Results 91 to 100 of about 4,202 (211)

Reversible hypogammaglobulinaemia.

open access: yesThe Netherlands journal of medicine, 2007
Contains fulltext : 51746.pdf (Publisher’s version ) (Open Access)
Desar, I.M.E.   +3 more
openaire   +3 more sources

Allogeneic transplantation after failure of chimeric antigen receptor‐T cells and exposure to bispecific antibodies: Feasibility, safety and survival outcomes

open access: yesBritish Journal of Haematology, Volume 207, Issue 3, Page 956-964, September 2025.
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]

open access: yes, 2017
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

open access: yesJournal of the Pakistan Medical Association
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]

open access: yes, 2016
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]

open access: yes, 2018
© 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]

open access: yes, 2015
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]

open access: yes, 2006
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

open access: yes
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]

open access: yes, 2014
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

Home - About - Disclaimer - Privacy