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1. SARS-CoV-2 brainstem encephalitis in human inherited DBR1 deficiency.

3. Human TMEFF1 is a restriction factor for herpes simplex virus in the brain

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

6. Frequency and clinical relevance of MOG-antibodies in CSF in pediatric patients with MOG antibody-associated diseases

8. JAK Inhibition in Aicardi-Goutières Syndrome: a Monocentric Multidisciplinary Real-World Approach Study

12. Juvenile neuropsychiatric systemic lupus erythematosus: A specific clinical phenotype and proposal of a probability score

13. Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants.

14. Ceroid lipofuscinosis type 2 disease: Effective presymptomatic therapy—Oldest case of a presymptomatic enzyme therapy.

16. Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)

17. Autoantibodies neutralizing type I IFNs underlie West Nile virus encephalitis in ∼40% of patients

18. Encephalitis and poor neuronal death–mediated control of herpes simplex virus in human inherited RIPK3 deficiency

19. Prospective Multicenter Validation of a Simple Blood Test for the Diagnosis of Glut1 Deficiency Syndrome

20. Long Term Clinical and Biological Prognostic Factors of Anti-Nmda Receptor Encephalitis in Children

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

22. Indications and Safety of Rituximab in Pediatric Neurology: A 10-Year Retrospective Study

23. Periodic electroencephalographic discharges and epileptic spasms involve cortico-striatal-thalamic loops on Arterial Spin Labeling Magnetic Resonance Imaging

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

25. Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome

28. Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis

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

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

31. Une infection antérieure par des coronavirus saisonniers n’empêche pas la COVID-19 chez les enfants

33. Prior infection by seasonal coronaviruses, as assessed by serology, does not prevent SARS-CoV-2 infection and disease in children, France, April to June 2020

34. Neuroimaging manifestations in children with SARS-CoV-2 infection: a multinational, multicentre collaborative study

35. Herpes simplex encephalitis in a patient with a distinctive form of inherited IFNAR1 deficiency

36. Prior infection by seasonal coronaviruses does not prevent SARS-CoV-2 infection and associated Multisystem Inflammatory Syndrome in children

37. Quantifying the Genetic Basis of Marfan Syndrome Clinical Variability

38. Therapeutic Plasma Exchange in Pediatrics for Immunologic Disorders; Tolerated and Safe Process for Pediatric Life-Threatening Conditions

39. Marfan Syndrome Variability: Investigation of the Roles of Sarcolipin and Calcium as Potential Transregulator of FBN1 Expression

41. Severe paediatric conditions linked with EV-A71 and EV-D68, France, May to October 2016

43. Homozygous and compound heterozygous mutations in theFBN1gene: unexpected findings in molecular diagnosis of Marfan syndrome

45. Liste des auteurs

46. MFAP5 Loss-of-Function Mutations Underscore the Involvement of Matrix Alteration in the Pathogenesis of Familial Thoracic Aortic Aneurysms and Dissections

47. Early-Onset Osteoarthritis, Charcot-Marie-Tooth Like Neuropathy, Autoimmune Features, Multiple Arterial Aneurysms and Dissections: An Unrecognized and Life Threatening Condition

48. Homozygous and compound heterozygous mutations in the FBN1gene: unexpected findings in molecular diagnosis of Marfan syndrome

49. Severe and fatal neonatal infections linked to a new variant of echovirus 11, France, July 2022 to April 2023.

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