Beta-synuclein gene alterations in dementia with Lewy bodies
Ohtake, H, Limprasert, P, Fan, Y, Onodera, O, Kakita, A, Takahashi, H, Bonner, L T, Tsuang, D W, Murray, I V J, Lee, V M-Y, Trojanowski, J Q, Ishikawa, A, Idezuka, J, Murata, M, Toda, T, Bird, T D, Leverenz, J B, Tsuji, S, La Spada, A R
Published in Neurology (14.09.2004)
Published in Neurology (14.09.2004)
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Journal Article
Familial transmission of the FMR1 CGG repeat
NOLIN, S. L, LEWIS, F. A, SHERMAN, S. L, BROWN, W. T, LING LING YE, HOUCK, G. E, GLICKSMAN, A. E, LIMPRASERT, P, SHU YUN LI, ZHONG, N, ASHLEY, A. E, FEINGOLD, E
Published in American journal of human genetics (01.12.1996)
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Published in American journal of human genetics (01.12.1996)
Journal Article
A new method for FMR1 gene methylation screening by multiplex methylation-specific real-time polymerase chain reaction
Elias, Marjanu Hikmah, Ankathil, Ravindran, Salmi, Abdul Razak, Sudhikaran, Wanna, Limprasert, Pornprot, Zilfalil, Bin Alwi
Published in Genetic testing and molecular biomarkers (01.06.2011)
Published in Genetic testing and molecular biomarkers (01.06.2011)
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Journal Article
Prenatal diagnosis of deletion of chromosome 6p presenting with hydrops fetalis
Suwanrath‐Kengpol, Chitkasaem, Limprasert, Pornprot, Mitarnun, Winyou
Published in Prenatal diagnosis (01.11.2004)
Published in Prenatal diagnosis (01.11.2004)
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Journal Article
Autism
J Wirojanan, J Sangkool, P Limprasert
Published in Journal of Health Science and Medical Research (JHSMR) (01.08.2006)
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Published in Journal of Health Science and Medical Research (JHSMR) (01.08.2006)
Journal Article
Familial dementia with Lewy bodies with an atypical clinical presentation
Bonner, Lauren T, Tsuang, Debby W, Cherrier, Monique M, Eugenio, Charisma J, Du Jennifer, Q, Steinbart, Ellen J, Limprasert, Pornprot, La Spada, Albert R, Seltzer, Benjamin, Bird, Thomas D, Leverenz, James B
Published in Journal of geriatric psychiatry and neurology (01.03.2003)
Published in Journal of geriatric psychiatry and neurology (01.03.2003)
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Journal Article
Analysis of CAG Repeat of the Machado-Joseph Gene in Human, Chimpanzee and Monkey Populations: A Variant Nucleotide is Associated with the Number of CAG Repeats
Limprasert, Pornprot, Nouri, Nassim, Heyman, Rock A., Nopparatana, Chamnong, Kamonsilp, Mahatana, Deininger, Prescott L., Keats, Bronya J. B.
Published in Human molecular genetics (01.02.1996)
Published in Human molecular genetics (01.02.1996)
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Journal Article
A clinical checklist for fragile X syndrome: screening of Thai boys with developmental delay of unknown cause
Limprasert, P, Ruangdaraganon, N, Vasiknanonte, P, Sura, T, Jaruratanasirikul, S, Sriwongpanich, N, Sriplung, H
Published in Journal of the Medical Association of Thailand (01.10.2000)
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Published in Journal of the Medical Association of Thailand (01.10.2000)
Journal Article
Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene
Limprasert, P, Nouri, N, Nopparatana, C, Deininger, P L, Keats, B J
Published in American journal of medical genetics (19.09.1997)
Published in American journal of medical genetics (19.09.1997)
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Journal Article
Prevalence and clinical characteristics of fragile X syndrome at child development clinic, Ramathibodi Hospital
Ruangdaraganon, N, Limprasert, P, Sura, T, Sombuntham, T, Sriwongpanich, N, Kotchabhakdi, N
Published in Journal of the Medical Association of Thailand (01.01.2000)
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Published in Journal of the Medical Association of Thailand (01.01.2000)
Journal Article
Analysis of CAG repeat of the Machado-Joseph gene in human, chimpanzee and monkey populations : a variant nucleoside is associated with the number of CAG repeats
LIMPRASERT, P, NASSIM NOURI, HEYMAN, R. A, CHAMNONG NOPPARATANA, MAHATANA KAMONSILP, DEININGER, P. L, KEATS, B. J. B
Published in Human molecular genetics (1996)
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Published in Human molecular genetics (1996)
Journal Article
Familial Dementia With Lewy Bodies: A Clinical and Neuropathological Study of 2 Families
Tsuang, Debby W, Dalan, Aaron M, Eugenio, Charisma J, Poorkaj, Parvonah, Limprasert, Pornprot, La Spada, Albert R, Steinbart, Ellen J, Bird, Thomas D, Leverenz, James B
Published in Archives of neurology (Chicago) (01.10.2002)
Published in Archives of neurology (Chicago) (01.10.2002)
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Journal Article
The frequency of Fragile X Syndrome among selected patients at Songklanagarind Hospital during 1991-1996, studied by cytogenetic and molecular methods
JINOROSE, U, VASIKNANONTE, P, LIMPRASERT, P, BROWN, W. T, PANICH, V
Published in Southeast Asian journal of tropical medicine and public health (1997)
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Published in Southeast Asian journal of tropical medicine and public health (1997)
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Journal Article
Unilateral macroorchidism in fragile X syndrome
Limprasert, P, Jaruratanasirikul, S, Vasiknanonte, P
Published in American journal of medical genetics (18.12.2000)
Published in American journal of medical genetics (18.12.2000)
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Journal Article
Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier
Yamada, K, Limprasert, P, Ratanasukon, M, Tengtrisorn, S, Yingchareonpukdee, J, Vasiknanonte, P, Kitaoka, T, Ghadami, M, Niikawa, N, Kishino, T
Published in American journal of medical genetics (15.04.2001)
Published in American journal of medical genetics (15.04.2001)
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Journal Article
Haplotype analysis at the FRAXA locus in Thai subjects
Limprasert, P, Saechan, V, Ruangdaraganon, N, Sura, T, Vasiknanote, P, Jaruratanasirikul, S, Brown, W T
Published in American journal of medical genetics (22.01.2001)
Published in American journal of medical genetics (22.01.2001)
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Journal Article
Possible founder effects for FRAXE alleles
Limprasert, P, Zhong, N, Currie, J R, Brown, W T
Published in American journal of medical genetics (28.05.1999)
Published in American journal of medical genetics (28.05.1999)
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Journal Article
Polymorphism of FXR1 showing lack of association with autism
Limprasert, P, Zhong, N, Dobkin, C, Brown, W T
Published in American journal of medical genetics (25.07.1997)
Published in American journal of medical genetics (25.07.1997)
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Journal Article