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1. MSL2 variants lead to a neurodevelopmental syndrome with lack of coordination, epilepsy, specific dysmorphisms, and a distinct episignature.

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

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

6. Clinical and biological landscape of constitutional mismatch-repair deficiency syndrome: an International Replication Repair Deficiency Consortium cohort study

9. Clinical outcomes after 4.5 years of eliglustat therapy for Gaucher disease type 1: Phase 3 ENGAGE trial final results.

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

15. Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency

19. Bi-allelic variants in neuronal cell adhesion molecule cause a neurodevelopmental disorder characterized by developmental delay, hypotonia, neuropathy/spasticity

22. The CHD4-related syndrome: a comprehensive investigation of the clinical spectrum, genotype–phenotype correlations, and molecular basis

25. Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction Rates

28. A Unique Presentation of Infantile-Onset Colitis and Eosinophilic Disease without Recurrent Infections Resulting from a Novel Homozygous CARMIL2 Variant

29. Telemedicine Versus Traditional In-Person Consultations: Comparison of Patient Satisfaction Rates.

31. Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia

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

35. Additional file 1 of Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19

36. Utility of Genetic Testing in Children with Leukodystrophy

37. SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetrance.

38. Autoantibodies against type I IFNs in patients with critical influenza pneumonia

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

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 similar to 4% of uninfected individuals over 70 years old and account for similar to 20% of COVID-19 deaths

45. Experts’ views on COVID‐19 vaccination and the impact of the pandemic on patients with Gaucher disease

46. A Novel Homozygous In-Frame Deletion in Complement Factor 3 Underlies Early-Onset Autosomal Recessive Atypical Hemolytic Uremic Syndrome - Case Report

48. Diagnostic criteria for constitutional mismatch repair deficiency (CMMRD): recommendations from the international consensus working group

50. Heterozygous loss of WBP11 function causes multiple congenital defects in humans and mice

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