Association between apolipoprotein E genotypes and Parkinson’s disease von Pulkes, T, Papsing, C, Mahasirimongkol, S, Busabaratana, M, Kulkantrakorn, K, Tiamkao, S

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Mutation and haplotype analysis of oculopharyngeal muscular dystrophy in Thai patients von Pulkes, T, Papsing, C, Busabaratana, M, Dejthevaporn, C, Witoonpanich, R

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P34-18 Electrophysiological and immunological tests in myasthenia gravis: Their diagnostic sensitivities and correlation von Dejthevaporn, C, Witoonpanich, R, Sriphrapradang, A, Pulkes, T

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CTG repeat lengths of the DMPK gene in myotonic dystrophy patients compared to healthy controls in Thailand von Theerasasawat, S, Papsing, C, Pulkes, T

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Human mitochondrial DNA diseases von Pulkes, T, Hanna, M G

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Phenotypic heterogeneity in a large Thai slow-channel congenital myasthenic syndrome kinship: Correction von Witoonpanich, R, Pulkes, T, Dejthevaporn, C, Witoonpanich, P, Yodnopklao, P, Wetchaphanphesat, S, Brengman, J, Engel, A.G

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P2.39 Mutation of alpha subunit of acetylcholine receptor causing slow-channel congenital myasthenic syndrome in a Thai family von Witoonpanich, R, Pulkes, T, Dejthevaporn, C, Yodnopklao, P, Witoonpanich, P, Wetchaphanphesat, S, Brengman, J, Engel, A

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Increased risk of stroke in patients with the A12308G polymorphism in mitochondria von Pulkes, T, Sweeney, MG, Hanna, MG

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Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance von PULKES, T, LIOLITSA, D, WILLS, A. J, HARGREAVES, I, HEALES, S, HANNA, M. G

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New phenotypic diversity associated with the mitochondrial tRNA(SerUCN) gene mutation von Pulkes, T, Liolitsa, D, Eunson, L H, Rose, M, Nelson, I P, Rahman, S, Poulton, J, Marchington, D R, Landon, D N, Debono, A G, Morgan-Hughes, J A, Hanna, M G

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Evaluation of Retinal Nerve Fiber Layer and Ganglion Cell Layer Thickness in Alzheimer's Disease Using Optical Coherence Tomography von Jindahra, Panitha, Hengsiri, Nitchanan, Witoonpanich, Pirada, Poonyathalang, Anuchit, Pulkes, Teeratorn, Tunlayadechanont, Supoch, Thadanipon, Kunlawat, Vanikieti, Kavin

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Radiological Characteristics of Extraocular Muscles in Myasthenia Gravis Patients with Ocular Manifestations: A Case-Control Study von Lueangaram, Sirin, Tritanon, Oranan, Siriyotha, Sukanya, Vanikieti, Kavin, Padungkiatsagul, Tanyatuth, Preechawat, Pisit, Poonyathalang, Anuchit, Dejthevaporn, Charungthai, Pulkes, Teeratorn, Tunlayadechanont, Supoch, Jindahra, Panitha

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Restricted diffusion of the optic nerve in NMO optic neuritis von Jindahra, P., Tritanon, O., Savangned, P., Chokthaweesak, W., Vanikieti, K., Preechawat, P., Poonyathalang, A., Apiwattanakul, M., Laothamatas, J., Pulkes, T., Tunlayadechanont, S.

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Etiologies of Acute Optic Neuritis in Thailand: An Observational Study of 171 Patients von Vanikieti, Kavin, Janyaprasert, Pavarut, Lueangram, Sirin, Nimworaphan, Jirat, Rattanathamsakul, Natthapon, Tiraset, Nanida, Chokthaweesak, Wimonwan, Samipak, Narong, Padungkiatsagul, Tanyatuth, Preechawat, Pisit, Poonyathalang, Anuchit, Pulkes, Teeratorn, Tunlayadechanont, Supoch, Siriyotha, Sukanya, Jindahra, Panitha

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Frequencies of LRRK2 variants in Thai patients with Parkinson's disease: evidence for an R1628P founder von Pulkes, Teeratorn, Papsing, Chutima, Mahasirimongkol, Surakameth, Busabaratana, Manisa, Kulkantrakorn, Kongkiat, Tiamkao, Somsak

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Clinical Characteristics of HIV-Associated Optic Neuritis von Jindahra, Panitha, Phuphuakrat, Angsana, Tangjaisanong, Thanapol, Siriyotha, Sukanya, Padungkiatsagul, Tanyatuth, Vanikieti, Kavin, Preechawat, Pisit, Poonyathalang, Anuchit, Sungkanuparph, Somnuek, Pulkes, Teeratorn, Tunlayadechanont, Supoch

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P01.4 Electrophysiological and immunological studies in patients with myasthenia gravis von Witoonpanich, R., Sriphrapradang, A., Pulkes, T.

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The mitochondrial DNA G13513A transition in ND5 is associated with a LHON/MELAS overlap syndrome and may be a frequent cause of MELAS von Pulkes, Teeratorn, Eunson, Louise, Patterson, Victor, Siddiqui, Asra, Wood, Nicholas W., Nelson, Isabelle P., Morgan-Hughes, John A., Hanna, Michael G.

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Classical mitochondrial phenotypes without mtDNA mutations: The possible role of nuclear genes von PULKES, Teeratorn, LIOLITSA, Danae, NELSON, Isabelle P, HANNA, Michael G

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Human mitochondrial DNA diseases: Drug and DNA delivery to mitochondria von PULKES, T, HANNA, M. G

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