Search

Your search keyword '"Sullivan, Kathleen"' showing total 108 results

Search Constraints

Start Over You searched for: Author "Sullivan, Kathleen" Remove constraint Author: "Sullivan, Kathleen" Publication Year Range This year Remove constraint Publication Year Range: This year
108 results on '"Sullivan, Kathleen"'

Search Results

5. COVID-19 Vaccination in Patients with Inborn Errors of Immunity Reduces Hospitalization and Critical Care Needs Related to COVID-19: a USIDNET Report

7. Correction to: Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development

9. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

10. Dominant missense variants in SREBF2 are associated with complex dermatological, neurological, and skeletal abnormalities

11. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

12. The common variable immunodeficiency IgM repertoire narrowly recognizes erythrocyte and platelet glycans

14. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

15. De novo variants in DENND5B cause a neurodevelopmental disorder

17. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

18. Serum cytokine panels in pediatric clinical practice

20. Nuclear-free NYC: How New Yorkers are disarming the legacies of the Manhattan Project.

21. Exome and genome sequencing in a heterogeneous population of patients with rare disease: Identifying predictors of a diagnosis

22. 108 PU.1-associated inborn errors of immunity: new mutations, phenotypes, and inheritance patterns

27. De novo variants in DENND5B cause a neurodevelopmental disorder

29. Humoral And Cellular Immune Response To Covid-19 Vaccines After Primary Vaccination With A 3-dose Scheme And Boosters Vaccines (4th And 5th Doses) In 55 Brazilian Patients With Inborn Errors Of Immunity Compared To Healthy Controls

30. Impact of medications on salivary flow rate and oral signs and symptoms in patients with Sjogren's Disease: a retrospective study by the Xeromeds Consortium

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

33. A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

35. A patient with Pitt–Hopkins syndrome with concomitant common variable immunodeficiency.

36. BRIEF OF CONSTITUTIONAL LAW SCHOLARS AS AMICI CURIAE IN VIRGINIA V. FERRIERO.

37. Rubella virus chronic inflammatory disease and other unusual viral phenotypes in inborn errors of immunity.

41. Surveillance for rubella virus in samples obtained from non‐immunodeficient individuals.

43. The Undiagnosed Diseases Network: Characteristics of solvable applicants and diagnostic suggestions for nonaccepted ones

44. Dominant missense variants in SREBF2are associated with complex dermatological, neurological, and skeletal abnormalities

45. Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorder

48. TNFSF13 insufficiency disrupts human colonic epithelial cell-mediated B cell differentiation.

49. Health assessment of nesting loggerhead sea turtles ( Caretta caretta ) in one of their largest rookeries (central eastern Florida coast, USA).

50. Germline mutations in a G protein identify signaling cross-talk in T cells.

Catalog

Books, media, physical & digital resources