نتایج جستجو برای: diagnostic criteria
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S ir, I read the article “Mildly Elevated Transaminases: Excellent diagnostic c l u e f o r A n i c t e r i c L e p t o s p i r o s i s ” with interest.1 Leptospirosis can be diagnosed only by laboratory tests as clinical features are non specific. But the laboratory tests are complex and hence definite guidelines for diagnosis of human leptospirosis is necessary. I fully agree that microscopic...
1 Coeliac disease (CD) is a chronic, multisystemic, autoimmune disorder, induced by gluten exposure, in genetically sensitive individuals (1-3). Its clinical presentation is extremely various, and changes considerably from full-blown malabsorption syndrome, seen in the classic childhood-onset disease, to subtle and atypical symptomatology, especially in the lateonset forms. The prevalence of CD...
In a recent review paper, Adriaenssens et al. (2015) cluded that about 26% of emergency nurses (EN) suffer burnout and described their results as alarming. ile we applaud Adriaenssens et al.’s efforts to provide a rer picture of ill-health in EN, we think that these hors’ conclusions are weakened by a fundamental fact, ely, the absence of consensual, clinically valid gnostic criteria for burnou...
Snoring is a significant problem with social and medical manifestations. After snoring has been confirmed, other nocturnal respiratory diseases should be excluded so that the appropriate treatment can be instituted. This chapter addresses the current management of snoring and its treatment.
Neurocysticercosis is the most common helminthic infection of the CNS but its diagnosis remains difficult. Clinical manifestations are nonspecific, most neuroimaging findings are not pathognomonic, and some serologic tests have low sensitivity and specificity. The authors provide diagnostic criteria for neurocysticercosis based on objective clinical, imaging, immunologic, and epidemiologic data...
In 1993 diagnostic criteria for incontinentia pigmenti (IP), a genodermatosis in which skin changes are usually combined with anomalies of other organs, were established. Approximately a decade ago, IKBKG gene mutation was discovered as a cause for IP. This finding has not been included in IP diagnosis so far. In addition, literature data pointed out a few other clinical findings as possible IP...
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