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10.1002/ccr3.1427 http://scihub22266oqcxt.onion/10.1002/ccr3.1427 C5889233!5889233!29636940     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 243.2 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Clin+Case+Rep 2018 ; 6 (4): 686-9 Nephropedia Template TP {{tp|p=29636940|t=2018. A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard?Soulier syndrome: case report |pdf=|usr=}}{{29636940}} gab.com Text A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard Soulier syndrome: case report JO: Clin Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=29636940 #FOAvip We need to be aware of rare causes of persistent thrombocytopenia as Bernard?Soulier syndrome (BSS). When BSS is suspected based on family history and giant platelets, genetic test for mutations of GPIbIXV is necessary. Management varies once you recognize the cause. Platelets transfusion and antifibrinolytics are the mainstay of therapy. Twit Text FOAVip A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard Soulier syndrome: case report ????Clin Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=29636940 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29636940 #FOAvip English Wikipedia <ref>{{Cite pmid|29636940}}</ref> A point mutation in Phe71Ser in glycoprotein IX as a genetic cause of Bernard?Soulier syndrome: case report #MMPMID29636940 Alsahafi IK; Al?Harbi I; Aldor SM; Albarakati BA; Alahmadi GB Clin Case Rep 2018[Apr]; 6 (4): 686-9 PMID29636940show ga We need to be aware of rare causes of persistent thrombocytopenia as Bernard?Soulier syndrome (BSS). When BSS is suspected based on family history and giant platelets, genetic test for mutations of GPIbIXV is necessary. Management varies once you recognize the cause. Platelets transfusion and antifibrinolytics are the mainstay of therapy. äA point mutation in Phe71Ser in glycoprotein IX as a genetic cause of (epmc).pdf DeepDyve Pubget Overpricing