Genetic errors of immunity distinguish pediatric nonmalignant lymphoproliferative disorders
Journal
Journal of Allergy and Clinical Immunology
ISSN
0091-6749
Date Issued
2022
Author(s)
Lisa R. Forbes
Olive S. Eckstein
Nitya Gulati
Erin C. Peckham-Gregory
Nmazuo W. Ozuah
Joseph Lubega
Nader K. El-Mallawany
Jennifer E. Agrusa
M. Cecilia Poli
Tiphanie P. Vogel
Natalia S. Chaimowitz
Nicholas L. Rider
Emily M. Mace
Jordan S. Orange
Jason W. Caldwell
Juan C. Aldave-Becerra
Stephen Jolles
Francesco Saettini
Hey J. Chong
Asbjorg Stray-Pedersen
Helen E. Heslop
Kala Y. Kamdar
R. Helen Rouce
Donna M. Muzny
Shalini N. Jhangiani
Richard A. Gibbs
Zeynep H. Coban-Akdemir
James R. Lupski
Kenneth L. McClain
Carl E. Allen
Ivan K. Chinn
Type
Resource Types::text::journal::journal article
URL Institutional Repository
Cite this document
Forbes, L. R., Eckstein, O. S., Gulati, N., Peckham-Gregory, E. C., Ozuah, N. W., Lubega, J., El-Mallawany, N. K., Agrusa, J. E., Poli, M. C., Vogel, T. P., Chaimowitz, N. S., Rider, N. L., Mace, E. M., Orange, J. S., Caldwell, J. W., Aldave-Becerra, J. C., Jolles, S., Saettini, F., Chong, H. J., … Chinn, I. K. (2022). Genetic errors of immunity distinguish pediatric nonmalignant lymphoproliferative disorders. Journal of Allergy and Clinical Immunology, 149(2), 758-766. https://doi.org/10.1016/j.jaci.2021.07.015
Subjects
primary immunodeficiency
;
classification
;
guidelines
;
adolescent
;
autoimmunity
;
child
;
child, preschool
;
female
;
genetic association studies
;
genetic testing
;
herpesvirus 4, human
;
humans
;
immunity
;
infant
;
lymphoproliferative disorders
;
male
;
whole exome sequencing
;
young adult
;
biological product
;
steroid
;
adolescent
;
adult
;
age
;
article
;
autoimmune disease
;
autoinflammatory disease
;
biological therapy
;
chemotherapy
;
child
;
clinical feature
;
clinical outcome
;
cohort analysis
;
controlled study
;
diffuse large b cell lymphoma
;
epstein barr virus infection
;
female
;
genetic association
;
genetic disorder
;
genetic screening
;
genotype phenotype correlation
;
hemophagocytic syndrome
;
human
;
immunity
;
lymphadenopathy
;
lymphocytic infiltration
;
lymphoproliferative disease
;
major clinical study
;
male
;
molecular diagnosis
;
pediatric nonmalignant lymphoproliferative disorder
;
pediatric nonmalignant lymphoproliferative disorder
;
splenomegaly
;
survival rate
;
thyroid papillary carcinoma
;
whole exome sequencing
;
autoimmunity
;
epstein barr virus
;
genetic association study
;
genetics
;
immunity
;
immunology
;
infant
;
isolation and purification
;
lymphoproliferative disease
;
mortality
;
preschool child
;
young adult