269 related articles for article (PubMed ID: 12410386)
1. Bilateral periventricular nodular heterotopia due to filamin 1 gene mutation: widespread glomeruloid microvascular anomaly and dysplastic cytoarchitecture in the cerebral cortex.
Kakita A; Hayashi S; Moro F; Guerrini R; Ozawa T; Ono K; Kameyama S; Walsh CA; Takahashi H
Acta Neuropathol; 2002 Dec; 104(6):649-57. PubMed ID: 12410386
[TBL] [Abstract][Full Text] [Related]
2. Filamin a, periventricular nodular heterotopia, and West syndrome.
Robertson SP
Epilepsia; 2006 Jun; 47(6):1082; author reply 1082-3. PubMed ID: 16822260
[No Abstract] [Full Text] [Related]
3. Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males.
Masruha MR; Caboclo LO; Carrete H; Cendes IL; Rodrigues MG; Garzon E; Yacubian EM; Sakamoto AC; Sheen V; Harney M; Neal J; Hill RS; Bodell A; Walsh C; Vilanova LC
Epilepsia; 2006 Jan; 47(1):211-4. PubMed ID: 16417552
[TBL] [Abstract][Full Text] [Related]
4. Gene symbol: FLNA. Disease: Ehlers-Danlos syndrome and periventricular nodular heterotopia.
Gomez-Garre P; Serratosa JM
Hum Genet; 2005 Dec; 118(3-4):545. PubMed ID: 16521297
[No Abstract] [Full Text] [Related]
5. 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]
6. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
Fox JW; Lamperti ED; Ekşioğlu YZ; Hong SE; Feng Y; Graham DA; Scheffer IE; Dobyns WB; Hirsch BA; Radtke RA; Berkovic SF; Huttenlocher PR; Walsh CA
Neuron; 1998 Dec; 21(6):1315-25. PubMed ID: 9883725
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Ehlers-Danlos syndrome and periventricular nodular heterotopia in a Spanish family with a single FLNA mutation.
Gómez-Garre P; Seijo M; Gutiérrez-Delicado E; Castro del Río M; de la Torre C; Gómez-Abad C; Morales-Corraliza J; Puig M; Serratosa JM
J Med Genet; 2006 Mar; 43(3):232-7. PubMed ID: 15994863
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. A glial origin for periventricular nodular heterotopia caused by impaired expression of Filamin-A.
Carabalona A; Beguin S; Pallesi-Pocachard E; Buhler E; Pellegrino C; Arnaud K; Hubert P; Oualha M; Siffroi JP; Khantane S; Coupry I; Goizet C; Gelot AB; Represa A; Cardoso C
Hum Mol Genet; 2012 Mar; 21(5):1004-17. PubMed ID: 22076441
[TBL] [Abstract][Full Text] [Related]
11. Multiple pterygium syndrome, bilateral periventricular nodular heterotopia and epileptic seizures--a syndrome?
Holtmann M; Woermann FG; Boenigk HE
Neuropediatrics; 2001 Oct; 32(5):264-6. PubMed ID: 11748498
[TBL] [Abstract][Full Text] [Related]
12. Familial periventricular heterotopia: missense and distal truncating mutations of the FLN1 gene.
Moro F; Carrozzo R; Veggiotti P; Tortorella G; Toniolo D; Volzone A; Guerrini R
Neurology; 2002 Mar; 58(6):916-21. PubMed ID: 11914408
[TBL] [Abstract][Full Text] [Related]
13. Epilepsy and malformations of the cerebral cortex.
Guerrini R; Sicca F; Parmeggiani L
Epileptic Disord; 2003 Sep; 5 Suppl 2():S9-26. PubMed ID: 14617417
[TBL] [Abstract][Full Text] [Related]
14. Periventricular nodular heterotopia in patients with filamin-1 gene mutations: neuroimaging findings.
Poussaint TY; Fox JW; Dobyns WB; Radtke R; Scheffer IE; Berkovic SF; Barnes PD; Huttenlocher PR; Walsh CA
Pediatr Radiol; 2000 Nov; 30(11):748-55. PubMed ID: 11100490
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Epilepsy and genetic malformations of the cerebral cortex.
Guerrini R; Carrozzo R
Am J Med Genet; 2001; 106(2):160-73. PubMed ID: 11579436
[TBL] [Abstract][Full Text] [Related]
17. Periventricular nodular heterotopia: report of a pediatric series.
Spalice A; Taddeucci G; Perla FM; Pascali MP; Iannetti P
J Child Neurol; 2002 Apr; 17(4):300-4. PubMed ID: 12088088
[TBL] [Abstract][Full Text] [Related]
18. Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.
Fink JM; Dobyns WB; Guerrini R; Hirsch BA
Am J Hum Genet; 1997 Aug; 61(2):379-87. PubMed ID: 9311743
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Bilateral periventricular heterotopias in an X-linked dominant transmission in a family with two affected males.
Gérard-Blanluet M; Sheen V; Machinis K; Neal J; Apse K; Danan C; Sinico M; Brugières P; Mage K; Ratsimbazafy L; Elbez A; Janaud JC; Amselem S; Walsh C; Encha-Razavi F
Am J Med Genet A; 2006 May; 140(10):1041-6. PubMed ID: 16596669
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]