Here are entered works on mortgage loans offered at a higher interest rate than the prime rate, primarily to individuals with low credit scores who do not qualify for traditional financing
Sub-Saharan African People : Atlas of dermatological conditions in populations of African ancestry / Claudia M.Y.A. Donkor, Jeannette Aryee-Boi, Itohan Roseline Osazuwa, Francis Kwame Afflu, Andrew F. Alexis
Suba Colombia : Propuesta de mitigación para los sectores críticos de inundación en la localidad de Suba / autores, Ronal Orlando Serrano Romero, Daniel Hernando Hernández Gómez
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Suba Emergency management Colombia : Propuesta de mitigación para los sectores críticos de inundación en la localidad de Suba / autores, Ronal Orlando Serrano Romero, Daniel Hernando Hernández Gómez
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Suba Flood control Colombia : Propuesta de mitigación para los sectores críticos de inundación en la localidad de Suba / autores, Ronal Orlando Serrano Romero, Daniel Hernando Hernández Gómez
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Subacute Care. : Nursing the highly dependent child or infant : a manual of care
A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous system overactivity. It may result from toxic/metabolic conditions or structural brain lesions. (From Adams et al., Principles of Neurology, 6th ed, pp411-2)
A disorder characterized by CONFUSION; inattentiveness; disorientation; ILLUSIONS; HALLUCINATIONS; agitation; and in some instances autonomic nervous system overactivity. It may result from toxic/metabolic conditions or structural brain lesions. (From Adams et al., Principles of Neurology, 6th ed, pp411-2)
An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement
A rare transmissible encephalopathy most prevalent between the ages of 50 and 70 years. Affected individuals may present with sleep disturbances, personality changes, ATAXIA; APHASIA, visual loss, weakness, muscle atrophy, MYOCLONUS, progressive dementia, and death within one year of disease onset. A familial form exhibiting autosomal dominant inheritance and a new variant CJD (potentially associated with ENCEPHALOPATHY, BOVINE SPONGIFORM) have been described. Pathological features include prominent cerebellar and cerebral cortical spongiform degeneration and the presence of PRIONS. (From N Engl J Med, 1998 Dec 31;339(27))