Meow-Keong Thong

Meow-Keong Thong

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Meow-Keong Thong

Meow-Keong Thong

Publications by authors named "Meow-Keong Thong"

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54Publications

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Quality of life of children with tuberous sclerosis complex.

Arch Dis Child 2019 Oct 23;104(10):972-978. Epub 2019 May 23.

Paediatric Department, Hospital Raja Perempuan Zainab II, Kelantan, Malaysia.

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http://dx.doi.org/10.1136/archdischild-2018-316394DOI Listing
October 2019

Infantile neuroaxonal dystrophy in a pair of Malaysian siblings with progressive cerebellar atrophy: Description of an expanded phenotype with novel PLA2A6 variants.

J Clin Neurosci 2019 Sep 4. Epub 2019 Sep 4.

Genetics and Metabolism Unit, Department of Paediatrics, Faculty of Medicine, University Malaya, Kuala Lumpur, Malaysia. Electronic address:

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http://dx.doi.org/10.1016/j.jocn.2019.08.111DOI Listing
September 2019

Ten-year trend in prevalence and outcome of Down syndrome with congenital heart disease in a middle-income country.

Eur J Pediatr 2019 Aug 20;178(8):1267-1274. Epub 2019 Jun 20.

Department of Pediatrics, Faculty of Medicine, University of Malaya, Jalan Universiti, 50603, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1007/s00431-019-03403-xDOI Listing
August 2019

Sandhoff disease in two siblings of a Malaysian family: Description of novel beta hexosaminidase mutations, magnetic resonance imaging, and spectroscopic findings.

Neurol India 2017;65(Supplement):S98-S100

Department of Biomedical Imaging, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.4103/neuroindia.NI_1121_15DOI Listing
July 2019

Deregulation of microRNAs in blood and skeletal muscles of myotonic dystrophy type 1 patients.

Neurol India 2017 May-Jun;65(3):512-517

Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.4103/neuroindia.NI_237_16DOI Listing
July 2019

A comparative study of patients' perceptions of genetic and genomic medicine services in California and Malaysia.

J Community Genet 2019 Jul 3;10(3):351-361. Epub 2018 Dec 3.

Department of Genetic and Genomic Medicine, University of California Irvine, Irvine, CA, 92697, USA.

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http://dx.doi.org/10.1007/s12687-018-0399-8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6591353PMC
July 2019

Achieving the targets of sustainable development goals (2030 agenda) for congenital disorders in Asia: Bottlenecks and interventions.

Authors:
Meow-Keong Thong

Am J Med Genet C Semin Med Genet 2019 06 23;181(2):254-261. Epub 2019 Feb 23.

Genetics and Metabolism Unit, Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1002/ajmg.c.31690DOI Listing
June 2019

Training in clinical genetics and genetic counseling in Asia.

Am J Med Genet C Semin Med Genet 2019 06 29;181(2):177-186. Epub 2019 Apr 29.

Department of Pediatrics, College of Medicine, University of the Philippines Manila, Manila, Philippines.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/ajmg.c.31703
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http://dx.doi.org/10.1002/ajmg.c.31703DOI Listing
June 2019

Asia Pacific Society of Human Genetics (APSHG) from conception to 2019: 13 years of collaboration to tackle congenital malformation and genetic disorders in Asia.

Am J Med Genet C Semin Med Genet 2019 06 3;181(2):155-165. Epub 2019 May 3.

Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

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http://dx.doi.org/10.1002/ajmg.c.31701DOI Listing
June 2019

Medical genetics in developing countries in the Asia-Pacific region: challenges and opportunities.

Genet Med 2018 10 10;20(10):1114-1121. Epub 2018 Aug 10.

Department of Biomedical Science, Kulliyyah of Allied Health Sciences, International Islamic University Malaysia, Kuantan, Malaysia.

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http://dx.doi.org/10.1038/s41436-018-0135-0DOI Listing
October 2018

Is BRCA Mutation Testing Cost Effective for Early Stage Breast Cancer Patients Compared to Routine Clinical Surveillance? The Case of an Upper Middle-Income Country in Asia.

Appl Health Econ Health Policy 2018 06;16(3):395-406

Center of Pharmaceutical Outcomes Research (CPOR), Department of Pharmacy Practice, Faculty of Pharmaceutical Sciences, Naresuan University, Muang, Phitsanulok, Thailand.

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http://dx.doi.org/10.1007/s40258-018-0384-8DOI Listing
June 2018

An audiological evaluation of syndromic and non-syndromic craniosynostosis in pre-school going children.

Int J Pediatr Otorhinolaryngol 2018 Jun 14;109:50-53. Epub 2018 Mar 14.

Department of Otorhinolaryngology, University of Malaya, Kuala Lumpur, Malaysia. Electronic address:

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http://dx.doi.org/10.1016/j.ijporl.2018.03.010DOI Listing
June 2018

Williams-Beuren syndrome in diverse populations.

Am J Med Genet A 2018 05;176(5):1128-1136

Medical Genetics Branch, National Human Genome Research Institute, The National Institutes of Health, Bethesda, Maryland.

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http://doi.wiley.com/10.1002/ajmg.a.38672
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http://dx.doi.org/10.1002/ajmg.a.38672DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6007881PMC
May 2018

Growth hormone therapy for people with thalassaemia.

Cochrane Database Syst Rev 2017 09 18;9:CD012284. Epub 2017 Sep 18.

Jeffrey Cheah School of Medicine and Health Sciences, Monash University Malaysia, Johor Bahru, Malaysia.

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http://dx.doi.org/10.1002/14651858.CD012284.pub2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353149PMC
September 2017

3-Methylglutaconic aciduria, a frequent but underrecognized finding in carbamoyl phosphate synthetase I deficiency.

Clin Chim Acta 2017 Aug 17;471:95-100. Epub 2017 May 17.

Department of Human Genetics, Technical University Munich, Munich, Germany; Institute of Human Genetics, Helmholtz Zentrum, Neuherberg, Germany; Department of Pediatrics, Salzburger Landeskliniken (SALK) and Paracelsus Medical University (PMU), Salzburg, Austria. Electronic address:

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http://dx.doi.org/10.1016/j.cca.2017.05.023DOI Listing
August 2017

Effects of sharing information on drug administration errors in pediatric wards: a pre-post intervention study.

Ther Clin Risk Manag 2017 23;13:345-353. Epub 2017 Mar 23.

Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.2147/TCRM.S128504DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5367452PMC
March 2017

Methylmalonic Aciduria: A Treatable Disorder of Which Adult Neurologists Need to Be Aware.

Mov Disord Clin Pract 2016 Jan-Feb;3(1):104-105. Epub 2015 Sep 16.

Division of Neurology and the Mah Pooi Soo & Tan Chin Nam Center for Parkinson's & Related Disorders University of Malaya Kuala Lumpur Malaysia.

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http://dx.doi.org/10.1002/mdc3.12237DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6353345PMC
September 2015

Birth defects registries in the genomics era: challenges and opportunities for developing countries.

Authors:
Meow-Keong Thong

Front Pediatr 2014 16;2:60. Epub 2014 Jun 16.

Department of Paediatrics, Faculty of Medicine, University of Malaya , Kuala Lumpur , Malaysia.

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http://dx.doi.org/10.3389/fped.2014.00060DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4058635PMC
July 2014

Genetic counseling services and development of training programs in Malaysia.

J Genet Couns 2013 Dec 25;22(6):911-6. Epub 2013 Apr 25.

Department of Medical Social Work, University Malaya Medical Centre, 59100, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1007/s10897-013-9589-zDOI Listing
December 2013

Genetic counseling/consultation in South-East Asia: a report from the workshop at the 10th Asia pacific conference on human genetics.

J Genet Couns 2013 Dec 19;22(6):917-24. Epub 2013 Sep 19.

School of English, The University of Hong Kong, Faculty of Arts, Centennial Campus, the University of Hong Kong, Room 738, 7/F, Run Run Shaw Tower (Building B, Arts) Pokfulam Road, Hong Kong SAR, China,

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http://dx.doi.org/10.1007/s10897-013-9646-7DOI Listing
December 2013

Neural tube defects in Malaysia: data from the Malaysian National Neonatal Registry.

J Trop Pediatr 2013 Oct 12;59(5):338-42. Epub 2013 Apr 12.

Faculty of Medicine and Health Sciences, Universiti Tunku Abdul Rahman, 43000 Kajang, Selangor, Malaysia.

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http://dx.doi.org/10.1093/tropej/fmt026DOI Listing
October 2013

Current diagnosis and management of mucopolysaccharidosis VI in the Asia-Pacific region.

Mol Genet Metab 2012 Sep 20;107(1-2):136-44. Epub 2012 Jul 20.

Department of Pediatrics and Medical Genetics, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei 100, Taiwan.

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http://dx.doi.org/10.1016/j.ymgme.2012.07.019DOI Listing
September 2012

A tribute to Keiko Kobayashi and her work on citrin deficiency.

Authors:
Meow-Keong Thong

Mol Genet Metab 2012 Apr 10;105(4):551-2. Epub 2012 Jan 10.

Genetics & Metabolism Unit, Department of Pediatrics, University of Malaya, 50603 Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1016/j.ymgme.2012.01.003DOI Listing
April 2012

Genetic counseling for patients and families with hereditary breast and ovarian cancer in a developing Asian country: an observational descriptive study.

Fam Cancer 2011 Jun;10(2):199-205

Cancer Research Initiatives Foundation, 2nd Floor Outpatient Centre, Sime Darby Medical Centre, 1 Jalan SS12/1A, 47500 Subang Jaya, Selangor, Malaysia.

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http://link.springer.com/content/pdf/10.1007/s10689-011-9420
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http://link.springer.com/10.1007/s10689-011-9420-7
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http://dx.doi.org/10.1007/s10689-011-9420-7DOI Listing
June 2011

Adenylosuccinate lyase deficiency in a Malaysian patient, with novel adenylosuccinate lyase gene mutations.

J Inherit Metab Dis 2010 Dec 23;33 Suppl 3:S159-62. Epub 2010 Feb 23.

Biochemical Genetic Unit, Department of Genetics, Kuala Lumpur Hospital, Jalan Pahang 50586, Malaysia.

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http://dx.doi.org/10.1007/s10545-010-9056-zDOI Listing
December 2010

Large BRCA1 and BRCA2 genomic rearrangements in Malaysian high risk breast-ovarian cancer families.

Breast Cancer Res Treat 2010 Nov 9;124(2):579-84. Epub 2010 Jul 9.

Cancer Research Initiatives Foundation, Sime Darby Medical Centre, 2nd Floor, Outpatient Centre, 1 Jalan SS12/1A, Subang Jaya, 47500, Selangor, Malaysia.

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http://dx.doi.org/10.1007/s10549-010-1018-5DOI Listing
November 2010

Spectrum of inherited metabolic disorders in Malaysia.

Ann Acad Med Singapore 2008 Dec;37(12 Suppl):66-5

Genetics & Metabolism Unit, Department of Paediatrics, University of Malaya, Kuala Lumpur, Malaysia.

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December 2008

Prenatal detection of birth defects in a Malaysian population: estimation of the influence of termination of pregnancy on birth prevalence in a developing country.

Aust N Z J Obstet Gynaecol 2006 Feb;46(1):55-7

Paediatric Department, Royal College of Medicine Perak, Ipoh, Perak, Malaysia.

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http://dx.doi.org/10.1111/j.1479-828X.2006.00516.xDOI Listing
February 2006

Characterisation of beta-globin gene mutations in Malaysian children: a strategy for the control of beta-thalassaemia in a developing country.

J Trop Pediatr 2005 Dec 20;51(6):328-33. Epub 2005 Jun 20.

Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1093/tropej/fmi052DOI Listing
December 2005

Diagnosis and management of Duchenne muscular dystrophy in a developing country over a 10-year period.

Dev Med Child Neurol 2005 Jul;47(7):474-7

Department of Paediatrics, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1017/s0012162205000915DOI Listing
July 2005

Further delineation of Al-Gazali syndrome (multiple skeletal abnormalities with anterior segment anomalies of the eye and early lethality) in a Malaysian family.

Clin Dysmorphol 2005 Jan;14(1):1-5

Genetics Unit, Department of Paediatrics, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.

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http://dx.doi.org/10.1097/00019605-200501000-00001DOI Listing
January 2005