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33 results on '"the Jeffrey Modell Foundation"'

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1. COVID-19 Vaccine Responses in PIDD Subjects

4. Single-cell Atlas of common variable immunodeficiency shows germinal center-associated epigenetic dysregulation in B-cell responses.

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

6. A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

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

8. FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

9. A loss-of-function IFNAR1 allele in Polynesia underlies severe viral diseases in homozygotes

10. Three Copies of Four Interferon Receptor Genes Underlie a Mild Type I Interferonopathy in Down Syndrome

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

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

13. COVID-19 infection in first trimester of pregnancy marked by a liver cytolysis in a woman previously treated by hydroxychloroquine for repeated implantation failure : a case report

14. Tuberculosis and impaired IL-23–dependent IFN-γ immunity in humans homozygous for a common TYK2 missense variant

15. Inherited CARD9 deficiency in 2 unrelated patients with invasive Exophiala infection

16. Age-dependent association between pulmonary tuberculosis and common TOX variants in the 8q12-13 linkage region

17. Inherited IL-12p40 Deficiency Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds

18. Immunodeficiency, autoinflammation and amylopectinosis in humans with inherited HOIL-1 and LUBAC deficiency

19. Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both

20. Blacklisting variants common in private cohorts but not in public databases optimizes human exome analysis

21. A pleiotropic recurrent dominant ITPR3 variant causes a complex multisystemic disease.

22. Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling.

23. SARS-CoV-2 spike antibody concentration in gamma globulin products from high-prevalence COVID-19 countries are transmitted to X-linked agammaglobulinemia patients.

24. Care of patients with inborn errors of immunity in thirty J Project countries between 2004 and 2021.

25. Hematopoietic Stem Cell Transplantation in ARPC1B Deficiency.

27. GATA2 Deficiency in Adult Life Is Characterized by Phenotypic Diversity and Delayed Diagnosis.

28. Genetic workup as a complementary tool for the diagnosis of primary complement component deficiencies: a multicenter experience.

29. Minor Clinical Impact of COVID-19 Pandemic on Patients With Primary Immunodeficiency in Israel.

30. Correction to: Primary immunodeficiencies in Central and Eastern Europe-the power of networking Report on the activity of the Jeffrey Modell Foundation Centers Network in Central and Eastern Europe.

31. Primary immunodeficiencies in Central and Eastern Europe-the power of networking Report on the activity of the Jeffrey Modell Foundation Centers Network in Central and Eastern Europe.

32. Calculation of a Primary Immunodeficiency "Risk Vital Sign" via Population-Wide Analysis of Claims Data to Aid in Clinical Decision Support.

33. First Year of Israeli Newborn Screening for Severe Combined Immunodeficiency-Clinical Achievements and Insights.

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