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INFARTO ESPLENICO PDF

Infarto esplénico asociado a cocaína y úlcera gástrica por tuberculosis. Visits. Download PDF. D. Dobarro, F. Montoya Lozano, J.M. Fraile Vicente, J. García. Infarto esplénico asociado a cocaína y úlcera gástrica por tuberculosis. D. Dobarro, F. Montoya Lozano, J.M. Fraile Vicente, J. García Puig. Servicio de Medicina. Request PDF on ResearchGate | On Mar 1, , D. Dobarro and others published Infarto esplénico asociado a cocaína y úlcera gástrica por tuberculosis .

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The following tests were done: Mayo Clin Proc, 61pp. Hospital de Infecciosas F. A year-old woman from Ecuador reported episodes of abdominal pain accompanied by anaemia, always in high-altitude places.

Infarto esplénico masivo como debut de hemoglobinopatía S

Two weeks later the patient was readmitted for a pain in the left hypochondrium and a temperature of 38 o C. Thromb Hemost, 61pp. CiteScore measures average citations received per document published. Sickle cell disease is an autosomal recessive hereditary disease characterised by the presence of Haemoglobin S HbS 1which when deoxygenated is less soluble and polymerises, giving rise to sickled red blood cells or drepanocytes, which become rigid and join with other red blood cells to cause vascular occlusion 2,3.

SRJ is a prestige metric based on the idea that not all citations are the same. 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.

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Circulating coagulation inhibitors in the acquired immunodeficiency syndrome.

SRJ is a prestige metric based on the idea that not all citations are the same. Anticardiolipin antibodies are elevated in HIV-1 infected haemophilics but not predict for disease progression. Nucleation and growth of fibres and gel formation in sickle cell haemoglobin. Initial treatment for splenic infarction must be conservative, aimed at correcting the precipitating factors and achieving an adequate oxygenation and hydration.

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Discussion Sickle cell disease is an autosomal recessive hereditary disease characterised by the presence of Haemoglobin S HbS 1which when deoxygenated is less soluble and polymerises, giving rise to sickled red blood cells or drepanocytes, which become rigid and join with other red blood cells to cause vascular occlusion 2,3. The journal fully endorses the goals of updating knowledge and facilitating the acquisition of key developments in internal medicine applied to clinical practice.

Massive splenic infarction in Saudi patients with sickle cell anemia: Indian J Surg ; Si continua navegando, consideramos que acepta su uso. A new thrombotic manifestation of the circulating lupus anticoagulant. Anticardiolipin antibodies directed not to cardiolipin but to a plasma protein factor.

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Continuing navigation will be considered as acceptance of this use. Servicio de Medicina Interna. J Pediatr Surg ; Hospital Universitario La Paz. Hospital Universitario La Paz.

infarto esplênico

Surgical treatment will only be necessary in the presence of complications haemorrhage, abscess or pseudocyst and in massive infarction when symptoms persist Se continuar a navegar, consideramos que aceita o seu uso.

Rev Esp Enferm Dig ;7: Full text is only aviable in PDF.

Neurology, 40pp. Continuing navigation will be considered as acceptance of this use. To improve our services and products, we use “cookies” own or third parties authorized to infaeto advertising related to client preferences through the analyses of navigation customer behavior.

Ann Int Med ; The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the infqrto receding years. Previous article Next article.

Montoya LozanoJ. SRJ is a prestige metric based on the idea that not all citations are the same.