Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Clara G.C. Ooi"'
Autor:
Chak Sing Lau, Yui Ming Lam, Clara G.C. Ooi, Hung-Fat Tse, Peter Chin Wah Fung, Woon Sing Wong, Mo Yin Mok, Yik Wong
Publikováno v:
Clinical Rheumatology. 27:315-322
There is no surrogate marker in serum for defining disease activity in scleroderma (SSc). Nitric oxide (NO), which regulates vasodilation and possesses pro-inflammatory actions, has been implicated in the pathogenesis of SSc. We compared serum NO x (
Use of the oral chelator deferiprone in the treatment of iron overload in patients with Hb H disease
Autor:
Chor Sang Chim, T. K. Chan, Raymond Liang, Bernard M.Y. Cheung, J. C. W. Chan, Vivian Chan, Clara G.C. Ooi
Publikováno v:
British Journal of Haematology. 133:198-205
Seventeen non-transfusion-dependent Chinese haemoglobin H (Hb H) disease patients (age 29-76 years) with serum ferritin900 microg/l were treated with deferiprone for up to 18 months. One patient withdrew and data from 16 patients were analysed. Sixte
Autor:
Joyce Y. H. Hui, Yip Fai Chan, Eva L. H. Tsui, Lilian L Y Leong, Tai Pang Wong, Gregory E. Antonio, K. T. Wong, Alan N L Sy, Jane C K Chan, Henry Y H Huang, Anil T. Ahuja, Cho Yin Chan, Joyce S. W. Wong, Clara G.C. Ooi
Publikováno v:
Radiology. 237:1081-1090
To retrospectively analyze serial chest radiographs in all patients with severe acute respiratory syndrome (SARS) in Hong Kong for temporal changes and differences between patients who died and those who were discharged from the hospital and to compa
Publikováno v:
Current Infectious Disease Reports
Severe acute respiratory syndrome (SARS) is a highly contagious and predominantly pneumonic illness caused by a novel coronavirus now commonly known as SARS-CoV. This article describes the key diagnostic clinical features, radiologic features, and in
Autor:
Chi F Wong, Wai M Wong, Pek L. Khong, Kam Sze Tsang, Wai C. Yiu, Poon C. Wong, James Chung-Man Ho, Kar N. Lai, Bing Lam, Clara G.C. Ooi
Publikováno v:
Radiology. 229:500-506
To evaluate the relationship among chest radiographs, oxygen supplementation requirement, and treatment response in severe acute respiratory syndrome (SARS).Forty patients (20 women, 20 men; mean age, 42.90 years +/- 14.01 [SD]; median age, 41.5 year
Autor:
Wai Man Wong, Clara G.C. Ooi, Man-Fung Yuen, Chee-Kin Hui, Ching-Lung Lai, Annie On-On Chan, Benjamin C.Y. Wong
Publikováno v:
Cancer. 97:2776-2782
BACKGROUND Systemic, high–dose interferon-α treatment given three times per week subcutaneously induces tumor regression in approximately 30% of patients with inoperable hepatocellular carcinoma (HCC). The objective of the current study was to det
Publikováno v:
Pediatric Neurology. 26:205-209
We studied the in vivo cerebral metabolites and documented the presence of MECP2 gene mutations in six Chinese females with Rett syndrome. Magnetic resonance spectroscopy spectra from the frontal lobe (gray and white matter) and deep gray nuclei (bas
Autor:
Wilfred Hing Sang Wong, Clara G.C. Ooi, Susan S. Chiu, Lok-Yee So, Pak-Leung Ho, Pek-Lan Khong, Eunice L.Y. Chan
Publikováno v:
Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi. 49(2)
Objectives We sought to document the incidence of pediatric hospitalization for bacterial pneumonia before universal childhood conjugate pneumococcal vaccination using two different methods of diagnosis. Methods By following the World Health Organiza
Autor:
Bing Lam, Clara G.C. Ooi, James Chung-Man Ho, Kwok N. Chan, Kenneth W. Tsang, Maria Pik Wong, Wah K. Lam
Publikováno v:
Respirology. 5:265-270
Objectives: The aim was to study the yield of malignant or suspicious cells from bronchoalveolar lavage (BAL), endobronchial biopsy (BX) and endobronchial brushing (BR) specimens obtained at bronchoscopy. Methodology: We prospectively followed up all
Autor:
Sau Yin Ha, Bernard M.Y. Cheung, Vivian Chan, Raymond Liang, Tai Kwong Chan, Clara G.C. Ooi, FE Chen, David Todd
Publikováno v:
New England Journal of Medicine. 343:544-550
Background Normally, one pair of each of the two α-globin genes, α1 and α2, resides on each copy of chromosome 16. In hemoglobin H disease, three of these four α-globin genes are affected by a deletion, a mutation, or both. We studied the α-glob