213 results on '"Markert, M. Louise"'
Search Results
2. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy
3. Clinical Practice Guidelines for the Immunological Management of Chromosome 22q11.2 Deletion Syndrome and Other Defects in Thymic Development
4. Diagnostic assay to assist clinical decisions for unclassified severe combined immune deficiency
5. Newborn Screening for Severe Combined Immunodeficiency and T-cell Lymphopenia in California, 2010-2017.
6. 29 Safety and feasibility of the use of dual cardiac-thymus transplant in a child with cardiac failure requiring heart transplant
7. Care of Children with DiGeorge Before and After Cultured Thymus Tissue Implantation
8. Biallelic variants in ribonuclease inhibitor (RNH1), an inflammasome modulator, are associated with a distinctive subtype of acute, necrotizing encephalopathy
9. Defects in thymic development
10. Contributors
11. Cultured thymus tissue transplantation
12. FOXN1 compound heterozygous mutations cause selective thymic hypoplasia in humans
13. Introducing thymus for promoting transplantation tolerance
14. Thymus Transplantation
15. Induction of donor-specific tolerance to heart transplantation: From concept to clinical translation.
16. Disseminated Mycobacterium kansasii Disease in Complete DiGeorge Syndrome
17. 22q11.2 Deletion Syndrome Causes a Thymus Hypoplasia Corrected by Mesenchymal Cell Replacement
18. Characterization of Human FOXN1 Mutations Uncovers both Loss- and Gain-of-Function Outcomes
19. First use of thymus transplantation therapy for FOXN1 deficiency (nude/SCID): a report of 2 cases
20. Experience with cultured thymus tissue in 105 children
21. Induction of donor-specific tolerance to heart transplantation: From concept to clinical translation
22. Mechanisms of tolerance to parental parathyroid tissue when combined with human allogeneic thymus transplantation
23. Mutation of Jak3 in a Patient with SCID: Essential Role of Jak3 in Lymphoid Development
24. Polymorphism of Human B-Cell Alloantigens: Evidence for Three Loci within the HLA System
25. Defects in Thymic Development
26. List of Contributors
27. Diagnosis of 22q11.2 Deletion Syndrome and Artemis Deficiency in Two Children with T-B-NK+ Immunodeficiency
28. Thymus transplantation in complete DiGeorge anomaly
29. Characterization of cultured thymus tissue used for transplantation with emphasis on promiscuous expression of thyroid tissue-specific genes
30. Thymic reconstitution
31. Contributors
32. Cultured thymus tissue implementation promotes donor-specific tolerance to allogeneic heart transplants
33. Histopathologic assessment of cultured human thymus
34. Predicting Autoimmunity Development in 22q11.2DS
35. Transplantation of thymus tissue in complete DiGeorge syndrome
36. Hematopoietic stem-cell transplantation for the treatment of severe combined immunodeficiency
37. Normalization of the Peripheral Blood T Cell Receptor Vβ Repertoire After Cultured Postnatal Human Thymic Transplantation in DiGeorge Syndrome
38. Postnatal thymus transplantation with immunosuppression as treatment for DiGeorge syndrome
39. SpA: web-accessible spectratype analysis: data management, statistical analysis and visualization
40. Statistical analysis of antigen receptor spectratype data
41. Complete DiGeorge syndrome: Development of rash, lymphadenopathy, and oligoclonal T cells in 5 cases
42. Thymus transplantation in complete DiGeorge syndrome: immunologic and safety evaluations in 12 patients
43. Complete DiGeorge syndrome: Persistence of profound immunodeficiency
44. Compound Heterozygous Mutations in Forkhead Box N1 (FOXN1) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients
45. Thymus transplantation for complete DiGeorge syndrome: European experience
46. Thymus transplantation
47. Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development
48. Thymus Transplantation for Chronic Graft Versus Host Disease
49. Adenosine deaminase and purine nucleoside phosphorylase deficiencies: Evaluation of therapeutic interventions in eight patients
50. Functional variants in TBX2 are associated with a syndromic cardiovascular and skeletal developmental disorder.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.