159 related articles for article (PubMed ID: 12199736)
1. Mild generalized epilepsy and developmental disorder associated with large inv dup(15).
Chifari R; Guerrini R; Pierluigi M; Cavani S; Sgrò V; Elia M; Canger R; Canevini MP
Epilepsia; 2002 Sep; 43(9):1096-100. PubMed ID: 12199736
[TBL] [Abstract][Full Text] [Related]
2. Symptomatic generalized epilepsy associated with an inverted duplication of chromosome 15.
Takeda Y; Baba A; Nakamura F; Ito M; Honma H; Koyama T
Seizure; 2000 Mar; 9(2):145-50. PubMed ID: 10845741
[TBL] [Abstract][Full Text] [Related]
3. Unusual features in children with inv dup(15) supernumerary marker: a study of genotype-phenotype correlation in Taiwan.
Hou JW; Wang TR
Eur J Pediatr; 1998 Feb; 157(2):122-7. PubMed ID: 9504785
[TBL] [Abstract][Full Text] [Related]
4. Partial hexasomy of chromosome 15.
Huang B; Bartley J
Am J Med Genet A; 2003 Sep; 121A(3):277-80. PubMed ID: 12923871
[TBL] [Abstract][Full Text] [Related]
5. The inv dup (15) or idic (15) syndrome (Tetrasomy 15q).
Battaglia A
Orphanet J Rare Dis; 2008 Nov; 3():30. PubMed ID: 19019226
[TBL] [Abstract][Full Text] [Related]
6. Inv dup (15): is the electroclinical phenotype helpful for this challenging clinical diagnosis?
Valente KD; Freitas A; Fridman C; Varela M; Silva AE; Fett AC; Koiffmann CP
Clin Neurophysiol; 2006 Apr; 117(4):803-9. PubMed ID: 16495142
[TBL] [Abstract][Full Text] [Related]
7. FISH characterisation of dynamic mosaicism involving an inv dup(15) in a patient with mental retardation.
Cockwell AE; Dávalos IP; Rivera HR; Crolla JA
Am J Med Genet; 2001 Nov; 103(4):289-94. PubMed ID: 11746008
[TBL] [Abstract][Full Text] [Related]
8. Molecular cytogenetic analysis of inv dup(15) chromosomes, using probes specific for the Prader-Willi/Angelman syndrome region: clinical implications.
Leana-Cox J; Jenkins L; Palmer CG; Plattner R; Sheppard L; Flejter WL; Zackowski J; Tsien F; Schwartz S
Am J Hum Genet; 1994 May; 54(5):748-56. PubMed ID: 8178816
[TBL] [Abstract][Full Text] [Related]
9. Simultaneous formation of inv dup(15) and dup(15q) in a girl with developmental delay: origin of the abnormal chromosomes.
Abeliovich D; Dagan J; Werner M; Lerer I; Shapira Y; Meiner V
Eur J Hum Genet; 1995; 3(1):49-55. PubMed ID: 7767656
[TBL] [Abstract][Full Text] [Related]
10. Cytogenetic and molecular characterization of inverted duplicated chromosomes 15 from 11 patients.
Cheng SD; Spinner NB; Zackai EH; Knoll JH
Am J Hum Genet; 1994 Oct; 55(4):753-9. PubMed ID: 7942854
[TBL] [Abstract][Full Text] [Related]
11. Absence epilepsy with fast rhythmic discharges during sleep: an intermediary form of generalized epilepsy?
Guye M; Bartolomei F; Gastaut JL; Chauvel P; Dravet C
Epilepsia; 2001 Mar; 42(3):351-6. PubMed ID: 11442152
[TBL] [Abstract][Full Text] [Related]
12. The inv dup(15) syndrome: a clinically recognizable syndrome with altered behavior, mental retardation, and epilepsy.
Battaglia A; Gurrieri F; Bertini E; Bellacosa A; Pomponi MG; Paravatou-Petsotas M; Mazza S; Neri G
Neurology; 1997 Apr; 48(4):1081-6. PubMed ID: 9109904
[TBL] [Abstract][Full Text] [Related]
13. Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures.
Trevathan E; Kerls SP; Hammer AE; Vuong A; Messenheimer JA
Pediatrics; 2006 Aug; 118(2):e371-8. PubMed ID: 16847080
[TBL] [Abstract][Full Text] [Related]
14. Maternal uniparental disomy in a patient with Prader-Willi syndrome with an additional small inv dup(15) chromosome.
Wang YM; Chuang L; Wang BT; Kuo PL
J Formos Med Assoc; 2004 Dec; 103(12):943-7. PubMed ID: 15624046
[TBL] [Abstract][Full Text] [Related]
15. [A case of inv dup (15) mosaic with mental retardation and symptomatic generalized epilepsy].
Kobayashi Y; Yoshino A
No To Shinkei; 1999 Mar; 51(3):259-62. PubMed ID: 10226291
[TBL] [Abstract][Full Text] [Related]
16. Absence status epilepsy: delineation of a distinct idiopathic generalized epilepsy syndrome.
Genton P; Ferlazzo E; Thomas P
Epilepsia; 2008 Apr; 49(4):642-9. PubMed ID: 18093147
[TBL] [Abstract][Full Text] [Related]
17. Two inv dup(15) chromosomes in a woman with repeated abortions.
Shim SH; Lee CH; Park YJ; Lee HJ; Park WI; Cho YH
Am J Med Genet; 2001 Dec; 104(4):303-6. PubMed ID: 11754065
[TBL] [Abstract][Full Text] [Related]
18. The syndrome of inv dup (15): clinical, electroencephalographic, and imaging findings.
Buoni S; Sorrentino L; Farnetani MA; Pucci L; Fois A
J Child Neurol; 2000 Jun; 15(6):380-5. PubMed ID: 10868780
[TBL] [Abstract][Full Text] [Related]
19. Uniparental disomy explains the occurrence of the Angelman or Prader-Willi syndrome in patients with an additional small inv dup(15) chromosome.
Robinson WP; Wagstaff J; Bernasconi F; Baccichetti C; Artifoni L; Franzoni E; Suslak L; Shih LY; Aviv H; Schinzel AA
J Med Genet; 1993 Sep; 30(9):756-60. PubMed ID: 8411071
[TBL] [Abstract][Full Text] [Related]
20. Efficacy of lamotrigine in idiopathic generalized epilepsy syndromes: a video-EEG-controlled, open study.
Gericke CA; Picard F; de Saint-Martin A; Strumia S; Marescaux C; Hirsch E
Epileptic Disord; 1999 Sep; 1(3):159-65. PubMed ID: 10937148
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]