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List of works by Teeratorn Pulkes

Analysis of SCA8, SCA10, SCA12, SCA17 and SCA19 in patients with unknown spinocerebellar ataxia: a Thai multicentre study.

scientific article published on 15 September 2015

Association between apolipoprotein E genotypes and Parkinson's disease

scientific article published on 22 July 2011

CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand ⬇️

scientific article published on August 30, 2010

Clinical Characteristics of HIV-Associated Optic Neuritis

scientific article published on 11 November 2020

Clinical analysis of adult-onset spinocerebellar ataxias in Thailand.

scientific article

Confirmation of the association between LRRK2 R1628P variant and susceptibility to Parkinson's disease in the Thai population.

scientific article

Diagnostic utility of NMO/AQP4-IgG in evaluating CNS inflammatory disease in Thai patients.

scientific article

Electrophysiological and immunological study in myasthenia gravis: Diagnostic sensitivity and correlation ⬇️

scientific article published on March 17, 2011

Etiologies of Acute Optic Neuritis in Thailand: An Observational Study of 171 Patients

scientific article published on 30 September 2020

Evaluation of Retinal Nerve Fiber Layer and Ganglion Cell Layer Thickness in Alzheimer's Disease Using Optical Coherence Tomography

scientific article published on 02 October 2020

Frequencies of LRRK2 variants in Thai patients with Parkinson's disease: evidence for an R1628P founder

scientific article published on 22 June 2010

Glucocerebrosidase mutations in Thai patients with Parkinson's disease

scientific article published on 23 June 2014

Idiopathic hypertrophic cranial pachymeningitis.

scientific article published on 30 January 2008

Increased risk of stroke in patients with the A12308G polymorphism in mitochondria

scientific article published on 01 December 2000

Long-term effectiveness of acetazolamide on permanent weakness in hyperkalemic periodic paralysis

scientific article

Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patients.

scientific article published in May 2011

New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation.

scientific article published in May 2005

Paroxysmal neuromyotonia: a new sporadic channelopathy

scientific article published on 03 February 2012

Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship.

scientific article published in March 2011

Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction

scientific article published on 07 March 2012

The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS

article

Trinucleotide repeat expansion of TATA-binding protein gene associated with Parkinson's disease: A Thai multicenter study

scientific article

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