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138 results on '"de Leeuw A"'

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1. Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole exome sequencing from Central Brazil

2. Sharp increase in inequality in education in times of the COVID-19-pandemic

3. Acceptability, effectiveness and cost-effectiveness of blended cognitive-behavioural therapy (bCBT) versus face-to-face CBT (ftfCBT) for anxiety disorders in specialised mental health care: A 15-week randomised controlled trial with 1-year follow-up

4. Re-evaluating randomized clinical trials of psychological interventions: Impact of response shift on the interpretation of trial results

5. Re-evaluating randomized clinical trials of psychological interventions: Impact of response shift on the interpretation of trial results

6. Concerns of older patients and their caregivers in the emergency department

8. The efficacy of Life Review Therapy combined with Memory Specificity Training (LRT-MST) targeting cancer patients in palliative care: A randomized controlled trial

9. The need for information among patients with hematological malignancies: Psychometric analyses of the 62-item Hematology Information Needs Questionnaire (HINQ-62)

12. The efficacy of Life Review Therapy combined with Memory Specificity Training (LRT-MST) targeting cancer patients in palliative care: A randomized controlled trial

13. An In Vivo Study of Self-Regulated Study Sequencing in Introductory Psychology Courses

14. Towards Development of Small Molecule Lipid II Inhibitors as Novel Antibiotics

16. Gender Differentiated Preferences for a Community-Based Conservation Initiative

17. A dissociation between engagement and learning: Enthusiastic instructions fail to reliably improve performance on a memory task

18. Towards Development of Small Molecule Lipid II Inhibitors as Novel Antibiotics

20. A Randomised Controlled Trial of Consent Procedures for the Use of Residual Tissues for Medical Research: Preferences of and Implications for Patients, Research and Clinical Practice

23. Functional gene group analysis indicates no role for heterotrimeric G proteins in cognitive ability

24. Impact of serum high mobility group box 1 and soluble receptor for advanced glycation end-products on subclinical atherosclerosis in patients with granulomatosis with polyangiitis

25. Spotting East African mammals in open savannah from space

26. Post-stroke epilepsy in young adults: a long-term follow-up study

27. Meaning making in cancer survivors: a focus group study

28. Combining next-generation sequencing and microarray technology into a transcriptomics approach for the non-model organism Chironomus riparius

29. Lower Ipsilateral Hippocampal Integrity after Ischemic Stroke in Young Adults: A Long-Term Follow-Up Study

30. Coexistence of flexibility and stability of proteins: an equation of state

31. The M235T polymorphism in the AGT gene and CHD risk: evidence of a Hardy-Weinberg equilibrium violation and publication bias in a meta-analysis

35. Development and Validation of a Prediction Model for Tube Feeding Dependence after Curative (Chemo-) Radiation in Head and Neck Cancer

36. Functional Gene Group Analysis Indicates No Role for Heterotrimeric G Proteins in Cognitive Ability

43. Protective Efficacy of Newcastle Disease Virus Expressing Soluble Trimeric Hemagglutinin against Highly Pathogenic H5N1 Influenza in Chickens and Mice

44. Protective Efficacy of Newcastle Disease Virus Expressing Soluble Trimeric Hemagglutinin against Highly Pathogenic H5N1 Influenza in Chickens and Mice

47. Lock, Stock and Two Different Barrels: Comparing the Genetic Composition of Morphotypes of the Indo-Pacific Sponge Xestospongia testudinaria.

48. Eggs in the Freezer: Energetic Consequences of Nest Site and Nest Design in Arctic Breeding Shorebirds.

49. Sharp increase in inequality in education in times of the COVID-19-pandemic.

50. Diagnostic yield of patients with undiagnosed intellectual disability, global developmental delay and multiples congenital anomalies using karyotype, microarray analysis, whole exome sequencing from Central Brazil.

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