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Pediatrics International : Official Journal of the Japan Pediatric Society
|
October 19, 2011
Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia
Nithiwat Vatanavicharn, Somporn Liammongkolkul, Osamu Sakamoto, et al.
Clinical Chemistry and Laboratory Medicine
|
September 18, 2007
Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients
Moltira Promkan, Somporn Teingtat, Atchara Stheinkijkarnchai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 26, 2001
A sensitive and simplified method to analyze free fatty acids in children with mitochondrial beta oxidation disorders using gas chromatography/mass spectrometry and dried blood spots
Masahiko Kimura, Hye Ran Yoon, Pornswan Wasant, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
August 9, 2005
Retrospective study of patients with suspected inborn errors of metabolism at Siriraj Hospital, Bangkok, Thailand (1997-2001)
Pornswan Wasant, Nithiwat Vatanavicharn, Chantragan Srisomsap, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 4, 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
Pornswan Wasant, Carmencita Padilla, Stephen Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 2008
Organic acid disorders detected by urine organic acid analysis: twelve cases in Thailand over three-year experience
Pornswan Wasant, Somporn Liammongkolkul, Chulaluck Kuptanon, et al.
World Journal of Pediatrics : WJP
|
January 28, 2014
Clinical characteristics and mutation analysis of propionic acidemia in Thailand
Nithiwat Vatanavicharn, Somporn Liammongkolkul, Osamu Sakamoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
November 2, 2022
Phenotypic and molecular features of Thai patients with primary carnitine deficiency
Somporn Liammongkolkul, Boonchai Boonyawat, Chodchanok Vijarnsorn, et al.
Pediatric Neurology
|
September 15, 2010
Glutaric aciduria type 2, late onset type in Thai siblings with myopathy
Pornswan Wasant, Chulaluck Kuptanon, Nithiwat Vattanavicharn, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
August 30, 2005
Argininosuccinate synthetase deficiency: mutation analysis in 3 Thai patients
Pornswan Wasant, Vip Viprakasit, Chantragan Srisomsap, et al.
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Search research articles
Search
Showing results (11-20 of 32) with videos related to
Sort By:
Page
of 4
Pediatrics International : Official Journal of the Japan Pediatric Society
|
October 19, 2011
Phenotypic and mutation spectrums of Thai patients with isovaleric acidemia
Nithiwat Vatanavicharn, Somporn Liammongkolkul, Osamu Sakamoto, et al.
Clinical Chemistry and Laboratory Medicine
|
September 18, 2007
Highest accuracy of combined consensus clinical criteria and SNRPN gene molecular markers in diagnosis of Prader-Willi syndrome in Thai patients
Moltira Promkan, Somporn Teingtat, Atchara Stheinkijkarnchai, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 26, 2001
A sensitive and simplified method to analyze free fatty acids in children with mitochondrial beta oxidation disorders using gas chromatography/mass spectrometry and dried blood spots
Masahiko Kimura, Hye Ran Yoon, Pornswan Wasant, et al.
Journal of the Medical Association of Thailand = Chotmaihet Thangphaet
|
August 9, 2005
Retrospective study of patients with suspected inborn errors of metabolism at Siriraj Hospital, Bangkok, Thailand (1997-2001)
Pornswan Wasant, Nithiwat Vatanavicharn, Chantragan Srisomsap, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics
|
May 4, 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
Pornswan Wasant, Carmencita Padilla, Stephen Lam, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 15, 2008
Organic acid disorders detected by urine organic acid analysis: twelve cases in Thailand over three-year experience
Pornswan Wasant, Somporn Liammongkolkul, Chulaluck Kuptanon, et al.
World Journal of Pediatrics : WJP
|
January 28, 2014
Clinical characteristics and mutation analysis of propionic acidemia in Thailand
Nithiwat Vatanavicharn, Somporn Liammongkolkul, Osamu Sakamoto, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society
|
November 2, 2022
Phenotypic and molecular features of Thai patients with primary carnitine deficiency
Somporn Liammongkolkul, Boonchai Boonyawat, Chodchanok Vijarnsorn, et al.
Pediatric Neurology
|
September 15, 2010
Glutaric aciduria type 2, late onset type in Thai siblings with myopathy
Pornswan Wasant, Chulaluck Kuptanon, Nithiwat Vattanavicharn, et al.
The Southeast Asian Journal of Tropical Medicine and Public Health
|
August 30, 2005
Argininosuccinate synthetase deficiency: mutation analysis in 3 Thai patients
Pornswan Wasant, Vip Viprakasit, Chantragan Srisomsap, et al.
Page
of 4