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http://scihub22266oqcxt.onion/ 7489971!ä!7489971 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=7489971&cmd=llinks): Failed to open stream: HTTP request failed! 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Parvovirus B19 as a possible causative agent of fulminant liver failure and associated aplastic anemia |pdf=|usr=}}{{7489971}} gab.com Text Parvovirus B19 as a possible causative agent of fulminant liver failure and associated aplastic anemia JO: Hepatology http://www.kidney.de/pget.php?&tw=1&pmid=7489971 #FOAvip We recently observed that more than one third of pediatric patients who presented with non-A, non-B fulminant liver failure (FLF) also developed aplastic anemia (AA) either before or shortly after liver transplantation. Factors involved in the suppression of bone marrow could be the same as those causing hepatic failure. We considered parvovirus B19 a candidate etiologic agent because of the known tropism of B19 for erythroid precursors. Archived liver and serum from six patients undergoing liver transplantation for non-A, non-B, non-C FLF with associated AA were analyzed for the presence of B19 DNA and anti-B19 serology. An age- and gender-matched control group (N = 44) was analyzed in parallel. B19 DNA studies and anti-B19 serology were performed in a blinded fashion. B19 serologies were performed by antibody capture enzyme-linked immunosorbent assay (ELISA). B19 DNA was detected after polymerase chain reaction (PCR) amplification of target B19 DNA sequences in liver and serum. Liver tissue showed evidence of B19 DNA in four of six (66%) patients with FLF and associated AA. Two of 4 patients with cryptogenic FLF but without AA had B19 DNA detected in the liver tissue. Of the 34 remaining controls, only 5 (15%) showed evidence of B19 DNA in liver tissue (66% vs. 15%, P = .016). B19 DNA was not detected in any of the test or control sera. This study provides evidence to support the role of parvovirus B19 in the development of FLF and associated AA. Twit Text FOAVip Parvovirus B19 as a possible causative agent of fulminant liver failure and associated aplastic anemia ????Hepatology http://www.kidney.de/pget.php?&tw=1&pmid=7489971 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=7489971 #FOAvip English Wikipedia <ref>{{Cite pmid|7489971}}</ref> Parvovirus B19 as a possible causative agent of fulminant liver failure and associated aplastic anemia #MMPMID7489971 Langnas AN; Markin RS; Cattral MS; Naides SJ Hepatology 1995[Dec]; 22 (6): 1661-5 PMID7489971show ga We recently observed that more than one third of pediatric patients who presented with non-A, non-B fulminant liver failure (FLF) also developed aplastic anemia (AA) either before or shortly after liver transplantation. Factors involved in the suppression of bone marrow could be the same as those causing hepatic failure. We considered parvovirus B19 a candidate etiologic agent because of the known tropism of B19 for erythroid precursors. Archived liver and serum from six patients undergoing liver transplantation for non-A, non-B, non-C FLF with associated AA were analyzed for the presence of B19 DNA and anti-B19 serology. An age- and gender-matched control group (N = 44) was analyzed in parallel. B19 DNA studies and anti-B19 serology were performed in a blinded fashion. B19 serologies were performed by antibody capture enzyme-linked immunosorbent assay (ELISA). B19 DNA was detected after polymerase chain reaction (PCR) amplification of target B19 DNA sequences in liver and serum. Liver tissue showed evidence of B19 DNA in four of six (66%) patients with FLF and associated AA. Two of 4 patients with cryptogenic FLF but without AA had B19 DNA detected in the liver tissue. Of the 34 remaining controls, only 5 (15%) showed evidence of B19 DNA in liver tissue (66% vs. 15%, P = .016). B19 DNA was not detected in any of the test or control sera. This study provides evidence to support the role of parvovirus B19 in the development of FLF and associated AA. |*Erythema Infectiosum[MESH] |*Parvovirus B19, Human/genetics/immunology[MESH] |Anemia, Aplastic/pathology/*virology[MESH] |Antibodies, Viral/blood[MESH] |Bone Marrow/pathology[MESH] |Child[MESH] |Chronic Disease[MESH] |DNA, Viral/analysis[MESH] |Humans[MESH] |Immunoglobulin G/blood[MESH] |Liver Diseases/virology[MESH] |Liver Failure, Acute/surgery/*virology[MESH] |Liver Transplantation[MESH]Parvovirus B19 as a possible causative agent of fulminant liver failur(epmc).pdf DeepDyve Pubget Overpricing