Dobyns WB - Search Results

1

Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy.

Syrbe S, Harms FL, Parrini E, Montomoli M, Mütze U, Helbig KL, Polster T, Albrecht B, Bernbeck U, van Binsbergen E, Biskup S, Burglen L, Denecke J, Heron B, Heyne HO, Hoffmann GF, Hornemann F, Matsushige T, Matsuura R, Kato M, Korenke GC, Kuechler A, Lämmer C, Merkenschlager A, Mignot C, Ruf S, Nakashima M, Saitsu H, Stamberger H, Pisano T, Tohyama J, Weckhuysen S, Werckx W, Wickert J, Mari F, Verbeek NE, Møller RS, Koeleman B, Matsumoto N, Dobyns WB, Battaglia D, Lemke JR, Kutsche K, Guerrini R. Syrbe S, et al. Among authors: dobyns wb. Brain. 2017 Sep 1;140(9):2322-2336. doi: 10.1093/brain/awx195. Brain. 2017. PMID: 29050398 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. Neurology. 1996 Aug;47(2):331-9. doi: 10.1212/wnl.47.2.331. Neurology. 1996. PMID: 8757001 Review.

3

Olivopontocerebellar atrophy leading to recognition of carbohydrate-deficient glycoprotein syndrome type I.

Pavone L, Fiumara A, Barone R, Rizzo R, Buttitta P, Dobyns WB, Jaeken J. Pavone L, et al. Among authors: dobyns wb. J Neurol. 1996 Oct;243(10):700-5. doi: 10.1007/BF00873975. J Neurol. 1996. PMID: 8923302

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. 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. Among authors: dobyns wb. 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. Among authors: dobyns wb. Neurologia. 1999 May;14 Suppl 3:32-47. Neurologia. 1999. PMID: 10379165 Review.

7

Differences in the gyral pattern distinguish chromosome 17-linked and X-linked lissencephaly.

Dobyns WB, Truwit CL, Ross ME, Matsumoto N, Pilz DT, Ledbetter DH, Gleeson JG, Walsh CA, Barkovich AJ. Dobyns WB, et al. Neurology. 1999 Jul 22;53(2):270-7. doi: 10.1212/wnl.53.2.270. Neurology. 1999. PMID: 10430413

8

Cortical dysplasias, genetics, and epileptogenesis.

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

9

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: dobyns wb. Ann Neurol. 2000 Feb;47(2):265-9. Ann Neurol. 2000. PMID: 10665503

10

Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome.

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

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