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Results: 1-9 |
Results: 9
'Mitotic drive' of expanded CTG repeats in myotonic dystrophy type 1 (DM1)
Authors: Khajavi, M Tari, AM Patel, NB Tsuji, K Siwak, DR Meistrich, ML Terry, NHA Ashizawa, T
Citation: M. Khajavi et al., 'Mitotic drive' of expanded CTG repeats in myotonic dystrophy type 1 (DM1), HUM MOL GEN, 10(8), 2001, pp. 855-863
Alcohol dehydrogenase polymorphism and Parkinson's disease
Authors: Tan, EK Nagamitsu, S Matsuura, T Khajavi, M Jankovic, J Ondo, W Ashizawa, T
Citation: Ek. Tan et al., Alcohol dehydrogenase polymorphism and Parkinson's disease, NEUROSCI L, 305(1), 2001, pp. 70-72
Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
Authors: Matsuura, T Yamagata, T Burgess', DL Rasmussen, A Grewal, RP Watase, K Khajavi, M McCall, AE Davis, CF Zu, L Achari, M Pulst, SM Alonso, E Noebels, JL Nelson, DL Zoghbi, HY Ashizawa, T
Citation: T. Matsuura et al., Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10, NAT GENET, 26(2), 2000, pp. 191-194
Variability and validity of polymorphism association studies in Parkinson's disease
Authors: Tan, EK Khajavi, M Thornby, JI Nagamitsu, S Jankovic, J Ashizawa, T
Citation: Ek. Tan et al., Variability and validity of polymorphism association studies in Parkinson's disease, NEUROLOGY, 55(4), 2000, pp. 533-538
A "dystrophic" variant of autosomal recessive myotonia congenita caused bynovel mutations in the CLCN1 gene
Authors: Nagamitsu, S Matsuura, T Khajavi, M Armstrong, R Gooch, C Harati, Y Ashizawa, T
Citation: S. Nagamitsu et al., A "dystrophic" variant of autosomal recessive myotonia congenita caused bynovel mutations in the CLCN1 gene, NEUROLOGY, 55(11), 2000, pp. 1697-1703
New nomenclature and DNA testing guidelines for myotonic dystrophy type 1(DM1)
Authors: Gonzalez, I Ohsawa, N Singer, RH Devillers, M Ashizawa, T Balasubramanyam, A Cooper, TA Khajavi, M Lia-Baldini, AS Miller, G Philips, AV Timchenko, LT Waring, J Yamagata, H Barbet, JP Klesert, TR Tapscott, SJ Roses, AD Wagner, M Baiget, M Martorell, L Browne, GB Eymard, B Gourdon, G Junien, C Seznec, H Carey, N Gosling, M Maire, P Gennarelli, M Sato, S Ansved, T Kvist, U Eriksson, M Furling, D Chen, EJ Housman, DE Luciano, B Siciliano, M Spring, N Shimizu, M Eddy, E Morris, GE Krahe, R Furuya, H Adelman, J Pribnow, D Furutama, D Mathieu, J Hilton-Jones, D Kinoshita, M Abbruzzese, C Sinden, RR Wells, RD Pearson, CE Kobayashi, T Johansson, A Salvatori, S Perryman, B Swanson, MS Gould, FK Harris, SE Johnson, K Mitchell, AM Monckton, DG Winchester, CL Antonini, G Day, JW Liquori, C Ranum, LPW Westerlaken, J Wieringa, B Griffith, JD Michalowski, S Moore, H Hamshere, M Korade, Z Thornton, CA Jaeger, H Lehmann, F Moorman, JR Mounsey, JP Mahadevan, MS
Citation: I. Gonzalez et al., New nomenclature and DNA testing guidelines for myotonic dystrophy type 1(DM1), NEUROLOGY, 54(6), 2000, pp. 1218-1221
Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?
Authors: Tan, EK Matsuura, T Nagamitsu, S Khajavi, M Jankovic, J Ashizawa, T
Citation: Ek. Tan et al., Polymorphism of NACP-Rep1 in Parkinson's disease: An etiologic link with essential tremor?, NEUROLOGY, 54(5), 2000, pp. 1195-1198
Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy
Authors: Matsuura, T Achari, M Khajavi, M Bachinski, LL Zoghbi, HY Ashizawa, T
Citation: T. Matsuura et al., Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy, ANN NEUROL, 45(3), 1999, pp. 407-411
The G209A mutation in the alpha-synuclein gene is not detected in familialcases of Parkinson disease in non-Greek and/or Italian populations
Authors: Wang, WW Khajavi, M Patel, BJ Beach, J Jankovic, J Ashizawa, T
Citation: Ww. Wang et al., The G209A mutation in the alpha-synuclein gene is not detected in familialcases of Parkinson disease in non-Greek and/or Italian populations, ARCH NEUROL, 55(12), 1998, pp. 1521-1523
Risultati: 1-9 |