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Publications by Edgar Borges de Oliveira Junior
A C126R De Novo Mutation in CYBB Leads to X-Linked Chronic Granulomatous Disease With Recurrent Pneumonia and BCGitis
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
A Novel Mutation in the NCF2 Gene in a CGD Patient With Chronic Recurrent Pneumopathy
Frontiers in Pediatrics
Child Health
Pediatrics
Perinatology
Related publications
Unusual Late Presentation of X-Linked Chronic Granulomatous Disease in an Adult Female With a Somatic Mosaic for a Novel Mutation in CYBB
Blood
Biochemistry
Immunology
Cell Biology
Hematology
Gene Therapy for X-Linked Chronic Granulomatous Disease (Net4CGD)
Human gene therapy. Clinical development
Genetics
X-Linked Carriers of Chronic Granulomatous Disease: Illness, Lyonization, and Stability
Journal of Allergy and Clinical Immunology
Allergy
Immunology
The First De Novo Mutation of the Connexin 32 Gene Associated With X Linked Charcot-Marie-Tooth Disease.
Journal of Medical Genetics
Genetics
288. Dual-Regulated Lentiviral Vector for Gene Therapy of X-Linked Chronic Granulomatous Disease
Molecular Therapy
Molecular Medicine
Molecular Biology
Pharmacology
Medicine
Genetics
Drug Discovery
Transient, Recurrent, White Matter Lesions in X-Linked Charcot-Marie-Tooth Disease With Novel Connexin 32 Mutation
Archives of Neurology
AB027. Newly Diagnosed Chronic Granulomatous Disease in a Thirty Four Year Old Woman With Pneumocystis Jiroveci Pneumonia
Annals of Translational Medicine
Medicine
Chronic Granulomatous Disease
New England Journal of Medicine
Medicine
Chronic Granulomatous Disease
Clinical Reviews in Allergy and Immunology
Medicine
Allergy
Immunology