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Literature DB >> 26861558

A case of Bilateral Perisylvian Syndrome with reading disability.

Mark A Eckert¹, Virginia W Berninger², Fumiko Hoeft³, Kenneth I Vaden⁴.

Abstract

Entities: Chemical Disease Gene Species

Keywords: Bilateral Perisylvian Syndrome; Dyslexia; Reading disability; Sylvian fissure

Mesh：

Year: 2016 PMID： 26861558 PMCID： PMC4776332 DOI： 10.1016/j.cortex.2016.01.004

Source DB: PubMed Journal: Cortex ISSN： 0010-9452 Impact factor: 4.027

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14 in total

1. Bilateral perisylvian polymicrogyria with cerebellar dysplasia and ectopic neurohypophysis.

Authors: Irene Toldo; Milena Calderone; Stefano Sartori; Rodica Mardari; Michela Gatta; Clementina Boniver; Renzo Guerrini; Pier Antonio Battistella
Journal: J Child Neurol Date: 2011-01-27 Impact factor: 1.987

2. Bilateral agenesis of arcuate fasciculus demonstrated by fiber tractography in congenital bilateral perisylvian syndrome.

Authors: Ozden Kilinc; Gazanfer Ekinci; Ezgi Demirkol; Kadriye Agan
Journal: Brain Dev Date: 2014-05-20 Impact factor: 1.961

3. A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27.

Authors: Neide F Santos; Rodrigo Secolin; Iara L Brandão-Almeida; Marilza S Silva; Fábio R Torres; Simone S Tsuneda; Catarina A Guimarães; Simone R V Hage; Fernando Cendes; Marilisa M Guerreiro; Iscia Lopes-Cendes
Journal: Am J Med Genet A Date: 2008-05-01 Impact factor: 2.802

4. Voxel-based morphometry and intellectual assessment in patients with congenital bilateral perisylvian syndrome.

Authors: Clarissa L Yasuda; Catarina A Guimarães; Marilisa M Guerreiro; Mirela Boscariol; Ecila P M Oliveira; Karine C Teixeira; André L F Costa; Guilherme C Beltramini; Fernando Cendes
Journal: J Neurol Date: 2014-04-30 Impact factor: 4.849

5. Developmental Foix-Chavany-Marie syndrome in identical twins.

Authors: N R Graff-Radford; E P Bosch; J C Stears; D Tranel
Journal: Ann Neurol Date: 1986-11 Impact factor: 10.422

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

Authors: R Kuzniecky; F Andermann; R Guerrini
Journal: Lancet Date: 1993-03-06 Impact factor: 79.321

Review 7. Dyslexia: The evolution of a scientific concept.

Authors: Jack M Fletcher
Journal: J Int Neuropsychol Soc Date: 2009-07 Impact factor: 2.892

8. Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

Authors: C G F de Kovel; F A Hol; J G A M Heister; J J H T Willemen; L A Sandkuijl; B Franke; G W Padberg
Journal: J Med Genet Date: 2004-09 Impact factor: 6.318

9. Xq27 FRAXA locus is a strong candidate for dyslexia: evidence from a genome-wide scan in French families.

Authors: M Huc-Chabrolle; C Charon; A Guilmatre; P Vourc'h; G Tripi; M A Barthez; E Sizaret; R A Thepault; S Le Gallic; J Hager; A Toutain; M Raynaud; C Andres; D Campion; F Laumonnier; F Bonnet-Brilhault
Journal: Behav Genet Date: 2013-01-11 Impact factor: 2.805

10. Characterisation of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next-generation sequencing study.

Authors: Ghayda M Mirzaa; Valerio Conti; Andrew E Timms; Christopher D Smyser; Sarah Ahmed; Melissa Carter; Sarah Barnett; Robert B Hufnagel; Amy Goldstein; Yoko Narumi-Kishimoto; Carissa Olds; Sarah Collins; Kathreen Johnston; Jean-François Deleuze; Patrick Nitschké; Kathryn Friend; Catharine Harris; Allison Goetsch; Beth Martin; Evan August Boyle; Elena Parrini; Davide Mei; Lorenzo Tattini; Anne Slavotinek; Ed Blair; Christopher Barnett; Jay Shendure; Jamel Chelly; William B Dobyns; Renzo Guerrini
Journal: Lancet Neurol Date: 2015-10-29 Impact factor: 44.182

3 in total