• 234 Citations
  • 8 h-Index
20082019
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Research Output 2008 2019

  • 234 Citations
  • 8 h-Index
  • 21 Article
  • 1 Conference contribution
  • 1 Review article

Acanthamoeba encephalitis in an immunocompetent child and review of the imaging features of intracranial acanthamoebic infections in immunocompetent patients

Hanafiah, M., Mohamed Mukari, S. A., Hamdan, M. F., Wong, S. W. & P. Yoganathan, K., 1 Jun 2018, In : Neurology Asia. 23, 2, p. 179-184 6 p.

Research output: Contribution to journalReview article

Acanthamoeba
Encephalitis
Infection
Immunocompromised Host
Brain
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
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
5 Citations (Scopus)

Congenital hepatic fibrosis in a child with autosomal dominant polycystic kidney disease

P. Yoganathan, K., Abdul Hamid, H. & Wong, S. W., Aug 2008, In : Medical Journal of Malaysia. 63, 3, p. 251-253 3 p.

Research output: Contribution to journalArticle

Autosomal Dominant Polycystic Kidney
Autosomal Recessive Polycystic Kidney
Portal Hypertension
Hypertension
Congenital Hepatic Fibrosis
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
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

Health-related quality of life in paediatric spina bifida

Thong, P. L., Wong, S. W., Abdul Manaf, M. R., Lee, M. L. & P. Yoganathan, K., 1 Aug 2019, In : Medical Journal of Malaysia. 74, 4, p. 281-287 7 p.

Research output: Contribution to journalArticle

Spinal Dysraphism
Neurogenic Bowel
Quality of Life
Pediatrics
Only Child
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
23 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
12 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
1 Citation (Scopus)

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
5 Citations (Scopus)

Malignant hypertension in a child with phakomatosis pigmentovascularis type II b

P. Yoganathan, K., Abdul Hamid, H., Wong, S. W. & Zulfiqar, A., Nov 2008, In : Acta Paediatrica, International Journal of Paediatrics. 97, 11, p. 1589-1591 3 p.

Research output: Contribution to journalArticle

Neurocutaneous Syndromes
Malignant Hypertension
Nevus of Ota
Sturge-Weber Syndrome
Klippel-Trenaunay-Weber Syndrome
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
63 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 others, Szepetowski, 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
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

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
21 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
32 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
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

Transition care readiness among patients in a tertiary paediatric department

Chong, D. L. S., Azim, E., Latiff, Z., Zakaria, S. Z. S., Wong, S. W., Wu, L. L., Hong, J. S. S., Alias, H., Loh, C-K., Shri Abd. Aziz, B. B., Rasat, R. & P. Yoganathan, K., 1 Dec 2018, In : Medical Journal of Malaysia. 73, 6, p. 382-387 6 p.

Research output: Contribution to journalArticle

Pediatrics
Delivery of Health Care
Patient Transfer
Time and Motion Studies
Thalassemia
11 Citations (Scopus)
Sialorrhea
Type A Botulinum Toxins
Cerebral Palsy
Caregivers
Quality of Life