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1.
Acad Med ; 74(1 Suppl): S136-40, 1999 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-9934324

RESUMEN

Locum tenens programs were independently developed by the University of New Mexico Health Sciences Center and East Carolina University School of Medicine to address health care needs within their states. The programs represent distinct models to provide locum tenens services for practices in rural and medically underserved regions through collaboration with stage government representatives and agencies. Differences between programs include years of operation, days of coverage provided, types of learners and providers involved, sources of funding, costs of the programs, and extent of institutional support. Common beneficial outcomes of the programs include coverage for struggling practices, training in rural medicine for locum tenens providers, recruitment of physicians to rural practice sites, and improved relationships with program partners. Adequate funding and institutional support are essential for success of locum tenens programs.


Asunto(s)
Área sin Atención Médica , Modelos Organizacionales , Facultades de Medicina , Selección de Profesión , Gobierno , Humanos , New Mexico , North Carolina , Desarrollo de Programa , Evaluación de Programas y Proyectos de Salud , Población Rural
2.
Neurology ; 36(11): 1465-70, 1986 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-2945125

RESUMEN

We studied a girl with an infantile syndrome of limb weakness, seizures, cortical blindness, and corneal opacifications; she died at age 7 months of respiratory failure. There was no consanguinity or family history of neuromuscular diseases. Histochemical and biochemical studies of muscle showed mildly increased glycogen content and markedly decreased PFK activity (1.4% of the normal mean). Anaerobic glycolysis in vitro confirmed the metabolic block. Immunofluorescence and immunotitration by ELISA using monoclonal antibodies against subunit M of PFK showed a normal amount of cross-reacting material. The brain showed typical features of neuroaxonal dystrophy. This variant of PFK deficiency may be due to a distinct genetic defect.


Asunto(s)
Enfermedad del Almacenamiento de Glucógeno Tipo VII/patología , Enfermedad del Almacenamiento de Glucógeno/patología , Músculos/enzimología , Fosfofructoquinasa-1/deficiencia , Encefalopatías/enzimología , Femenino , Enfermedad del Almacenamiento de Glucógeno/metabolismo , Humanos , Lactante , Músculos/patología
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