Pornprot limprasert
Pornprot limprasert
Faculty of Medicine, KMITL
Підтверджена електронна адреса в
Familial transmission of the FMR1 CGG repeat.
SL Nolin, FA Lewis 3rd, LL Ye, GE Houck Jr, AE Glicksman, P Limprasert, ...
American journal of human genetics 59 (6), 1252, 1996
β-synuclein gene alterations in dementia with Lewy bodies
H Ohtake, P Limprasert, Y Fan, O Onodera, A Kakita, H Takahashi, ...
Neurology 63 (5), 805-811, 2004
β-synuclein modulates α-synuclein neurotoxicity by reducing α-synuclein protein expression
Y Fan, P Limprasert, IVJ Murray, AC Smith, VMY Lee, JQ Trojanowski, ...
Human molecular genetics 15 (20), 3002-3011, 2006
Familial dementia with lewy bodies: a clinical and neuropathological study of 2 families
DW Tsuang, AM Dalan, CJ Eugenio, P Poorkaj, P Limprasert, ...
Archives of neurology 59 (10), 1622-1630, 2002
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
P Limprasert, N Nouri, RA Heyman, C Nopparatana, M Kamonsilp, ...
Human molecular genetics 5 (2), 207-213, 1996
De novo subtelomeric deletion of 15q associated with satellite translocation in a child with developmental delay and severe growth retardation
S Rujirabanjerd, W Suwannarat, T Sripo, P Dissaneevate, ...
American Journal of Medical Genetics Part A 143 (3), 271-276, 2007
Familial dementia with Lewy bodies with an atypical clinical presentation
LT Bonner, DW Tsuang, MM Cherrier, CJ Eugenio, JQ Du, EJ Steinbart, ...
Journal of geriatric psychiatry and neurology 16 (1), 59-64, 2003
HLA-B* 15: 21 and carbamazepine-induced Stevens-Johnson syndrome: pooled-data and in silico analysis
K Jaruthamsophon, V Tipmanee, A Sangiemchoey, C Sukasem, ...
Scientific reports 7 (1), 1-7, 2017
Mutation screening of the CDKL5 gene in cryptogenic infantile intractable epilepsy and review of clinical sensitivity
U Intusoma, F Hayeeduereh, O Plong-On, T Sripo, P Vasiknanonte, ...
european journal of paediatric neurology 15 (5), 432-438, 2011
Two Thai families with Norrie disease (ND): association of two novel missense mutations with severe ND phenotype, seizures, and a manifesting carrier
K Yamada, P Limprasert, M Ratanasukon, S Tengtrisorn, ...
American journal of medical genetics 100 (1), 52-55, 2001
Mutation screening of the neurexin 1 gene in thai patients with intellectual disability and autism spectrum disorder
S Yangngam, O Plong-On, T Sripo, R Roongpraiwan, T Hansakunachai, ...
Genetic testing and molecular biomarkers 18 (7), 510-515, 2014
Comparative studies of the CAG repeats in the spinocerebellar ataxia type 1 (SCA1) gene
P Limprasert, N Nouri, C Nopparatana, PL Deininger, BJB Keats
American journal of medical genetics 74 (5), 488-493, 1997
A New Method for FMR1 Gene Methylation Screening by Multiplex Methylation-Specific Real-Time Polymerase Chain Reaction
MH Elias, R Ankathil, AR Salmi, W Sudhikaran, P Limprasert, BA Zilfalil
Genetic testing and molecular biomarkers 15 (6), 387-393, 2011
A case with a ring chromosome 13 in a cohort of 203 children with non-syndromic autism and review of the cytogenetic literature
C Charalsawadi, W Maisrikhaw, V Praphanphoj, J Wirojanan, ...
Cytogenetic and genome research 144 (1), 1-8, 2014
Mutation screening of the Aristaless-related homeobox (ARX) gene in Thai pediatric patients with delayed development: first report from Thailand
S Rujirabanjerd, K Tongsippunyoo, T Sripo, P Limprasert
European journal of medical genetics 50 (5), 346-354, 2007
Clinical abnormalities, intervention program, and school attendance of Down syndrome children in southern Thailand
E Unit
J Med Assoc Thai 87 (10), 1199-204, 2004
Haplotype analysis at the FRAXA locus in Thai subjects
P Limprasert, V Saechan, N Ruangdaraganon, T Sura, P Vasiknanote, ...
American journal of medical genetics 98 (3), 224-229, 2001
Significant changes in plasma alpha-Synuclein and Beta-Synuclein levels in male children with autism Spectrum disorder
W Sriwimol, P Limprasert
BioMed research international 2018, 2018
A genome wide pattern of population structure and admixture in peninsular Malaysia Malays
WI Hatin, A Etemad, W Jin, P Qin, S Xu, L Jin, SG Tan, P Limprasert, ...
The HUGO journal 8 (1), 1-18, 2014
Novel compound heterozygous mutations in the TRAPPC9 gene in two siblings with autism and intellectual disability
A Hnoonual, P Graidist, S Kritsaneepaiboon, P Limprasert
Frontiers in genetics 10, 61, 2019
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Статті 1–20