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2. Cystathionine beta synthase deficiency and brain edema associated with methionine excess under betaine supplementation: Four new cases and a review of the evidence

3. Mutations in RNU7-1 Weaken Secondary RNA Structure, Induce MCP-1 and CXCL10 in CSF, and Result in Aicardi-Goutières Syndrome with Severe End-Organ Involvement

5. Shortcutting the diagnostic odyssey: the multidisciplinary Program for Undiagnosed Rare Diseases in adults (UD-PrOZA)

7. A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

8. Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

12. Ignoring people: The micro-politics of misrecognition in participatory governance

13. Micro- and Macrolevel Determinants of Women's Employment in Six Arab Countries

14. On the Compatibility of Islam and Gender Equality: Effects of Modernization, State Islamization, and Democracy on Women's Labor Market Participation in 45 Muslim Countries

17. Diagnosing pediatric mitochondrial disease: lessons from 2,000 exomes

18. Integration of proteomics with genomics and transcriptomics increases the diagnostic rate of Mendelian disorders

32. Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation (Nature Communications, (2019), 10, 1, (4779), 10.1038/s41467-019-12704-6)

33. A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

34. A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation

35. The Phenomenology of Change: How Conflict Drives Urban Transformation.

36. Learning from Conflict.

39. Galactokinase deficiency: lessons from the GalNet registry

40. VOICE: Design of a State Vocational Education Computer Network.

41. Recurrent arterial ischemic stroke with good response to mycophenolate mofetil.

46. ATP2B2de novo variants as a cause of variable neurodevelopmental disorders that feature dystonia, ataxia, intellectual disability, behavioral symptoms, and seizures

48. Mitochondrial abnormalities in a newborn with lactic acidosis and adrenal calcifications

49. Prevalence of (potentially) BH4 responsive mutations in PKU patients from Ghent, Belgium

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