Hayes, et al.Plos One|February 26, 2013
SNPs identified as modulators of ECG traits in the general population do not markedly affect ECG traits during acute myocardial infarction nor ventricular fibrillation risk in this conditionRaha Pazoki, Jonas S S G de Jong, Roos F Marsman, et al.Plos One|January 21, 2022
Intermediate-term outcome of cryoballoon ablation of persistent atrial fibrillation and improvements in quality of life of patientsDaniel Mol, Anchee M Boersma, Wouter R Berger, et al.Open Heart|January 4, 2018
Heart failure following STEMI: a contemporary cohort study of incidence and prognostic factorsJohannes M I H Gho, Pieter G Postema, Maartje Conijn, et al.Platelets|January 11, 2013
Altered platelet contents in survivors of early ischemic ventricular fibrillation: preliminary findingsJonas S S G De Jong, Rienk Nieuwland, Joost C M Meijers, et al.Journal of Inherited Metabolic Disease|March 21, 1998
Oligosaccharide excretion in adult Gaucher diseaseJ G de Jong, J M Aerts, S van Weely, et al.Neuromuscular Disorders : NMD|September 8, 2004
Increased risk for cardiorespiratory failure associated with the A3302G mutation in the mitochondrial DNA encoded tRNALeu(UUR) geneB J C van den Bosch, I F M de Coo, A T M Hendrickx, et al.Endocrine|December 29, 1998
Prolactin-regulated apoptosis of Nb2 lymphoma cells: pim-1, bcl-2, and bax expressionJ S Krumenacker, D J Buckley, M A Leff, et al.Nature Genetics|June 16, 1999
Mutations in the gene encoding mevalonate kinase cause hyper-IgD and periodic fever syndrome. International Hyper-IgD Study GroupJ P Drenth, L Cuisset, G Grateau, et al.Pageof 37