239 related articles for article (PubMed ID: 10515162)
1. Genes that regulate neuronal migration in the cerebral cortex.
Allen KM; Walsh CA
Epilepsy Res; 1999 Sep; 36(2-3):143-54. PubMed ID: 10515162
[TBL] [Abstract][Full Text] [Related]
2. Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein.
Gleeson JG; Allen KM; Fox JW; Lamperti ED; Berkovic S; Scheffer I; Cooper EC; Dobyns WB; Minnerath SR; Ross ME; Walsh CA
Cell; 1998 Jan; 92(1):63-72. PubMed ID: 9489700
[TBL] [Abstract][Full Text] [Related]
3. Neuronal migration disorders, genetics, and epileptogenesis.
Guerrini R; Filippi T
J Child Neurol; 2005 Apr; 20(4):287-99. PubMed ID: 15921228
[TBL] [Abstract][Full Text] [Related]
4. Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defects.
Sossey-Alaoui K; Hartung AJ; Guerrini R; Manchester DK; Posar A; Puche-Mira A; Andermann E; Dobyns WB; Srivastava AK
Hum Mol Genet; 1998 Aug; 7(8):1327-32. PubMed ID: 9668176
[TBL] [Abstract][Full Text] [Related]
5. A novel CNS gene required for neuronal migration and involved in X-linked subcortical laminar heterotopia and lissencephaly syndrome.
des Portes V; Pinard JM; Billuart P; Vinet MC; Koulakoff A; Carrié A; Gelot A; Dupuis E; Motte J; Berwald-Netter Y; Catala M; Kahn A; Beldjord C; Chelly J
Cell; 1998 Jan; 92(1):51-61. PubMed ID: 9489699
[TBL] [Abstract][Full Text] [Related]
6. Genetic malformations of cortical development.
Guerrini R; Marini C
Exp Brain Res; 2006 Aug; 173(2):322-33. PubMed ID: 16724181
[TBL] [Abstract][Full Text] [Related]
7. Doublecortin functions at the extremities of growing neuronal processes.
Friocourt G; Koulakoff A; Chafey P; Boucher D; Fauchereau F; Chelly J; Francis F
Cereb Cortex; 2003 Jun; 13(6):620-6. PubMed ID: 12764037
[TBL] [Abstract][Full Text] [Related]
8. Neuronal migration, cerebral cortical development, and cerebral cortical anomalies.
Pilz D; Stoodley N; Golden JA
J Neuropathol Exp Neurol; 2002 Jan; 61(1):1-11. PubMed ID: 11829339
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Genetic mechanisms underlying abnormal neuronal migration in classical lissencephaly.
Kerjan G; Gleeson JG
Trends Genet; 2007 Dec; 23(12):623-30. PubMed ID: 17997185
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse.
Ware ML; Fox JW; González JL; Davis NM; Lambert de Rouvroit C; Russo CJ; Chua SC; Goffinet AM; Walsh CA
Neuron; 1997 Aug; 19(2):239-49. PubMed ID: 9292716
[TBL] [Abstract][Full Text] [Related]
13. Malformations of cortical development.
Pang T; Atefy R; Sheen V
Neurologist; 2008 May; 14(3):181-91. PubMed ID: 18469675
[TBL] [Abstract][Full Text] [Related]
14. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
Guerrini R; Carrozzo R
Seizure; 2002 Apr; 11 Suppl A():532-43; quiz 544-7. PubMed ID: 12185771
[TBL] [Abstract][Full Text] [Related]
15. Epileptogenic brain malformations: clinical presentation, malformative patterns and indications for genetic testing.
Guerrini R; Carrozzo R
Seizure; 2001 Oct; 10(7):532-43; quiz 544-7. PubMed ID: 11749114
[TBL] [Abstract][Full Text] [Related]
16. Genetic malformations of the cerebral cortex and epilepsy.
Guerrini R
Epilepsia; 2005; 46 Suppl 1():32-7. PubMed ID: 15816977
[TBL] [Abstract][Full Text] [Related]
17. doublecortin is the major gene causing X-linked subcortical laminar heterotopia (SCLH).
des Portes V; Francis F; Pinard JM; Desguerre I; Moutard ML; Snoeck I; Meiners LC; Capron F; Cusmai R; Ricci S; Motte J; Echenne B; Ponsot G; Dulac O; Chelly J; Beldjord C
Hum Mol Genet; 1998 Jul; 7(7):1063-70. PubMed ID: 9618162
[TBL] [Abstract][Full Text] [Related]
18. Linkage and physical mapping of X-linked lissencephaly/SBH (XLIS): a gene causing neuronal migration defects in human brain.
Ross ME; Allen KM; Srivastava AK; Featherstone T; Gleeson JG; Hirsch B; Harding BN; Andermann E; Abdullah R; Berg M; Czapansky-Bielman D; Flanders DJ; Guerrini R; Motté J; Mira AP; Scheffer I; Berkovic S; Scaravilli F; King RA; Ledbetter DH; Schlessinger D; Dobyns WB; Walsh CA
Hum Mol Genet; 1997 Apr; 6(4):555-62. PubMed ID: 9097958
[TBL] [Abstract][Full Text] [Related]
19. Isolated lissencephaly sequence and double-cortex syndrome in a German family with a novel doublecortin mutation.
Aigner L; Fluegel D; Dietrich J; Ploetz S; Winkler J
Neuropediatrics; 2000 Aug; 31(4):195-8. PubMed ID: 11071144
[TBL] [Abstract][Full Text] [Related]
20. Subcortical band heterotopia (SBH) in males: clinical, imaging and genetic findings in comparison with females.
D'Agostino MD; Bernasconi A; Das S; Bastos A; Valerio RM; Palmini A; Costa da Costa J; Scheffer IE; Berkovic S; Guerrini R; Dravet C; Ono J; Gigli G; Federico A; Booth F; Bernardi B; Volpi L; Tassinari CA; Guggenheim MA; Ledbetter DH; Gleeson JG; Lopes-Cendes I; Vossler DG; Malaspina E; Franzoni E; Sartori RJ; Mitchell MH; Mercho S; Dubeau F; Andermann F; Dobyns WB; Andermann E
Brain; 2002 Nov; 125(Pt 11):2507-22. PubMed ID: 12390976
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
