Guerrini R - Search Results

1

Profiling PI3K-AKT-MTOR variants in focal brain malformations reveals new insights for diagnostic care.

Pirozzi F, Berkseth M, Shear R, Gonzalez L, Timms AE, Sulc J, Pao E, Oyama N, Forzano F, Conti V, Guerrini R, Doherty ES, Saitta SC, Lockwood CM, Pritchard CC, Dobyns WB, Novotny E, Wright JNN, Saneto RP, Friedman S, Hauptman J, Ojemann J, Kapur RP, Mirzaa GM. Pirozzi F, et al. Among authors: guerrini r. Brain. 2022 Apr 29;145(3):925-938. doi: 10.1093/brain/awab376. Brain. 2022. PMID: 35355055 Free PMC article.

2

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.

3

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.

4

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.

5

Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.

Guerrini R, Dobyns WB. Guerrini R, et al. Neurology. 1998 Aug;51(2):499-503. doi: 10.1212/wnl.51.2.499. Neurology. 1998. PMID: 9710025

6

Epilepsy and malformations of the cerebral cortex.

Guerrini R, Canapicchi R, Dobyns WB. Guerrini R, et al. Neurologia. 1999 May;14 Suppl 3:32-47. Neurologia. 1999. PMID: 10379165 Review.

7

Cortical dysplasias, genetics, and epileptogenesis.

Guerrini R, Andermann E, Avoli M, Dobyns WB. Guerrini R, et al. Adv Neurol. 1999;79:95-121. Adv Neurol. 1999. PMID: 10514808 Review. No abstract available.

8

Genetic and neuroradiological heterogeneity of double cortex syndrome.

Gleeson JG, Luo RF, Grant PE, Guerrini R, Huttenlocher PR, Berg MJ, Ricci S, Cusmai R, Wheless JW, Berkovic S, Scheffer I, Dobyns WB, Walsh CA. Gleeson JG, et al. Among authors: guerrini r. Ann Neurol. 2000 Feb;47(2):265-9. Ann Neurol. 2000. PMID: 10665503

9

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome.

Guerrini R, Barkovich AJ, Sztriha L, Dobyns WB. Guerrini R, et al. Neurology. 2000 Feb 22;54(4):909-13. doi: 10.1212/wnl.54.4.909. Neurology. 2000. PMID: 10690985

10

Familial perisylvian polymicrogyria: a new familial syndrome of cortical maldevelopment.

Guerreiro MM, Andermann E, Guerrini R, Dobyns WB, Kuzniecky R, Silver K, Van Bogaert P, Gillain C, David P, Ambrosetto G, Rosati A, Bartolomei F, Parmeggiani A, Paetau R, Salonen O, Ignatius J, Borgatti R, Zucca C, Bastos AC, Palmini A, Fernandes W, Montenegro MA, Cendes F, Andermann F. Guerreiro MM, et al. Among authors: guerrini r. Ann Neurol. 2000 Jul;48(1):39-48. Ann Neurol. 2000. PMID: 10894214

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