JA
Juan Aldave
Research areas: Immunology and Microbiology · Immunology · Immunodeficiency and Autoimmune Disorders · Blood disorders and treatments · T-cell and B-cell Immunology
0000-0003-3548-0385
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Publications (19)
- Calidad de vida relacionada con la salud en niños peruanos con errores innatos de la inmunidad durante la pandemia de COVID-19: estudio transversal en dos hospitales de referencia de Lima, Perú Save
- Improved outcome of HSCT in STAT1 gain-of-function disease following JAK inhibition bridging Save
- DIAGNÓSTICO OPORTUNO DE UNA VARIANTE PATOGÉNICA POTENCIALMENTE MORTAL EN EL GEN DEL RECEPTOR GAMMA DE INTERLEUCINA-2 EN UN NEONATO DIAGNÓSTICO NEONATAL DE UNA INMUNODEFICIENCIA COMBINADA GRAVE Save
- Uso de interferón gamma en un paciente con enfermedad granulomatosa crónica posterior a falla primaria de trasplante de progenitores hematopoyéticos en un hospital público en Perú: reporte de un caso Save
- COVID-19 y oftalmología: rol del sistema inmunitario Save
- Genetic diagnosis of patients with primary agammaglobulinemia treated at third level peruvian centers Save
- Latin American consensus on the supportive management of patients with severe combined immunodeficiency Save
- Lentiviral gene therapy combined with low-dose busulfan in infants with SCID-X1 Save
- X-linked agammaglobulinemia (XLA):Phenotype, diagnosis, and therapeutic challenges around the world Save
- Genetic and mechanistic diversity in pediatric hemophagocytic lymphohistiocytosis Save
- Hematopoietic stem cell transplantation in patients with gain-of-function signal transducer and activator of transcription 1 mutations Save
- Registration of patients with primary immunodeficiencies in the three main reference centers in Peru,Registro de pacientes con inmunodeficiencias primarias en los tres principales centros de referencia del Perú Save
- A 3-year-old girl with recurrent infections and autoimmunity due to a STAT1 gain-of-function mutation: The expanding clinical presentation of primary immunodeficiencies Save
- Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders Save
- Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype Save
- International survey on skin patch test procedures, attitudes and interpretation Save
- Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia Save
- First report of the hyper-IgM syndrome registry of the latin american society for immunodeficiencies: Novel mutations, unique infections, and outcomes Save
- A 1-year-old girl with a gain-of-function STAT1 mutation treated with hematopoietic stem cell transplantation Save