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61.
Rocio T. Martinez-Nunez Fethi Louafi Peter S. Friedmann Tilman Sanchez-Elsner 《The Journal of biological chemistry》2009,284(24):16334-16342
62.
Sukriye Ilkay Guner Savas Guner Erdal Peker Mehmet Fethi Ceylan Ayse Guler Ugur Turktas Barıs Kaki 《The Journal of membrane biology》2013,246(2):115-119
The purpose of this study was to investigate prospectively the effects of swaddling and consanguineous marriage on developmental dysplasia of the hip and associated risk factors. We screened by ultrasound 265 infants using the Graf method. The Pediatrics Department referred all newborn infants with suspected instability or a recognized risk factor to the orthopedic clinic. Risk factors of developmental dysplasia of the hip were searched and noted in these patients. Swaddling and consanguineous marriage were also determined and noted. We observed 164 of 265 infants (61.9 %) who had been swaddled and that 64 of 265 infants’ parents were in a consanguineous marriage (24.2 %). In the statistical analysis that was conducted for swaddling and consanguineous marriage, highly significant differences were found. Our study showed that the rate of developmental dysplasia of the hip is very high, 11.7 %, in our region, eastern Turkey. Also, we commonly see improper swaddling and consanguineous marriage in our region, which affects many infants. 相似文献
63.
Fethi Ben Abdallah Rihab Lagha Amina Bakhrouf 《World journal of microbiology & biotechnology》2008,24(8):1507-1512
Salmonella bovismorbificans, rare serovar, isolated from patient in Tunisia were incubated during 13 years in soil. After its resuscitation, the cells
showed a biochemical profile completely inactive on Api 20E system. These cells recuperated their initial characters after
6 months of incubation in Tryptic Soy broth. The atomic force micrographs showed a reduction of the cells size and an evolution
to coccoid-shapes. After resuscitation S. bovismorbificans cells recuperated their original rod shape. These cells showed an altered envelope. The resuscitate cells were identified
by PCR following the amplification of the internal transcribed spacer (ITS) region of 16S–23S rRNA gene. 相似文献