يعرض 1 - 10 نتائج من 54 نتيجة بحث عن '"Kar Hui, Ng"', وقت الاستعلام: 1.01s تنقيح النتائج
  1. 1
    دورية أكاديمية
    SARS-CoV-2 Humoral Immunity Persists Following Rituximab Therapy

    المؤلفون: Liangjian Lu, Chang Yien Chan, Yi Yang Lim, Mya Than, Sharon Teo, Perry Y. W. Lau, Kar Hui Ng, Hui Kim Yap

    المصدر: Vaccines, Vol 11, Iss 12, p 1864 (2023)

    مصطلحات موضوعية: SARS-CoV-2, mRNA vaccines, long-lived plasma cells, Rituximab, Medicine

    وصف الملف: electronic resource

    Relation: https://www.mdpi.com/2076-393X/11/12/1864; https://doaj.org/toc/2076-393X

    URL الوصول: https://doaj.org/article/a9d5ecd823194a77be51a8438d10d983

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  2. 2
    دورية أكاديمية
    Heterogenous antibody and T‐cell responses to SARS‐CoV‐2 mRNA vaccines among immunocompromised young people

    المؤلفون: Liangjian Lu, Chang Yien Chan, Pauline P. L. Chan‐Ng, Mya Than, Pamela S. Y. Tan, Lee Kean Lim, Sharon Teo, Perry YW Lau, Kar Hui Ng, Elizabeth Y. Ang, Sivaramakrishnan Venkatesh Karthik, Marion M. Aw, Paul A. Tambyah, Hui Kim Yap, Bee Wah Lee

    المصدر: Clinical and Translational Medicine, Vol 13, Iss 1, Pp n/a-n/a (2023)

    مصطلحات موضوعية: Medicine (General), R5-920

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2001-1326

    URL الوصول: https://doaj.org/article/7f2c63741e7447edac6ecf22058e47d3

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  3. 3
    دورية أكاديمية
    Angiomotin mutation causes glomerulopathy and renal cysts by upregulating hepatocyte nuclear factor transcriptional activity

    المؤلفون: Yaochun Zhang, Liangjian Lu, Zhenhua Hu, Yu Dai, Nurul Jannah Binti Ahmad, Jun Li Ng, Chang Yien Chan, Md. Zakir Hossain, Alwin Hwai Liang Loh, Jerrold M. Ward, Puay Hoon Tan, Sonia Davila, Vikrant Kumar, Walter Hunziker, Haishu Lin, Hui Kim Yap, Kar Hui Ng

    المصدر: Clinical and Translational Medicine, Vol 12, Iss 6, Pp n/a-n/a (2022)

    مصطلحات موضوعية: Medicine (General), R5-920

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2001-1326

    URL الوصول: https://doaj.org/article/c110950dde334c4596491e14d171efd7

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  4. 4
    دورية أكاديمية
    Hepatocyte nuclear factors play an important role in the pathogenesis of nephropathy

    المؤلفون: Yaochun Zhang, Liangjian Lu, Hui Kim Yap, Kar Hui Ng

    المصدر: Clinical and Translational Discovery, Vol 2, Iss 2, Pp n/a-n/a (2022)

    مصطلحات موضوعية: Therapeutics. Pharmacology, RM1-950

    وصف الملف: electronic resource

    Relation: https://doaj.org/toc/2768-0622

    URL الوصول: https://doaj.org/article/ebf29321bbbf48a58cd844c1e4712892

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  5. 5
    Pioglitazone enhances proteinuria reduction in complicated pediatric nephrotic syndrome

    المؤلفون: Tracy E, Hunley, Guillermo, Hidalgo, Kar Hui, Ng, Yoko, Shirai, Kenichiro, Miura, Hostensia M, Beng, Qiang, Wu, Motoshi, Hattori, William E, Smoyer

    المصدر: Pediatric Nephrology. 38:1127-1138

    مصطلحات موضوعية: Nephrology, Pediatrics, Perinatology and Child Health

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::476d477d0b2bb025541bd82d9bdea663
    https://doi.org/10.1007/s00467-022-05637-8

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  6. 6
    Low regulatory T-cells: A distinct immunological subgroup in minimal change nephrotic syndrome with early relapse following rituximab therapy

    المؤلفون: Sharon Teo, Kar-Hui Ng, Perry Yew-Weng Lau, Stanley C. Jordan, Yiong-Huak Chan, Chang-Yien Chan, Liangjian Lu, Mya Than, Hui-Kim Yap, Kong-Peng Lam

    المصدر: Translational Research. 235:48-61

    مصطلحات موضوعية: Adult, Male, 0301 basic medicine, medicine.medical_specialty, Adolescent, Cyclophosphamide, medicine.medical_treatment, Calcineurin Inhibitors, Lymphocyte Activation, T-Lymphocytes, Regulatory, Gastroenterology, Young Adult, 03 medical and health sciences, 0302 clinical medicine, Recurrence, Physiology (medical), Internal medicine, medicine, Humans, Child, Glucocorticoids, business.industry, Nephrosis, Lipoid, Biochemistry (medical), Public Health, Environmental and Occupational Health, FOXP3, General Medicine, medicine.disease, Calcineurin, 030104 developmental biology, Cytokine, Child, Preschool, 030220 oncology & carcinogenesis, Toxicity, Cytokines, Female, Rituximab, business, Nephrotic syndrome, Glucocorticoid, medicine.drug

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd2103960d2b1f32b6a7fcaea267d78a
    https://doi.org/10.1016/j.trsl.2021.03.019

    View record from ScienceDirect Full Text via ClinicalKey
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  7. 7
    Paediatric living-donor liver and kidney transplantation during COVID-19

    المؤلفون: Vidyadhar Padmakar, Mali, Marion, Aw, Kar Hui, Ng, Sivaramakrishnan Venkatesh, Karthik, Michelle, Tan, Sharon, Teo, Perry Yew Weng, Lau, Yoke Lin, Nyo, Dale Ser Kheng Lincoln, Loh, Ho Yee, Tiong, Seng Hock, Quak, Hui Kim, Yap

    المصدر: Annals of the Academy of Medicine, Singapore. 51:119-121

    مصطلحات موضوعية: Liver, SARS-CoV-2, Living Donors, COVID-19, Humans, Kidney Failure, Chronic, General Medicine, Child, Kidney Transplantation, Liver Transplantation

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82a71df3435b30a64006eeccc30b7d1b
    https://doi.org/10.47102/annals-acadmedsg.2021272

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  8. 8
    Structured re-training to reduce peritonitis in a pediatric peritoneal dialysis program: a quality improvement intervention

    المؤلفون: Mya Than, Azizur Rahman, Charmaine Yan-Pin Goh, Yiong-Huak Chan, Tin Wei Yuen, Jing Geng, Clarissa Wei Shuen Cheong, Neha Bhandari, Hui-Kim Yap, Hamidah Mistam, Noor-Haziah Hussain, Kar-Hui Ng, Sharon Teo

    المصدر: Pediatric Nephrology. 36:3191-3200

    مصطلحات موضوعية: Nephrology, medicine.medical_specialty, Quality management, medicine.medical_treatment, 030232 urology & nephrology, Peritonitis, 030204 cardiovascular system & hematology, Peritoneal dialysis, 03 medical and health sciences, 0302 clinical medicine, Internal medicine, medicine, Humans, Prospective Studies, Child, Retrospective Studies, Exit site, business.industry, University hospital, medicine.disease, Quality Improvement, Pediatrics, Perinatology and Child Health, Emergency medicine, Kidney Failure, Chronic, business, Peritoneal Dialysis

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8aee862cb8fb68e56a0718cb5c04b95
    https://doi.org/10.1007/s00467-021-05039-2

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  9. 9
    Multicenter study on the genetics of glomerular diseases among southeast and south Asians: Deciphering Diversities - Renal Asian Genetics Network (DRAGoN)

    المؤلفون: Liangjian, Lu, Yok-Chin, Yap, Duc Quang, Nguyen, Yiong-Huak, Chan, Jun-Li, Ng, Yao-Chun, Zhang, Chang-Yien, Chan, Mya, Than, Isaac Desheng, Liu, Sadaf, Asim, Khemchand, Moorani, Bilquis, Naeem, Iftikhar, Ijaz, Thi Minh Tan, Nguyen, Ming-Lee, Lee, Caroline, Eng, Syed Saimul, Huque, Yong-Hong, Ng, Indra, Ganesan, Sing-Ming, Chao, Siew-Le, Chong, Puay-Hoon, Tan, Alwin, Loh, Sonia, Davila, Vikrant, Kumar, Joanna Zhi-Jie, Ling, Rajesh Babu, Moorakonda, Karen Mei-Ling, Tan, Alvin Yu-Jin, Ng, Kok-Siong, Poon, Franz, Schaefer, Beata, Lipska-Zietkiewicz, Hui-Kim, Yap, Kar-Hui, Ng

    المصدر: Clinical geneticsREFERENCES. 101(5-6)

    مصطلحات موضوعية: Collagen Type IV, Male, Proteinuria, Nephrotic Syndrome, Asian People, Mutation, Genetics, Humans, Female, Nephritis, Hereditary, Child, Genetics (clinical)

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8e066c7c89daac4804864b4dad8fe2
    https://pubmed.ncbi.nlm.nih.gov/35064937

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  10. 10
    Variation of the clinical spectrum and genotype-phenotype associations in Coenzyme Q10 deficiency associated glomerulopathy

    المؤلفون: Stefania Drovandi, Beata S. Lipska-Ziętkiewicz, Fatih Ozaltin, Francesco Emma, Bora Gulhan, Olivia Boyer, Agnes Trautmann, Szymon Ziętkiewicz, Hong Xu, Qian Shen, Jia Rao, Korbinian M. Riedhammer, Uwe Heemann, Julia Hoefele, Sarah L. Stenton, Alexey N. Tsygin, Kar-Hui Ng, Svitlana Fomina, Elisa Benetti, Manon Aurelle, Larisa Prikhodina, Anne M. Schijvens, Mansoureh Tabatabaeifar, Maciej Jankowski, Sergey Baiko, Jianhua Mao, Chunyue Feng, Fang Deng, Caroline Rousset-Rouviere, Małgorzata Stańczyk, Irena Bałasz-Chmielewska, Marc Fila, Anne M. Durkan, Tanja Kersnik Levart, Ismail Dursun, Nasrin Esfandiar, Dorothea Haas, Anna Bjerre, Ali Anarat, Marcus R. Benz, Saeed Talebi, Nakysa Hooman, Gema Ariceta, Franz Schaefer, Lina Maria Serna Higuita, Alaleh Gheissari, Nazym Nigmatullina, Marcin Tkaczyk, Halina Borzecka, Radovan Bogdanovic, Sevgi Mir, Thomas Klopstock, Holger Prokisch, Cornelia Kornblum, Cui-Hua Liu, Shu-Zhen Sun, Yang Dong, Xiao-Wen Wang, Jiang-Wei Luan

    المساهمون: Institut Català de la Salut, [Drovandi S] Division of Pediatric Nephrology, Center for Pediatrics and Adolescent Medicine, University of Heidelberg, Heidelberg, Germany. Division of Nephrology, Dialysis and Transplantation, Department of Internal Medicine, Ospedale Policlinico San Martino and University of Genoa, Genoa, Italy. Division of Nephrology, Dialysis, Transplantation, Giannina Gaslini Children's Hospital, Genoa, Italy. [Lipska-Ziętkiewicz BS] Rare Diseases Centre, Medical University of Gdańsk, Gdańsk, Poland. Department of Biology and Medical Genetics, Clinical Genetics Unit, Medical University of Gdańsk, Gdańsk, Poland. [Ozaltin F, Gulhan B] Division of Pediatric Nephrology, Department of Pediatrics, Hacettepe University Faculty of Medicine, Ankara, Turkey. [Emma F] Department of Pediatric Subspecialties, Division of Nephrology and Dialysis, Bambino Gesù Childrens Hospital, IRCCS, Rome, Italy. [Boyer O] APHP, Necker-Enfants Malades Hospital, Pediatric Nephrology, MARHEA and SNI Reference Centers, Paris, France. Imagine Institute, Paris University, Paris, France. [Ariceta G] Servei de Nefrologia Pediàtrica, Vall d'Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus

    المصدر: Kidney Int. 102, 592-603 (2022)
    Scientia

    مصطلحات موضوعية: técnicas de investigación::técnicas genéticas::estudios de asociación genética [TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS], Mitochondrial Diseases, Muscle Weakness, Nephrotic Syndrome, Otros calificadores::Otros calificadores::/genética [Otros calificadores], Ubiquinone, Mitocondris - Malalties - Aspectes genètics, enfermedades urogenitales masculinas::enfermedades urológicas::enfermedades renales::nefrosis::síndrome nefrótico [ENFERMEDADES], Male Urogenital Diseases::Urologic Diseases::Kidney Diseases::Nephrosis::Nephrotic Syndrome [DISEASES], Nutritional and Metabolic Diseases::Metabolic Diseases::Mitochondrial Diseases [DISEASES], Ronyons - Malalties - Aspectes genètics, Coenzyme Q10, Mitochondria, Steroid-resistant Nephrotic Syndrome, Nephrology, Mutation, Other subheadings::Other subheadings::/genetics [Other subheadings], Humans, Ataxia, Steroids, Investigative Techniques::Genetic Techniques::Genetic Association Studies [ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT], enfermedades nutricionales y metabólicas::enfermedades metabólicas::enfermedades mitocondriales [ENFERMEDADES], Genetic Association Studies

    وصف الملف: application/pdf

    URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e1e37391fef1cc876f8e121f4381fe
    http://hdl.handle.net/10852/99032

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