Response of levetiracetam in neonatal seizures

Por Yau, Maggie Lo-Yee, Fung, Eva Lai-Wah, Ng, Pak Cheung
Publicado no World J Clin Pediatr (2015)

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

Por Yang, Hongqian, Fung, Eva Y. M., Zubarev, Alexander R., Zubarev, Roman A.
Publicado em 2009

Hirayama disease in a 17-year-old Chinese man

Por Sitt, Jacqueline Ching Man, Fung, Eva Lai Wah, Yuen, Edmund Hok-Yuen, Ahuja, Anil Tejbhan
Publicado no 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

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

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

Por 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.
Publicado no Child Neurol Open (2015)

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

Por 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
Publicado no Nat Commun (2015)

Exome sequencing in paediatric patients with movement disorders

Por 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
Publicado no Orphanet J Rare Dis (2021)

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

Por 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
Publicado no Neurol Genet (2019)