Reversible hypogammaglobulinaemia.
Contains fulltext : 51746.pdf (Publisher’s version ) (Open Access)
Desar, I.M.E. +3 more
openaire +3 more sources
Summary Clinical outcome after chimeric antigen receptor (CAR)‐T‐cell failure in large B‐cell lymphoma (LBCL) is dismal. Allogeneic stem cell transplantation (alloSCT) represents a potentially curative salvage for relapsed/refractory LBCL, although concerns remain regarding its feasibility and safety in patients exposed to CAR‐T and bispecific ...
Angelica Barone +10 more
wiley +1 more source
ANCA-associated vasculitis [PDF]
The vasculitides are a heterogeneous group of conditions typified by their ability to cause vessel inflammation with or without necrosis. They present with a wide variety of signs and symptoms and, if left untreated, carry a significant burden of ...
Watts, Richard, Yates, Max
core +1 more source
Common variable immunodeficiency associated enteropathy: a diagnostic enigma in developing countries
Common variable immunodeficiency (CVID) is the most prevalent primary immunodeficiency disorder with different phenotypes and aetiologies. It is characterised by hypogammaglobulinaemia, defects in specific antibody response, erroneous activation and ...
Muhammad Aftab Hassan +4 more
doaj +1 more source
Severe EBV Infection In Primary Immunodeficiency And The Normal Host [PDF]
Epstein–Barr virus (EBV) infection is ubiquitous in humans, but the majority of infections have an asymptomatic or self-limiting clinical course.
Booth, C, Houldcroft, C, Worth, A
core
What is the burden of immunoglobulin replacement therapy in adult patients with primary immunodeficiencies? A systematic review [PDF]
© 2018 Jones, Vogt, Chambers, Clowes and Shrimpton. Background: Primary immunodeficiency disorders (PIDs) are a group of heterogeneous rare disorders, whereby the immune system is missing or not functioning adequately.
Ballow +40 more
core +4 more sources
Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 gene [PDF]
Spondyloenchondrodysplasia (SPENCD) is a rare skeletal dysplasia, characterized by metaphyseal lesions, neurological impairment and immune dysregulation associated with lupus-like features.
Christine Wolf +4 more
core +1 more source
Adults with spontaneous aerobic Gram-negative bacillary meningitis admitted to the intensive care unit [PDF]
The characteristics of spontaneous aerobic Gram-negative bacillary meningitis (AGNBM) were determined in 40 adults requiring admission to an intensive care unit (ICU) during a 16-year period in ten French ICUs. Eight infections were hospital-acquired and
L. Bouadma +24 more
core +2 more sources
Tandem combination of ASCT and CAR T‐cell therapy in highly refractory CNS lymphomas
British Journal of Haematology, Volume 207, Issue 5, Page 2178-2182, November 2025.
Lydia Montes +19 more
wiley +1 more source
A de novo atypical ring sSMC(22) characterized by array CGH in a boy with cat-eye syndrome. [PDF]
BACKGROUND: Microduplications 22q11 have been characterized as a genomic duplication syndrome mediated by nonallelic homologous recombination between region-specific low-copy repeats.
Fekete, György +5 more
core +3 more sources

