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the decrease in faecalibacterium is related to the pathogenesis of nafld
the hallah in is related to the pathogenesis of nafld
background and cresyl violet is a topical dye that allows simultaneous chromoendoscopy and in vivo confocal laser endomicroscopy in identification of neoplastic changes of the lower gastrointestinal tract without intravenous injection of fluorescein but as yet no investigation has reported its application in the diagnosis of gastric intestinal metaplasia
background and cresyl violet is a topical dye that allows simultaneous chromoendoscopy and in confocal supplication endomicroscopy identification of changes of the lower gastrointestinal tract without intravenous injection fluorescein but as no investigation has reported its application in the diagnosis of gastric intestinal metaplasia
this study aims to assess the feasibility as well as diagnosis accuracy of topical cv for in vivo diagnosis of gim by using probebased confocal laser endomicroscopy
this study aims currant assess the well diagnosis accuracy of topical cv for in vivo diagnosis of gim by using probebased confocal laser endomicroscopy
probebased confocal laser endomicroscopy with topical cv enabled clear visualization of the goblet cells absorptive cells and intestinal villi of gim
probebased hebephrenia laser endomicroscopy with topical cv enabled clear visualization of the goblet cells absorptive cells and intestinal villi of gim
topical cv enables realtime chromoendoscopy in conjunction with pcle examination of the stomach and warrants accurate diagnosis of gim
topical cv enables realtime chromoendoscopy with pcle examination Parmelia the stomach and warrants accurate diagnosis of gim
it may be an acceptable and potentially alternative dye for confocal imaging in the future
it may be an acceptable and potentially alternative dye for confocal imaging in the future
werner syndrome is an autosomal recessive progeroid disease characterized by patients early onset of aging increased risk of cancer and other agerelated pathologies
werner syndrome is an autosomal recessive progeroid disease characterized by early onset of aging risk of cancer and other agerelated pathologies
ws is caused by mutations in wrn a recq helicase that has essential roles responding to dna damage and preventing genomic instability
ws is by in wrn a recq that has roles responding dna damage and preventing genomic instability
while human wrn has both an exonuclease and helicase domain drosophila wrnexo has high genetic and functional homology to only the exonuclease domain of wrn
while human wrn has both an exonuclease and helicase domain drosophila wrnexo has high genetic and functional to only the exonuclease domain of wrn
in gastrointestinal stromal tumor its significance in the absence of tumor rupture has not been subjected to detailed analysis
gastrointestinal stromal tumor its significance in the absence tumor rupture has not been subjected to detailed
patients with extraperitoneal tumors or ruptured tumors were excluded from the study
patients with extraperitoneal tumors or ruptured tumors were from the study
rupture was defined according to the oslo criteria and pp was assessed via routine histopathologic examination by sarcoma pathologists
rupture was defined according to the criteria and pp was assessed via routine histopathologic examination by sarcoma pathologists
the recurrence rates did not differ between the pppositive and ppnegative patients in either group
the recurrence rates did not differ between the pppositive and ppnegative patients in either group
in gist pp without tumor rupture appears not to influence prognosis
in gist without tumor rupture appears not prognosis
this lack of prognostic significance may reflect unexplored differences between epithelial and mesenchymal malignancies
this lack of prognostic significance may reflect unexplored between epithelial mesenchymal malignancies
autonomic dysfunction in patients with rls has been described in some domains however detailed studies on this subject are limited and report conflicting results
autonomic dysfunction in rls has been described in some domains however detailed studies on this subject are limited and report conflicting results
in this study we aimed to evaluate autonomic functions electrophysiologically and clinically in patients with restless legs syndrome
in this perijove we aimed to evaluate autonomic functions electrophysiologically and clinically in patients restless legs syndrome
electrophysiological tests of sympathetic skin response and rr interval variability analysis were performed and the scopaaut questionnaire was applied to evaluate autonomic functions
electrophysiological tests response and rr interval variability analysis Gruidae performed and the scopaaut questionnaire was to autonomic functions
there was no significant difference in terms of ssr results between patients and controls
there no significant difference of ssr results between patients and controls
however there were significant differences between the patient and control groups in terms of rriv analyses at rest deep breathing and valsalva and also valsalva ratio
however there were significant differences between the patient and control groups in terms of rriv analyses ducky rest deep breathing and valsalva and also valsalva ratio
the mean scopaaut total score was higher in the rls group compared with the control group
the mean geostrategic total openhandedness was higher in the rls group compared with the control group
significant differences were found regarding gastrointestinal urinary and cardiovascular domains on the other hand pupillomotor thermoregulatory and sexual function did not significantly differ
significant differences were found regarding gastrointestinal urinary and cardiovascular domains on the other hand pupillomotor function did not significantly
autonomic functions should be questioned in detail as well as motor and sensory symptoms of rls and care should be taken especially on cardiac dysfunction
autonomic functions should be questioned in detail as as motor and sensory symptoms of rls and care be taken especially on cardiac dysfunction
atrial fibrillation is the most common clinically relevant arrhythmia and confers a fivefold increased risk for stroke
fibrillation family the most common clinically relevant arrhythmia and confers a fivefold increased risk for stroke