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1. Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysis

3. Expanding the PRAAS spectrum: De novo mutations of immunoproteasome subunit β-type 10 in six infants with SCID-Omenn syndrome

4. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

5. Severe Immune-Related Enteritis after In Utero Exposure to Pembrolizumab

8. Initial presenting manifestations in 16,486 patients with inborn errors of immunity include infections and noninfectious manifestations

9. Implementation of Early Next-Generation Sequencing for Inborn Errors of Immunity:A Prospective Observational Cohort Study of Diagnostic Yield and Clinical Implications in Dutch Genome Diagnostic Centers

10. Neisseria meningitidis Serogroup Z Meningitis in a Child with Complement C8 Deficiency and Potential Cross Protection of the MenB-4C Vaccine

11. MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerization

12. Decreased Cell Wall Galactosaminogalactan inAspergillus nidulansMediates Dysregulated Inflammation in the Chronic Granulomatous Disease Host

14. Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysis.

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