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

6. Safety and efficacy of rivaroxaban in pediatric cerebral venous thrombosis (EINSTEIN-Jr CVT): for the EINSTEIN-Jr Cerebral Venous Thrombosis trial investigators

9. Safety and efficacy of anticoagulant therapy in pediatric catheter-related venous thrombosis (EINSTEIN-Jr CVC-VTE)

10. Position paper concerning the competence, performance and environment required for the practice of ablation in children and in congenital heart disease

11. Rivaroxaban for treatment of pediatric venous thromboembolism. An Einstein‐Jr phase 3 dose‐exposure‐response evaluation

12. Impact of Sophrology on cardiopulmonary fitness in teenagers and young adults with a congenital heart disease: The SOPHROCARE study rationale, design and methods

13. CYP2C9, VKORC1, and CYP4F2 polymorphisms and pediatric warfarin maintenance dose: a systematic review and meta-analysis

16. Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries

22. Acute Heart Failure in Multisystem Inflammatory Syndrome in Children in the Context of Global SARS-CoV-2 Pandemic

24. Multisystem inflammatory syndrome in children during the COVID-19 waves: data from the Juvenile Inflammatory Rheumatism cohort

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

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

29. Additional file 1 of Expanding the phenome and variome of the ROBO-SLIT pathway in congenital heart defects: toward improving the genetic testing yield of CHD

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

31. Correction to “Hyper inflammatory syndrome following COVID-19 mRNA vaccine in children: A national post-authorization pharmacovigilance study”

32. Hyper inflammatory syndrome following COVID-19 mRNA vaccine in children: A national post-authorization pharmacovigilance study

34. Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans

35. PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families

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

39. PPA2-associated sudden cardiac death: extending the clinical and allelic spectrum in 20 new families

41. Biallelic alterations in PLXND1 cause common arterial trunk and other cardiac malformations in humans.

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

44. Cohort profile: the ESC EURObservational Research Programme Atrial Fibrillation III (AF III) Registry

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

50. Acute heart failure in multisystem inflammatory syndrome in children (MIS-C) in the context of global SARS-CoV-2 pandemi

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