Literature DB >> 20331705

Genetic malformations of the human frontal lobe.

Dina Amrom1, Christopher A Walsh.   

Abstract

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Year:  2010        PMID： 20331705      PMCID： PMC4271974          DOI： 10.1111/j.1528-1167.2009.02435.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN： 0013-9580            Impact factor:   5.864


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  31 in total

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3.  Magnetic resonance imaging abnormalities of the brain in Goldberg-Shprintzen syndrome (Hirschsprung disease, microcephaly, and iris coloboma)

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

Authors:  W B Dobyns; C L Truwit; M E Ross; N Matsumoto; D T Pilz; D H Ledbetter; J G Gleeson; C A Walsh; A J Barkovich
Journal:  Neurology       Date:  1999-07-22       Impact factor: 9.910

5.  Bilateral frontal polymicrogyria: a newly recognized brain malformation syndrome.

Authors:  R Guerrini; A J Barkovich; L Sztriha; W B Dobyns
Journal:  Neurology       Date:  2000-02-22       Impact factor: 9.910

6.  Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.

Authors:  N Matsumoto; R J Leventer; J A Kuc; S K Mewborn; L L Dudlicek; M B Ramocki; D T Pilz; P L Mills; S Das; M E Ross; D H Ledbetter; W B Dobyns
Journal:  Eur J Hum Genet       Date:  2001-01       Impact factor: 4.246

Review 7.  Lissencephaly and other malformations of cortical development: 1995 update.

Authors:  W B Dobyns; C L Truwit
Journal:  Neuropediatrics       Date:  1995-06       Impact factor: 1.947

8.  Characterization of mutations in the gene doublecortin in patients with double cortex syndrome.

Authors:  J G Gleeson; S R Minnerath; J W Fox; K M Allen; R F Luo; S E Hong; M J Berg; R Kuzniecky; P J Reitnauer; R Borgatti; A P Mira; R Guerrini; G L Holmes; C M Rooney; S Berkovic; I Scheffer; E C Cooper; S Ricci; R Cusmai; T O Crawford; R Leroy; E Andermann; J W Wheless; W B Dobyns; C A Walsh
Journal:  Ann Neurol       Date:  1999-02       Impact factor: 10.422

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

Authors:  Renzo Guerrini; Francesca Moro; Eva Andermann; Elaine Hughes; Daniela D'Agostino; Romeo Carrozzo; Andrea Bernasconi; Frances Flinter; Lucio Parmeggiani; Anna Volzone; Elena Parrini; Davide Mei; Jozef M Jarosz; Robin G Morris; Polly Pratt; Gaetano Tortorella; François Dubeau; Frederick Andermann; William B Dobyns; Soma Das
Journal:  Ann Neurol       Date:  2003-07       Impact factor: 10.422

10.  The location of DCX mutations predicts malformation severity in X-linked lissencephaly.

Authors:  Pierre-Louis Leger; Isabelle Souville; Nathalie Boddaert; Caroline Elie; Jean Marc Pinard; Perrine Plouin; Marie Laure Moutard; Vincent des Portes; Hilde Van Esch; Sylvie Joriot; Jean Louis Renard; Jamel Chelly; Fiona Francis; Cherif Beldjord; Nadia Bahi-Buisson
Journal:  Neurogenetics       Date:  2008-08-07       Impact factor: 2.660
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