Results 41 to 50 of about 4,202 (211)
A difficult diagnosis of coeliac disease: Repeat duodenal histology increases diagnostic yield in patients with concomitant causes of villous atrophy [PDF]
, 2017 Villous atrophy in absence of coeliac disease (CD)-specific antibodies represents a diagnostic dilemma. We report a case of a woman with anaemia, weight loss and diarrhoea with an initial diagnosis of seronegative CD and a histological documented villous
Cappello, Maria +5 more
core +1 more source
THE ROLE OF IgM-ENRICHED INTRAVENOUS IMMUNOGLOBULIN IN TRANSPLANTATION [PDF]
Sanamed, 2014 After organ transplantation, gamma globulin and intravenous immunoglobulin enriched with IgM are most frequently used in septic shock as early immune-support.
Szabó Judit +2 more
doaj +3 more sources
Case Reports in Oncology, 2010 A case of persistent B-cell lymphocytopenia in a 40-year-old woman with lymphoid-epithelial thymoma treated with chemotherapy, surgery and irradiation is described.
Klas Raaschou-Jensen +4 more
doaj +1 more source
Helcococcus ovis associated with septic arthritis and bursitis in calves – a case report
BMC Veterinary Research, 2021 Background Septic arthritis often occurs in young calves when the passive transfer of maternal immunoglobulins has failed, which results in hypogammaglobulinaemia in the calf. Another important cause is suboptimal herd health management which often leads
Alexandra Jost, Marlene Sickinger
doaj +1 more source
International Journal of Infectious Diseases, 2021 Objectives: Enterovirus (EV) is a frequent cause of encephalitis. The optimal therapeutic approach remains a matter of debate. We present the case of an immunosuppressed patient with EV encephalitis treated successfully with intravenous immunoglobulin ...
Judith N. Wagner +4 more
doaj +1 more source
Lung disease in primary antibody deficiency. [PDF]
, 2015 This Review summarises current knowledge on the pulmonary manifestations of primary antibody deficiency (PAD) syndromes in adults. We describe the major PAD syndromes, with a particular focus on common variable immunodeficiency (CVID).
Grimbacher, B, Hurst, JR, Verma, N
core +1 more source
TRNT1 deficiency: clinical, biochemical and molecular genetic features [PDF]
, 2016 BACKGROUND: TRNT1 (CCA-adding transfer RNA nucleotidyl transferase) enzyme deficiency is a new metabolic disease caused by defective post-transcriptional modification of mitochondrial and cytosolic transfer RNAs (tRNAs).
Chong, WK +14 more
core +2 more sources
Acquired hypogammaglobulinaemia and sarcoidosis [PDF]
Postgraduate Medical Journal, 1984 Summary A syndrome has been described in which hypogammaglobulinaemia is associated with splenomegaly and haemolytic anaemia and also non-caseating granulomata in lymph nodes, liver, spleen and skin. This report describes a patient with this syndrome who in addition had a positive Kveim and elevated serum angiotensin converting enzyme ...
openaire +2 more sources
Primary `acquired' hypogammaglobulinaemia and amyloidosis [PDF]
Journal of Clinical Pathology, 1968 The clinical details and post-mortem findings are given of a patient who had primary `acquired' hypogammaglobulinaemia and was found at necropsy to have amyloidosis. The relationship of gamma globulin deficiency to amyloidosis is discussed, and the possible relevance of the hypogammaglobulinaemia to the formation and nature of amyloid is noted.
W D, Murray, I A, Cook
openaire +2 more sources
Treatment of immune thrombocytopenia with intravenous immunoglobulin and insights for other diseases
Swiss Medical Weekly, 2012 Since 1946 the development of fractionation and purification methods of human plasma led to biologic immunoglobulin for intravenous use (IVIG).
Paul Imbach
doaj +1 more source