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Pornprot Limprasert

Research Profile

Disorders

Geographic Areas

Thailand

Chemicals & Drugs

Concepts & Ideas

Pedigree

Procedures

Living Beings

Infants

Genes & Molecular Sequences

Alleles

Physiology

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Publications

TOP 3
Utcharee Intusoma; Supachai Janjindamai; Fadell Hayeeduereh; Apasri Lusawat; Oradawan Plong-On; Thanya Sripo; Sasipa Thammongkol; Punnee Vasiknanonte; Anannit Visudtibhan; Pornprot Limprasert
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity.
Marjanu Hikmah Elias; Ravindran Ankathil; Abdul Razak Salmi; Wanna Sudhikaran; Pornprot Limprasert; Bin Alwi Zilfalil
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.
Sinitdhorn Rujirabanjerd; Kobkul Tongsippunyoo; Thanya Sripo; Pornprot Limprasert
Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.

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All Publications

2011: Utcharee Intusoma; Supachai Janjindamai; Fadell Hayeeduereh; Apasri Lusawat; Oradawan Plong-On; Thanya Sripo; Sasipa Thammongkol; Punnee Vasiknanonte; Anannit Visudtibhan; Pornprot Limprasert
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2011;15(5):432-8.
2011: Marjanu Hikmah Elias; Ravindran Ankathil; Abdul Razak Salmi; Wanna Sudhikaran; Pornprot Limprasert; Bin Alwi Zilfalil
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction.
Genetic testing and molecular biomarkers 2011;15(6):387-93.
2007: Sinitdhorn Rujirabanjerd; Kobkul Tongsippunyoo; Thanya Sripo; Pornprot Limprasert
Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand.
European journal of medical genetics 2007;50(5):346-54.
2007: Sinitdhorn Rujirabanjerd; Warapong Suwannarat; Thanya Sripo; Pathikan Dissaneevate; Wutichai Permsirivanich; Pornprot Limprasert
De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardation.
American journal of medical genetics. Part A 2007;143(3):271-6.
2006: Yuxin Fan; Pornprot Limprasert; Ian V J Murray; Annette C Smith; Virginia M-Y Lee; John Q Trojanowski; Bryce L Sopher; Albert R La Spada
Beta-synuclein modulates alpha-synuclein neurotoxicity by reducing alpha-synuclein protein expression.
Human molecular genetics 2006;15(20):3002-11.
2005: Chariyawan Charalsawadi; Thanya Sripo; Pornprot Limprasert
Multiplex methylation specific PCR analysis of fragile X syndrome: experience in Songklanagarind Hospital.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2005;88(8):1057-61.
2004: Chitkasaem Suwanrath-Kengpol; Pornprot Limprasert; Winyou Mitarnun
Prenatal diagnosis of deletion of chromosome 6p presenting with hydrops fetalis.
Prenatal diagnosis 2004;24(11):887-9.
2004: Somchit Jaruratanasirikul; Somkiat Soponthammarak; Prasin Chanvitan; Pornprot Limprasert; Hutcha Sriplung; Wipawan Leelasamran; Seesuda Winothai
Clinical abnormalities, intervention program, and school attendance of Down syndrome children in southern Thailand.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2004;87(10):1199-204.
2004: H Ohtake; Pornprot Limprasert; Y Fan; Osamu Onodera; Akiyoshi Kakita; Hidenobu Takahashi; Lauren T Bonner; Debby W Tsuang; Ian V J Murray; Virginia M-Y Lee; John Q Trojanowski; A Ishikawa; J Idezuka; M Murata; T Toda; Thomas D Bird; James B Leverenz; Shoji Tsuji; Albert R La Spada
Beta-synuclein gene alterations in dementia with Lewy bodies.
Neurology 2004;63(5):805-11.
2003: Lauren T Bonner; Debby W Tsuang; Monique M Cherrier; Charisma J Eugenio; Q Du Jennifer; Ellen J Steinbart; Pornprot Limprasert; Albert R La Spada; Benjamin Seltzer; Thomas D Bird; James B Leverenz
Familial dementia with Lewy bodies with an atypical clinical presentation.
Journal of geriatric psychiatry and neurology 2003;16(1):59-64.
2002: Debby W Tsuang; Aaron M Dalan; Charisma J Eugenio; Parvoneh Poorkaj-Navas; Pornprot Limprasert; Albert R La Spada; Ellen J Steinbart; Thomas D Bird; James B Leverenz
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 families.
Archives of neurology 2002;59(10):1622-30.
2001: Koki Yamada; Pornprot Limprasert; Mansing Ratanasukon; Supaporn Tengtrisorn; J Yingchareonpukdee; Punnee Vasiknanonte; T Kitaoka; Mohsen Ghadami; Norio Niikawa; Tatsuya Kishino
Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier.
American journal of medical genetics 2001;100(1):52-5.
2001: Pornprot Limprasert; Vannarat Saechan; Nichara Ruangdaraganon; Thanyachai Sura; P Vasiknanote; Somchit Jaruratanasirikul; W Ted Brown
Haplotype analysis at the FRAXA locus in Thai subjects.
American journal of medical genetics 2001;98(3):224-9.
2000: Pornprot Limprasert; Somchit Jaruratanasirikul; Punnee Vasiknanonte
Unilateral macroorchidism in fragile X syndrome.
American journal of medical genetics 2000;95(5):516-7.
2000: Pornprot Limprasert; Nichara Ruangdaraganon; Punnee Vasiknanonte; Thanyachai Sura; Somchit Jaruratanasirikul; N Sriwongpanich; Hutcha Sriplung
A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2000;83(10):1260-6.
2000: Nichara Ruangdaraganon; Pornprot Limprasert; Thanyachai Sura; Tasnawat Sombuntham; N Sriwongpanich; Naiphinich Kotchabhakdi
Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital.
Journal of the Medical Association of Thailand = Chotmaihet thangphaet 2000;83(1):69-76.
1999: Pornprot Limprasert; Nanbert Zhong; Julia R Currie; W Ted Brown
Possible founder effects for FRAXE alleles.
American journal of medical genetics 1999;84(3):286-90.
1999: Pornprot Limprasert; Nichara Ruangdaraganon; Thanyachai Sura; Punnee Vasiknanonte; U Jinorose
Molecular screening for fragile X syndrome in Thailand.
The Southeast Asian journal of tropical medicine and public health 1999;30 Suppl 2():114-8.
1997: Pornprot Limprasert; Nanbert Zhong; Carl Dobkin; W Ted Brown
Polymorphism of FXR1 showing lack of association with autism.
American journal of medical genetics 1997;74(4):453-4.
1997: U Jinorose; Punnee Vasiknanonte; Pornprot Limprasert; W Ted Brown; V Panich
The frequency of fragile X syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods.
The Southeast Asian journal of tropical medicine and public health 1997;28 Suppl 3():69-74.
1996: Sarah L Nolin; F A Lewis; L L Ye; George E Houck; A E Glicksman; Pornprot Limprasert; S Y Li; Nanbert Zhong; A E Ashley; Eleanor Feingold; Stephanie L Sherman; W Ted Brown
Familial transmission of the FMR1 CGG repeat.
American journal of human genetics 1996;59(6):1252-61.

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