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Your search keyword '"Ma, Kam-hung"' showing total 6 results
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6 results on '"Ma, Kam-hung"'

1. Mitochondrial diseases in Hong Kong: prevalence, clinical characteristics and genetic landscape

Author

Wong, Tsz-sum, Belaramani, Kiran M., Chan, Chun-kong, Chan, Wing-ki, Chan, Wai-lun Larry, Chang, Shek-kwan, Cheung, Sing-ngai, Cheung, Ka-yin, Cheung, Yuk-fai, Chong, Shuk-ching Josephine, Chow, Chi-kwan Jasmine, Chung, Hon-yin Brian, Fan, Sin-ying Florence, Fok, Wai-ming Joshua, Fong, Ka-wing, Fung, Tsui-hang Sharon, Hui, Kwok-fai, Hui, Ting-hin, Hui, Joannie, Ko, Chun-hung, Kwan, Min-chung, Kwok, Mei-kwan Anne, Kwok, Sung-shing Jeffrey, Lai, Moon-sing, Lam, Yau-on, Lam, Ching-wan, Lau, Ming-chung, Law, Chun-yiu Eric, Lee, Wing-cheong, Lee, Han-chih Hencher, Lee, Chin-nam, Leung, Kin-hang, Leung, Kit-yan, Li, Siu-hung, Ling, Tsz-ki Jacky, Liu, Kam-tim Timothy, Lo, Fai-man, Lui, Hiu-tung, Luk, Ching-on, Luk, Ho-ming, Ma, Che-kwan, Ma, Karen, Ma, Kam-hung, Mew, Yuen-ni, Mo, Alex, Ng, Sui-fun, Poon, Wing-kit Grace, Rodenburg, Richard, Sheng, Bun, Smeitink, Jan, Szeto, Cheuk-ling Charing, Tai, Shuk-mui, Tse, Choi-ting Alan, Tsung, Li-yan Lilian, Wong, Ho-ming June, Wong, Wing-yin Winnie, Wong, Kwok-kui, Wong, Suet-na Sheila, Wong, Chun-nei Virginia, Wong, Wai-shan Sammy, Wong, Chi-kin Felix, Wu, Shun-ping, Wu, Hiu-fung Jerome, Yau, Man-mut, Yau, Kin-cheong Eric, Yeung, Wai-lan, Yeung, Hon-ming Jonas, Yip, Kin-keung Edwin, Young, Pui-hong Terence, Yuan, Gao, Yuen, Yuet-ping Liz, Yuen, Chi-lap, and Fung, Cheuk-wing

Published
2023
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2. Guillain-Barré syndrome in children – High occurrence of Miller Fisher syndrome in East Asian region

Author

Chiu, Annie Ting Gee, Chan, Ricky Wing Ki, Yau, Maggie Lo Yee, Yuen, Angus Chi Lap, Lam, Alva King Fai, Lau, Shirley Wai Yin, Lau, Alan Ming Chung, Fung, Sharon Tsui Hang, Ma, Kam Hung, Lau, Christine Wai Ling, Yau, Man Mut, Ko, Chun Hung, Tsui, Kwing Wan, Ma, Che Kwan, Tai, Shuk Mui, Yau, Eric Kin Cheong, Fung, Eva, Wu, Shun Ping, Kwong, Karen Ling, and Chan, Sophelia Hoi Shan

Published
2022
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5. Reduction in Myoclonus and Ataxia Following the Use of Perampanel in Patient With Sialidosis Type 1.

Author

So, Enoch C.T., Mak, Chloe M., Ng, Grace S.F., Tsui, Kwing Wan, Ma, Kam Hung, and Yeung, Wai Lan

Subjects
*MYOCLONUS, *ATAXIA, *NEUROLOGICAL disorders, *PYRIDINE, *ANTICONVULSANTS, *INBORN errors of metabolism, *PHARMACODYNAMICS, *DISEASE complications
Abstract

Keywords: Sialidosis; Perampanel; Myoclonus; Ataxia EN Sialidosis Perampanel Myoclonus Ataxia 91 93 3 07/24/20 20200801 NES 200801 Introduction Sialidosis is a rare autosomal recessive disorder under the umbrella of lysosomal storage diseases. Adjunctive perampanel showed clinically swift and meaningful reduction in myoclonus and ataxia, leading to restoration of our patient's independence of daily living. [Extracted from the article]

Published
2020
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6. Isolated adrenocorticotropin deficiency in a child with Kabuki syndrome.

Author

Ma KH, Chow SN, and Yau FT

Subjects
Abnormalities, Multiple genetics, Child, Corticotropin-Releasing Hormone, Cosyntropin, Dermatoglyphics, Fingers abnormalities, Hormones blood, Humans, Hypoglycemia complications, Hyponatremia complications, Intellectual Disability genetics, Male, Seizures complications, Syndrome, Water-Electrolyte Imbalance genetics, Water-Electrolyte Imbalance physiopathology, Abnormalities, Multiple physiopathology, Adrenocorticotropic Hormone deficiency, Intellectual Disability physiopathology
Abstract

A 6 year-old Chinese boy with Kabuki syndrome presented with hypoglycemic seizure. He was diagnosed to have isolated adrenocorticotropin deficiency. To our knowledge, this is the first case of Kabuki syndrome with isolated adrenocorticotropin deficiency in the literature.

Published
2005
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