yuka miyata-nozaka, hui jan tan, sau wei wong, azman ali raymond, haslyna omar, shamsul mohd zain.  (2021).  cyp3a5 genetic variants and their associations with carbamazepine and valproic acid response in malaysian epileptic patients.  - international journal of clinical pharmacology and therapeutics.  8-16. 

pui ling thong, sau wei wong, mohd rizal abdul manaf, ming lee lee, kanaheswari yoganathan.  (2019).  health-related quality of life in paediatric spina bifida.  - medical journal of malaysia.  281-287. 

emilia rosniza mohammed rusli, juriza ismail, wong saw wei, shareena ishak, rohana jaafar, faizah mohd zaki.  (2019).  neonatal hypoxic encephalopathy: correlation between post-cooling brain mri findings and 2 years neurodevelopmental outcome.  - the indian journal of radiology and imaging.  350-355. 

doris lau sie chong, ezdiani azim, zarina latiff, syed zulkifli syed zakaria, sau wei wong, loo ling wu, joyce soo synn hong, hamidah alias, c-khai loh, bilkis abd aziz, rahmah rasat, kanaheswari yoganathan.  (2018).  transition care readiness among patients in a tertiary paediatric department.  - medical journal of malaysia.  . 

farin masra, sau wei wong, kanaheswari yoganathan, swee fong tang.  (2018).  streptococcus pneumoniae haemolytic uraemic syndrome: a case report.  - brunei international medical journal.  . 

mohammad hanafiah, azura mohamed mukari shahizon, mohd farhan hamdan, sau wei wong, yoganathan kanaheswari.  (2018).  acanthamoeba encephalitis in an immunocompetent child and review of the imaging features of intracranial acanthamoebic infections in immunocompetent patients.  - neurology asia.  . 

siti aishah abdul wahab, yusnita yakob,teik-beng khoo, sangita dharshini terumalay, vigneswari ganesan, chee-ming teh, nor azni bin yahya, hock-sin heng, manonmani vaithialingam, sau-wei wong.  (2017).  lack of meaningful genotype-phenotype association in scn1a-related infantile-onset epileptic encephalopathies.  - neurology asia.  99-111. 

batoul sadat haerian, hidayati mohd sha`ari, choong yi fong, hui jan tan, sau wei wong, lai choo ong, azman ali raymond, chong tin tan, zahurin mohamed.  (2015).  contribution of timp4 rs3755724 polymorphism to susceptibility to focal epilepsy in malaysian chinese.  - journal of neuroimmonology.  137-143. 

batoul sadat haerian, hidayati mohd sha`ari, hui jan tan, choong yi fong, sau wei wong, lai choo ong, azman ali raymond, chong tin tan, zahurin mohamed.  (2015).  rora gene rs12912233 and rs880626 polymorphisms and their interaction with scn1a rs3812718 in the risk of epilepsy: a case-control study in malaysia.  - genomics.  229-236. 

raymond warouw atmawidjaja, sau wei wong, wai wai yang, lai choo ong.  (2014).  sleep disturbances in malaysian children with cerebral palsy.  - developmental medicine and child neurology.  681-685. 

zarina a. latiff, sharifah azween s. omar, doris lau, sau wei wong.  (2013).  alpha-thalassemia mental retardation syndrome: a case report of two affected siblings.  - journal of pediatric neurology.  11(1):67-70. 

cloarec r, bruneau n, rudolf g, massacrier a, salmi m, bataillard m, boulay c, caraballo r, fejerman n, genton p, hirsch e, hunter a, lesca g, motte j, roubertie a, sanlaville d, wong sw, fu yh, roche.  (2012).  prrt2 links infantile convulsions and paroxysmal dyskinesia with migraine.  - neurology.  79(21):2097-2103. 

b.s. haerian, k.s.lim, e.h.m.mohamed, h.j.tan, c.t.tan, a.a.raymond, c.p. wong, s.w.wong, z.mohamed.  (2011).  lack of association of abcb1 haplotypes on five loci with response to treatment in epilepsy.  - seizure.  20(7):546-53. 

b.s. haerian, k.s.lim, e.h.m.mohameda, h.j.tan, c.t.tan, a.a.raymond, c.p. wong, s.w.wong, z.mohamed.  (2011).  lack of association of abcb1 and pxr polymorphisms with response to treatment in epilepsy.  - seizure-european journal of epilepsy.  20(5):387-394. 

sau wei wong, linn kyaw, lai choo ong and annuar m zulfiqar.  (2011).  sturge-weber syndrome without facial nevus: an unusual cause of neonatal seizures.  - journal of paediatrics and child health.  47(4):237-239. 

haerian bs, lim ks, tan hj, wong cp, wong sw, tan ct, raymond aa, mohamed z.  (2011).  lack of association between synapsin ii (syn2) gene polymorphism and susceptibility epilepsy: a case-control study and meta-analysis.  - synapse.  65(10):1073-1079. 

batoul sadat haerian, kheng seang lim, hui jan tan, elsa hanifa mejia mohamed, chong tin tan, azman ali raymond, chee piau wong, sau wei wong, haslyna omar, harun roslan , zahurin mohamed.  (2011).  association between abcb1 polymorphism and response to sodium valproate treatment in malaysian epilepsy patients.  - epileptic disorders.  13(1): 65-75. 

azlina ahmad annuar, kum thong wong, ai sze ching , meow keong thong, sau wei wong, feizel alsiddiq, lai choo ong, khean jin goh.  (2010).  exercise induced cramps and myoglobinuria in dystrophinopathy - a report of three malaysian patients.  - neurology asia.  15(2):125-131. 

lai choo ong, wai wai yang, sau wei wong, feizel alsiddiq and yi soon khu.  (2010).  sleep habits and disturbances in malaysian children with epilepsy.  - journal of paediatrics and child health.  46(3):80-84. 

rochette j, roll p, fu yh, lemoing ag, rover b, roubertie a, berquin p, motte j, wong sw, hunter a, robaglia-schlupp a, ptacek lj, szepetowski p.  (2010).  novel familial cases of icca (infantile convulsions with paroxysmal choreoathetosis) syndrome.  - epileptic disorders.  12(3):199-204. 

raja juanita raja lope, sau wei wong and loo ling wu.  (2010).  episodic vomiting and headache in children: consider occipital epilepsy.  - journal of paediatrics and child health.  46(4):204-206. 

ong lai choo, wong sau wei, hamzaini abdul hamid.  (2009).  treatment of drooling in children with cerebral palsy using ultrasound guided intraglandular injections of botulinum toxin a.  - journal of pediatric neurology.  7(2):141-145. 

kanaheswari y, hamzaini ah,wong sw.  (2008).  congenital hepatic fibrosis in a child with autosomal dominant polycystic kidney disease.  - medical journal of malaysia.  63(3):251-253. 

y kanaheswari, ah hamzaini , sw wong , a zulfiqar.  (2008).  malignant hypertension in a child with phakomatosis pigmentovascularis type ii b.  - acta paediatrica.  97(11):1589-1591.