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642 results on '"Lee, Hung-chang"'

1. Evaluating Self-Management Behaviors of Diabetic Patients in a Telehealthcare Program: Longitudinal Study Over 18 Months

Author

Chen, Lichin, Chuang, Lee-Ming, Chang, Chia-Hsiun, Wang, Chiou-Shiang, Wang, I-Ching, Chung, Yufang, Peng, Hui-Yu, Chen, Hui-Chuen, Hsu, Yu-Ling, Lin, Yu-Sheng, Chen, Huang-Jen, Chang, Tieng-Chun, Jiang, Yi-Der, Lee, Hung-Chang, Tan, Ching-Ting, Chang, Hsin-Lu, and Lai, Feipei

Subjects
Computer applications to medicine. Medical informatics, R858-859.7, Public aspects of medicine, RA1-1270
Abstract

BackgroundSelf-management is an important skill for patients with diabetes, and it involves frequent monitoring of glucose levels and behavior modification. Techniques to enhance the behavior changes of diabetic patients have been developed, such as diabetes self-management education and telehealthcare. Although the patients are engaged in self-management activities, barriers to behavior changes remain and additional work is necessary to address the impact of electronic media and telehealthcare on patient self-care behaviors. ObjectiveThe aims of this study were to (1) explore the behaviors of diabetic patients interacting with online applications, (2) determine the impact of a telehealthcare program among 7 self-care behaviors of the patients, and (3) determine the changes in glycosylated hemoglobin (HbA1c) levels. MethodsA telehealthcare program was conducted to assist the patients with 7 self-care activities. The telehealthcare program lasted for 18 months and included the use of a third-generation mobile telecommunications glucometer, an online diabetes self-management system, and a teleconsultant service. We analyzed the data of 59 patients who participated in the telehealthcare program and 103 who did not. The behavioral assessments and the HbA1c data were collected and statistically analyzed to determine whether the telehealthcare services had an impact on the patients. We divided the 18-month period into 3 6-month intervals and analyzed the parameters of patients assisted by the telehealthcare service at different time points. We also compared the results of those who were assisted by the telehealthcare service with those who were not. ResultsThere was a significant difference in monitoring blood glucose between the beginning and the end of the patient participation (P=.046) and between the overall period and the end of patient participation (P

Published
2013
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13. Multisystem disorder associated with a pathogenic variant in CLCN7 in the absence of osteopetrosis.

Author

Lee, Chung‐Lin, Chang, Yeun‐Wen, Lin, Hsiang‐Yu, Lee, Hung‐Chang, Yeh, Ting‐Chi, Fang, Li‐Ching, Lee, Ni‐Chung, Tsai, Jeng‐Daw, and Lin, Shuan‐Pei

Subjects
OSTEOPETROSIS, DEVELOPMENTAL delay, AGAMMAGLOBULINEMIA, DRUG target, PHENOTYPES
Abstract

Background: We clinically and genetically evaluated a Taiwanese boy presenting with developmental delay, organomegaly, hypogammaglobulinemia and hypopigmentation without osteopetrosis. Whole‐exome sequencing revealed a de novo gain‐of‐function variant, p.Tyr715Cys, in the C‐terminal domain of ClC‐7 encoded by CLCN7. Methods: Nicoli et al. (2019) assessed the functional impact of p.Tyr715Cys by heterologous expression in Xenopus oocytes and evaluating resulting currents. Results: The variant led to increased outward currents, indicating it underlies the patient's phenotype of lysosomal hyperacidity, storage defects and vacuolization. This demonstrates the crucial physiological role of ClC‐7 antiporter activity in maintaining appropriate lysosomal pH. Conclusion: Elucidating mechanisms by which CLCN7 variants lead to lysosomal dysfunction will advance understanding of genotype–phenotype correlations. Identifying modifier genes and compensatory pathways may reveal therapeutic targets. Ongoing functional characterization of variants along with longitudinal clinical evaluations will continue advancing knowledge of ClC‐7's critical roles and disease mechanisms resulting from its dysfunction. Expanded cohort studies are warranted to delineate the full spectrum of associated phenotypes. [ABSTRACT FROM AUTHOR]

Published
2024
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23. Associations between Vitamin D Deficiency and Carbohydrate Intake and Dietary Factors in Taiwanese Pregnant Women

Author

Lin, Chao-Hsu, primary, Lin, Pei-Shun, additional, Lee, Meei-Shyuan, additional, Lin, Chien-Yu, additional, Sung, Yi-Hsiang, additional, Li, Sung-Tse, additional, Weng, Shun-Long, additional, Chang, Shing-Jyh, additional, Lee, Hung-Chang, additional, Lee, Yann-Jinn, additional, Chang, Hung-Yang, additional, and Lin, Chih-Sheng, additional

Published
2023
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24. Levels of bioavailable, and free forms of 25(OH)D after supplementation with vitamin D3 in primary hyperparathyroidism

Author

dos Santos, Lívia Marcela, primary, Ohe, Monique Nakayama, additional, Pallone, Sthefanie Giovanna, additional, Nacaguma, Isabela Ohki, additional, Kunii, Ilda Sizue, additional, da Silva, Renata Elen Costa, additional, Maeda, Sergio Setsuo, additional, Vieira, José Gilberto Henriques, additional, Lazaretti-Castro, Marise, additional, Chang, Szu-Wen, additional, and Lee, Hung-Chang, additional

Published
2022
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33. Handwritten Numeral Recognition Based on Simplified Feature Extraction, Structural Classification and Fuzzy Memberships

Author

Jou, Chichang, Lee, Hung-Chang, Kanade, Takeo, editor, Kittler, Josef, editor, Kleinberg, Jon M., editor, Mattern, Friedemann, editor, Mitchell, John C., editor, Nierstrasz, Oscar, editor, Pandu Rangan, C., editor, Steffen, Bernhard, editor, Sudan, Madhu, editor, Terzopoulos, Demetri, editor, Tygar, Dough, editor, Vardi, Moshe Y., editor, Weikum, Gerhard, editor, Carbonell, Jaime G., editor, Siekmann, Jörg, editor, Orchard, Bob, editor, Yang, Chunsheng, editor, and Ali, Moonis, editor

Published
2004
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44. sj-pdf-1-imr-10.1177_03000605221129102 - Supplemental material for A rare case of pancreatic macrocystic serous cystadenoma in an adolescent: a case report and literature review

Author

Chang, Yu-Jui, Lee, Hung-Chang, Yeung, Chun-Yan, Chen, Wai-Tao, and Jiang, Chuen-Bin

Subjects
111199 Nutrition and Dietetics not elsewhere classified, Cardiology, 170199 Psychology not elsewhere classified, 111799 Public Health and Health Services not elsewhere classified, 110604 Sports Medicine, FOS: Health sciences, 110306 Endocrinology, 110308 Geriatrics and Gerontology, 111099 Nursing not elsewhere classified, 111708 Health and Community Services, 160807 Sociological Methodology and Research Methods, 111702 Aged Health Care, 111403 Paediatrics, 110904 Neurology and Neuromuscular Diseases, 110203 Respiratory Diseases, 110315 Otorhinolaryngology, FOS: Clinical medicine, 110319 Psychiatry (incl. Psychotherapy), FOS: Sociology, FOS: Psychology, 110599 Dentistry not elsewhere classified, 110323 Surgery, 110305 Emergency Medicine, 111599 Pharmacology and Pharmaceutical Sciences not elsewhere classified, 111299 Oncology and Carcinogenesis not elsewhere classified, 110314 Orthopaedics
Abstract

Supplemental material, sj-pdf-1-imr-10.1177_03000605221129102 for A rare case of pancreatic macrocystic serous cystadenoma in an adolescent: a case report and literature review by Yu-Jui Chang, Hung-Chang Lee, Chun-Yan Yeung, Wai-Tao Chen and Chuen-Bin Jiang in Journal of International Medical Research

Published
2022
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47. Localization and Laparoscopic Excision of Gastric Heterotopic Pancreas in a Child by Endoscopic SPOT ® Tattooing.

Author

Liou, Yu-Jung, Weng, Shu-Chao, Chang, Paul Chia-Yu, Jiang, Chuen-Bin, Lee, Hung-Chang, Chan, Wai-Tao, Ho, Cheng-Yu, Wu, Pao-Shu, and Yeung, Chun-Yan

Subjects
PANCREATIC surgery, ECTOPIC tissue, X-rays, LIPASES, DIARRHEA, ULTRASONIC imaging, BLOOD vessels, TATTOOING, AMYLASES, ISLANDS of Langerhans, LAPAROSCOPY, ABDOMINAL pain, COMPUTED tomography, GASTRIC mucosa, CHILDREN
Abstract

Heterotopic pancreas (HP) is defined as pancreatic tissue lacking vascular or anatomic connection with the normal pancreas. Surgical resection is often indicated for symptomatic gastric HP. However, intraoperative identification of gastric HP is often difficult during laparoscopic surgery. Herein, we describe a patient with gastric HP, which was marked with SPOT® dye (GI Supply, Camp Hill, PA, USA). The dye was seen clearly laparoscopically facilitating total excision of the lesion. The final pathology report confirmed the presence of heterotopic pancreatic tissue including pancreatic acini, small pancreatic ducts tissue with islets of Langerhans in the deep gastric submucosal area. There were no postoperative complications, and the patient was symptom-free. To the best of our knowledge, this was the first case report in the literature in which endoscopic tattooing of gastric HP before laparoscopic resection was performed. This method of localization was simple and reliable in children. [ABSTRACT FROM AUTHOR]

Published
2023
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