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                    "lastName": "Pandey"
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            "abstractNote": "Objective\nTo study the diagnostic potential of fluorescence spectroscopy and its comparison with different screening methods, including Pap smear and colposcopy, in detecting early cervical neoplasia.\n\nMethod\nThe study was conducted on patients with gynecological complaints. A full gynecological workup of the patients was done along with Pap smear and colposcopy. Cervical biopsy was done in suspected cases and fresh tissue was sent to IIT for spectroscopy.\n\nResult\nThere is a definite increase in NADH fluorescence (67.4 %) and a decrease in collagen fluorescence (74 %) in dysplastic tissues. When epithelial fluorescence and stromal fluorescence are considered together, diagnostic accuracy is increased to 96.5 %.\n\nConclusion\nThe clinical diagnosis of cervical neoplasia by spectroscopic methods is potentially a reliable, fast, and cost-effective alternative to the conventional smear test which needs trained personnel for its interpretation. Research is still continuing to obtain a statistically significant cutoff value from in vitro studies and then use them for in vivo study.",
            "publicationTitle": "Journal of Obstetrics and Gynaecology of India",
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                    "lastName": "Gong"
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            "abstractNote": "Background\nMinimal deviation adenocarcinoma (MDA) of the uterine cervix is defined as an extremely well differentiated variant of cervical adenocarcinoma, with well-formed glands that resemble benign glands but show distinct nuclear anaplasia or evidence of stromal invasion. Thus, MDA is difficult to differentiate from other cervical hyperplastic lesions. Monoclonality is a major characteristic of most tumors, whereas normal tissue and reactive hyperplasia are polyclonal.\n\nMethods\nThe clinicopathological features and clonality of MDA were investigated using laser microdissection and a clonality assay based on the polymorphism of androgen receptor (AR) and X-chromosomal inactivation mosaicism in female somatic tissues. \n\nResults\nThe results demonstrated that the glands were positive for CEA, Ki-67, and p53 and negative for estrogen receptor (ER), progesterone receptor (PR), and high-risk human papilloma virus (HPV) DNA. The index of proliferation for Ki-67 was more than 50%. However, the stromal cells were positive for ER, PR, vimentin, and SM-actin. The clonal assay showed that MDA was monoclonal. Thus, our findings indicate that MDA is a true neoplasm but is not associated with high-risk HPV.\n\nConclusions\nDiagnosis of MDA depends mainly on its clinical manifestations, the pathological feature that MDA glands are located deeper than the lower level of normal endocervical glands, and immunostaining.",
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            "creators": [
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                    "creatorType": "author",
                    "firstName": "Jennifer J.",
                    "lastName": "Kiser"
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                {
                    "creatorType": "author",
                    "firstName": "Rui",
                    "lastName": "Zhu"
                },
                {
                    "creatorType": "author",
                    "firstName": "David Z.",
                    "lastName": "D'Argenio"
                },
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                    "creatorType": "author",
                    "firstName": "Mark F.",
                    "lastName": "Cotton"
                },
                {
                    "creatorType": "author",
                    "firstName": "Raziya",
                    "lastName": "Bobat"
                },
                {
                    "creatorType": "author",
                    "firstName": "George D.",
                    "lastName": "McSherry"
                },
                {
                    "creatorType": "author",
                    "firstName": "Shabir A",
                    "lastName": "Madhi"
                },
                {
                    "creatorType": "author",
                    "firstName": "Vincent J.",
                    "lastName": "Carey"
                },
                {
                    "creatorType": "author",
                    "firstName": "Heiner I.",
                    "lastName": "Seifart"
                },
                {
                    "creatorType": "author",
                    "firstName": "Cedric J.",
                    "lastName": "Werely"
                },
                {
                    "creatorType": "author",
                    "firstName": "Courtney V.",
                    "lastName": "Fletcher"
                }
            ],
            "abstractNote": "Aims\nThere are limited data on isoniazid (INH) pharmacokinetics in infants and young children and, therefore, uncertainty on appropriate dosing.\n\nMethods\nPharmacokinetic data were obtained from perinatally HIV-exposed South African infants ages 3–24 months receiving INH 10–20 mg/kg/day orally for Mycobacterium tuberculosis (TB) prophylaxis. INH pharmacokinetic parameters were characterized with a population pharmacokinetic approach. Dosing simulations were performed to evaluate weight-based INH doses in children based on N-acetyltransferase 2 enzyme (NAT2) genotype, age, maximum concentrations (Cmax) ≥ 3mg/L, and area under the curve (AUC0-24) ≥ 10.52 mg*hr/L.\n\nResults\nIn 151 infants (53% female, 48% HIV positive) receiving a mean INH dose of 14.5 mg/kg/day, mean (±SD) Cmax at 3, 6, and 23 months of age were 10.0 (3.5), 8.6 (2.6), and 9.3 (3.8) mg/L, respectively, mean (±SD) AUC0-24 were 53.6 (26.8), 42 (19.9), and 44 (30.7) mg*hr/L, respectively, and mean (±SD) half-life were 2.1 (0.7), 1.9 (0.6), and 1.8 (0.9) hours, respectively. A trimodal apparent oral clearance of INH as a function of NAT2 genotype was apparent as early as 3 months. INH was well tolerated. At an average INH dose of 14.5 mg/kg/day, 99% of infants ages 3–24 months have an INH Cmax ≥ 3 mg/L and 98% have an INH AUC0-24 ≥ 10.52 mg*hr/L.\n\nConclusions\nINH at an average dose of 14.5 mg/kg once daily was well tolerated in infants and achieved INH Cmax values ≥ 3 mg/L and AUC0-24 values ≥ 10.52 mg*hr/L.",
            "publicationTitle": "Therapeutic Drug Monitoring",
            "publisher": "",
            "place": "",
            "date": "2012-8",
            "volume": "34",
            "issue": "4",
            "section": "",
            "partNumber": "",
            "partTitle": "",
            "pages": "446-451",
            "series": "",
            "seriesTitle": "",
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