288 related articles for article (PubMed ID: 11829339)
1. 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]
2. The multipolar stage and disruptions in neuronal migration.
LoTurco JJ; Bai J
Trends Neurosci; 2006 Jul; 29(7):407-413. PubMed ID: 16713637
[TBL] [Abstract][Full Text] [Related]
3. Cerebral developmental disorders.
Lian G; Sheen V
Curr Opin Pediatr; 2006 Dec; 18(6):614-20. PubMed ID: 17099359
[TBL] [Abstract][Full Text] [Related]
4. Molecular genetics of neuronal migration disorders.
Liu JS
Curr Neurol Neurosci Rep; 2011 Apr; 11(2):171-8. PubMed ID: 21222180
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Genotype-phenotype correlation in lissencephaly and subcortical band heterotopia: the key questions answered.
Leventer RJ
J Child Neurol; 2005 Apr; 20(4):307-12. PubMed ID: 15921231
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Lissencephaly and subcortical band heterotopia: molecular basis and diagnosis.
Leventer RJ; Pilz DT; Matsumoto N; Ledbetter DH; Dobyns WB
Mol Med Today; 2000 Jul; 6(7):277-84. PubMed ID: 10859564
[TBL] [Abstract][Full Text] [Related]
9. Neuronal migration defects of the cerebral cortex: a destination debacle.
Uher BF; Golden JA
Clin Genet; 2000 Jul; 58(1):16-24. PubMed ID: 10945656
[TBL] [Abstract][Full Text] [Related]
10. Enhanced expression of Pafah1b1 causes over-migration of cerebral cortical neurons into the marginal zone.
Katayama KI; Hayashi K; Inoue S; Sakaguchi K; Nakajima K
Brain Struct Funct; 2017 Dec; 222(9):4283-4291. PubMed ID: 28836069
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Molecular mechanisms of neuronal migration disorders, quo vadis?
Couillard-Despres S; Winkler J; Uyanik G; Aigner L
Curr Mol Med; 2001 Dec; 1(6):677-88. PubMed ID: 11899256
[TBL] [Abstract][Full Text] [Related]
13. Malformations of Cortical Development: From Postnatal to Fetal Imaging.
Lerman-Sagie T; Leibovitz Z
Can J Neurol Sci; 2016 Sep; 43(5):611-8. PubMed ID: 27670206
[TBL] [Abstract][Full Text] [Related]
14. Lissencephaly and the molecular basis of neuronal migration.
Kato M; Dobyns WB
Hum Mol Genet; 2003 Apr; 12 Spec No 1():R89-96. PubMed ID: 12668601
[TBL] [Abstract][Full Text] [Related]
15. Normal and abnormal neuronal migration in the developing cerebral cortex.
Sun XZ; Takahashi S; Cui C; Zhang R; Sakata-Haga H; Sawada K; Fukui Y
J Med Invest; 2002 Aug; 49(3-4):97-110. PubMed ID: 12323012
[TBL] [Abstract][Full Text] [Related]
16. Multiple dose-dependent effects of Lis1 on cerebral cortical development.
Gambello MJ; Darling DL; Yingling J; Tanaka T; Gleeson JG; Wynshaw-Boris A
J Neurosci; 2003 Mar; 23(5):1719-29. PubMed ID: 12629176
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Drebrin-like (Dbnl) Controls Neuronal Migration via Regulating N-Cadherin Expression in the Developing Cerebral Cortex.
Inoue S; Hayashi K; Fujita K; Tagawa K; Okazawa H; Kubo KI; Nakajima K
J Neurosci; 2019 Jan; 39(4):678-691. PubMed ID: 30504273
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Location and type of mutation in the LIS1 gene do not predict phenotypic severity.
Uyanik G; Morris-Rosendahl DJ; Stiegler J; Klapecki J; Gross C; Berman Y; Martin P; Dey L; Spranger S; Korenke GC; Schreyer I; Hertzberg C; Neumann TE; Burkart P; Spaich C; Meng M; Holthausen H; Adès L; Seidel J; Mangold E; Buyse G; Meinecke P; Schara U; Zeschnigk C; Muller D; Helland G; Schulze B; Wright ML; Kortge-Jung S; Hehr A; Bogdahn U; Schuierer G; Kohlhase J; Aigner L; Wolff G; Hehr U; Winkler J
Neurology; 2007 Jul; 69(5):442-7. PubMed ID: 17664403
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
