Documentos relacionados

1. [Primary immunodeficiencies in seriously ill children: Report of 3 clinical cases].
2. Allogeneic HSCT for Symptomatic Female X-linked Chronic Granulomatous Disease Carriers.
3. A Novel Assay in Whole Blood Demonstrates Restoration of Mitochondrial Activity in Phagocytes After Successful HSCT in Hyperinflamed X-Linked Chronic Granulomatous Disease.
4. Practical guidance for the diagnosis and management of secondary hypogammaglobulinemia: A Work Group Report of the AAAAI Primary Immunodeficiency and Altered Immune Response Committees.
5. Chronic granulomatous disease: a 25-year patient registry based on a multistep diagnostic procedure, from the referral center for primary immunodeficiencies in Greece.
6. [A case report of chronic granulomatous disease with <i>CYBB</i> gene mutation in an adult].
7. Late Onset of Chronic Granulomatous Disease Revealed by Paecilomyces lilacinus Cutaneous Infection.
8. X-linked chronic granulomatous disease secondary to skewed X-chromosome inactivation in female patients.
9. Selective IgM deficiency: Follow-up and outcome.
10. Chronic Granulomatous Disease: an Updated Experience, with Emphasis on Newly Recognized Features.