150 related articles for article (PubMed ID: 12654978)
1. Periventricular heterotopia associated with chromosome 5p anomalies.
Sheen VL; Wheless JW; Bodell A; Braverman E; Cotter PD; Rauen KA; Glenn O; Weisiger K; Packman S; Walsh CA; Sherr EH
Neurology; 2003 Mar; 60(6):1033-6. PubMed ID: 12654978
[TBL] [Abstract][Full Text] [Related]
2. Periventricular nodular heterotopia: report of a pediatric series.
Spalice A; Taddeucci G; Perla FM; Pascali MP; Iannetti P
J Child Neurol; 2002 Apr; 17(4):300-4. PubMed ID: 12088088
[TBL] [Abstract][Full Text] [Related]
3. Trisomy of the short arm of chromosome 5 due to a de novo inversion and duplication (5)(p15.3 p13.3).
Cervera M; Sánchez S; Molina B; Alcántara MA; Del Castillo V; Carnevale A; González-del Angel A
Am J Med Genet A; 2005 Aug; 136A(4):381-5. PubMed ID: 16001443
[TBL] [Abstract][Full Text] [Related]
4. Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus.
Sheen VL; Basel-Vanagaite L; Goodman JR; Scheffer IE; Bodell A; Ganesh VS; Ravenscroft R; Hill RS; Cherry TJ; Shugart YY; Barkovich J; Straussberg R; Walsh CA
Brain Dev; 2004 Aug; 26(5):326-34. PubMed ID: 15165674
[TBL] [Abstract][Full Text] [Related]
5. Bilateral periventricular nodular heterotopia with mental retardation and frontonasal malformation.
Guerrini R; Dobyns WB
Neurology; 1998 Aug; 51(2):499-503. PubMed ID: 9710025
[TBL] [Abstract][Full Text] [Related]
6. Mutation in filamin A causes periventricular heterotopia, developmental regression, and West syndrome in males.
Masruha MR; Caboclo LO; Carrete H; Cendes IL; Rodrigues MG; Garzon E; Yacubian EM; Sakamoto AC; Sheen V; Harney M; Neal J; Hill RS; Bodell A; Walsh C; Vilanova LC
Epilepsia; 2006 Jan; 47(1):211-4. PubMed ID: 16417552
[TBL] [Abstract][Full Text] [Related]
7. Periventricular heterotopia, mental retardation, and epilepsy associated with 5q14.3-q15 deletion.
Cardoso C; Boys A; Parrini E; Mignon-Ravix C; McMahon JM; Khantane S; Bertini E; Pallesi E; Missirian C; Zuffardi O; Novara F; Villard L; Giglio S; Chabrol B; Slater HR; Moncla A; Scheffer IE; Guerrini R
Neurology; 2009 Mar; 72(9):784-92. PubMed ID: 19073947
[TBL] [Abstract][Full Text] [Related]
8. Steroid sulfatase deficiency with bilateral periventricular nodular heterotopia.
Ozawa H; Osawa M; Nagai T; Sakura N
Pediatr Neurol; 2006 Mar; 34(3):239-41. PubMed ID: 16504797
[TBL] [Abstract][Full Text] [Related]
9. A patient with an interstitial duplication of chromosome 5p11-p13.3 further confirming a critical region for 5p duplication syndrome.
Loscalzo ML; Becker TA; Sutcliffe M
Eur J Med Genet; 2008; 51(1):54-60. PubMed ID: 18006398
[TBL] [Abstract][Full Text] [Related]
10. Bilateral periventricular nodular heterotopia with mental retardation and syndactyly in boys: a new X-linked mental retardation syndrome.
Dobyns WB; Guerrini R; Czapansky-Beilman DK; Pierpont ME; Breningstall G; Yock DH; Bonanni P; Truwit CL
Neurology; 1997 Oct; 49(4):1042-7. PubMed ID: 9339687
[TBL] [Abstract][Full Text] [Related]
11. Multiple pterygium syndrome, bilateral periventricular nodular heterotopia and epileptic seizures--a syndrome?
Holtmann M; Woermann FG; Boenigk HE
Neuropediatrics; 2001 Oct; 32(5):264-6. PubMed ID: 11748498
[TBL] [Abstract][Full Text] [Related]
12. Partial tetrasomy with triplication of chromosome (5) (p14-p15.33) in a patient with severe multiple congenital anomalies.
Harrison KJ; Teshima IE; Silver MM; Jay V; Unger S; Robinson WP; James A; Levin A; Chitayat D
Am J Med Genet; 1998 Sep; 79(2):103-7. PubMed ID: 9741467
[TBL] [Abstract][Full Text] [Related]
13. Identification of a duplication of Xq28 associated with bilateral periventricular nodular heterotopia.
Fink JM; Dobyns WB; Guerrini R; Hirsch BA
Am J Hum Genet; 1997 Aug; 61(2):379-87. PubMed ID: 9311743
[TBL] [Abstract][Full Text] [Related]
14. Trisomy of the short arm of chromosome 5: autopsy data in a malformed newborn with inv dup (5) (p13.1----p15.3).
Kleczkowska A; Fryns JP; Moerman P; Vandenberghe K; Van den Berghe H
Clin Genet; 1987 Jul; 32(1):49-56. PubMed ID: 3621654
[TBL] [Abstract][Full Text] [Related]
15. Two sibs with different phenotypes due to adjacent-1 segregation of a subtle translocation t(4;5)(p16.3;p15.3)mat.
Qumsiyeh MB; Stevens CA
Am J Med Genet; 1993 Sep; 47(3):387-91. PubMed ID: 8135287
[TBL] [Abstract][Full Text] [Related]
16. Molecular studies of segmental aneusomy: FISHing for the atypical cry in del(5)(p15.3).
Hodge JC; Lawson-Yuen A; Stoler JM; Ligon AH
Cytogenet Genome Res; 2007; 119(1-2):15-20. PubMed ID: 18160776
[TBL] [Abstract][Full Text] [Related]
17. Molecular characterisation of a mosaicism with a complex chromosome rearrangement: evidence for coincident chromosome healing by telomere capture and neo-telomere formation.
Chabchoub E; Rodríguez L; Galán E; Mansilla E; Martínez-Fernandez ML; Martínez-Frías ML; Fryns JP; Vermeesch JR
J Med Genet; 2007 Apr; 44(4):250-6. PubMed ID: 17172463
[TBL] [Abstract][Full Text] [Related]
18. Mutations in filamin 1 prevent migration of cerebral cortical neurons in human periventricular heterotopia.
Fox JW; Lamperti ED; Ekşioğlu YZ; Hong SE; Feng Y; Graham DA; Scheffer IE; Dobyns WB; Hirsch BA; Radtke RA; Berkovic SF; Huttenlocher PR; Walsh CA
Neuron; 1998 Dec; 21(6):1315-25. PubMed ID: 9883725
[TBL] [Abstract][Full Text] [Related]
19. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
Shi S; Pan G; Yang Y; Yan R; Li W
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
[TBL] [Abstract][Full Text] [Related]
20. Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation.
Grosso S; Fichera M; Galesi O; Luciano D; Pucci L; Giardini F; Berardi R; Balestri P
Dev Med Child Neurol; 2008 Jun; 50(6):473-6. PubMed ID: 18384621
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
