These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 19384555)
1. Movement disorder and neuronal migration disorder due to ARFGEF2 mutation. de Wit MC; de Coo IF; Halley DJ; Lequin MH; Mancini GM Neurogenetics; 2009 Oct; 10(4):333-6. PubMed ID: 19384555 [TBL] [Abstract][Full Text] [Related]
2. The expanding phenotypic spectrum of ARFGEF2 gene mutation: Cardiomyopathy and movement disorder. Yilmaz S; Gokben S; Serdaroglu G; Eraslan C; Mancini GM; Tekin H; Tekgul H Brain Dev; 2016 Jan; 38(1):124-7. PubMed ID: 26126837 [TBL] [Abstract][Full Text] [Related]
3. Periventricular nodular heterotopia and dystonia due to an ARFGEF2 mutation. Bardón-Cancho EJ; Muñoz-Jiménez L; Vázquez-López M; Ruíz-Martín Y; García-Morín M; Barredo-Valderrama E Pediatr Neurol; 2014 Sep; 51(3):461-4. PubMed ID: 25160555 [TBL] [Abstract][Full Text] [Related]
4. Elaborating the phenotypic spectrum associated with mutations in ARFGEF2: case study and literature review. Tanyalçin I; Verhelst H; Halley DJ; Vanderhasselt T; Villard L; Goizet C; Lissens W; Mancini GM; Jansen AC Eur J Paediatr Neurol; 2013 Nov; 17(6):666-70. PubMed ID: 23755938 [TBL] [Abstract][Full Text] [Related]
5. Periventricular heterotopia in 6q terminal deletion syndrome: role of the C6orf70 gene. Conti V; Carabalona A; Pallesi-Pocachard E; Parrini E; Leventer RJ; Buhler E; McGillivray G; Michel FJ; Striano P; Mei D; Watrin F; Lise S; Pagnamenta AT; Taylor JC; Kini U; Clayton-Smith J; Novara F; Zuffardi O; Dobyns WB; Scheffer IE; Robertson SP; Berkovic SF; Represa A; Keays DA; Cardoso C; Guerrini R Brain; 2013 Nov; 136(Pt 11):3378-94. PubMed ID: 24056535 [TBL] [Abstract][Full Text] [Related]
6. Disruption of neural progenitors along the ventricular and subventricular zones in periventricular heterotopia. Ferland RJ; Batiz LF; Neal J; Lian G; Bundock E; Lu J; Hsiao YC; Diamond R; Mei D; Banham AH; Brown PJ; Vanderburg CR; Joseph J; Hecht JL; Folkerth R; Guerrini R; Walsh CA; Rodriguez EM; Sheen VL Hum Mol Genet; 2009 Feb; 18(3):497-516. PubMed ID: 18996916 [TBL] [Abstract][Full Text] [Related]
7. Mutations in ARFGEF2 implicate vesicle trafficking in neural progenitor proliferation and migration in the human cerebral cortex. Sheen VL; Ganesh VS; Topcu M; Sebire G; Bodell A; Hill RS; Grant PE; Shugart YY; Imitola J; Khoury SJ; Guerrini R; Walsh CA Nat Genet; 2004 Jan; 36(1):69-76. PubMed ID: 14647276 [TBL] [Abstract][Full Text] [Related]
8. Periventricular heterotopia: phenotypic heterogeneity and correlation with Filamin A mutations. Parrini E; Ramazzotti A; Dobyns WB; Mei D; Moro F; Veggiotti P; Marini C; Brilstra EH; Dalla Bernardina B; Goodwin L; Bodell A; Jones MC; Nangeroni M; Palmeri S; Said E; Sander JW; Striano P; Takahashi Y; Van Maldergem L; Leonardi G; Wright M; Walsh CA; Guerrini R Brain; 2006 Jul; 129(Pt 7):1892-906. PubMed ID: 16684786 [TBL] [Abstract][Full Text] [Related]
9. West syndrome, microcephaly, grey matter heterotopia and hypoplasia of corpus callosum due to a novel ARFGEF2 mutation. Banne E; Atawneh O; Henneke M; Brockmann K; Gärtner J; Elpeleg O; Edvardson S J Med Genet; 2013 Nov; 50(11):772-5. PubMed ID: 23812912 [TBL] [Abstract][Full Text] [Related]
11. Bilateral periventricular nodular heterotopia in France: frequency of mutations in FLNA, phenotypic heterogeneity and spectrum of mutations. Solé G; Coupry I; Rooryck C; Guérineau E; Martins F; Devés S; Hubert C; Souakri N; Boute O; Marchal C; Faivre L; Landré E; Debruxelles S; Dieux-Coeslier A; Boulay C; Chassagnon S; Michel V; Routon MC; Toutain A; Philip N; Lacombe D; Villard L; Arveiler B; Goizet C J Neurol Neurosurg Psychiatry; 2009 Dec; 80(12):1394-8. PubMed ID: 19917821 [TBL] [Abstract][Full Text] [Related]
12. Atypical male and female presentations of FLNA-related periventricular nodular heterotopia. Fergelot P; Coupry I; Rooryck C; Deforges J; Maurat E; Solé G; Boute O; Dieux-Coeslier A; David A; Marchal C; Thambo JB; Lacombe D; Arveiler B; Goizet C Eur J Med Genet; 2012 May; 55(5):313-8. PubMed ID: 22366253 [TBL] [Abstract][Full Text] [Related]
13. A new missense mutation found in the FLNA gene in a family with bilateral periventricular nodular heterotopia (BPNH) alters the splicing process. Tsuneda SS; Torres FR; Montenegro MA; Guerreiro MM; Cendes F; Lopes-Cendes I J Mol Neurosci; 2008 Jun; 35(2):195-200. PubMed ID: 18427995 [TBL] [Abstract][Full Text] [Related]
14. Familial periventricular nodular heterotopia, epilepsy and Melnick-Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects. Parrini E; Mei D; Pisanti MA; Catarzi S; Pucatti D; Bianchini C; Mascalchi M; Bertini E; Morrone A; Cavaliere ML; Guerrini R J Med Genet; 2015 Jun; 52(6):405-12. PubMed ID: 25755106 [TBL] [Abstract][Full Text] [Related]
15. Xq26.1-26.2 gain identified on array comparative genomic hybridization in bilateral periventricular nodular heterotopia with overlying polymicrogyria. Abe Y; Kikuchi A; Kobayashi S; Wakusawa K; Tanaka S; Inui T; Kunishima S; Kure S; Haginoya K Dev Med Child Neurol; 2014 Dec; 56(12):1221-1224. PubMed ID: 25052774 [TBL] [Abstract][Full Text] [Related]
16. FLNA p.V528M substitution is neither associated with bilateral periventricular nodular heterotopia nor with macrothrombocytopenia. Kunishima S; Ito-Yamamura Y; Hayakawa A; Yamamoto T; Saito H J Hum Genet; 2010 Dec; 55(12):844-6. PubMed ID: 20844545 [TBL] [Abstract][Full Text] [Related]
17. Reelin and human nodular heterotopia. Thom M; Garbelli R; Spreafico R Epilepsia; 2011 Mar; 52(3):650-2. PubMed ID: 21395570 [No Abstract] [Full Text] [Related]
18. Lung disease associated with periventricular nodular heterotopia and an FLNA mutation. Masurel-Paulet A; Haan E; Thompson EM; Goizet C; Thauvin-Robinet C; Tai A; Kennedy D; Smith G; Khong TY; Solé G; Guerineau E; Coupry I; Huet F; Robertson S; Faivre L Eur J Med Genet; 2011; 54(1):25-8. PubMed ID: 20888935 [TBL] [Abstract][Full Text] [Related]
19. Phenotypic and imaging features of FLNA-negative patients with bilateral periventricular nodular heterotopia and epilepsy. Fallil Z; Pardoe H; Bachman R; Cunningham B; Parulkar I; Shain C; Poduri A; Knowlton R; Kuzniecky R; Epilepsy Behav; 2015 Oct; 51():321-7. PubMed ID: 26340046 [TBL] [Abstract][Full Text] [Related]
20. Overlapping expression of ARFGEF2 and Filamin A in the neuroependymal lining of the lateral ventricles: insights into the cause of periventricular heterotopia. Lu J; Tiao G; Folkerth R; Hecht J; Walsh C; Sheen V J Comp Neurol; 2006 Jan; 494(3):476-84. PubMed ID: 16320251 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]