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2. Lack of association between classical HLA genes and asymptomatic SARS-CoV-2 infection

3. Untangling adaptive functioning of PMM2-CDG across age and its impact on parental stress: a cross-sectional study

4. ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization

5. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

6. Epigenetic profiling linked to multisystem inflammatory syndrome in children (MIS-C): A multicenter, retrospective study

7. Shaping current European mitochondrial haplogroup frequency in response to infection: the case of SARS-CoV-2 severity.

8. Epigenome-wide association study of COVID-19 severity with respiratory failure

9. Delineating the motor phenotype of SGCE-myoclonus dystonia syndrome

11. Associations of paediatric demyelinating and encephalitic syndromes with myelin oligodendrocyte glycoprotein antibodies: a multicentre observational study

12. L-serine treatment in patients with GRIN-related encephalopathy: A phase 2A, non-randomized study

14. PLA2G6-associated neurodegeneration: New insights into brain abnormalities and disease progression

15. Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy

16. Frequency, symptoms, risk factors, and outcomes of autoimmune encephalitis after herpes simplex encephalitis: a prospective observational study and retrospective analysis

18. Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy

19. Genetic Heterogeneity Underlying Phenotypes with Early-Onset Cerebellar Atrophy

20. A second update on mapping the human genetic architecture of COVID-19

21. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

22. HLA‐A*11:01 and HLA‐C*04:01 are associated with severe COVID‐19.

24. Clinical and electrophysiological features of SCN8A variants causing episodic or chronic ataxia

25. Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)

26. Relationship Between Epileptic Activity and Developmental Outcome in KCNQ2-Related Epilepsy

27. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

28. Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

29. Clinical description, molecular delineation and genotype–phenotype correlation in 340 patients with KBG syndrome: addition of 67 new patients

30. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

31. Clinical rating scale for pantothenate kinase‐associated neurodegeneration: A pilot study

32. Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3

33. Novel genes and sex differences in COVID-19 severity

34. Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization

35. Epigenetic profiling linked to multisystem inflammatory syndrome in children (MIS-C): A multicenter, retrospective study

36. Supplementary files of the article 'Novel genes and sex differences in COVID-19 severity' [Dataset]

37. Novel genes and sex differences in COVID-19 severity

38. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

39. Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias

40. Protein misfolding and clearance in the pathogenesis of a new infantile onset ataxia caused by mutations in PRDX3

41. Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy

42. Diagnosis of Genetic White Matter Disorders by Singleton Whole-Exome and Genome Sequencing Using Interactome-Driven Prioritization

43. The risk of COVID-19 death is much greater and age-dependent with type I IFN autoantibodies

44. Autoantibodies neutralizing type I IFNs are present in ~4% of uninfected individuals over 70 years old and account for ~20% of COVID-19 deaths

45. X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

46. Erratum to: Longitudinal volumetric and 2D assessment of cerebellar atrophy in a large cohort of children with phosphomannomutase deficiency (PMM2-CDG)

48. SARS-CoV-2-related MIS-C:A key to the viral and genetic causes of Kawasaki disease?

49. Expanding the β-III Spectrin-Associated Phenotypes toward Non-Progressive Congenital Ataxias with Neurodegeneration

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