Nabbout R - Search Results

1

A novel locus for generalized epilepsy with febrile seizures plus in French families.

Baulac S, Gourfinkel-An I, Couarch P, Depienne C, Kaminska A, Dulac O, Baulac M, LeGuern E, Nabbout R. Baulac S, et al. Among authors: nabbout r. Arch Neurol. 2008 Jul;65(7):943-51. doi: 10.1001/archneur.65.7.943. Arch Neurol. 2008. PMID: 18625863

2

Vigabatrin in partial seizures in children.

Nabbout RC, Chiron C, Mumford J, Dumas C, Dulac O. Nabbout RC, et al. J Child Neurol. 1997 Apr;12(3):172-7. doi: 10.1177/088307389701200304. J Child Neurol. 1997. PMID: 9130090 Clinical Trial.

3

The right brain hemisphere is dominant in human infants.

Chiron C, Jambaque I, Nabbout R, Lounes R, Syrota A, Dulac O. Chiron C, et al. Among authors: nabbout r. Brain. 1997 Jun;120 ( Pt 6):1057-65. doi: 10.1093/brain/120.6.1057. Brain. 1997. PMID: 9217688

4

Early diagnosis of subependymal giant cell astrocytoma in children with tuberous sclerosis.

Nabbout R, Santos M, Rolland Y, Delalande O, Dulac O, Chiron C. Nabbout R, et al. J Neurol Neurosurg Psychiatry. 1999 Mar;66(3):370-5. doi: 10.1136/jnnp.66.3.370. J Neurol Neurosurg Psychiatry. 1999. PMID: 10084537 Free PMC article.

5

Pyridoxine dependent epilepsy: a suggestive electroclinical pattern.

Nabbout R, Soufflet C, Plouin P, Dulac O. Nabbout R, et al. Arch Dis Child Fetal Neonatal Ed. 1999 Sep;81(2):F125-9. doi: 10.1136/fn.81.2.f125. Arch Dis Child Fetal Neonatal Ed. 1999. PMID: 10448181 Free PMC article.

6

A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31.

Cormier-Daire V, Dagoneau N, Nabbout R, Burglen L, Penet C, Soufflet C, Desguerre I, Munnich A, Dulac O. Cormier-Daire V, et al. Among authors: nabbout r. Am J Hum Genet. 2000 Oct;67(4):991-3. doi: 10.1086/303087. Epub 2000 Sep 7. Am J Hum Genet. 2000. PMID: 10978228 Free PMC article.

7

Genetic predisposition to severe myoclonic epilepsy in infancy.

Benlounis A, Nabbout R, Feingold J, Parmeggiani A, Guerrini R, Kaminska A, Dulac O. Benlounis A, et al. Among authors: nabbout r. Epilepsia. 2001 Feb;42(2):204-9. Epilepsia. 2001. PMID: 11240590 Free article.

8

A locus for simple pure febrile seizures maps to chromosome 6q22-q24.

Nabbout R, Prud'homme JF, Herman A, Feingold J, Brice A, Dulac O, LeGuern E. Nabbout R, et al. Brain. 2002 Dec;125(Pt 12):2668-80. doi: 10.1093/brain/awf281. Brain. 2002. PMID: 12429594

9

Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancy.

Nabbout R, Gennaro E, Dalla Bernardina B, Dulac O, Madia F, Bertini E, Capovilla G, Chiron C, Cristofori G, Elia M, Fontana E, Gaggero R, Granata T, Guerrini R, Loi M, La Selva L, Lispi ML, Matricardi A, Romeo A, Tzolas V, Valseriati D, Veggiotti P, Vigevano F, Vallée L, Dagna Bricarelli F, Bianchi A, Zara F. Nabbout R, et al. Neurology. 2003 Jun 24;60(12):1961-7. doi: 10.1212/01.wnl.0000069463.41870.2f. Neurology. 2003. PMID: 12821740

10

Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy.

Nabbout R, Kozlovski A, Gennaro E, Bahi-Buisson N, Zara F, Chiron C, Bianchi A, Brice A, Leguern E, Dulac O. Nabbout R, et al. Epilepsy Res. 2003 Oct;56(2-3):127-33. doi: 10.1016/j.eplepsyres.2003.08.007. Epilepsy Res. 2003. PMID: 14642997

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