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Archives of Disease in Childhood. Education and Practice Edition|December 23, 2020
BCG lymphadenitis: a potential complication of immune reconstitution following haematopoietic stem cell transplantChristo Tsilifis, Ina Schim van der Loeff, Eleri Williams, et al.
Frontiers in Pediatrics|March 7, 2022
Management of Chronic Graft-vs.-Host Disease in Children and Adolescents With ALL: Present Status and Model for a Personalised Management PlanAgnieszka Sobkowiak-Sobierajska, Caroline Lindemans, Tomas Sykora, et al.
Research Square|February 13, 2023
What Causes Aplastic Anaemia: Results of Transplants from Genetically-Identical TwinsRobert Gale, Wolfgang Hinterberger, Neal S Young, et al.
Journal of Pediatric Hematology/Oncology|September 10, 2002
CD3+CD4-CD8+NK- large granular lymphocytosis with neutropenia and evidence for clonality and T-cell receptor gene rearrangement: two pediatric casesMamidipudi T Krishna, Elizabeth Hodges, Frances L Lavender, et al.
BMJ Open Gastroenterology|August 17, 2024
Gut microbiota and intestinal rehabilitation: a prospective childhood cohort longitudinal study of short bowel syndrome (the MIRACLS study): study protocolJemma S Cleminson, Julian Thomas, Christopher J Stewart, et al.
The Journal of Allergy and Clinical Immunology. in Practice|February 2, 2020
Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine-Derived Complications: A Systematic ReviewSaba Fekrvand, Reza Yazdani, Peter Olbrich, et al.
Stem Cells (Dayton, Ohio)|July 3, 2013
Brief report: a human induced pluripotent stem cell model of cernunnos deficiency reveals an important role for XLF in the survival of the primitive hematopoietic progenitorsKatarzyna Tilgner, Irina Neganova, Chatchawan Singhapol, et al.
The Journal of Allergy and Clinical Immunology|January 11, 2014
Human syndromes of immunodeficiency and dysregulation are characterized by distinct defects in T-cell receptor repertoire developmentXiaomin Yu, Jorge R Almeida, Sam Darko, et al.
European Journal of Pediatrics|January 4, 2014
Towards a safety net for management of 22q11.2 deletion syndrome: guidelines for our timesAlex Habel, Richard Herriot, Dinakantha Kumararatne, et al.
Human Molecular Genetics|July 17, 2014
Selective demethylation and altered gene expression are associated with ICF syndrome in human-induced pluripotent stem cells and mesenchymal stem cellsKevin Huang, Zhourui Wu, Zhenshan Liu, et al.
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