156 related articles for article (PubMed ID: 38045215)
1.
Gao C; Liu N; Ma J; Zhao J; Zhao B; Song F; Dong R; Li Z; Lv Y; Liu Y; Gai Z
Heliyon; 2023 Nov; 9(11):e22323. PubMed ID: 38045215
[TBL] [Abstract][Full Text] [Related]
2. Phenotypic Variability in Novel Doublecortin Gene Variants Associated with Subcortical Band Heterotopia.
Procopio R; Fortunato F; Gagliardi M; Talarico M; Sammarra I; Sarubbi MC; Malanga D; Annesi G; Gambardella A
Int J Mol Sci; 2024 May; 25(10):. PubMed ID: 38791543
[TBL] [Abstract][Full Text] [Related]
3. Mutation analysis of the DCX gene and genotype/phenotype correlation in subcortical band heterotopia.
Matsumoto N; Leventer RJ; Kuc JA; Mewborn SK; Dudlicek LL; Ramocki MB; Pilz DT; Mills PL; Das S; Ross ME; Ledbetter DH; Dobyns WB
Eur J Hum Genet; 2001 Jan; 9(1):5-12. PubMed ID: 11175293
[TBL] [Abstract][Full Text] [Related]
4. Subcortical band heterotopia in rare affected males can be caused by missense mutations in DCX (XLIS) or LIS1.
Pilz DT; Kuc J; Matsumoto N; Bodurtha J; Bernadi B; Tassinari CA; Dobyns WB; Ledbetter DH
Hum Mol Genet; 1999 Sep; 8(9):1757-60. PubMed ID: 10441340
[TBL] [Abstract][Full Text] [Related]
5. Identification of DCX gene mutation in lissencephaly spectrum with subcortical band heterotopia using whole exome sequencing.
Jang MA; Woo HI; Kim JW; Lee J; Ki CS
Pediatr Neurol; 2013 May; 48(5):411-4. PubMed ID: 23583063
[TBL] [Abstract][Full Text] [Related]
6. New insights into genotype-phenotype correlations for the doublecortin-related lissencephaly spectrum.
Bahi-Buisson N; Souville I; Fourniol FJ; Toussaint A; Moores CA; Houdusse A; Lemaitre JY; Poirier K; Khalaf-Nazzal R; Hully M; Leger PL; Elie C; Boddaert N; Beldjord C; Chelly J; Francis F;
Brain; 2013 Jan; 136(Pt 1):223-44. PubMed ID: 23365099
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Intragenic deletions and duplications of the LIS1 and DCX genes: a major disease-causing mechanism in lissencephaly and subcortical band heterotopia.
Haverfield EV; Whited AJ; Petras KS; Dobyns WB; Das S
Eur J Hum Genet; 2009 Jul; 17(7):911-8. PubMed ID: 19050731
[TBL] [Abstract][Full Text] [Related]
9. The location of DCX mutations predicts malformation severity in X-linked lissencephaly.
Leger PL; Souville I; Boddaert N; Elie C; Pinard JM; Plouin P; Moutard ML; des Portes V; Van Esch H; Joriot S; Renard JL; Chelly J; Francis F; Beldjord C; Bahi-Buisson N
Neurogenetics; 2008 Oct; 9(4):277-85. PubMed ID: 18685874
[TBL] [Abstract][Full Text] [Related]
10. Novel lissencephaly-associated DCX variants in the C-terminal DCX domain affect microtubule binding and dynamics.
Lin JR; Cheng JF; Liu YT; Hsu TR; Lin KM; Chen C; Lin CL; Tsai MH; Tsai JW
Epilepsia; 2022 May; 63(5):1253-1265. PubMed ID: 35213059
[TBL] [Abstract][Full Text] [Related]
11. A novel missense mutation of doublecortin: mutation analysis of Korean patients with subcortical band heterotopia.
Kim MK; Park MS; Kim BC; Cho KH; Kim YS; Kim JH; Lee MC; Heo T; Kim EY
J Korean Med Sci; 2005 Aug; 20(4):670-3. PubMed ID: 16100463
[TBL] [Abstract][Full Text] [Related]
12. [A male case of subcortical band heterotopia with somatic mosaicism of DCX mutation].
Igarashi A; Kawatani M; Ohta G; Kometani H; Ohshima Y; Kato M
No To Hattatsu; 2013 Sep; 45(5):371-4. PubMed ID: 24205692
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Mosaic mutations of the LIS1 gene cause subcortical band heterotopia.
Sicca F; Kelemen A; Genton P; Das S; Mei D; Moro F; Dobyns WB; Guerrini R
Neurology; 2003 Oct; 61(8):1042-6. PubMed ID: 14581661
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Mosaic DCX deletion causes subcortical band heterotopia in males.
Quélin C; Saillour Y; Souville I; Poirier K; N'guyen-Morel MA; Vercueil L; Millisher-Bellaiche AE; Boddaert N; Dubois F; Chelly J; Beldjord C; Bahi-Buisson N
Neurogenetics; 2012 Nov; 13(4):367-73. PubMed ID: 22833188
[TBL] [Abstract][Full Text] [Related]
17. Familial pachygyria in both genders related to a DCX mutation.
Kim YO; Nam TS; Park C; Kim SK; Yoon W; Choi SY; Kim MK; Woo YJ
Brain Dev; 2016 Jun; 38(6):585-9. PubMed ID: 26743950
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]
