Un servicio de:
Amoxidal
Amoxidal Plus
Pensando en el valor de la salud...
Solo el médico conoce el mejor tratamiento.
Annals of Internal Medicine: http://www.annals.org/
Diagnosis and Management of Stable Chronic Obstructive Pulmonary Disease: A Clinical Practice Guideline from the American College of Physicians
Amir Qaseem et al.
Recomendaciones cimentadas en la mejor evidencia disponible. (Código 42)
The Enigma of Pulmonary Arterial Hypertension: New Insights from Genetic Studies
John H. Newman et al.
Esta revisión explora las oportunidades terapéuticas y de investigación que emergen de los más recientes descubrimientos de la genética de la hipertensión pulmonar. (Código 27)
The American Journal of Medicine: http://www.amjmedicine.com
Alpha-1 Antitrypsin Deficiency: Pathogenesis, Clinical Presentation, Diagnosis, and Treatment
Thomas Köhnlein, Tobias Welte
Actualización sobre esta enfermedad hereditaria, que afecta preferentemente pulmones e hígado. (Código 22)
Puede solicitar estos los textos completos de estos artículos a través del mail: infouru@intramed.net
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Publicado el 27 de marzo de 2008
Artículos seleccionados
Puesta al Día en Neumología y Alergia
Selección de artículos de revisión recientemente publicados en las revistas de mayor impacto.
Autor/a: Dra. D. Dolinsky
Un servicio de:
Amoxidal
Amoxidal Plus
Pensando en el valor de la salud...
Solo el médico conoce el mejor tratamiento.
Annals of Internal Medicine: http://www.annals.org/
Diagnosis and Management of Stable Chronic Obstructive Pulmonary Disease: A Clinical Practice Guideline from the American College of Physicians
Amir Qaseem et al.
Recomendaciones cimentadas en la mejor evidencia disponible. (Código 42)
The Enigma of Pulmonary Arterial Hypertension: New Insights from Genetic Studies
John H. Newman et al.
Esta revisión explora las oportunidades terapéuticas y de investigación que emergen de los más recientes descubrimientos de la genética de la hipertensión pulmonar. (Código 27)
The American Journal of Medicine: http://www.amjmedicine.com
Alpha-1 Antitrypsin Deficiency: Pathogenesis, Clinical Presentation, Diagnosis, and Treatment
Thomas Köhnlein, Tobias Welte
Actualización sobre esta enfermedad hereditaria, que afecta preferentemente pulmones e hígado. (Código 22)
Puede solicitar estos los textos completos de estos artículos a través del mail: infouru@intramed.net