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4.
Clin Orthop Relat Res ; (347): 93-104, 1998 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-9520879

RESUMO

Although nonoperative treatment is indicated and successful for the majority of diaphyseal humeral fractures, operative intervention is indicated in several situations. Either intramedullary nail or plate fixation commonly is used for the operative management of this problem. Familiarity with the surgical techniques and application of both types (and subtypes) of implants is necessary to allow optimal treatment for the widest range of fracture patterns. In most indications for operative management, internal fixation with plates is preferred. Stable fixation, sparing adjacent joints from iatrogenic injuries, and direct visualization and protection of the radial nerve are of critical importance in maximizing postoperative function and in most cases outweight the potential advantages of a loadsharing implant inserted through a more limited incision.


Assuntos
Pinos Ortopédicos , Placas Ósseas , Fixação Interna de Fraturas , Fraturas do Úmero/cirurgia , Fenômenos Biomecânicos , Fixação Intramedular de Fraturas , Fraturas Espontâneas/cirurgia , Fraturas não Consolidadas/cirurgia , Humanos , Fraturas do Úmero/diagnóstico por imagem , Fraturas do Úmero/fisiopatologia , Nervo Radial/lesões , Radiografia
6.
Psychopharmacology (Berl) ; 113(2): 257-61, 1993.
Artigo em Inglês | MEDLINE | ID: mdl-7855191

RESUMO

The effects of adenosine A1 and A2 receptors on catalepsy were studied in mice. The adenosine agonists 5-N'-ethylcarboxamide-adenosine (NECA), N6-phenylisopropyladenosine (PIA) and N6-cyclohexyladenosine (CHA) induced dose dependent catalepsy. The A1 adenosine antagonist 8-phenyltheophylline (8-PT) potentiated catalepsy induced by NECA, R-PIA and CHA. However, theophylline did not potentiate but inhibited the responses induced by NECA, R-PIA and CHA. Neither 8-PT nor theophylline alone has any effect on catalepsy in mice. It is concluded that catalepsy induced by the adenosine agonists may be due to A2 receptor stimulation and that the A1 antagonism may potentiate the response.


Assuntos
Catalepsia/induzido quimicamente , Agonistas do Receptor Purinérgico P1 , Antagonistas de Receptores Purinérgicos P1 , Adenosina/análogos & derivados , Adenosina/antagonistas & inibidores , Adenosina/farmacologia , Adenosina-5'-(N-etilcarboxamida) , Animais , Relação Dose-Resposta a Droga , Interações Medicamentosas , Camundongos , Fenilisopropiladenosina/antagonistas & inibidores , Fenilisopropiladenosina/farmacologia , Teofilina/análogos & derivados , Teofilina/farmacologia , Vasodilatadores/antagonistas & inibidores , Vasodilatadores/farmacologia
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