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  • About
  • The Global ETD Search service is a free service for researchers to find electronic theses and dissertations. This service is provided by the Networked Digital Library of Theses and Dissertations.
    Our metadata is collected from universities around the world. If you manage a university/consortium/country archive and want to be added, details can be found on the NDLTD website.
261

Ideal observer estimation and generalized ROC analysis for computer-aided diagnosis /

Edwards, Darrin C. January 2003 (has links)
Thesis (Ph. D.)--University of Chicago, Committee on Medical Physics, December 2003. / Includes bibliographical references. Also available on the Internet.
262

Detection of anti-aquaporin (AQP4) autoantibodies in the diagnosis of neuromyelitis optica (NMO)

Chan, Ka-man, 陳嘉雯 January 2010 (has links)
published_or_final_version / Pathology / Master / Master of Medical Sciences
263

Validating a quantified clinical screening tool in detecting aspiration

Ching, K. Y., 程潔怡. January 2005 (has links)
published_or_final_version / Medical Sciences / Master / Master of Medical Sciences
264

Micrometastases of esophageal cancer

Chan, Pui-man, Poemen, 陳培文 January 2006 (has links)
published_or_final_version / Surgery / Master / Master of Research in Medicine
265

Molecular characterization of multi-drug resistance mechanisms in mycobacterium tuberculosis

Siu, Kit-hang., 蕭傑恆. January 2010 (has links)
published_or_final_version / Microbiology / Doctoral / Doctor of Philosophy
266

Comparison between tissue-based indirect immunofluorescence andenzyme-linked immunosorbent assays, two detection methods for anti-aquaporin-4 antibodies in neuromyelitis optica spectrum disorders

Lo, Yuk-fai., 盧育輝. January 2011 (has links)
published_or_final_version / Medicine / Master / Master of Medical Sciences
267

Isolation of human leukocyte antigen G/cytokeratin 7 positive fetal cells from transcervical samples for potential use in prenatal genetic diagnosis

Wong, Hoi-hei, Vera, 王愷曦 January 2015 (has links)
There has been an increase in rates of chromosomal abnormalities in newborns as a result of reproductive aging. For the past decades, a lot of effort has been placed on identifying pregnancies at risk of genetic defects. Conventional prenatal genetic diagnosis is achieved by invasive procedures that have been associated with an increased risk of pregnancy loss. This has led the researchers to explore the use of non-/minimally invasive techniques for prenatal diagnosis. Trophoblasts are known to be shed from regressing chorionic villi into the lower uterine pole of pregnant women during the first trimester. These cells are trapped within cervical mucus, which can be retrieved with a cytobrush. By using human leukocyte antigen G (HLA-G) and cytokeratin-7 (CK7) as trophoblast markers, this study aims to investigate the possibility of isolating individual fetal trophoblast from transcervical samples for genetic diagnosis. 195 healthy pregnant women requesting for legal termination of pregnancy (TOP) were recruited in this study. Transcervical cells were collected from them with the use of a cytobrush before TOP. HLA-G+ or CK7+ cells were then isolated by a combination of mucolytic action, fluorescent immunohistochemistry, and micromanipulation. The origin of these cells was subsequently investigated by either fluorescent in situ hybridization (FISH) or allelic profiling by quantitative fluorescent polymerase chain reaction (QF-PCR) based on chromosome 16, chromosome X, amelogenin gene and sex determining region Y (SRY) gene. This study first demonstrated the presence of fetal cells in transcervical samples based on the detection of chromosome Y signal by ordinary PCR. Cells expressing HLA-G and CK7 were also identified among transcervical cells. Immunopositive cells were isolated by micromanipulation under fluorescent microscopy. One isolated cell expressing CK7 was shown to inherit paternal allele at a locus on chromosome 16, suggesting the possible fetal origin of this cell. However, this study was still hampered by a number of technical factors. Further optimization of the protocol is required before transcervical trophoblasts can be retrieved in a reliable manner. / published_or_final_version / Obstetrics and Gynaecology / Master / Master of Philosophy
268

NURSING DIAGNOSIS OF ACTUAL FLUID VOLUME EXCESS: VALIDATION OF DEFINING CHARACTERISTICS

Mackenzie, Kimberly Diane January 1984 (has links)
No description available.
269

Dynamic Model Based Diagnosis for Combustion Engines in RODON

Lundkvist, Joella, Wahnström, Stina January 2007 (has links)
Diagnosis is the task of finding faults or malfunctioning components in a technical system, e.g a car. When doing diagnosis on cars with combustion engines, a computer program can be used. The computer program, also called diagnosis system, needs information about the car. This information could be data sheets of all the electronic components in the car. It could also be a description of how the engine behaves in a nominal and a non-nominal case. This information is contained in a model of the engine. RODON, a diagnostic tool developed by Sörman Information and Media AB, uses models of systems for conflict detection diagnosis. RODON needs fault models of the components to do diagnosis. The diagnosis system is then used in workshops, factories, or other places where cars need to be surveyed. In this thesis, a Simulink model of the nominal behaviour of a combustion engine is given. The problem is how to make use of the model as well as the diagnostic tool RODON for combustion engine diagnosis. To solve this, the Simulink model is translated into a RODON model. Translating a Simulink model into a RODON model requires a new library in RODON. The library developed in this thesis is called AdvancedBlocks library. The Simulink model describes the nominal behaviour of a combustion engine but for diagnosis with RODON, fault models are needed as well. Several types of faults that can occur in an engine have been studied and fault models have been implemented in RODON. The conclusion is that diagnosis in RODON with a translated engine model is possible.
270

Aids for the early diagnosis of tuberculous meningitis (TBM)

Ramkissoon, Arthi. January 1985 (has links)
Mortality and morbidity rates associated with tuberculous meningitis (TBM) are substantial. The average duration of the untreated disease from onset to death is about 17 days. The prognosis of TBM is known to correlate with the stage of the disease at the time of diagnosis and commencement of chemotherapy. Early diagnosis improves the chances of recovery without neurological sequelae. Early diagnosis is a problem because the presenting symptoms are non-specific and the onset of the disease is typically insidious. To date no single test is available that is totally reliable and specific for TBM. I have attempted to develop a reliable and easily applicable test for the diagnosis of TBM. In fulfilling this objective, the work undertaken may be divided into three major sections:- 1. Detection of soluble Mycobacterium tuberculosis antigens in the cerebrospinal fluid (CSF) of patients with TBM and in control groups by using Mycobacterium bovis BCG antigens. The technique used was that of inhibition enzyme-linked immunosorbent assay (ELISA). The principle of this technique is illustrated in Fig. 5. 2. Detection of soluble M. tuberculosis antigens in the CSF of tuberculous and control groups of patients by using antibodies raised against M.bovis BCG. The technique used was that of the double antibody sandwich ELISA. An outline of this ELISA is given in Fig. 6. 3. Correlation of chloride levels in the blood and CSF of patients with tuberculous and other forms of meningitis. It has been established that the SERUM/CSF ratio of bromide tends towards unity in patients with TBM because the permeability of the blood-brain barrier is impaired. Since both bromide and chloride are chemically similar (both being halides), it was thought that a similar pattern may exist for BLOOD/CSF chloride ratios; and this was investigated. The method used for the INHIBITION ELISA had to be standardized before the samples could be tested. This involved investigating the acceptability of various microtitre plates; determination of the optimal working dilutions for the coating solution and conjugate; and determination of optimal conditions for the various incubation periods, both in terms of time and temperature. A total of 70 specimens was tested. These consisted of 25 normal CSF controls; 25 pleural and ascitic fluid samples; 10 TBM samples, and 10 bacterial meningitis CSF samples. It was found that a distinction existed between the absorbance values obtained from positive TBM CSF samples (Mean 0,658 + 0,043) and that from normal CSF samples (Mean 1,089 + 0,224). The mean absorbance of the culture-positive bacterial CSF's also differed significantly from the other 2 groups (Tables VII; IX). Some overlap occurred amongst the absorbance values of bacterial culture positive CSF's (Range 0,975-0,879) and normal CSF's (Range 1,486-0,934). The mean absorbance value for bacterial positive CSF samples (0,920 _+ 0,029) differed significantly (p <0,01) from those of normal CSF (1,089 + 0,224) and TBM CSF's (0,658 + 0,043). The difference between the mean values obtained with tuberculous and non-tuberculous groups of pleural and ascitic fluid was also significant (p < 0,01). The method used for the DOUBLE ANTIBODY SANDWICH ELISA was that of Sada et al. (1983). Before the samples could be tested, the method had to be standardized and similar investigations to those for the INHIBITION ELISA were performed. In addition, antibodies raised against M.bovis BCG were conjugated to alkaline phosphatase since no commercial preparation was available. Unfortunately no distinction was recorded between negative and positive test specimens, even on repetition of the entire procedure. Measurement of chloride was done by a fully automated procedure using the BECKMAN ASTRA-8. A total of 149 samples were tested. Of these 10 were tuberculous, 34 were viral, and the remainder were bacterial meningitis. No pattern was established that could differentiate TBM from viral or bacterial meningitis. The results obtained are tabulated in Table III and illustrated in Figures 9, 10, and 11. In summarizing, the use of the INHIBITION ELISA technique for the accurate diagnosis of TBM seems promising. However, its validity in the clinical situation will have to be assessed further and with greater numbers of specimens before it can be adopted as a diagnostic procedure for TBM. OBJECTIVE. To determine 1. The ability and reliability of the INHIBITION ELISA1 technique to detect mycobacterial antigens in pleural, ascitic, and cerebrospinal fluids. 2. The accuracy and reproducibility of the double antibody sandwich ELISA in the detection of mycobacterial antigens in CSF of patients with tuberculous meningitis (TBM). 3. Whether a correlation exists between blood and CSF chloride levels in patients with tuberculous and other forms of meningitis. / Thesis (M.Med.Sc.)-University of Natal, Durban, 1985.

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