Guerrini R - Search Results

1

Nonsyndromic mental retardation and cryptogenic epilepsy in women with doublecortin gene mutations.

Guerrini R, Moro F, Andermann E, Hughes E, D'Agostino D, Carrozzo R, Bernasconi A, Flinter F, Parmeggiani L, Volzone A, Parrini E, Mei D, Jarosz JM, Morris RG, Pratt P, Tortorella G, Dubeau F, Andermann F, Dobyns WB, Das S. Guerrini R, et al. Ann Neurol. 2003 Jul;54(1):30-7. doi: 10.1002/ana.10588. Ann Neurol. 2003. PMID: 12838518

2

Infantile spasms: an early epileptic manifestation in some patients with the congenital bilateral perisylvian syndrome.

Kuzniecky R, Andermann F, Guerrini R. Kuzniecky R, et al. Among authors: guerrini r. J Child Neurol. 1994 Oct;9(4):420-3. doi: 10.1177/088307389400900418. J Child Neurol. 1994. PMID: 7822736

3

Congenital bilateral perisylvian syndrome: study of 31 patients. The CBPS Multicenter Collaborative Study.

Kuzniecky R, Andermann F, Guerrini R. Kuzniecky R, et al. Among authors: guerrini r. Lancet. 1993 Mar 6;341(8845):608-12. doi: 10.1016/0140-6736(93)90363-l. Lancet. 1993. PMID: 8094839

4

The epileptic spectrum in the congenital bilateral perisylvian syndrome. CBPS Multicenter Collaborative Study.

Kuzniecky R, Andermann F, Guerrini R. Kuzniecky R, et al. Among authors: guerrini r. Neurology. 1994 Mar;44(3 Pt 1):379-85. doi: 10.1212/wnl.44.3_part_1.379. Neurology. 1994. PMID: 8145902

5

Cortical myoclonus in Angelman syndrome.

Guerrini R, De Lorey TM, Bonanni P, Moncla A, Dravet C, Suisse G, Livet MO, Bureau M, Malzac P, Genton P, Thomas P, Sartucci F, Simi P, Serratosa JM. Guerrini R, et al. Ann Neurol. 1996 Jul;40(1):39-48. doi: 10.1002/ana.410400109. Ann Neurol. 1996. PMID: 8687190

6

X-linked malformations of neuronal migration.

Dobyns WB, Andermann E, Andermann F, Czapansky-Beilman D, Dubeau F, Dulac O, Guerrini R, Hirsch B, Ledbetter DH, Lee NS, Motte J, Pinard JM, Radtke RA, Ross ME, Tampieri D, Walsh CA, Truwit CL. Dobyns WB, et al. Among authors: guerrini r. Neurology. 1996 Aug;47(2):331-9. doi: 10.1212/wnl.47.2.331. Neurology. 1996. PMID: 8757001 Review.

7

Bilateral parasagittal parietooccipital polymicrogyria and epilepsy.

Guerrini R, Dubeau F, Dulac O, Barkovich AJ, Kuzniecky R, Fett C, Jones-Gotman M, Canapicchi R, Cross H, Fish D, Bonanni P, Jambaqué I, Andermann F. Guerrini R, et al. Ann Neurol. 1997 Jan;41(1):65-73. doi: 10.1002/ana.410410112. Ann Neurol. 1997. PMID: 9005867

8

Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.

Ross ME, Allen KM, Srivastava AK, Featherstone T, Gleeson JG, Hirsch B, Harding BN, Andermann E, Abdullah R, Berg M, Czapansky-Bielman D, Flanders DJ, Guerrini R, Motté J, Mira AP, Scheffer I, Berkovic S, Scaravilli F, King RA, Ledbetter DH, Schlessinger D, Dobyns WB, Walsh CA. Ross ME, et al. Among authors: guerrini r. Hum Mol Genet. 1997 Apr;6(4):555-62. doi: 10.1093/hmg/6.4.555. Hum Mol Genet. 1997. PMID: 9097958

9

Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.

Fink JM, Dobyns WB, Guerrini R, Hirsch BA. Fink JM, et al. Among authors: guerrini r. Am J Hum Genet. 1997 Aug;61(2):379-87. doi: 10.1086/514863. Am J Hum Genet. 1997. PMID: 9311743 Free PMC article.

10

Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome.

Dobyns WB, Guerrini R, Czapansky-Beilman DK, Pierpont ME, Breningstall G, Yock DH Jr, Bonanni P, Truwit CL. Dobyns WB, et al. Among authors: guerrini r. Neurology. 1997 Oct;49(4):1042-7. doi: 10.1212/wnl.49.4.1042. Neurology. 1997. PMID: 9339687 Review.

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