9 research outputs found

    The effects of music and guided imagery on self-esteem of elderly female care home residents

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    Thesis (M.M.Ed.)--University of Kansas, Art, Music Education and Music Therapy, 1984

    Analysis of the Effect of Current Ratio (CR), Return on Assets (RoA), Debt to Equity Ratio (DER) and Net Profit Margin (NPM) on Stock Price (Empirical Study on Lq45 Companies Listed on the Indonesia Stock Exchange for the 2017-2020 Period)

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    Investments are made with the aim of obtaining profits as expected. Therefore, to achieve this goal the company must increase the value of the company. This study aims to determine the effect of financial ratios represented by Current Ratio (CR), Return On Assets (ROA), Debt to Equity (DER) and Net Profit Margin (NPM) on stock prices. The sample selection method in this study was purposive sampling method and obtained 26 companies as research samples. The results showed that the Current Ratio (CR) and Net Profit Margin (NPM) had an effect on stock prices. Meanwhile, Return on Assets (ROA) and Debt to Equity (DER) have no effect on stock prices. Keywords: current ratio, return on assets, debt to equity, net profit margin, stock pric

    EDUKASI MENGENAI PENYAKIT JANTUNG KORONER KEPADA PASIEN DI PUSKESMAS KELURAHAN SUNTER AGUNG I

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    Penyakit Jantung Koroner (PJK) merupakan suatu penyakit dimana jantung tidak mampu untuk memompa darah secara efektif ke seluruh tubuh dalam memenuhi perfusi darah ke organ. PJK merupakan penyakit yang berbahaya bagi masyarakat dimana berpengaruh erat pada kehidupan dan kebiasaan buruk masyarakat, mulai dari kebiasaan hidup yang tidak sehat ditambah lagi dengan pola makan yang tidak sehat. Dalam pencegahan PJK dengan melakukan diet sehat, olahraga, aktivitas fisik, penurunan berat badan, tidak merokok, dan melakukan pengendalian hipertensi, serta melaksanakan terapi non farmakologi dalam tatalaksana PJK. Penyuluhan Kesehatan ini dilakukan dengan pemaparan materi secara langsung menggunakan power point dengan melibatkan sebanyak 30 audiens pasien Puskesmas Sunter Agung 1. Keberhasilan dalam kegiatan ini dinilai berdasarkan nilai pre-test dan post-test dengan total masing-masing sebanyak 10 pertanyaan dalam menghitung tingkat pemahaman pasien sebelum dan sesudah dilaksanakannya pemaparan materi. Hasil yang diperoleh berdasarkan peningkatan rata-rata presentase jawaban pertanyaan yang benar yaitu 43,23% saat pre-test menjadi 81,33% saat post-test.  Dengan demikian dapat disimpulkan kegiatan penyuluhan yang sudah dilakukan mampu meningkatkan pengetahuan dan kesadaran masyarakat mengenai penyakit jantung koroner, dimana memberikan dampak positif bagi masyarakat ditunjukkan berdasarkan peningkatan presentasi jumlah pertanyaan benar

    X Chromosome Dose and Sex Bias in Autoimmune Diseases:Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

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    OBJECTIVE: More than 80% of autoimmune disease is female dominant, but the mechanism for this female bias is poorly understood. We suspected an X chromosome dose effect and hypothesized that trisomy X (47,XXX , 1 in ~1,000 live female births) would be increased in female predominant diseases (e.g. systemic lupus erythematosus [SLE], primary Sjögren’s syndrome [SS], primary biliary cirrhosis [PBC] and rheumatoid arthritis [RA]) compared to diseases without female predominance (sarcoidosis) and controls. METHODS: We identified 47,XXX subjects using aggregate data from single nucleotide polymorphism (SNP) arrays and confirmed, when possible, by fluorescent in situ hybridization (FISH) or quantitative polymerase chain reaction (q-PCR). RESULTS: We found 47,XXX in seven of 2,826 SLE and three of 1,033 SS female patients, but only in two of the 7,074 female controls (p=0.003, OR=8.78, 95% CI: 1.67-86.79 and p=0.02, OR=10.29, 95% CI: 1.18-123.47; respectively). One 47,XXX subject was present for ~404 SLE women and ~344 SS women. 47,XXX was present in excess among SLE and SS subjects. CONCLUSION: The estimated prevalence of SLE and SS in women with 47,XXX was respectively ~2.5 and ~2.9 times higher than in 46,XX women and ~25 and ~41 times higher than in 46,XY men. No statistically significant increase of 47,XXX was observed in other female-biased diseases (PBC or RA), supporting the idea of multiple pathways to sex bias in autoimmunity

    X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

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    Objective More than 80% of autoimmune disease predominantly affects females, but the mechanism for this female bias is poorly understood. We suspected that an X chromosome dose effect accounts for this, and we undertook this study to test our hypothesis that trisomy X (47,XXX; occurring in ?1 in 1,000 live female births) would be increased in patients with female-predominant diseases (systemic lupus erythematosus [SLE], primary Sjögren's syndrome [SS], primary biliary cirrhosis, and rheumatoid arthritis [RA]) compared to patients with diseases without female predominance (sarcoidosis) and compared to controls. Methods All subjects in this study were female. We identified subjects with 47,XXX using aggregate data from single-nucleotide polymorphism arrays, and, when possible, we confirmed the presence of 47,XXX using fluorescence in situ hybridization or quantitative polymerase chain reaction. Results We found 47,XXX in 7 of 2,826 SLE patients and in 3 of 1,033 SS patients, but in only 2 of 7,074 controls (odds ratio in the SLE and primary SS groups 8.78 [95% confidence interval 1.67-86.79], P = 0.003 and odds ratio 10.29 [95% confidence interval 1.18-123.47], P = 0.02, respectively). One in 404 women with SLE and 1 in 344 women with SS had 47,XXX. There was an excess of 47,XXX among SLE and SS patients. Conclusion The estimated prevalence of SLE and SS in women with 47,XXX was ?2.5 and ?2.9 times higher, respectively, than that in women with 46,XX and ?25 and ?41 times higher, respectively, than that in men with 46,XY. No statistically significant increase of 47,XXX was observed in other female-biased diseases (primary biliary cirrhosis or RA), supporting the idea of multiple pathways to sex bias in autoimmunity. © 2016, American College of Rheumatology

    X Chromosome Dose and Sex Bias in Autoimmune Diseases: Increased Prevalence of 47,XXX in Systemic Lupus Erythematosus and Sjögren's Syndrome

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    Objective More than 80% of autoimmune disease predominantly affects females, but the mechanism for this female bias is poorly understood. We suspected that an X chromosome dose effect accounts for this, and we undertook this study to test our hypothesis that trisomy X (47,XXX; occurring in ?1 in 1,000 live female births) would be increased in patients with female-predominant diseases (systemic lupus erythematosus [SLE], primary Sjögren's syndrome [SS], primary biliary cirrhosis, and rheumatoid arthritis [RA]) compared to patients with diseases without female predominance (sarcoidosis) and compared to controls. Methods All subjects in this study were female. We identified subjects with 47,XXX using aggregate data from single-nucleotide polymorphism arrays, and, when possible, we confirmed the presence of 47,XXX using fluorescence in situ hybridization or quantitative polymerase chain reaction. Results We found 47,XXX in 7 of 2,826 SLE patients and in 3 of 1,033 SS patients, but in only 2 of 7,074 controls (odds ratio in the SLE and primary SS groups 8.78 [95% confidence interval 1.67-86.79], P = 0.003 and odds ratio 10.29 [95% confidence interval 1.18-123.47], P = 0.02, respectively). One in 404 women with SLE and 1 in 344 women with SS had 47,XXX. There was an excess of 47,XXX among SLE and SS patients. Conclusion The estimated prevalence of SLE and SS in women with 47,XXX was ?2.5 and ?2.9 times higher, respectively, than that in women with 46,XX and ?25 and ?41 times higher, respectively, than that in men with 46,XY. No statistically significant increase of 47,XXX was observed in other female-biased diseases (primary biliary cirrhosis or RA), supporting the idea of multiple pathways to sex bias in autoimmunity. © 2016, American College of Rheumatology
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