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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]
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]
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. Abnormal network activity in a targeted genetic model of human double cortex. Ackman JB; Aniksztejn L; Crépel V; Becq H; Pellegrino C; Cardoso C; Ben-Ari Y; Represa A J Neurosci; 2009 Jan; 29(2):313-27. PubMed ID: 19144832 [TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. 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] [Next] [New Search]