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Mostrando ítems 31-40 de 16015
Pompe disease: Clinical perspectives
(Dove Medical, 2017)
Pompe disease (acid alpha-glucosidase deficiency, OMIM 232300) is a rare lysosomal storage disorder due to autosomal recessive mutations in the GAA gene. It has also been called acid maltase deficiency and glycogen storage ...
Revisiting the chronic renal disease in pediatric patients
(Universidade Federal de Minas GeraisBrasilFAR - DEPARTAMENTO DE ANÁLISES CLÍNICAS E TOXICOLÓGICASMED - DEPARTAMENTO DE PEDIATRIAUFMG, 2016)
Oxidative stress: a possible link between periodontal disease and cardiovascular disease
(Universidade Federal de UberlândiaBrasilOdontologia, 2017)
Swallowing endoscopy findings in Huntington's disease: A case report
(2016-01-01)
Huntington's disease (HD) is a degenerative genetic disorder with autosomal-dominant transmission. The triad of symptoms of this disease consists of psychiatric disorders, jerky movements, and dementia. Oropharyngeal ...
Apatia na doença de alzheimer: Contribuição para uma visão clínica da progressão da demência
(2010-10-27)
In addition to cognitive impairment, apathy is increasingly recognized as an important neuropsychiatric syndrome in Alzheimer's disease (AD). Aims: To identify the relationship between dementia severity and apathy levels, ...
Apatia na doença de alzheimer: Contribuição para uma visão clínica da progressão da demência
(2010-10-27)
In addition to cognitive impairment, apathy is increasingly recognized as an important neuropsychiatric syndrome in Alzheimer's disease (AD). Aims: To identify the relationship between dementia severity and apathy levels, ...