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Role of Urinary Neutrophil Gelatinase–Associated Lipocalin for Predicting the Severity of Renal Functions in Patients With Autosomal-Dominant Polycystic Kidney Disease

Transplantation proceedings, 2017-06, Vol.49 (5), p.950-954

2017

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Genetic variant screening of MC3R and MC4R genes in early-onset obese children and their relatives among a Thai population: family-based study

Genetics and molecular research, 2015-12, Vol.14 (4), p.18090-18102

2015

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Association between rs155971 in the PCSK1 gene and the lipid profile of obese Thai children: a family-based study

Genetics and molecular research, 2015-08, Vol.14 (3), p.9136-9144

2015

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The first study of plasma voriconazole concentration in Thai patient with invasive aspergillosis

International journal of infectious diseases, 2014-04, Vol.21 (S1), p.36-36

2014

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High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals

Clinical genetics, 2004-11, Vol.66 (5), p.452-460

2004

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AOSP36 PREVALENCE OF DMMR IN SPORADIC COLORECTAL CANCER PATIENTS AT SIRIRAJ HOSPITAL

European journal of cancer (1990), 2013-03, Vol.49, p.S19-S19

2013

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PO19-WE-14 Analysis of homozygous deletions in SMN1 of Thai SMA patients and the use of DHPLC-based technique for SMN1 copy number determination

Journal of the neurological sciences, 2009, Vol.285, p.S268-S268

2009

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PO19-WE-15 Molecular study of ATP7B gene mutations in Thai patients with Wilson disease

Journal of the neurological sciences, 2009, Vol.285, p.S269-S269

2009

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PO19-WE-08 Clinical and electrophysiological features in Thai patients with Kennedy's disease

Journal of the neurological sciences, 2009, Vol.285, p.S267-S267

2009

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Influence of CYP2D6, CYP3A5, ABCB1, APOE polymorphisms and nongenetic factors on donepezil treatment in patients with Alzheimer's disease and vascular dementia

Pharmacogenomics and personalized medicine, 2019-01, Vol.12, p.209-224

2019

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An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of theRMRP gene associated with chondrodysplasia and severe immunodeficiency

Journal of applied genetics, 2010-12, Vol.51 (4), p.523-528

2010

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An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of the RMRP gene associated with chondrodysplasia and severe immunodeficiency

Journal of applied genetics, 2010, Vol.51 (4), p.523

2010

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Identification of a novel mutation in APP gene in a Thai subject with early-onset Alzheimer's disease

Neuropsychiatric disease and treatment, 2018-01, Vol.14, p.3015-3023

2018

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An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy

European journal of neurology, 2005-05, Vol.12 (5), p.388-391

2005

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Cardiac disease in Costello syndrome

Pediatrics (Evanston), 1998-04, Vol.101 (4 Pt 1), p.706-708

1998

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Genetic testing for renal diseases: Medical and ethical considerations

American journal of kidney diseases, 1998-12, Vol.32 (6), p.934-945

1998

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Pharmacokinetics and safety of a new paediatric fixed-dose combination of zidovudine/lamivudine/ nevirapine in HIV-infected children

Antiviral therapy, 2011-01, Vol.16 (8), p.1287-1295

2011

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Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridia

Molecular vision, 2011, Vol.17, p.1305-1309

2011

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A Novel Mutation in the β-Subunit of the Epithelial Sodium Channel Gene (SCNNIB) in a Thai Family with Liddle's Syndrome

Journal of Pediatric Endocrinology and Metabolism, 2009, Vol.22 (1), p.85-90

2009

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Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literature

Prenatal diagnosis, 2005-03, Vol.25 (3), p.210-215

2005

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Association between ADAM33 polymorphisms and asthma in a Thai population

Asian Pacific journal of allergy and immunology, 2008-12, Vol.26 (4), p.205

2008

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Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian population

Haematologica (Roma), 2006-05, Vol.91 (5), p.675

2006

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Hemoglobin pakse: Presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism

International journal of hematology, 2004-08, Vol.80 (2), p.136-139

2004

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Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis

American journal of medical genetics, 2005-02, Vol.133A (1), p.103-105

2005

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Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome

Genes chromosomes & cancer, 1998-02, Vol.21 (2), p.113-118

1998

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Role of Urinary Neutrophil Gelatinase–Associated Lipocalin for Predicting the Severity of Renal Functions in Patients With Autosomal-Dominant Polycystic Kidney Disease

Genetic variant screening of MC3R and MC4R genes in early-onset obese children and their relatives among a Thai population: family-based study

Association between rs155971 in the PCSK1 gene and the lipid profile of obese Thai children: a family-based study

The first study of plasma voriconazole concentration in Thai patient with invasive aspergillosis

High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals

AOSP36 PREVALENCE OF DMMR IN SPORADIC COLORECTAL CANCER PATIENTS AT SIRIRAJ HOSPITAL

PO19-WE-14 Analysis of homozygous deletions in SMN1 of Thai SMA patients and the use of DHPLC-based technique for SMN1 copy number determination

PO19-WE-15 Molecular study of ATP7B gene mutations in Thai patients with Wilson disease

PO19-WE-08 Clinical and electrophysiological features in Thai patients with Kennedy's disease

Influence of CYP2D6, CYP3A5, ABCB1, APOE polymorphisms and nongenetic factors on donepezil treatment in patients with Alzheimer's disease and vascular dementia

An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of theRMRP gene associated with chondrodysplasia and severe immunodeficiency

An infant with cartilage-hair hypoplasia due to a novel homozygous mutation in the promoter region of the RMRP gene associated with chondrodysplasia and severe immunodeficiency

Identification of a novel mutation in APP gene in a Thai subject with early-onset Alzheimer's disease

An unusual family with Leber's hereditary optic neuropathy and facioscapulohumeral muscular dystrophy

Cardiac disease in Costello syndrome

Genetic testing for renal diseases: Medical and ethical considerations

Pharmacokinetics and safety of a new paediatric fixed-dose combination of zidovudine/lamivudine/ nevirapine in HIV-infected children

Run-on mutation in the PAX6 gene and chorioretinal degeneration in autosomal dominant aniridia

A Novel Mutation in the β-Subunit of the Epithelial Sodium Channel Gene (SCNNIB) in a Thai Family with Liddle's Syndrome

Ectrodactyly-ectodermal dysplasia-clefting (EEC) syndrome presenting with a large nephrogenic cyst, severe oligohydramnios and hydrops fetalis: a case report and review of the literature

Association between ADAM33 polymorphisms and asthma in a Thai population

Mutations of AML1 in non-M0 acute myeloid leukemia: six novel mutations and a high incidence of cooperative events in a South-east Asian population

Hemoglobin pakse: Presence on red blood cell membrane and detection by polymerase chain reaction-single-strand conformational polymorphism

Novel contributions to the Asian CFTR mutation spectrum: Genotype and phenotype in Thai patients with cystic fibrosis

Deletion 10q23.2-q23.33 in a patient with gastrointestinal juvenile polyposis and other features of a Cowden-like syndrome

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