• 220 Citations
  • 8 h-Index
20082018
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Research Output 2008 2018

  • 220 Citations
  • 8 h-Index
  • 19 Article
  • 1 Conference contribution
  • 1 Review article
2018
Acanthamoeba
Encephalitis
Infection
Immunocompromised Host
Brain
2017

Lack of meaningful genotype-phenotype association in SCN1A-related infantile-onset epileptic encephalopathies

Wahab, S. A. A., Yakob, Y., Khoo, T. B., Terumalay, S. D., Ganesan, V., Teh, C. M., bin Yahaya, N. A., Heng, H. S., Vaithialingam, M. & Wong, S. W., 2017, In : Neurology Asia. 22, 2, p. 99-111 13 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Brain Diseases
Mutation
Seizures
Myoclonic Epilepsy
2015
3 Citations (Scopus)

Contribution of TIMP4 rs3755724 polymorphism to susceptibility to focal epilepsy in Malaysian Chinese

Haerian, B. S., Sha'ari, H. M., Fong, C. Y., Tan, H. J., Wong, S. W., Ong, L. C., Ali, R. A., Tan, C. T. & Mohamed, Z., 15 Jan 2015, In : Journal of Neuroimmunology. 278, p. 137-143 7 p.

Research output: Contribution to journalArticle

Partial Epilepsy
Epilepsy
Haplotypes
Alleles
Genotype
5 Citations (Scopus)

RORA gene rs12912233 and rs880626 polymorphisms and their interaction with SCN1A rs3812718 in the risk of epilepsy: A case-control study in Malaysia

Haerian, B. S., Sha'ari, H. M., Tan, H. J., Fong, C. Y., Wong, S. W., Ong, L. C., Ali, R. A., Tan, C. T. & Mohamed, Z., 1 Apr 2015, In : Genomics. 105, 4, p. 229-236 8 p.

Research output: Contribution to journalArticle

Orphaned Children
Malaysia
Case-Control Studies
Epilepsy
Genes
2014
18 Citations (Scopus)

Sleep disturbances in Malaysian children with cerebral palsy

Atmawidjaja, R. W., Wong, S. W., Wai Wai, Y. & Ong, L. C., 2014, In : Developmental Medicine and Child Neurology. 56, 7, p. 681-685 5 p.

Research output: Contribution to journalArticle

Cerebral Palsy
Sleep
Caregivers
Siblings
Sleep-Wake Transition Disorders
2013
2 Citations (Scopus)

Alpha-thalassemia mental retardation syndrome: A case report of two affected siblings

Abdul Latiff, Z., Omar, S. A. S., Lau, S. C. D., Wong, S. W., Ong, L. C., Abdul Aziz, D. A. & Akmal, S. N., 2013, In : Journal of Pediatric Neurology. 11, 1, p. 67-70 4 p.

Research output: Contribution to journalArticle

alpha-Thalassemia
Intellectual Disability
Hemoglobin H
X-Linked Mental Retardation
Inheritance Patterns

Screening of polymorphisms for MTHFR and DHFR genes in spina bifida children and their mothers

Husna, M. Z., Ismail, E., Ibrahim, S., Selvi Naicker, A., Fakhrurazi, H., Htwe, R. O., Kanehaswari, Y., Abd Rashid, A. H., Wong, S. W., Subashini, K., Syahira, O. N. & Aishah, S., 2013, AIP Conference Proceedings. Vol. 1571. p. 271-276 6 p.

Research output: Chapter in Book/Report/Conference proceedingConference contribution

polymorphism
folic acid
genes
deletion
screening
2012
58 Citations (Scopus)

PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine

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, S. W., Fu, Y. H., Rochette, J., Ptáček, L. J. & 1 othersSzepetowski, P., 20 Nov 2012, In : Neurology. 79, 21, p. 2097-2103 7 p.

Research output: Contribution to journalArticle

Chorea
Migraine Disorders
Seizures
Mutation
Migraine without Aura
2011
17 Citations (Scopus)

Association between ABCB1 polymorphism and response to sodium valproate treatment in Malaysian epilepsy patients

Haerian, B. S., Lim, K. S., Tan, H. J., Mohamed, E. H. M., Tan, C. T., Ali, R. A., Wong, C. P., Wong, S. W., Omar, H., Roslan, H. & Mohamed, Z., Mar 2011, In : Epileptic Disorders. 13, 1, p. 65-75 11 p.

Research output: Contribution to journalArticle

Valproic Acid
Epilepsy
Genotype
Genes
P-Glycoprotein
7 Citations (Scopus)

Lack of association between synapsin II (SYN2) gene polymorphism and susceptibility epilepsy: A case-control study and meta-analysis

Haerian, B. S., Lim, K. S., Tan, H. J., Wong, C. P., Wong, S. W., Tan, C. T., Ali, R. A. & Mohamed, Z., Oct 2011, In : Synapse. 65, 10, p. 1073-1079 7 p.

Research output: Contribution to journalArticle

Synapsins
Meta-Analysis
Case-Control Studies
Epilepsy
Genes
22 Citations (Scopus)

Lack of association of ABCB1 and PXR polymorphisms with response to treatment in epilepsy

Haerian, B. S., Lim, K. S., Mohamed, E. H. M., Tan, H. J., Tan, C. T., Ali, R. A., Wong, C. P., Wong, S. W. & Mohamed, Z., Jun 2011, In : Seizure. 20, 5, p. 387-394 8 p.

Research output: Contribution to journalArticle

Epilepsy
Anticonvulsants
Carbamazepine
Valproic Acid
Haplotypes
11 Citations (Scopus)

Lack of association of ABCB1 haplotypes on five loci with response to treatment in epilepsy

Haerian, B. S., Lim, K. S., Mohamed, E. H. M., Tan, H. J., Tan, C. T., Ali, R. A., Wong, C. P., Wong, S. W. & Mohamed, Z., Sep 2011, In : Seizure. 20, 7, p. 546-553 8 p.

Research output: Contribution to journalArticle

Haplotypes
Carbamazepine
Valproic Acid
Epilepsy
Adenosine Triphosphate
6 Citations (Scopus)

Sturge-Weber syndrome without facial nevus: An unusual cause of neonatal seizures

Wong, S. W., Kyaw, L., Ong, L. C. & Zulfiqar, A. M., Apr 2011, In : Journal of Paediatrics and Child Health. 47, 4, p. 237-239 3 p.

Research output: Contribution to journalArticle

Sturge-Weber Syndrome
Nevus
Seizures
Eye Abnormalities
Port-Wine Stain
2010
3 Citations (Scopus)

Episodic vomiting and headache in children: Consider occipital epilepsy

Lope, R. J. R., Wong, S. W. & Wu, L. L., Apr 2010, In : Journal of Paediatrics and Child Health. 46, 4, p. 204-206 3 p.

Research output: Contribution to journalArticle

Vomiting
Headache
Epilepsy
Diagnostic Errors
Seizures

Exercise induced cramps and myoglobinuria in dystrophinopathy - A report of three Malaysian patients

Annuar, A. A., Wong, K. T., Ching, A. S., Thong, M. K., Wong, S. W., Alsiddiq, F., Ong, L. C. & Goh, K. J., Aug 2010, In : Neurology Asia. 15, 2, p. 125-131 7 p.

Research output: Contribution to journalArticle

Myoglobinuria
Muscle Cramp
Dystrophin
Exercise
Phenotype
12 Citations (Scopus)

Novel familial cases of ICCA (infantile convulsions with paroxysmal choreoathetosis) syndrome

Rochette, J., Roll, P., Fu, Y. H., Lemoing, A. G., Royer, B., Roubertie, A., Berquin, P., Motte, J., Wong, S. W., Hunter, A., Robaglia-Schlupp, A., Ptacek, L. J. & Szepetowski, P., Sep 2010, In : Epileptic Disorders. 12, 3, p. 199-204 6 p.

Research output: Contribution to journalArticle

Chorea
Seizures
Epilepsy
Chromosomes
Genes
30 Citations (Scopus)

Sleep habits and disturbances in Malaysian children with epilepsy

Ong, L. C., Wai Wai, Y., Wong, S. W., Alsiddiq, F. & Khu, Y. S., Mar 2010, In : Journal of Paediatrics and Child Health. 46, 3, p. 80-84 5 p.

Research output: Contribution to journalArticle

Habits
Epilepsy
Sleep
Siblings
Confidence Intervals
6 Citations (Scopus)

Sleep position and infant care practices in an urban community in Kuala Lumpur

Raja Lope, R. J., Kong, W. K., Lee, V. W. M., Tiew, W. T. & Wong, S. W., Mar 2010, In : Medical Journal of Malaysia. 65, 1, p. 45-48 4 p.

Research output: Contribution to journalArticle

Infant Care
Sleep
Sudden Infant Death
Play and Playthings
Prenatal Care
2009
10 Citations (Scopus)
Sialorrhea
Type A Botulinum Toxins
Cerebral Palsy
Caregivers
Quality of Life
2008
5 Citations (Scopus)
Autosomal Dominant Polycystic Kidney
Autosomal Recessive Polycystic Kidney
Portal Hypertension
Hypertension
Congenital Hepatic Fibrosis
5 Citations (Scopus)
Neurocutaneous Syndromes
Malignant Hypertension
Nevus of Ota
Sturge-Weber Syndrome
Klippel-Trenaunay-Weber Syndrome