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(21 - 40 of 4,758)

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Non-invasive assessment of atherosclerotic coronary lesion length using multidetector computed tomography angiography: comparison to quantitative coronary angiography
Relationship between specific adverse events and efficacy of exemestane therapy in early postmenopausal breast cancer patients
SUB-CLONAL CYTOGENETIC HETEROGENEITY IN HIGH HYPERDIPLOID ACUTE LYMPHOBLASTIC LEUKAEMIA
Effect of Small Molecule Supplements during In Vitro Culture of Mouse Zygotes and Parthenogenetic Embryos on Hypoblast Formation and Stem Cell Derivation
Alba shapes the archaeal genome using a delicate balance of bridging and stiffening the DNA
Risk Factors for Alloimmunisation after red blood Cell Transfusions (R-FACT): a case cohort study
The Marburg I polymorphism of factor VII activating protease is associated with low proteolytic and low pro-coagulant activity
The quality of bone surfaces may govern the use of model based fluoroscopy in the determination of joint laxity
Pleconaril revisited: clinical course of chronic enteroviral meningoencephalitis after treatment correlates with in vitro susceptibility
Reference Intervals of Spinal Mobility Measures in Normal Individuals - The Mobility Study
Contribution of donor and recipient characteristics to short- and long-term pancreas graft survival
Focusing illusion, adaptation and EQ-5D health state descriptions: the difference between patients and public
Increase in short-chain ceramides correlates with an altered lipid organization and decreased barrier function in atopic eczema patients
Reduced CD26 expression is associated with improved cardiac function after acute myocardial infarction Insights from the REPERATOR study
Interruption of CD28-mediated costimulation during allergen challenge protects mice from allergic airway disease
Digenic inheritance of an SMCHD1 mutation and an FSHD-permissive D4Z4 allele causes facioscapulohumeral muscular dystrophy type 2
Evaluation of the effect of genetic variations in GATA-4 on the phenprocoumon and acenocoumarol maintenance dose
Severe disseminated mycobacterial infection in a boy with a novel mutation leading to IFN-gamma R2 deficiency
Self-management to support hypertensive kidney patients: The ESMO study
Presynaptic Ca(v)2.1 calcium channels carrying familial hemiplegic migraine mutation R192Q allow faster recovery from synaptic depression in mouse calyx of Held

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