Related references
Note: Only part of the references are listed.A new genetic subgroup of chronic granulomatous disease with autosomal recessive mutations in p40phox and selective defects in neutrophil NADPH oxidase activity
Juan D. Matute et al.
BLOOD (2009)
Reconstructing Indian population history
David Reich et al.
NATURE (2009)
Chronic Granulomatous Disease: The European Experience
J. Merlijn van den Berg et al.
PLOS ONE (2009)
Fatal Hemophagocytic Lymphohistiocytosis in X-Linked Chronic Granulomatous Disease Associated With a Perforin Gene Variant
Joris A. van Montfrans et al.
PEDIATRIC BLOOD & CANCER (2009)
A 24-Year-Old Man With Giddiness, Hemoptysis, and Skin Lesions
Lancelot Mark Pinto et al.
CHEST (2008)
Clinical features, long-term follow-up and outcome of a large cohort of patients with Chronic Granulomatous Disease: An Italian multicenter study
Baldassarre Martire et al.
CLINICAL IMMUNOLOGY (2008)
Spectrum of primary immune deficiency at a tertiary care hospital
Sumit Verma et al.
INDIAN JOURNAL OF PEDIATRICS (2008)
Susceptibility to mycobacterial infections in children with X-linked chronic granulomatous disease - A review of 17 patients living in a region endemic for tuberculosis
Pamela P. W. Lee et al.
PEDIATRIC INFECTIOUS DISEASE JOURNAL (2008)
BCG-osis and tuberculosis in a child with chronic granulomatous disease
Jacinta Bustamante et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2007)
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
R. El Kares et al.
JOURNAL OF HUMAN GENETICS (2006)
Long-term follow-up and outcome of 39 patients with chronic granulomatous disease
J Liese et al.
JOURNAL OF PEDIATRICS (2000)
Chronic granulomatous disease - Report on a national registry of 368 patients
JA Winkelstein et al.
MEDICINE (2000)