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Molecular approaches to fungal infections in immunocompromised patientsWilliamson, Emma Charlotte Mary January 2001 (has links)
No description available.
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Human haemopoietic progenitor cell mobilizationWatts, Michael John January 2000 (has links)
No description available.
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Generation and analysis of a mouse model of #beta#-cell-specific TGF-receptor type II-deficiencyCazac, Balthazar Bernard January 2000 (has links)
No description available.
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Adhesive interactions of leukaemic cells with endotheliumCavenagh, James Durrell January 1996 (has links)
No description available.
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Applications of the Cre-LoxP technology to the study of megakaryocytesEmambokus, Nikla R. January 2000 (has links)
No description available.
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Regulation of macrophage inflammatory protein-1#alpha# expression by haemopoietic growth factorsJarmin, David Ian January 1998 (has links)
No description available.
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Modeling bone marrow sub-structures at power-line frequenciesChiu, Roanna Sum-Wan. 10 April 2008 (has links)
No description available.
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The differentiation of osteogenic cells from bone marrowBennett, Jonathan Hilary January 1991 (has links)
No description available.
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the practice and usefulness of bone marrow examinations in a cohort of human immunodeficiency virus infected children in South Africa: a descriptive studyRowe, Biance 11 January 2012 (has links)
INTRODUCTION: Bone marrow examination (BME) is performed in Human Immunodeficiency Virus-infected (HIV+) children with haematologic abnormalities to exclude specific disease (SD).
AIMS: To describe the:
(1) indications for BME , (2) utility of BME to diagnose SD, (3) patient characteristics associated with SD or non-specific disease (NSD).
METHODS:
Design: Retrospective review.
Definitions:
SD: BME positive for opportunistic infection (OI) or HIV-related malignancy. NSD: HIV-related changes only.
RESULTS:
Eighty six BME’s were done. Suspected SD in 56/86(65.1%) was the most common clinical indication. Bicytopaenia(n=32) and isolated cytopaenia(n=31) were the most common haematologic indications. NSD 48/86 (55.8%) was a more common finding than SD 32/86 (37.2%). Granulomas, pure red cell aplasia and malignancy were the SD identified. Pre- highly active antiretroviral therapy (HAART), advanced stage, and not being virally suppressed were significantly associated with NSD.
CONCLUSION:
The yield of SD (37.2%) on BME is comparable to adult studies. HAART should be instituted before BME as NSD will be the most likely finding.
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Mieloma múltiple con osteoesclerosis difusa: reporte de casoValdivieso Herrera, Marco Antonio Josué, Vargas Ruiz, Luis Oswaldo, Morales Luna, Domingo Antonio, Piscoya, Alejandro, del Carpio Jayo, Daniel Rubén 06 1900 (has links)
The case is presented of a female patient with history of anaemia (haemoglobin 9 g/dL) of 4 years onset, who was referred to the Internal Medicine department complaining of fatigue, dyspnoea, and syncope. She also had a burning pain in the costal region radiating to dorsal and lumbar spine, and lower limbs, which persisted for more than 6 months. The laboratory results reported a haemoglobin value of 8.4 g / dL. There were also high levels of immunoglobulin A (2087). The serum protein electrophoresis revealed the presence of a monoclonal peak, with immunofixation showing the presence of Kappa type IgA. The histopathological examination of the bone marrow biopsy showed the presence of osteosclerosis and few plasma cells. Multiple myeloma was confirmed by CD 138 immunohistochemical staining. A review is presented on multiple myeloma, its clinical presentation, and differential diagnosis. / Revisión por pares
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