Publications

Found 12 results

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Journal Article
Angelman syndrome: correlations between epilepsy phenotypes and genotypes., Minassian, B. A., DeLorey T. M., Olsen R. W., Philippart M., Bronstein Y., Zhang Q., Guerrini R., Van Ness P., Livet M. O., and Delgado-Escueta A. V. , Annals of neurology, 1998 Apr, Volume 43, Issue 4, p.485-93, (1998) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9546330?dopt=Abstract

Cortical myoclonus in Angelman syndrome., Guerrini, R., DeLorey T. M., Bonanni P., Moncla A., Dravet C., Suisse G., Livet M. O., Bureau M., Malzac P., Genton P., et al. , Annals of neurology, 1996 Jul, Volume 40, Issue 1, p.39-48, (1996) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8687190?dopt=Abstract

Early clinical and EEG features of infantile spasms in Down syndrome., Silva, M. L., Cieuta C., Guerrini R., Plouin P., Livet M. O., and Dulac O. , Epilepsia, 1996 Oct, Volume 37, Issue 10, p.977-82, (1996) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8822696?dopt=Abstract

Early-onset benign occipital seizure susceptibility syndrome., Ferrie, C. D., Beaumanoir A., Guerrini R., Kivity S., Vigevano F., Takaishi Y., Watanabe K., Mira L., Capizzi G., Costa P., et al. , Epilepsia, 1997 Mar, Volume 38, Issue 3, p.285-93, (1997) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9070590?dopt=Abstract

Epilepsy and focal gyral anomalies detected by MRI: electroclinico-morphological correlations and follow-up., Guerrini, R., Dravet C., Raybaud C., Roger J., Bureau M., Battaglia A., Livet M. O., Gambarelli D., and Robain O. , Developmental medicine and child neurology, 1992 Aug, Volume 34, Issue 8, p.706-18, (1992) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/1644233?dopt=Abstract

Epilepsy, antiepileptic drugs, and malformations in children of women with epilepsy: a French prospective cohort study., Dravet, C., Julian C., Legras C., Magaudda A., Guerrini R., Genton P., Soulayrol S., Giraud N., Mesdjian E., and Trentin G. , Neurology, 1992 Apr, Volume 42, Issue 4 Suppl 5, p.75-82, (1992) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/1574181?dopt=Abstract

Identification and characterization of three calmodulin binding sites of the skeletal muscle ryanodine receptor., Menegazzi, P., Larini F., Treves S., Guerrini R., Quadroni M., and Zorzato F. , Biochemistry, 1994 Aug 9, Volume 33, Issue 31, p.9078-84, (1994) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8049209?dopt=Abstract

Ketamine in refractory convulsive status epilepticus in children avoids endotracheal intubation., Ilvento, Lucrezia, Rosati Anna, Marini Carla, L'Erario Manuela, Mirabile Lorenzo, and Guerrini Renzo , Epilepsy & behavior : E&B, 2015 Jul 16, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/26189786?dopt=Abstract

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain., Ross, M. E., Allen K. M., Srivastava A. K., Featherstone T., Gleeson J. G., Hirsch B., Harding B. N., Andermann E., Abdullah R., Berg M., et al. , Human molecular genetics, 1997 Apr, Volume 6, Issue 4, p.555-62, (1997) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/9097958?dopt=Abstract

Mutations of protocadherin 19 in female epilepsy (PCDH19-FE) lead to allopregnanolone deficiency., Tan, Chuan, Shard Chloe, Ranieri Enzo, Hynes Kim, Pham Duyen H., Leach Damian, Buchanan Grant, Corbett Mark, Shoubridge Cheryl, Kumar Raman, et al. , Human molecular genetics, 2015 Jun 29, (2015) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/26123493?dopt=Abstract

Neurological findings and seizure outcome in children with bilateral opercular macrogyric-like changes detected by MRI., Guerrini, R., Dravet C., Raybaud C., Roger J., Bureau M., Battaglia A., Livet M. O., Colicchio G., and Robain O. , Developmental medicine and child neurology, 1992 Aug, Volume 34, Issue 8, p.694-705, (1992) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/1644232?dopt=Abstract

X-linked malformations of neuronal migration., Dobyns, W. B., Andermann E., Andermann F., Czapansky-Beilman D., Dubeau F., Dulac O., Guerrini R., Hirsch B., Ledbetter D. H., Lee N. S., et al. , Neurology, 1996 Aug, Volume 47, Issue 2, p.331-9, (1996) Abstract

http://www.ncbi.nlm.nih.gov/pubmed/8757001?dopt=Abstract