CONCLUSIONS: In the year after implementation of the 2011 ACGME standards, graduating pediatrics residents report no changes or a worsening in multiple components of their working and learning environments, as well CBL0137 datasheet as no changes in the amount of sleep they receive each day.”
“Hypertrophic cardiomyopathy (HCM), characterized by myocardial hypertrophy, is the most common cause of sudden cardiac arrest in young individuals. More than 270 mutations have been found to be responsible

for familial HCM to date; mutations in MYH7, which encodes the beta-myosin heavy chain (beta-MHC) and MYBPC3, which encodes the myosin binding protein C, are seen most often. This study aimed to screen a pathogenic mutation causing HCM in a large family and assess its possible impact on the function screening assay of the specific protein. Exome sequencing was applied in the proband for searching a novel mutation; segments bearing the specific mutation were analyzed by polymerase chain reaction and direct sequencing. A novel p. G407C mutation in the beta-MHC gene (MYH7) was identified to be responsible for familial HCM in this family. The mutation may cause damage

to the second structure of the protein despite the fact that patients bearing the mutation may have a relatively benign prognosis in this family. The clinical details of the p. G407C mutation are described for the first time in this study. Our report shows a good genotype-phenotype consistency and makes it possible for genetic counseling in this family.”
“Background: In this experimental study, the vasorelaxant effects of levosimendan and dobutamine on isolated rat thoracic aorta preparations were compared. Methods:

Sixteen Wistar albino type male rats were used. The thoracic aortas were removed carefully and were transferred to petri dishes Cl-amidine molecular weight containing Krebs solution. Aortic rings of approximately 5 mm in length were prepared and placed in the organ bath. Contraction and relaxation forces of the aortic rings were recorded. Contraction response was obtained by applying 10(-5)M phenylephrine to aortic rings. Subsequently, cumulative doses of levosimendan (10(-8)M-10(-4)M) was applied to eight aortic rings and cumulative doses of dobutamine (10(-8)M-10(-3)M) was applied to the other eight aortic rings and dose-response curves were recorded. The EC50 and pD2 values were calculated by the computer program named Graph Pad Prisim 4.0. The Mann-Whitney U-test was performed for statistical analysis. Results: The relaxation response of the aortic rings with levosimendan 10(-4)M administration was %92.33 while the relaxation response with dobutamine 10-4M administration was %82.48. It did not show a significant difference between both relaxation responses (p=0.059). The EC50 value was calculated as 6.605×10(-6)M for dobutamine and 5.093×10(-5)M for levosimendan. The pD2 value was found to be 5.2 +/- 0.4 for levosimendan and 4.3 +/- 0.2 for dobutamine.