Response of levetiracetam in neonatal seizures

per Yau, Maggie Lo-Yee, Fung, Eva Lai-Wah, Ng, Pak Cheung
Publicat a World J Clin Pediatr (2015)

Toward proteome-scale identification and quantification of isoaspartyl residues in biological samples

per Yang, Hongqian, Fung, Eva Y. M., Zubarev, Alexander R., Zubarev, Roman A.
Publicat 2009

Hirayama disease in a 17-year-old Chinese man

per Sitt, Jacqueline Ching Man, Fung, Eva Lai Wah, Yuen, Edmund Hok-Yuen, Ahuja, Anil Tejbhan
Publicat a Singapore Med J (2014)

Proteomics and Pathway Analysis Identifies JNK Signaling as Critical for High Linear Energy Transfer Radiation-induced Apoptosis in Non-small Lung Cancer Cells

per Ståhl, Sara, Fung, Eva, Adams, Christopher, Lengqvist, Johan, Mörk, Birgitta, Stenerlöw, Bo, Lewensohn, Rolf, Lehtiö, Janne, Zubarev, Roman, Viktorsson, Kristina
Publicat 2009

Prevalence and Characteristics of Chinese Patients With Duchenne and Becker Muscular Dystrophy: A Territory Wide Collaborative Study in Hong Kong

per Chan, Sophelia H. S., Lo, Ivan F. M., Cherk, Sharon W. W., Cheng, Wai Wai, Fung, Eva L. W., Yeung, Wai Lan, Ngan, Mary, Lee, Wing Cheong, Kwong, Ling, Wong, Suet Na, Ma, Che Kwan, Tai, Shuk Mui, Ng, Grace S. F., Wu, Shun Ping, Wong, Virginia C. N.
Publicat a Child Neurol Open (2015)

Recessive mutations in POLR1C cause a leukodystrophy by impairing biogenesis of RNA polymerase III

per Thiffault, Isabelle, Wolf, Nicole I., Forget, Diane, Guerrero, Kether, Tran, Luan T., Choquet, Karine, Lavallée-Adam, Mathieu, Poitras, Christian, Brais, Bernard, Yoon, Grace, Sztriha, Laszlo, Webster, Richard I., Timmann, Dagmar, van de Warrenburg, Bart P., Seeger, Jürgen, Zimmermann, Alíz, Máté, Adrienn, Goizet, Cyril, Fung, Eva, van der Knaap, Marjo S., Fribourg, Sébastien, Vanderver, Adeline, Simons, Cas, Taft, Ryan J., Yates III, John R., Coulombe, Benoit, Bernard, Geneviève
Publicat a Nat Commun (2015)

Exome sequencing in paediatric patients with movement disorders

per Kwong, Anna Ka-Yee, Tsang, Mandy Ho-Yin, Fung, Jasmine Lee-Fong, Mak, Christopher Chun-Yu, Chan, Kate Lok-San, Rodenburg, Richard J. T., Lek, Monkol, Huang, Shushu, Pajusalu, Sander, Yau, Man-Mut, Tsoi, Cheung, Fung, Sharon, Liu, Kam-Tim, Ma, Che-Kwan, Wong, Sheila, Yau, Eric Kin-Cheong, Tai, Shuk-Mui, Fung, Eva Lai-Wah, Wu, Nick Shun-Ping, Tsung, Li-Yan, Smeitink, Jan, Chung, Brian Hon-Yin, Fung, Cheuk-Wing
Publicat a Orphanet J Rare Dis (2021)

Clinical spectrum of POLR3-related leukodystrophy caused by biallelic POLR1C pathogenic variants

per Gauquelin, Laurence, Cayami, Ferdy K., Sztriha, László, Yoon, Grace, Tran, Luan T., Guerrero, Kether, Hocke, François, van Spaendonk, Rosalina M.L., Fung, Eva L., D'Arrigo, Stefano, Vasco, Gessica, Thiffault, Isabelle, Niyazov, Dmitriy M., Person, Richard, Lewis, Kara Stuart, Wassmer, Evangeline, Prescott, Trine, Fallon, Penny, McEntagart, Meriel, Rankin, Julia, Webster, Richard, Philippi, Heike, van de Warrenburg, Bart, Timmann, Dagmar, Dixit, Abhijit, Searle, Claire, Thakur, Nivedita, Kruer, Michael C., Sharma, Suvasini, Vanderver, Adeline, Tonduti, Davide, van der Knaap, Marjo S., Bertini, Enrico, Goizet, Cyril, Fribourg, Sébastien, Wolf, Nicole I., Bernard, Geneviève
Publicat a Neurol Genet (2019)