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Rhabdomyolysis and severe hypercalcemia. Report of one case
(SOC MEDICA SANTIAGO, 2019)
Rhabdomyolysis (RD) is the process that leads to cell destruction of striated muscle. Causes include inherited metabolic defects or acquired disorders. RD is frequently associated with acute kidney injury (AKI) and disorders ...
Analysis of the diagnostic presentation profile, parathyroidectomy indication and bone mineral density follow-up of Brazilian patients with primary hyperparathyroidism
(Associação Brasileira de Divulgação Científica, 2007-04-01)
Primary hyperparathyroidism is an endocrine disorder with variable clinical expression, frequently presenting as asymptomatic hypercalcemia in Western countries but still predominantly as a symptomatic disease in developing ...
Williams syndrome: Pediatric, neurologic, and cognitive development
(ELSEVIER SCIENCE INC, 2005-03)
This study examines the developmental history of 32 Williams syndrome patients, positive to the fluorescence in situ hybridization (FISH) test. The information is intended to provide help for early diagnosis and appropriate ...
Williams syndrome: Pediatric, neurologic, and cognitive development
(ELSEVIER SCIENCE INC, 2005)
This study examines the developmental history of 32 Williams syndrome patients, positive to the fluorescence in situ hybridization (FISH) test. The information is intended to provide help for early diagnosis and appropriate ...
Skeletal-related events due to bone metastases from differentiated thyroid cancer
(Oxford University Press, 2012)
BACKGROUND:
In oncology, the clinical impact of metastatic bone disease is conveyed via a composite end point termed skeletal-related events (SRE), which encompasses spinal cord compression, pathological fracture, a need ...
Skeletal-related events due to bone metastases from differentiated thyroid cancer
(Oxford University Press, 2012)
BACKGROUND:
In oncology, the clinical impact of metastatic bone disease is conveyed via a composite end point termed skeletal-related events (SRE), which encompasses spinal cord compression, pathological fracture, a need ...
Assessment of Intellectual and Visuo- Spatial Abilities in Children and Adults with Williams Syndrome
The Williams-Beuren syndrome (SWB), also known as Williams syndrome, is a contiguous gene deletion of the region 7q.11.23. The main clinical characteristics are typical faces, supravalvular aortic stenosis, failure to ...
Assessment of Intellectual and Visuo- Spatial Abilities in Children and Adults with Williams Syndrome
The Williams-Beuren syndrome (SWB), also known as Williams syndrome, is a contiguous gene deletion of the region 7q.11.23. The main clinical characteristics are typical faces, supravalvular aortic stenosis, failure to ...
Incidencia de la enfermedad pulmonar en pacientes con mieloma múltiple previo y posterior a trasplante de progenitores hematopoyéticos mediante un estudio de cohorte retrospectivo en la Clínica FOSCAL
(Universidad Autónoma de Bucaramanga UNABFacultad Ciencias de la SaludEspecialización en Medicina Interna, 2021)
Introducción: Los pacientes con Mieloma Múltiple (MM) pueden recibir diversos regímenes de quimioterapia y de acondicionamiento, que hacen parte del proceso de trasplante de progenitores hematopoyéticos (TPH). Este tratamiento ...