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1. Semiautomated approach focused on new genomic information results in time and effort-efficient reannotation of negative exome data

5. De novo variants in DENND5B cause a neurodevelopmental disorder

6. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

7. Early role for a Na+,K+-ATPase (ATP1A3) in brain development

8. Truncating SRCAP variants outside the Floating-Harbor syndrome locus cause a distinct neurodevelopmental disorder with a specific DNA methylation signature

9. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

10. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

11. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

12. Tracer metabolomics reveals the role of aldose reductase in glycosylation

13. De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features

14. Predominant and novel de novo variants in 29 individuals with ALG13 deficiency: Clinical description, biomarker status, biochemical analysis, and treatment suggestions

15. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

16. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

17. Galactose epimerase deficiency: lessons from the GalNet registry

20. From periphery immunity to central domain through clinical interview as a new insight on schizophrenia

21. De novo variants in DENND5B cause a neurodevelopmental disorder

22. Phenotypic expansion of CACNA1C-associated disorders to include isolated neurological manifestations

23. Heterozygous loss-of-function variants significantly expand the phenotypes associated with loss of GDF11

26. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

27. NEXMIF encephalopathy: an X-linked disorder with male and female phenotypic patterns

33. Efficacy and safety of D,L-3-hydroxybutyrate (D,L-3-HB) treatment in multiple acyl-CoA dehydrogenase deficiency

35. Case report: Novel genotype of ALG2-CDG and confirmation of the heptasaccharide glycan (NeuAc-Gal-GlcNAc- Man2-GlcNAc2) as a specific diagnostic biomarker.

37. Biallelic CRELD1 variants cause a multisystem syndrome including neurodevelopmental phenotypes, cardiac dysrhythmias, and frequent infections.

40. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy

43. Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male mice

44. Interplay of Impaired Cellular Bioenergetics and Autophagy in PMM2-CDG

45. HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder

46. De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling

49. Bi-allelic variants in INTS11 are associated with a complex neurological disorder

50. A concurrent dual analysis of genomic data augments diagnoses: Experiences of 2 clinical sites in the Undiagnosed Diseases Network

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