Zobrazeno 1 - 10
of 27
pro vyhledávání: '"Ka-chung Wong"'
Autor:
Johnny Yau Cheung Chang, Chariene Shao Lin Woo, Wing Sun Chow, Anne White, Ka Chung Wong, Po Tsui, Alan Chun Hong Lee, Eunice Ka Hong Leung, Yu Cho Woo, Kathryn Choon Beng Tan, Karen Siu Ling Lam, Chi Ho Lee, David Tak Wai Lui
Publikováno v:
Frontiers in Medicine, Vol 10 (2023)
Here, we report the first adult case of pancreatic yolk sac tumor with ectopic adrenocorticotropic hormone (ACTH) syndrome. The patient was a 27-year-old woman presenting with abdominal distension, Cushingoid features, and hyperpigmentation. Endogeno
Externí odkaz:
https://doaj.org/article/402c0cc4d8154c18af2bf39f4f24245d
Autor:
Yau Cheung Chang, Johnny, Shao Lin Woo, Chariene, Wing Sun Chow, White, Anne, Ka Chung Wong, Po Tsui, Chun Hong Lee, Alan, Ka Hong Leung, Eunice, Yu Cho Woo, Choon Beng Tan, Kathryn, Siu Ling Lam, Karen, Chi Ho Lee, Tak Wai Lui, David
Publikováno v:
Frontiers in Medicine; 2023, p1-7, 7p
Nuclear magnetic resonance spectroscopy-based urinalysis for a young girl with extreme hypoglycaemia
Autor:
Ka-chung Wong, Tsz-ki Ling, Grace Wing-kit Poon, Nike Kwai-Cheung Lau, Anne Mei-kwun Kwok, Chun-yiu Law, Ching-Wan Lam
Publikováno v:
Pathology. 54:505-508
Autor:
Yeow-Kuan Chong, Lai-Ka Lee, Tsz-ki Ling, Han-Chih Hencher Lee, Chun-Hung Ko, Candace Yim Chan, Ching-Wan Lam, Chloe Mak, Nike Kwai-Cheung Lau, Cheuk-Wing Fung, Sheila Suet-Na Wong, Sidney Tam, Chun-yiu Law, K M Cheung, Chi-Kong Lai, Kin-Cheong Eric Yau, Albert Y W Chan, Ka-chung Wong
Publikováno v:
Clinica Chimica Acta. 521:40-44
Background Aromatic L-amino acid decarboxylase deficiency is a rare neurometabolic disease due to impaired decarboxylation of neurotransmitter precursors to its active form. Case: We retrospectively reviewed 8 cases from 2008 to 2019 with cerebrospin
Publikováno v:
Pathology. 54(5)
Autor:
Ka-lok Lee, Tsz-ki Ling, Winnie C.W. Chu, Gloria Brea-Calvo, Ching-Wan Lam, Kin-wing Yan, Chun-Yiu Law, Ka-chung Wong, Nai-Chung Fong
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
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[Background]: Primary CoQ deficiency occurs because of the defective biosynthesis of coenzyme Q, one of the key components of the mitochondrial electron transport chain. Patients with this disease present with a myriad of non-specific symptoms and si
Autor:
Sik-Hon Tsui, Tsz-ki Ling, Ching-Lung Lai, Chun-yiu Law, SC Leung, Florence Loong, Nike Kwai-Cheung Lau, Ka-chung Wong, Ching-Wan Lam
Publikováno v:
Clinical toxicology (Philadelphia, Pa.). 60(2)
Colloidal silver packaged as a dietary supplement is readily available online and is thought to be safe. Literature describing its toxicity in humans is scarce.A 47-year-old man presented to us for sensory and gait problems. He had unremarkable past
Publikováno v:
Journal of human genetics. 66(8)
Hypomelanosis of Ito (HMI) is part of a neuroectodermal syndrome characterized by distinctive skin manifestations with or without multisystemic involvements. In our undiagnosed diseases program, we have encountered a 3-year-old girl presenting with c
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 496
Background Mitochondrial DNA depletion syndrome is a group of heterogeneous diseases with non-specific presentation. The common feature is the quantitative depletion of mitochondrial DNA without qualitative defects. Diagnosis of these diseases poses
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 200:105665