Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Tsz-ki Ling"'
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
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:
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
Autor:
Chun-Yiu Law, Ching-Wan Lam, Tsz Ki Ling, Patrick Siu-chung Leung, Florence Loong, Ka Chung Wong
Publikováno v:
Pathology. 52:S101
Publikováno v:
Pathology. 52:S107
Autor:
Tsz-Ki, Ling, Chun-Yiu, Law, Kin-Wing, Yan, Nai-Chung, Fong, Ka-Chung, Wong, Ka-Lok, Lee, Winnie Chiu-Wing, Chu, Gloria, Brea-Calvo, Ching-Wan, Lam
Publikováno v:
Clinica chimica acta; international journal of clinical chemistry. 497
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 signs, posing a
Autor:
Chun-Yiu Law, Winnie C.W. Chu, Gloria Brea-Calvo, Ka-lok Lee, Tsz-ki Ling, Chun-Hung Ko, Ka-chung Wong, Ching-Wan Lam, Nai-Chung Fong
Publikováno v:
Pathology. 51:S112-S113
Autor:
Y K Chong, Wing Lan Cheung, Tsz Ki Ling, Ling Yin Hung, Nike Kwai Cheung Lau, Chloe Miu Mak, KM Kwok, Bun Sheng
Publikováno v:
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia. 56
Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is an adult onset hereditary stroke syndrome characterized by recurrent stroke and progressive cognitive impairment caused by NOTCH3 mutations. We re