Correction of some misprints in our paper
- 作者P. Erdős; P. Vértesi
- 卷第38卷
- 印刷ISSN0236-5294
- 电子ISSN1588-2632
- 文件大小34.59KB
- 发表时间1981
- DOI10.1007/bf01917541
- 页码263-263
Case 18-2013Cabot, Richard C.; Harris, Nancy Lee; Rosenberg, Eric S.; Shepard, Jo-Anne O.; Cort, Alice M.; Ebeling, Sally H.; McDonald, Emily K.; Cole, Andrew J.; Eskandar, Emad; Mela, Theofanie; Noebels, Jeffrey L.; Gonzalez, R. Gilberto; McGuone, Declan · New England Journal of Medicine · 2013
PERSISTENT HYPERSYNCHRONIZATION OF NEOCORTICAL NEURONS IN THE <i>MOCHA</i> MUTANT OF MOUSENoebels, J. L.; Sidman, R. L. · Journal of Neurogenetics · 2007
Persistent Hypersynchronization of Neocortical Neurons in the Mocha Mutant of MouseNoebels, J. L.; Sidman, R. L. · Journal of Neurogenetics · 1989
Epilepsy in mice deficient in the 65-kDa isoform of glutamic acid decarboxylaseKash, S. F.; Johnson, R. S.; Tecott, L. H.; Noebels, J. L.; Mayfield, R. D.; Hanahan, D.; Baekkeskov, S. · Proceedings of the National Academy of Sciences · 1997
Inherited epilepsy: spike-wave and focal motor seizures in the mutant mouse totteringNoebels, J.; Sidman, R. · Science · 1979
Sensorineural Deafness and Seizures in Mice Lacking Vesicular Glutamate Transporter 3Rebecca P. Seal; Omar Akil; Eunyoung Yi; Christopher M. Weber; Lisa Grant; Jong Yoo; Amanda Clause; Karl Kandler; Jeffrey L. Noebels; Elisabeth Glowatzki; Lawrence R. Lustig; Robert H. Edwards · 2008
ILAE Genetics Commission Conference Report: Molecular Analysis of Complex Genetic EpilepsiesILAE Genetics Commission; E. Anderson; S. Berkovic; O. Dulac; M. Gardiner; S. Jain; M. Laue-Friis; D. Lindhout; J. Noebels; R. Ottman; A. Scaramelli; J. Serratosa; O. Steinlein; G. Avanzini; J. Bailey-Wilson; L. Cardon; R. Fischbach; K. Gwinn-Hardy; M. Leppert; J. Ott; K. Lindblad-Toh; K. Weiss · 2002