62 related articles for article (PubMed ID: 24145135)
1. Neuropsychological and neuroimaging phenotype induced by a CAMTA1 mutation.
Magnin E; Blagosklonov O; Sylvestre G; Minot D; Thevenon J; Faivre L; Boulahdour H; Thauvin-Robinet C; Rumbach L
Brain Dev; 2014 Sep; 36(8):711-5. PubMed ID: 24145135
[TBL] [Abstract][Full Text] [Related]
2. Intragenic CAMTA1 rearrangements cause non-progressive congenital ataxia with or without intellectual disability.
Thevenon J; Lopez E; Keren B; Heron D; Mignot C; Altuzarra C; Béri-Dexheimer M; Bonnet C; Magnin E; Burglen L; Minot D; Vigneron J; Morle S; Anheim M; Charles P; Brice A; Gallagher L; Amiel J; Haffen E; Mach C; Depienne C; Doummar D; Bonnet M; Duplomb L; Carmignac V; Callier P; Marle N; Mosca-Boidron AL; Roze V; Aral B; Razavi F; Jonveaux P; Faivre L; Thauvin-Robinet C
J Med Genet; 2012 Jun; 49(6):400-8. PubMed ID: 22693284
[TBL] [Abstract][Full Text] [Related]
3. De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability.
Wijnen IGM; Veenstra-Knol HE; Vansenne F; Gerkes EH; de Koning T; Vos YJ; Tijssen MAJ; Sival D; Darin N; Vanhoutte EK; Oosterloo M; Pennings M; van de Warrenburg BP; Kamsteeg EJ
Eur J Hum Genet; 2020 Jun; 28(6):763-769. PubMed ID: 32157189
[TBL] [Abstract][Full Text] [Related]
4. Intragenic CAMTA1 deletions are associated with a spectrum of neurobehavioral phenotypes.
Shinawi M; Coorg R; Shimony JS; Grange DK; Al-Kateb H
Clin Genet; 2015 May; 87(5):478-82. PubMed ID: 24738973
[TBL] [Abstract][Full Text] [Related]
5. A combined neuropsychological and brain imaging study of obstructive sleep apnea.
Yaouhi K; Bertran F; Clochon P; Mézenge F; Denise P; Foret J; Eustache F; Desgranges B
J Sleep Res; 2009 Mar; 18(1):36-48. PubMed ID: 19250174
[TBL] [Abstract][Full Text] [Related]
6. Myoclonic dystonia phenotype related to a novel calmodulin-binding transcription activator 1 sequence variant.
Dzinovic I; Serranová T; Prouteau C; Colin E; Ziegler A; Winkelmann J; Jech R; Zech M
Neurogenetics; 2021 May; 22(2):137-141. PubMed ID: 33677721
[TBL] [Abstract][Full Text] [Related]
7. Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.
Huentelman MJ; Papassotiropoulos A; Craig DW; Hoerndli FJ; Pearson JV; Huynh KD; Corneveaux J; Hänggi J; Mondadori CR; Buchmann A; Reiman EM; Henke K; de Quervain DJ; Stephan DA
Hum Mol Genet; 2007 Jun; 16(12):1469-77. PubMed ID: 17470457
[TBL] [Abstract][Full Text] [Related]
8. Allelic losses at 1p36 and 19q13 in gliomas: correlation with histologic classification, definition of a 150-kb minimal deleted region on 1p36, and evaluation of CAMTA1 as a candidate tumor suppressor gene.
Barbashina V; Salazar P; Holland EC; Rosenblum MK; Ladanyi M
Clin Cancer Res; 2005 Feb; 11(3):1119-28. PubMed ID: 15709179
[TBL] [Abstract][Full Text] [Related]
9. Expanding the molecular spectrum and the neurological phenotype related to CAMTA1 variants.
Jacobs EZ; Brown K; Byler MC; D'haenens E; Dheedene A; Henderson LB; Humberson JB; van Jaarsveld RH; Kanani F; Lebel RR; Millan F; Oegema R; Oostra A; Parker MJ; Rhodes L; Saenz M; Seaver LH; Si Y; Vanlander A; Vergult S; Callewaert B
Clin Genet; 2021 Feb; 99(2):259-268. PubMed ID: 33131045
[TBL] [Abstract][Full Text] [Related]
10. CAMTA1 T polymorphism is associated with neuropsychological test performance in older adults with cardiovascular disease.
Miller LA; Gunstad J; Spitznagel MB; McCaffery J; McGeary J; Poppas A; Paul RH; Sweet LH; Cohen RA
Psychogeriatrics; 2011 Sep; 11(3):135-40. PubMed ID: 21951953
[TBL] [Abstract][Full Text] [Related]
11. Identification and characterization of FLJ10737 and CAMTA1 genes on the commonly deleted region of neuroblastoma at human chromosome 1p36.31-p36.23.
Katoh M; Katoh M
Int J Oncol; 2003 Oct; 23(4):1219-24. PubMed ID: 12964007
[TBL] [Abstract][Full Text] [Related]
12. Allelic variants of CAMTA1 and FLJ10737 within a commonly deleted region at 1p36 in neuroblastoma.
Henrich KO; Claas A; Praml C; Benner A; Mollenhauer J; Poustka A; Schwab M; Westermann F
Eur J Cancer; 2007 Feb; 43(3):607-16. PubMed ID: 17222547
[TBL] [Abstract][Full Text] [Related]
13. CAMTA1-related disorder: Phenotypic and molecular characterization of 26 new individuals and literature review.
Al-Kateb H; Au PYB; Berland S; Cogne B; Demurger F; Fluss J; Isidor B; Frank LM; Varvagiannis K; Koolen DA; McDonald M; Montgomery S; Moortgat S; Deprez M; Karadurmus D; Paulsen J; Reis A; Rieger M; Vasileiou G; Willing M; Shinawi M
Clin Genet; 2024 Mar; 105(3):294-301. PubMed ID: 38044714
[TBL] [Abstract][Full Text] [Related]
14. Broader phenotypic traits and widespread brain hypometabolism in spinocerebellar ataxia 27.
Paucar M; Lundin J; Alshammari T; Bergendal Å; Lindefeldt M; Alshammari M; Solders G; Di Re J; Savitcheva I; Granberg T; Laezza F; Iwarsson E; Svenningsson P
J Intern Med; 2020 Jul; 288(1):103-115. PubMed ID: 32112487
[TBL] [Abstract][Full Text] [Related]
15. Behr syndrome with homozygous C19ORF12 mutation.
Kleffner I; Wessling C; Gess B; Korsukewitz C; Allkemper T; Schirmacher A; Young P; Senderek J; Husstedt IW
J Neurol Sci; 2015 Oct; 357(1-2):115-8. PubMed ID: 26187298
[TBL] [Abstract][Full Text] [Related]
16. CAMTA1, a 1p36 tumor suppressor candidate, inhibits growth and activates differentiation programs in neuroblastoma cells.
Henrich KO; Bauer T; Schulte J; Ehemann V; Deubzer H; Gogolin S; Muth D; Fischer M; Benner A; König R; Schwab M; Westermann F
Cancer Res; 2011 Apr; 71(8):3142-51. PubMed ID: 21385898
[TBL] [Abstract][Full Text] [Related]
17. MRI-guided flumazenil- and FDG-PET in temporal lobe epilepsy.
Szelies B; Weber-Luxenburger G; Pawlik G; Kessler J; Holthoff V; Mielke R; Herholz K; Bauer B; Wienhard K; Heiss WD
Neuroimage; 1996 Apr; 3(2):109-18. PubMed ID: 9345482
[TBL] [Abstract][Full Text] [Related]
18. Christianson syndrome: spectrum of neuroimaging findings.
Bosemani T; Zanni G; Hartman AL; Cohen R; Huisman TA; Bertini E; Poretti A
Neuropediatrics; 2014 Aug; 45(4):247-51. PubMed ID: 24285247
[TBL] [Abstract][Full Text] [Related]
19. Cell cycle-dependent transcriptional regulation of calmodulin-binding transcription activator 1 in neuroblastoma cells.
Nakatani K; Nishioka J; Itakura T; Nakanishi Y; Horinouchi J; Abe Y; Wada H; Nobori T
Int J Oncol; 2004 Jun; 24(6):1407-12. PubMed ID: 15138581
[TBL] [Abstract][Full Text] [Related]
20. Evaluation of focus laterality in temporal lobe epilepsy: a quantitative study comparing double inversion-recovery MR imaging at 3T with FDG-PET.
Morimoto E; Okada T; Kanagaki M; Yamamoto A; Fushimi Y; Matsumoto R; Takaya S; Ikeda A; Kunieda T; Kikuchi T; Paul D; Miyamoto S; Takahashi R; Togashi K
Epilepsia; 2013 Dec; 54(12):2174-83. PubMed ID: 24117006
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]