Leiden University Scholarly Publications

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(21 - 40 of 7,607)

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TECRL, a new life-threatening inherited arrhythmia gene associated with overlapping clinical features of both LQTS and CPVT
Assessment of causality between serum gamma-glutamyltransferase and type 2 diabetes mellitus using publicly available data: a Mendelian randomization study
Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease
Pre-clinical Evaluation of a Cyanine-Based SPECT Probe for Multimodal Tumor Necrosis Imaging
RE: BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers Response
Factors related to fatigue after paediatric acquired brain injury (ABI)
Growth hormone secretion is diminished and tightly controlled in humans enriched for familial longevity
PCR-based detection of Aspergillus fumigatus Cyp51A mutations on bronchoalveolar lavage: a multicentre validation of the AsperGenius assay (R) in 201 patients with haematological disease suspected for invasive aspergillosis
Prenatal Reflective Functioning and Accumulated Risk as Predictors of Maternal Interactive Behavior During Free Play, the Still-Face Paradigm, and Two Teaching Tasks
Internet-based self-management support for adults with asthma: a qualitative study among patients, general practitioners and practice nurses on barriers to implementation
Photo-crosslinking of clinically relevant kinases using H89-derived photo-affinity probes
The role of multimodality imaging in the selection of patients for aortic valve repair
Airway hyperresponsiveness in chronic obstructive pulmonary disease: A marker of asthma-chronic obstructive pulmonary disease overlap syndrome?
Using High-Field Magnetic Resonance Imaging to Estimate Distensibility of the Middle Cerebral Artery
Access for all: contextualising HIV treatment as prevention in Swaziland
Are disseminated tumor cells in bone marrow and tumor-stroma ratio clinically applicable for patients undergoing surgical resection of primary colorectal cancer? The Leiden MRD study
Hypomorphic MKS1 Mutation in a Pakistani Family with Mild Joubert Syndrome and Atypical Features: Expanding the Phenotypic Spectrum of MKS1-Related Ciliopathies
CT and MR Imaging in the Diagnosis of Scleritis
Early Magnetic Resonance Imaging and Cognitive Markers of Hereditary Cerebral Amyloid Angiopathy
In-depth site-specific N- and O-Glycosylation analysis of human C1-Inhibitor reveals extensive mucin-type O-glycosylation

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