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Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives

Hong Kong medical journal = Xianggang yi xue za zhi, 2019-02, Vol.25 (1), p.21-29

2019

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Identification of RASSF1A modulated genes in nasopharyngeal carcinoma

Oncogene, 2006-01, Vol.25 (2), p.310-316

2006

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A frequent activated smoothened mutation in sporadic basal cell carcinomas

Oncogene, 1999-01, Vol.18 (3), p.833-836

1999

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Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria

Kidney international, 2006-01, Vol.69 (1), p.123-128

2006

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Poor blood pressure control and its associated factors among older people with hypertension: A cross-sectional study in six public primary care clinics in Malaysia

Malaysian family physician, 2015, Vol.10 (1), p.19-25

2015

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The Accuracy of Mother's Touch to Detect Fever in Children: A Systematic Review

Journal of tropical pediatrics (1980), 2008-02, Vol.54 (1), p.70-73

2008

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Effect of Soil Burial on Mechanical Properties of Bamboo Fiber Reinforced Epoxy Composites

IOP conference series. Materials Science and Engineering, 2020-01, Vol.736 (5), p.52016

2020

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Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase gene

Neurology, 2003-02, Vol.60 (4), p.715-717

2003

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The roles of men in family planning - a study of married men at the UKM primary care clinic

Malaysian family physician, 2017, Vol.12 (1), p.2-13

2017

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Electrochemical Wastewater Disinfection: Identification of Its Principal Germicidal Actions

Journal of environmental engineering (New York, N.Y.), 2004-10, Vol.130 (10), p.1217-1221

2004

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MECP2 mutation in male patients with non-specific X-linked mental retardation

FEBS letters, 2000-09, Vol.481 (3), p.285-288

2000

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Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

Journal of medical genetics, 2000-12, Vol.37 (12), p.e41-41

2000

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Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese

Molecular genetics and metabolism, 2010-04, Vol.99 (4), p.431-433

2010

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Validity and reliability of the Malay version of the Hill-Bone compliance to high blood pressure therapy scale for use in primary healthcare settings in Malaysia: A cross-sectional study

Malaysian family physician, 2015, Vol.10 (2), p.36-44

2015

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Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC

Clinical chemistry (Baltimore, Md.), 2001-02, Vol.47 (2), p.343-346

2001

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Pantothenate kinase-associated neurodegeneration in two Chinese children: identification of a novel PANK2 gene mutation

Hong Kong medical journal = Xianggang yi xue za zhi, 2008-02, Vol.14 (1), p.70-73

2008

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Definition of the correct sequence in the donor splice site of intron 2 in the human glucose 6-phosphate translocase gene

FEBS letters, 1999-02, Vol.445 (2), p.449-450

1999

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Rarity of debrisoquine hydroxylase gene polymorphism in chinese patients with Parkinson's disease

Movement disorders, 1998-05, Vol.13 (3), p.529-532

1998

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Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness

Neurology, 2001-09, Vol.57 (6), p.1121-1124

2001

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Renewable Energy Generation by Full-Scale Biomass Gasification System Using Agricultural and Forestal Residues

Practice periodical of hazardous, toxic, and radioactive waste management, 2007-07, Vol.11 (3), p.177-183

2007

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Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a

Clinical genetics, 1998-03, Vol.53 (3), p.184-190

1998

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Gene symbol: BCHE

Human genetics, 2007-04, Vol.121 (2), p.288-288

2007

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Intention to seek professional help for depression and its associated factors among elderly patients in Tenkera Health Clinic, Melaka, Malaysia

Medical journal of Malaysia, 2021-01, Vol.76 (1), p.61-67

2021

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Mutation of Proline 409 to Arginine in the Meander Region of Cytochrome P450c17 Causes Severe 17α-Hydroxylase Deficiency

Molecular genetics and metabolism, 2001-03, Vol.72 (3), p.254-259

2001

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Factors Associated with Successful Fasting among Type 2 Diabetic Mellitus Patients during Ramadan: A Retrospective Recall Study

Medicine & health (Kuala Lumpur, Malaysia), 2019-12, Vol.14 (2), p.97-108

Shing Ni, Leow

2019

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Sudden arrhythmia death syndrome in young victims: a five-year retrospective review and two-year prospective molecular autopsy study by next-generation sequencing and clinical evaluation of their first-degree relatives

Identification of RASSF1A modulated genes in nasopharyngeal carcinoma

A frequent activated smoothened mutation in sporadic basal cell carcinomas

Heterogeneous mutations in the SLC3A1 and SLC7A9 genes in Chinese patients with cystinuria

Poor blood pressure control and its associated factors among older people with hypertension: A cross-sectional study in six public primary care clinics in Malaysia

The Accuracy of Mother's Touch to Detect Fever in Children: A Systematic Review

Effect of Soil Burial on Mechanical Properties of Bamboo Fiber Reinforced Epoxy Composites

Juvenile-onset glycogen storage disease type II with novel mutations in acid alpha-glucosidase gene

The roles of men in family planning - a study of married men at the UKM primary care clinic

Electrochemical Wastewater Disinfection: Identification of Its Principal Germicidal Actions

MECP2 mutation in male patients with non-specific X-linked mental retardation

Spectrum of mutations in the MECP2 gene in patients with infantile autism and Rett syndrome

Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese

Validity and reliability of the Malay version of the Hill-Bone compliance to high blood pressure therapy scale for use in primary healthcare settings in Malaysia: A cross-sectional study

Novel mutation and polymorphisms of the HMBS gene detected by denaturing HPLC

Pantothenate kinase-associated neurodegeneration in two Chinese children: identification of a novel PANK2 gene mutation

Definition of the correct sequence in the donor splice site of intron 2 in the human glucose 6-phosphate translocase gene

Rarity of debrisoquine hydroxylase gene polymorphism in chinese patients with Parkinson's disease

Atypical presentation of dopa-responsive dystonia: generalized hypotonia and proximal weakness

Renewable Energy Generation by Full-Scale Biomass Gasification System Using Agricultural and Forestal Residues

Glucose-6-phosphatase gene (727G→T) splicing mutation is prevalent in Hong Kong Chinese patients with glycogen storage disease type 1a

Gene symbol: BCHE

Intention to seek professional help for depression and its associated factors among elderly patients in Tenkera Health Clinic, Melaka, Malaysia

Mutation of Proline 409 to Arginine in the Meander Region of Cytochrome P450c17 Causes Severe 17α-Hydroxylase Deficiency

Factors Associated with Successful Fasting among Type 2 Diabetic Mellitus Patients during Ramadan: A Retrospective Recall Study

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