Zobrazeno 1 - 10
of 198
pro vyhledávání: '"GARDINER, R M"'
Autor:
Gardiner, R. M.
Publikováno v:
The British Medical Journal, 1978 Aug . 2(6136), 571-571.
Externí odkaz:
https://www.jstor.org/stable/25428779
Autor:
GOODFRIEND, ARTHUR, ARISMAN, F. H., HOUSTON, ELSIE, COLE, R. G., ORPE, GUNHILD, JR., HENRY ECKHARDT, GIESELER, MARGARETA, PETTINGILL, ALBERT G., FAGAN, MYRON C., JR., AFFONSO PENNA, PULS, ALEXANDER E., HEYN, LOUIS L., HOPKE, HERBERT, EARTH, O. E., LUCKE, JOHN B., GARDINER, R. M., TROTT, W. J. HOWARD
Publikováno v:
TIME Magazine; 11/13/1939, Vol. 34 Issue 20, p2-13, 5p
Autor:
Kjeldsen, Marianne Juel, Chioza, B., Everett, K., Ashauer, H., Brouwer, O., Callenback, P., Covanis, A., Dulac, O., Durner, M., Eeg-Olofsson, O., Feucht, M., Friis, Mogens Laue, Heils, A., Larsson, K., Lehesjoki, A. E., Nabbout, R., Olsson, I., Sander, T., Sirén, A., Robinson, R., Rees, M., Gardiner, R. M.
Publikováno v:
Kjeldsen, M J, Chioza, B, Everett, K, Ashauer, H, Brouwer, O, Callenback, P, Covanis, A, Dulac, O, Durner, M, Eeg-Olofsson, O, Feucht, M, Friis, M L, Heils, A, Larsson, K, Lehesjoki, A E, Nabbout, R, Olsson, I, Sander, T, Sirén, A, Robinson, R, Rees, M & Gardiner, R M 2006, ' Evaluation of CACNA1H in European patients with childhood abscence epilepsy ', Epilepsy Research, vol. 69, pp. 177-181 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::42e81c83ece17f0b9b8bd0ab8b0fd1f9
https://portal.findresearcher.sdu.dk/da/publications/bd972180-602f-11dc-9480-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/bd972180-602f-11dc-9480-000ea68e967b
Autor:
Elmslie, F. V., Williamson, M. P., Rees, M., Kerr, M., Kjeldsen, M. J., Pang, K. A., Sundqvist, A., Friis, M. L., Richens, A., Chadwick, D., Whitehouse, W. P., Gardiner, R. M.
Linkage analysis in separately ascertained families of probands with juvenile myoclonic epilepsy (JME) has previously provided evidence both for and against the existence of a locus (designated "EJM1"), on chromosome 6p, predisposing to a trait defin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d45e8d4d00e71d3e1e61f1f19b384510
https://europepmc.org/articles/PMC1914914/
https://europepmc.org/articles/PMC1914914/
Autor:
BAKER, G. F., BARRETT, ANNA M., VAN VILET, JAMES, SALOMON, IRVING, LEMANSKY, JULIUS, WELLES, BERRY, BURNHAM JR., W. A., CRUICKSHANK, j.s, GARDINER, R. M., BERGH, ANN, BAILEY, E.L.
Publikováno v:
TIME Magazine; 6/26/1933, Vol. 21 Issue 26, p3-6, 3p
mtDNA encodes subunits of the electron transport chain and is exclusively maternally inherited in mammals. It has been suggested that mtDNA might be the site of some of the mutations causing a group of human disorders called the "mitochondrial myopat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8afd060e2ad7adce7b5e7157c02435c6
https://europepmc.org/articles/PMC1682963/
https://europepmc.org/articles/PMC1682963/
Autor:
Wallace, R H, Hodgson, B L, Grinton, B E, Gardiner, R M, Robinson, R, Rodriguez-Casero, V, Sadleir, L, Morgan, J, Harkin, L A, Dibbens, L M, Yamamoto, T, Andermann, E, Mulley, J C, Berkovic, S F, Scheffer, I E
Publikováno v:
Neurology; 2003 Sep 23, Vol. 61 Issue 6, p765-769, 5p
Autor:
Meeks, M., Walne, A., Spiden, S., Simpson, H., Mussaffi-Georgy, H., Hamam, H. D., Fehaid, E. L., Cheehab, M., Al-Dabbagh, M., Polak-Charcon, S., Blau, H., O'Rawe, A., Mitchison, H. M., Gardiner, R. M., Chung, E.
Publikováno v:
Journal of Medical Genetics; Apr2000, p241-244, 4p, 2 Diagrams, 1 Chart