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Mostrando ítems 21-30 de 97
Polimorfismo de la proteína ligante de ácidos grasos intestinal (FABP2), obesidad e insulina resistencia
(2006)
The genetic components of insulin-resistance, diabetes and obesity
have been largely studied. These conditions are determined by multiple polygenic and
environmental factors. Certain candidate genes, that have common ...
Acute Pontine Infarct in a 16-Year-Old Man with Acute Posterior Multifocal Placoid Pigment Epitheliopathy. A Case Report
(2009)
A 16-year-old boy recently diagnosed with acute posterior multifocal placoid pigment epitheliopathy (APMPPE) developed an acute infarct in the left pontine region. No relevant abnormalities were found in the brain and ...
Cerebelous syndrome by infratentorial brain tuberculomas and mutisystemic tuberculosis in AIDS patient Síndrome cerebeloso secundario a granulomas de fosa posterior y tuberculosis multisistémica en un paciente con SIDA
(2008)
We present a clinical case of a patient who consulted for a cerebelous syndrome and diplopia associated to 10 kg weight loss in six months and multiple adenopathies. Cerebral imagenology study evidenced the presence of ...
Carotid ultrasound examination as an aging and disability marker
(Japan Geriatrics Society, 2014)
Aim: To explore the usefulness of carotid ultrasound examination as a marker of aging and predictor of disability
among older people.
Methods: Carotid ultrasound, measuring carotid intima media thickness (CIMT) and ...
Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) in the pre-Columbian culture of Colombia.
(2015-02-10)
Mucopolysaccharidosis type VI or Maroteaux Lamy syndrome is an autosomal recessive lysosomal storage disorder resulting from a deficiency of arylsulfatase B, the clinical features include short stature, hepatosplenomegaly, ...
Síndrome de Waardenburg tipo 1 en gemelos monocigóticos y su familia
(Universidad Nacional de Colombia - Sede Bogotá - Facultad de Medicina, 2016-04-01)
El síndrome de Waardenburg (SW) es un trastorno genético poco frecuente con una incidencia de 1 por 40000 habitantes. Es originado por mutaciones en múltiples genes como PAX3, MITF, SNAI2 y SOX10; estas alteraciones genéticas ...
A craniometry-based predictive model to determine occlusal vertical dimension
(Mosby-Elsevier, 2020)
Statement of problem. Craniometry is a method of determining the occlusal vertical dimension
(OVD); the current prediction models do not consider factors such as facial type and sex or normalizing the OVD by using 1 main ...
Pituitary gigantism: a case series from Hospital de San José (Bogotá, Colombia)
(Sociedad Brasileña de Endocrinología y MetabologíaBrasil, 2019-04)
Introduction: Gigantism is a rare pediatric disease characterized by increased production of growth
hormone (GH) before epiphyseal closure, that manifests clinically as tall stature, musculoskeletal
abnormalities, and ...
TRP channels regulation of Rho GTPases in brain context and diseases
(Frontiers Media, 2020)
Neurological and neuropsychiatric disorders are mediated by several pathophysiological mechanisms, including developmental and degenerative abnormalities caused primarily by disturbances in cell migration, structural ...
Poroqueratosis. Revisión de su etiopatogenia, manifestaciones clínicas, diagnóstico y tratamiento
(Elsevier España, 2020)
Las poroqueratosis son un grupo heterogéneo e infrecuente de dermatosis adquiridas o heredadas de etiología desconocida, caracterizadas por un trastorno de la queratinización
secundario a una expansión clonal anormal de ...