Hello, I am Carmen, My illness is Idiopathic Pulmonary Haemosiderosis , a disease of the lung causing unknown pulmonary hemorrhaging. PDF | On Nov 1, , María del Rosario García-Luzardo and others published Hemosiderosis pulmonar idiopática en la infancia: buena respuesta al. PDF | On Jan 1, , JULIO ESPINOZA and others published Hemosiderosis pulmonar idiopática.
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Thorax, 35pp. It is a monthly Journal that publishes a total of 12 issues, which hemosidfrosis these types of articles to different extents. Idiopathic pulmonary hemosiderosis and the Goodpasture syndrome. Translators working for the Journal are in charge of the corresponding translations. All manuscripts are sent to peer-review and handled by the Editor or an Associate Editor from the team.
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Idiopathic pulmonary hemosiderosis is a disease of unknown etiology and pathogenesis, and is characterized by recurrent pulmonary bleeding, iron defidency anaemia and respiratory failure. Check this box if you wish to receive a copy hmosiderosis your message. Diffuse microvascular lung hemorrhage in immune and idiopathic disorders. Therefore, the submission of manuscripts written in either Spanish or English is welcome.
Full text is only aviable in PDF. A report of four cases of acute, severe pulmonary hemorrhage in hemosiderois and support with extracorporeal membrane oxygenation. Therefore, the submission of manuscripts written in either Spanish or English is welcome.
Furthermore, the Journal is also present in Twitter and Facebook. Other types of articles such pulmonra reviews, editorials, special articles, clinical reports, and letters to the Editor are also published in the Journal. Si continua navegando, consideramos que acepta su uso. Chloroquine in idiopathic pulmonary haemosiderosis. We report on two adult patients, one male and one female.
Chest, 68pp. Summary and related texts. Chest, 65 pklmonar, pp. Other types of articles such as reviews, editorials, special articles, clinical reports, and letters to the Editor are also published in the Journal.
Hemosiderosis pulmonar idiopática | Archivos de Bronconeumología (English Edition)
Manuscripts will be submitted electronically using the following web site: J Cell Biol, 47pp. SNIP measures contextual citation impact by wighting hemosideroxis based on the total number of citations in a subject field. Acta Paed Scand, 73pp. To improve our services and products, we use “cookies” own or third parties authorized to show advertising related to client preferences through the analyses of navigation customer behavior.
Subscribe to our Newsletter. Continuing navigation will be considered as acceptance of this use. Detection of intrapulmonary hemorrhage with carbon monoxide uptake.
Am J Med, 32pp. The former is still alive while the latter died after six years follow up. Additional information Further information on this disease Classification s 0 Gene s 0 Other website s 0. Arch Dis Child, 67pp. See more Access to any published article, in either language, is possible through the Journal web page as well as from Pubmed, Science Direct, and other international databases.
Manuscripts will be submitted electronically using the following web site: The outcome and clinical features of the disease, its etiopathogenic implications and the current status of its medical treatment are discussed. Pulmonary function studies in idiopathic pulmonary hemosiderosis in children. Continuing navigation will be considered as acceptance of this use. Only comments seeking to improve the quality and accuracy of information on the Orphanet website are accepted.
Idiopathic pulmonary hemosiderosis treated by plasmapheresis. Print Send to a friend Export reference Mendeley Statistics. Medicine, 63pp. Speluking in the pediatric airway: The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two receding years. Borderias ClauJ. Am J Med, 42pp. Full text is only aviable in PDF.
July – August Pages Pediatric Pulmonology, 13pp. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment. Mayo Clin Proc, 53pp. For all other comments, please send your remarks via contact us.
Am J Med, 59pp. An Orphanet summary for this disease is currently under development.