Successful Artery Embolization in a Patient with Autoimmune Lymphoproliferative Syndrome Associated with Splenic Rupture
Sign Up to like & getrecommendations! Published in 2020 at "Journal of Clinical Immunology"
DOI: 10.1007/s10875-020-00809-3
Abstract: To the Editor, Autoimmune lymphoproliferative syndrome (ALPS) is an autosomal dominant disorder of lymphocyte homeostasis wherein patients present with splenomegaly and lymphadenopathy [1]. ALPS results from defective apoptosis of T lymphocytes and accumulation of the… read more here.
Keywords: rupture; splenic rupture; lymphoproliferative syndrome; cytopenia ... See more keywords
A comprehensive analysis of cytopenias and bone marrow morphology in patients with a history of bariatric and metabolic surgery.
Sign Up to like & getrecommendations! Published in 2021 at "International journal of laboratory hematology"
DOI: 10.1111/ijlh.13738
Abstract: INTRODUCTION Following bariatric and metabolic surgery (BMS), patients may develop persistent cytopenia(s) despite adequate micronutrient levels. A comprehensive analysis of laboratory and hematopathologic findings in BMS patients with unexplained cytopenia(s) has not been previously described.… read more here.
Keywords: surgery; bone; cytopenias; cytopenia ... See more keywords
P383 Transient postviral cytopenia in children: an experience of a tertiary paediatric clinic
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DOI: 10.1136/archdischild-2017-313273.471
Abstract: Introduction Postinfectious cytopenia occurs commonly in paediatric practice.The differential diagnosis ranges from transient benign aetiology to a life threatening disease. Among the causes of transient postinfectious cytopenia, viral infections contribute to a great percentage. Aims… read more here.
Keywords: p383 transient; viral infections; cytopenia children; cytopenia ... See more keywords
Immune Mediated Cytopenia's Following Cord Blood Transplantation for Hurler's Syndrome: A Failure of Pre-Transplant Immune Suppression
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DOI: 10.1182/blood-2018-99-112995
Abstract: Background: Hurler's syndrome is the most severe phenotype of Mucopolysaccharidosis 1 (MPS1H) with severe deficiency of the lysosomal enzyme alpha-L-iduronidase causing heparan and dermatan sulfate accumulation, CNS and somatic manifestations and premature death. Haematopoeitic Stem… read more here.
Keywords: risk; hurler syndrome; transplant; risk factors ... See more keywords
Peripheral Blood Cytopenia and Subsequent Risk of Cardiovascular Disease and Mortality
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DOI: 10.1182/blood-2019-125956
Abstract: INTRODUCTION: African-Americans (blacks) have higher risk of stroke and coronary heart disease (CHD) - collectively referred to here as cardiovascular disease (CVD), than Caucasian-Americans (whites). Though partly explained by traditional cardiovascular risk factors, half of… read more here.
Keywords: risk; cvd mortality; mortality; model ... See more keywords
The Potential of Molecular Genetic Analysis for Diagnostic and Prognostic Decision Making in Clonal Cytopenia of Undetermined Significance (CCUS) and MDS - a Study on 576 Patients
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DOI: 10.1182/blood-2020-136557
Abstract: Background: Several specific therapies for MDS are now available. Molecular genetics plays a key role, as some therapies target distinct mutations and others are particularly effective for molecularly defined subgroups (e.g. SF3B1). In parallel, broad… read more here.
Keywords: cytopenia; mds; ccus mds; molecular genetics ... See more keywords
Magnitude and associated factors of peripheral cytopenia among HIV-infected children attending at University of Gondar Specialized Referral Hospital, Northwest Ethiopia
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DOI: 10.1371/journal.pone.0247878
Abstract: Background Isolated or multi lineage cytopenia are the most common clinicopathological features and independently associated with increased risk of disease progression and death among human immunodeficiency virus infected children. In the study area, there is… read more here.
Keywords: peripheral cytopenia; associated factors; cytopenia; hiv infected ... See more keywords