Zobrazeno 1 - 10
of 166
pro vyhledávání: '"Gardiner, R.M"'
Autor:
Windemuth, C, Schulz, H, Saar, K, Gennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Nabbout-Tarantino, R, Prud'homme, J.-F, Dulac, O, Bate, L, Gardiner, R.M, Lindhout, D, Wienker, T.F, Janz, D, Sander, T *
Publikováno v:
In Epilepsy Research 2002 51(1):23-29
Autor:
Gardiner, R.M.
Publikováno v:
Neurological Sciences. Sep2000 Supplement 1, Vol. 21, pS15. 5p.
Autor:
Sander, T., Windemuth, C., Schultz, H., Saar, K., Gennaro, E., Bianchi, A., Zara, F., Bulteau, C., Kaminska, A., Ville, D., Cieuta, C., Prud'homme, J.F., Dulac, O., Bate, L., Gardiner, R.M., Haan, G.J., Janssen, G.A.M.A.J., Witte, J., Halley, D.J.J., Lindhout, D., Wienker, T.F., Janz, D., The European Consortium on the Genetics of Idiopathic Generalized Epilepsy: participating clinicians: Kjeldsen M.J., Friis M.L.
Publikováno v:
Sander, T, Windemuth, C, Schultz, H, Saar, K, Gennaro, E, Bianchi, A, Zara, F, Bulteau, C, Kaminska, A, Ville, D, Cieuta, C, Prud'homme, J F, Dulac, O, Bate, L, Gardiner, R M, Haan, G J, Janssen, G A M A J, Witte, J, Halley, D J J, Lindhout, D, Wienker, T F, Janz, D & The European Consortium on the Genetics of Idiopathic Generalized Epilepsy: participating clinicians: Kjeldsen M.J., Friis M.L. 2002, ' No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1 ', American Journal of Medical Genetics. Part A, vol. 114, no. 6, pp. 673-678 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::221e8f562d682c1e260882f3c10bd9aa
https://portal.findresearcher.sdu.dk/da/publications/81e1e300-a8af-11dc-9626-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/81e1e300-a8af-11dc-9626-000ea68e967b
Autor:
Taske, N.L., Williamson, M.P., Makoff, A., Bate, L., Curtis, D., Kerr, M., Kjeldsen, Marianne Juel, Pang, K.A., Sundqvist, A., Friis, M.L., Chadwich, D., Richens, A., Covanis, A., Santos, M., Arzimanuglou, A., Panayiotopoulos, C.P., Whitehouse, W.P., Rees, M., Gardiner, R.M..
Publikováno v:
Taske, N L, Williamson, M P, Makoff, A, Bate, L, Curtis, D, Kerr, M, Kjeldsen, M J, Pang, K A, Sundqvist, A, Friis, M L, Chadwich, D, Richens, A, Covanis, A, Santos, M, Arzimanuglou, A, Panayiotopoulos, C P, Whitehouse, W P, Rees, M & Gardiner, R M 2002, ' Evaluation of the positional candidate gene CHRNA7 at the juvenile myoclonic epilepsy locus (EJM2) on chromosome 15q13-14 ', Epilepsy Research, vol. 49, pp. 157-172 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::c46fc5646e0a825567775fb8d0a90bde
https://portal.findresearcher.sdu.dk/da/publications/8d250a90-6fcf-11db-81a9-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/8d250a90-6fcf-11db-81a9-000ea68e967b
Autor:
Robinson, R., Taske, N., Heils, A., Sander, T., Whitehouse, W., Goutières, F., Aicardi, J., Lehesjoki, A.-E., Friis, M.L., Kjeldsen, M.J., Panayiotopoulos, C., Kennedy, C., Ferrie, C., Rees, M., Gardiner, R.M..
Publikováno v:
Robinson, R, Taske, N, Heils, A, Sander, T, Whitehouse, W, Goutières, F, Aicardi, J, Lehesjoki, A-E, Friis, M L, Kjeldsen, M J, Panayiotopoulos, C, Kennedy, C, Ferrie, C, Rees, M & Gardiner, R M 2002, ' Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8q ', Epilepsy Research, vol. 48, pp. 169-179 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::5f7b93e0031153f1d4f0142151b0f5ca
https://portal.findresearcher.sdu.dk/da/publications/8ce91300-6fcf-11db-81a9-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/8ce91300-6fcf-11db-81a9-000ea68e967b
Autor:
Maiti, A.K., Bartoloni, L., Mitchison, H.M., Meeks, M., Chung, E., Spiden, S., Gehrig, C., Rossier, C., DeLozier-Blanchet, C.D., Blouin, J.-L., Gardiner, R.M., Antonarakis, S.E.
Publikováno v:
Cytogenetic & Genome Research; 2000, Vol. 90 Issue 1/2, p119-122, 4p
Publikováno v:
Nucleic Acids Research; 12/15/1989, Vol. 17 Issue 24, p10223-10229, 7p
Autor:
Gardiner, R.M.
Publikováno v:
Current Paediatrics; June 2002, Vol. 12 Issue: 3 p238-243, 6p
Autor:
Mitchell, W.A., Wheeler, R.B., Sharp, J.D., Bate, S.L., Gardiner, R.M., Ranta, U.S., Lonka, L., Williams, R.E., Lehesjoki, A.E., Mole, S.E.
Publikováno v:
European Journal of Paediatric Neurology; January 2001, Vol. 5 Issue: Supplement 1 p21-27, 7p
Autor:
Fehaid, E.L., Meeks, M., Cheehab, M., Walne, A., Al-Dabbagh, M., Spiden, S., Mussaggi-Georgy, H., O'Rawe, A., Blau, H., Mitchison, H.M., Polak-Charcon, S., Gardiner, R.M., Chung, E., Simpson, H., Hamam, H.D.
Publikováno v:
Journal of Medical Genetics (JMG); April 1, 2000, Vol. 37 Issue: 4 p241-244, 4p