ESFEROCITOSIS HEREDITARIA PDF

Esferocitosis hereditaria. Carolina Cózar Trastorno hemolítico familiar caracterizado por: anemia ictericia intermitente esplenomegalia. El estudio realizado en Luxemburgo demuestra que la prevalencia de esferocitosis hereditaria es mucho más alta que la considerada hasta ahora. Resumen. HERRERA GARCIA, Mayelín y ESTRADA DEL CUETO, Marianela. Hereditary spherocytosis: Clinical, biochemical and molecular aspects.

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The journal fully endorses the goals of updating knowledge and facilitating the acquisition of key developments in internal medicine applied to clinical practice.

Nine issues are published each year, including mostly originals, reviews and consensus documents. 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. CiteScore esferocitosi average citations received per document published. SRJ is a prestige metric based on the idea that not all citations are the same.

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Orphanet: Esferocitosis hereditaria

SJR uses a similar algorithm as the Google page rank; it provides a quantitative and qualitative measure of the journal’s impact. SNIP measures contextual citation impact by wighting citations based on the total number of citations in a subject field.

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Esferocitosis hereditaria by Jazmin Cózar Madero on Prezi

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