Introduction: Diarrhea remains a major cause of death in children under 5 years are considered. However, following the overuse of antibiotics and the arbitrary use of broad-spectrum antibiotic, as well as diarrhea associated with antibiotic use is increasing. This study aimed to determine the role of probiotics in the prevention and treatments of diarrhea in children have been conducted.   Mate...

21 22 23 24 25 26 27 28 29 Article history: Received 28 January 2010 Received in revised form 26 August 2011 Accepted 30 August 2011 Available online xxxx

Professional Original Effective Date: December 12, 2006 Institutional Original Effective Date: March 30, 2007 Revision Date(s): March 30, 2007; May 2, 2007; January 26, 2010; October 8, 2010; March 28, 2011; June 6, 2011; August 24, 2012; January 15, 2013; June 14, 2013 Revision Date(s): May 2, 2007; January 26, 2010; November 8, 2010; March 28, 2011; June 6, 2011; August 24, 2012; January 15, ...

4:20A 4:30A 4:34A 4:40A 4:44A 4:50A 4:56A 4:59A 5:04A 5:05A 5:09A 5:12A 5:17A 5:20A 5:24A 5:28A 5:32A 4:44 4:54 4:58 5:04 5:08 5:14 5:20 5:23 5:28 5:29 5:33 5:36 5:41 5:44 5:48 5:52 5:56 5:04 5:14 5:18 5:24 5:28 5:34 5:40 5:43 5:48 5:49 5:53 5:56 6:01 6:04 6:08 6:12 6:16 5:24 5:34 5:38 5:44 5:48 5:54 6:00 6:03 6:08 6:09 6:13 6:16 6:21 6:24 6:28 6:32 6:36 5:44 5:54 5:58 6:04 6:08 6:14 6:20 6:23 ...

Professional Institutional Original Effective Date: October 17, 2006 Original Effective Date: May 1, 2007 Revision Date(s): January 20, 2007; April 1, 2007; September 25, 2007; June 26, 2008; January 1, 2009; June 30, 2009; February 25, 2011; January 15, 2013; March 27, 2014; January 21, 2016; December 20, 2017 Revision Date(s): September 25, 2007; June 26, 2008; January 1, 2009; June 30, 2009;...

objective: hearing loss is the most frequent neurosensory defect in human. mutations in gjb2 and gjb6 are responsible for 50% of autosomal recessive non-syndromic hearing loss (arnshl) cases. here we report on the frequencies of gjb2 and gjb6 mutations and three large deletions spanning the gjb6 gene including del (gjb6-d13s1830), del (gjb6-d13s1854) and a >920 kb deletion in patients affected ...