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1.
Acad Med ; 74(1 Suppl): S136-40, 1999 Jan.
Article de Anglais | MEDLINE | ID: mdl-9934324

RÉSUMÉ

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.


Sujet(s)
Zone médicalement sous-équipée , Modèles d'organisation , Écoles de médecine , Choix de carrière , Gouvernement , Humains , Nouveau Mexique , Caroline du Nord , Mise au point de programmes , Évaluation de programme , Population rurale
2.
Neurology ; 36(11): 1465-70, 1986 Nov.
Article de Anglais | MEDLINE | ID: mdl-2945125

RÉSUMÉ

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.


Sujet(s)
Glycogénose de type VII/anatomopathologie , Glycogénose/anatomopathologie , Muscles/enzymologie , Phosphofructokinase-1/déficit , Encéphalopathies/enzymologie , Femelle , Glycogénose/métabolisme , Humains , Nourrisson , Muscles/anatomopathologie
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