Search

Your search keyword '"Martin-Nalda, Andrea"' showing total 102 results

Search Constraints

Start Over You searched for: Author "Martin-Nalda, Andrea" Remove constraint Author: "Martin-Nalda, Andrea"
102 results on '"Martin-Nalda, Andrea"'

Search Results

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

2. A longitudinal prospective study of active tuberculosis in a Western Europe setting: insights and findings

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

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

8. Interferon-Gamma Release Assays Differentiate between Mycobacterium avium Complex and Tuberculous Lymphadenitis in Children

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

11. Validation of Risk Factors for Early Mortality in Cartilage-Hair Hypoplasia.

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

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

20. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

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

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

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

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

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

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

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

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

30. Newborn screening for presymptomatic diagnosis of complement and phagocyte deficiencies

31. Clinical Outcomes of a Zika Virus Mother-Child Pair Cohort in Spain

32. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

34. Clinical Outcomes of a Zika Virus Mother–Child Pair Cohort in Spain

35. Newborn Screening for Presymptomatic Diagnosis of Complement and Phagocyte Deficiencies

36. Primary and Secondary Immunodeficiency Diseases in Oncohaematology: Warning Signs, Diagnosis, and Management

37. Genetic analyses of aplastic anemia and idiopathic pulmonary fibrosis patients with short telomeres, possible implication of DNA-repair genes

38. Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years’ experience in Catalonia (Spain)

39. Tuberculosis infection in children visiting friends and relatives in countries with high incidence of tuberculosis: A study protocol.

40. Extended immunophenotyping reference values in a healthy pediatric population

41. Laboratory evaluation of the IFN-γ circuit for the molecular diagnosis of Mendelian susceptibility to mycobacterial disease

43. Diagnostic Accuracy of QuantiFERON-TB Gold Plus Assays in Children and Adolescents with Tuberculosis Disease

47. Hyperlactatemia and in Utero Exposure to Antiretrovirals: Is the Control Group the Clue?

48. Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

49. Immunomolecular and reactivity landscapes of gut IgA subclasses in homeostasis and inflammatory bowel disease.

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

Catalog

Books, media, physical & digital resources