Molecular Basis of Pulmonary Disease [recurso electrónico] : Insights from Rare Lung Disorders / edited by Francis X. McCormack, Ralph J. Panos, Bruce C. Trapnell.

Por: McCormack, Francis X [editor.]Colaborador(es): Panos, Ralph J [editor.] | Trapnell, Bruce C [editor.] | SpringerLink (Online service)Tipo de material: TextoTextoSeries Respiratory MedicineEditor: Totowa, NJ : Humana Press, 2010Descripción: XI, 438 p. online resourceTipo de contenido: text Tipo de medio: computer Tipo de portador: online resourceISBN: 9781597453844Tema(s): Medicine | Pneumology | Medicine & Public Health | Pneumology/Respiratory SystemFormatos físicos adicionales: Printed edition:: Sin títuloClasificación CDD: 616.2 Clasificación LoC:RC705-779Recursos en línea: Libro electrónicoTexto
Contenidos:
A Clinical Approach to Rare Lung Diseases -- Clinical Trials for Rare Lung Diseases -- Idiopathic and Familial Pulmonary Arterial Hypertension -- Lymphangioleiomyomatosis -- Autoimmune Pulmonary Alveolar Proteinosis -- Mutations in Surfactant Protein C and Interstitial Lung Disease -- Hereditary Haemorrhagic Telangiectasia -- Hermansky–Pudlak Syndrome -- Alpha-1 Antitrypsin Deficiency -- The Marfan Syndrome -- Surfactant Deficiency Disorders: SP-B and ABCA3 -- Pulmonary Capillary Hemangiomatosis -- Anti-glomerular Basement Disease: Goodpasture’s Syndrome -- Primary Ciliary Dyskinesia -- Pulmonary Alveolar Microlithiasis -- Cystic Fibrosis -- Pulmonary Langerhans’ Cell Histiocytosis – Advances in the Understanding of a True Dendritic Cell Lung Disease -- Sarcoidosis -- Scleroderma Lung Disease.
En: Springer eBooksResumen: The study of rare lung disorders enhances our understanding of common pulmonary diseases such as fibrosis and emphysema. Molecular Basis of Pulmonary Disease: Insights from Rare Lung Disorders brings together a panel of distinguished clinicians and molecular scientists who are experts in a range of rare lung diseases and their underlying molecular defects. Each chapter focuses on the pathogenic mechanisms and therapeutic targets suggested by basic research and follows an easy-to-read format: brief introduction followed by discussion of epidemiology, genetic basis and molecular pathogenesis, animal models, clinical presentation, diagnostic approaches, conventional management and treatment strategies, as well as future therapeutic targets and directions. Disorders ranging from the Marfan and Goodpasture’s syndromes to Sarcoidosis and alpha one antitrypsin deficiency are treated in detail. Written for pulmonary clinicians and scientists alike, Molecular Basis of Pulmonary Disease: Insights from Rare Lung Disorders is a comprehensive and invaluable nesource that sheds new light on the molecular mechanisms influencing the clinical presentation and treatment strategies for these debilitating disorders.
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Existencias
Tipo de ítem Biblioteca actual Colección Signatura Copia número Estado Fecha de vencimiento Código de barras
Libro Electrónico Biblioteca Electrónica
Colección de Libros Electrónicos RC705 -779 (Browse shelf(Abre debajo)) 1 No para préstamo 372496-2001

A Clinical Approach to Rare Lung Diseases -- Clinical Trials for Rare Lung Diseases -- Idiopathic and Familial Pulmonary Arterial Hypertension -- Lymphangioleiomyomatosis -- Autoimmune Pulmonary Alveolar Proteinosis -- Mutations in Surfactant Protein C and Interstitial Lung Disease -- Hereditary Haemorrhagic Telangiectasia -- Hermansky–Pudlak Syndrome -- Alpha-1 Antitrypsin Deficiency -- The Marfan Syndrome -- Surfactant Deficiency Disorders: SP-B and ABCA3 -- Pulmonary Capillary Hemangiomatosis -- Anti-glomerular Basement Disease: Goodpasture’s Syndrome -- Primary Ciliary Dyskinesia -- Pulmonary Alveolar Microlithiasis -- Cystic Fibrosis -- Pulmonary Langerhans’ Cell Histiocytosis – Advances in the Understanding of a True Dendritic Cell Lung Disease -- Sarcoidosis -- Scleroderma Lung Disease.

The study of rare lung disorders enhances our understanding of common pulmonary diseases such as fibrosis and emphysema. Molecular Basis of Pulmonary Disease: Insights from Rare Lung Disorders brings together a panel of distinguished clinicians and molecular scientists who are experts in a range of rare lung diseases and their underlying molecular defects. Each chapter focuses on the pathogenic mechanisms and therapeutic targets suggested by basic research and follows an easy-to-read format: brief introduction followed by discussion of epidemiology, genetic basis and molecular pathogenesis, animal models, clinical presentation, diagnostic approaches, conventional management and treatment strategies, as well as future therapeutic targets and directions. Disorders ranging from the Marfan and Goodpasture’s syndromes to Sarcoidosis and alpha one antitrypsin deficiency are treated in detail. Written for pulmonary clinicians and scientists alike, Molecular Basis of Pulmonary Disease: Insights from Rare Lung Disorders is a comprehensive and invaluable nesource that sheds new light on the molecular mechanisms influencing the clinical presentation and treatment strategies for these debilitating disorders.

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