409 related articles for article (PubMed ID: 29062978)
1. INTERNEURONOPATHIES AND THEIR ROLE IN EARLY LIFE EPILEPSIES AND NEURODEVELOPMENTAL DISORDERS.
Katsarou AM; Moshé SL; Galanopoulou AS
Epilepsia Open; 2017 Sep; 2(3):284-306. PubMed ID: 29062978
[TBL] [Abstract][Full Text] [Related]
2. [Topics of brain malformation and epilepsy--age-dependent epileptic encephalopathies and interneuronopathies].
Kato M
No To Hattatsu; 2010 Sep; 42(5):333-8. PubMed ID: 20845763
[TBL] [Abstract][Full Text] [Related]
3. Aristaless-related homeobox gene disruption leads to abnormal distribution of GABAergic interneurons in human neocortex: evidence based on a case of X-linked lissencephaly with abnormal genitalia (XLAG).
Okazaki S; Ohsawa M; Kuki I; Kawawaki H; Koriyama T; Ri S; Ichiba H; Hai E; Inoue T; Nakamura H; Goto Y; Tomiwa K; Yamano T; Kitamura K; Itoh M
Acta Neuropathol; 2008 Oct; 116(4):453-62. PubMed ID: 18458920
[TBL] [Abstract][Full Text] [Related]
4. An epilepsy-related ARX polyalanine expansion modifies glutamatergic neurons excitability and morphology without affecting GABAergic neurons development.
Beguin S; Crépel V; Aniksztejn L; Becq H; Pelosi B; Pallesi-Pocachard E; Bouamrane L; Pasqualetti M; Kitamura K; Cardoso C; Represa A
Cereb Cortex; 2013 Jun; 23(6):1484-94. PubMed ID: 22628459
[TBL] [Abstract][Full Text] [Related]
5. X-linked lissencephaly with abnormal genitalia as a tangential migration disorder causing intractable epilepsy: proposal for a new term, "interneuronopathy".
Kato M; Dobyns WB
J Child Neurol; 2005 Apr; 20(4):392-7. PubMed ID: 15921244
[TBL] [Abstract][Full Text] [Related]
6. A new paradigm for West syndrome based on molecular and cell biology.
Kato M
Epilepsy Res; 2006 Aug; 70 Suppl 1():S87-95. PubMed ID: 16806828
[TBL] [Abstract][Full Text] [Related]
7. A triplet repeat expansion genetic mouse model of infantile spasms syndrome, Arx(GCG)10+7, with interneuronopathy, spasms in infancy, persistent seizures, and adult cognitive and behavioral impairment.
Price MG; Yoo JW; Burgess DL; Deng F; Hrachovy RA; Frost JD; Noebels JL
J Neurosci; 2009 Jul; 29(27):8752-63. PubMed ID: 19587282
[TBL] [Abstract][Full Text] [Related]
8. Genotype-phenotype correlation in neuronal migration disorders and cortical dysplasias.
Kato M
Front Neurosci; 2015; 9():181. PubMed ID: 26052266
[TBL] [Abstract][Full Text] [Related]
9. Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans.
Kitamura K; Yanazawa M; Sugiyama N; Miura H; Iizuka-Kogo A; Kusaka M; Omichi K; Suzuki R; Kato-Fukui Y; Kamiirisa K; Matsuo M; Kamijo S; Kasahara M; Yoshioka H; Ogata T; Fukuda T; Kondo I; Kato M; Dobyns WB; Yokoyama M; Morohashi K
Nat Genet; 2002 Nov; 32(3):359-69. PubMed ID: 12379852
[TBL] [Abstract][Full Text] [Related]
10. KCNT1-related epilepsies and epileptic encephalopathies: phenotypic and mutational spectrum.
Bonardi CM; Heyne HO; Fiannacca M; Fitzgerald MP; Gardella E; Gunning B; Olofsson K; Lesca G; Verbeek N; Stamberger H; Striano P; Zara F; Mancardi MM; Nava C; Syrbe S; Buono S; Baulac S; Coppola A; Weckhuysen S; Schoonjans AS; Ceulemans B; Sarret C; Baumgartner T; Muhle H; Portes VD; Toulouse J; Nougues MC; Rossi M; Demarquay G; Ville D; Hirsch E; Maurey H; Willems M; de Bellescize J; Altuzarra CD; Villeneuve N; Bartolomei F; Picard F; Hornemann F; Koolen DA; Kroes HY; Reale C; Fenger CD; Tan WH; Dibbens L; Bearden DR; Møller RS; Rubboli G
Brain; 2021 Dec; 144(12):3635-3650. PubMed ID: 34114611
[TBL] [Abstract][Full Text] [Related]
11. A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females.
Ekşioğlu YZ; Pong AW; Takeoka M
Epilepsia; 2011 May; 52(5):984-92. PubMed ID: 21426321
[TBL] [Abstract][Full Text] [Related]
12. Basal ganglia involvement in
Curie A; Friocourt G; des Portes V; Roy A; Nazir T; Brun A; Cheylus A; Marcorelles P; Retzepi K; Maleki N; Bussy G; Paulignan Y; Reboul A; Ibarrola D; Kong J; Hadjikhani N; Laquerrière A; Gollub RL
Neuroimage Clin; 2018; 19():454-465. PubMed ID: 29984154
[TBL] [Abstract][Full Text] [Related]
13. Mutations of ARX are associated with striking pleiotropy and consistent genotype-phenotype correlation.
Kato M; Das S; Petras K; Kitamura K; Morohashi KI; Abuelo DN; Barr M; Bonneau D; Brady AF; Carpenter NJ; Cipero KL; Frisone F; Fukuda T; Guerrini R; Iida E; Itoh M; Lewanda AF; Nanba Y; Oka A; Proud VK; Saugier-Veber P; Schelley SL; Selicorni A; Shaner R; Silengo M; Stewart F; Sugiyama N; Toyama J; Toutain A; Vargas AL; Yanazawa M; Zackai EH; Dobyns WB
Hum Mutat; 2004 Feb; 23(2):147-159. PubMed ID: 14722918
[TBL] [Abstract][Full Text] [Related]
14. An Emerging Female Phenotype with Loss-of-Function Mutations in the Aristaless-Related Homeodomain Transcription Factor ARX.
Mattiske T; Moey C; Vissers LE; Thorne N; Georgeson P; Bakshi M; Shoubridge C
Hum Mutat; 2017 May; 38(5):548-555. PubMed ID: 28150386
[TBL] [Abstract][Full Text] [Related]
15. Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies.
Galanopoulou AS; Moshé SL
Neurobiol Dis; 2015 Jul; 79():135-49. PubMed ID: 25968935
[TBL] [Abstract][Full Text] [Related]
16. Idiopathic focal epilepsies: the "lost tribe".
Pal DK; Ferrie C; Addis L; Akiyama T; Capovilla G; Caraballo R; de Saint-Martin A; Fejerman N; Guerrini R; Hamandi K; Helbig I; Ioannides AA; Kobayashi K; Lal D; Lesca G; Muhle H; Neubauer BA; Pisano T; Rudolf G; Seegmuller C; Shibata T; Smith A; Striano P; Strug LJ; Szepetowski P; Valeta T; Yoshinaga H; Koutroumanidis M
Epileptic Disord; 2016 Sep; 18(3):252-88. PubMed ID: 27435520
[TBL] [Abstract][Full Text] [Related]
17. The ARX story (epilepsy, mental retardation, autism, and cerebral malformations): one gene leads to many phenotypes.
Sherr EH
Curr Opin Pediatr; 2003 Dec; 15(6):567-71. PubMed ID: 14631200
[TBL] [Abstract][Full Text] [Related]
18. Agenesis of the corpus callosum, abnormal genitalia and intractable epilepsy due to a novel familial mutation in the Aristaless-related homeobox gene.
Hartmann H; Uyanik G; Gross C; Hehr U; Lücke T; Arslan-Kirchner M; Antosch B; Das AM; Winkler J
Neuropediatrics; 2004 Jun; 35(3):157-60. PubMed ID: 15248097
[TBL] [Abstract][Full Text] [Related]
19. The aristaless (Arx) gene: one gene for many "interneuronopathies".
Ruggieri M; Pavone P; Scapagnini G; Romeo L; Lombardo I; Li Volti G; Corsello G; Pavone L
Front Biosci (Elite Ed); 2010 Jan; 2(2):701-10. PubMed ID: 20036914
[TBL] [Abstract][Full Text] [Related]
20.
; ; . PubMed ID:
[No Abstract] [Full Text] [Related]
[Next] [New Search]