164 related articles for article (PubMed ID: 9738673)
1. Chromosome 20 ring: a chromosomal disorder associated with a particular electroclinical pattern.
Canevini MP; Sgro V; Zuffardi O; Canger R; Carrozzo R; Rossi E; Ledbetter D; Minicucci F; Vignoli A; Piazzini A; Guidolin L; Saltarelli A; dalla Bernardina B
Epilepsia; 1998 Sep; 39(9):942-51. PubMed ID: 9738673
[TBL] [Abstract][Full Text] [Related]
2. Electroclinical evolution in ring chromosome 20 epilepsy syndrome: a case with severe phenotypic features followed for 25 years.
de Falco FA; Olivieri P; de Falco A; Concolino D; Battaglia F; Verardi R; Grande G; Stabile M
Seizure; 2006 Sep; 15(6):449-53. PubMed ID: 16806995
[TBL] [Abstract][Full Text] [Related]
3. Specificity of electroclinical features in the diagnosis of ring chromosome 20.
Gago-Veiga AB; Toledano R; García-Morales I; Pérez-Jiménez MA; Bernar J; Gil-Nagel A
Epilepsy Behav; 2018 Mar; 80():215-220. PubMed ID: 29414555
[TBL] [Abstract][Full Text] [Related]
4. Ring chromosome 17 epilepsy may resemble that of ring chromosome 20 syndrome.
Ricard-Mousnier B; N'Guyen S; Dubas F; Pouplard F; Guichet A
Epileptic Disord; 2007 Sep; 9(3):327-31. PubMed ID: 17884758
[TBL] [Abstract][Full Text] [Related]
5. Epilepsy and ring chromosome 20: case report.
Gomes Mda M; Lucca I; Bezerra SA; Llerena J; Moreira DM
Arq Neuropsiquiatr; 2002 Sep; 60(3-A):631-5. PubMed ID: 12244405
[TBL] [Abstract][Full Text] [Related]
6. Genetic investigations on 8 patients affected by ring 20 chromosome syndrome.
Giardino D; Vignoli A; Ballarati L; Recalcati MP; Russo S; Camporeale N; Marchi M; Finelli P; Accorsi P; Giordano L; La Briola F; Chiesa V; Canevini MP; Larizza L
BMC Med Genet; 2010 Oct; 11():146. PubMed ID: 20939888
[TBL] [Abstract][Full Text] [Related]
7. [Electroclinical characteristics of a patient with ring chromosome 20 syndrome].
Vega-Zelaya L; Alonso-Cerezo C; Quesada JF; Sola RG; Pastor J
Rev Neurol; 2014 May; 58(10):450-4. PubMed ID: 24819941
[TBL] [Abstract][Full Text] [Related]
8. Ring 20 chromosome syndrome with epilepsy and dysmorphic features: a case report.
García DM; Ortiz R; Gómez A; Barriuso E
Epilepsia; 2001 Dec; 42(12):1607-10. PubMed ID: 11879375
[TBL] [Abstract][Full Text] [Related]
9. Ring chromosome 20 syndrome: electroclinical description of six patients and review of the literature.
Elens I; Vanrykel K; De Waele L; Jansen K; Segeren M; Van Paesschen W; Ceulemans B; Boel M; Frijns JP; Buyse G; Lagae L
Epilepsy Behav; 2012 Apr; 23(4):409-14. PubMed ID: 22424860
[TBL] [Abstract][Full Text] [Related]
10. Early pattern of epilepsy in the ring chromosome 20 syndrome.
Ville D; Kaminska A; Bahi-Buisson N; Biraben A; Plouin P; Telvi L; Dulac O; Chiron C
Epilepsia; 2006 Mar; 47(3):543-9. PubMed ID: 16529619
[TBL] [Abstract][Full Text] [Related]
11. Ring chromosome 20 with nonconvulsive status epilepticus: electroclinical correlation of a rare epileptic syndrome.
Locharernkul C; Ebner A; Promchainant C
Clin EEG Neurosci; 2005 Jul; 36(3):151-60. PubMed ID: 16128150
[TBL] [Abstract][Full Text] [Related]
12. 6q terminal deletion syndrome associated with a distinctive EEG and clinical pattern: a report of five cases.
Elia M; Striano P; Fichera M; Gaggero R; Castiglia L; Galesi O; Malacarne M; Pierluigi M; Amato C; Musumeci SA; Romano C; Majore S; Grammatico P; Zara F; Striano S; Faravelli F
Epilepsia; 2006 May; 47(5):830-8. PubMed ID: 16686647
[TBL] [Abstract][Full Text] [Related]
13. [Ring chromosome 20: a distinctive syndrome identifiable by electroclinical diagnosis].
Gonzalez-Delgado M; Salas J; Hernando I; Calleja S; Hernandez C
Neurologia; 2004 May; 19(4):215-9. PubMed ID: 15131740
[TBL] [Abstract][Full Text] [Related]
14. Ring-20-syndrome and loss of telomeric regions.
García-Cruz D; Vásquez AI; Perez-Rulfo D; Dávalos NO; Peñaloza J; García-Ortiz JE; Patiño-García B; Sánchez-Corona J
Ann Genet; 2000; 43(3-4):113-6. PubMed ID: 11164191
[TBL] [Abstract][Full Text] [Related]
15. Ring chromosome 20 with loss of telomeric sequences detected by multicolour PRINS.
Brandt CA; Kierkegaard O; Hindkjaer J; Jensen PK; Pedersen S; Therkelsen AJ
Clin Genet; 1993 Jul; 44(1):26-31. PubMed ID: 8403451
[TBL] [Abstract][Full Text] [Related]
16. Molecular analysis of ring chromosome 20 syndrome reveals two distinct groups of patients.
Conlin LK; Kramer W; Hutchinson AL; Li X; Riethman H; Hakonarson H; Mulley JC; Scheffer IE; Berkovic SF; Hosain SA; Spinner NB
J Med Genet; 2011 Jan; 48(1):1-9. PubMed ID: 20972251
[TBL] [Abstract][Full Text] [Related]
17. Ring chromosome 20 syndrome without deletions of the subtelomeric and CHRNA4--KCNQ2 genes loci.
Elghezal H; Hannachi H; Mougou S; Kammoun H; Triki C; Saad A
Eur J Med Genet; 2007; 50(6):441-5. PubMed ID: 17851150
[TBL] [Abstract][Full Text] [Related]
18. Characteristic EEG findings in ring 20 syndrome as a diagnostic clue.
Kobayashi K; Inagaki M; Sasaki M; Sugai K; Ohta S; Hashimoto T
Electroencephalogr Clin Neurophysiol; 1998 Oct; 107(4):258-62. PubMed ID: 9872443
[TBL] [Abstract][Full Text] [Related]
19. [Fluorescence in situ hybridization in 6 patients with alterations of chromosome 18 and in 7 with marker chromosomes].
Esmer MC; Carnevale A; Gómez L; del Castillo V; Frías S
Rev Invest Clin; 1996; 48(1):27-33. PubMed ID: 8815483
[TBL] [Abstract][Full Text] [Related]
20. Presence of telomeric and subtelomeric sequences at the fusion points of ring chromosomes indicates that the ring syndrome is caused by ring instability.
Pezzolo A; Gimelli G; Cohen A; Lavaggetto A; Romano C; Fogu G; Zuffardi O
Hum Genet; 1993 Aug; 92(1):23-7. PubMed ID: 8365723
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
