99 related articles for article (PubMed ID: 7573359)
1. Lissencephaly gene product. Localization in the central nervous system and loss of immunoreactivity in Miller-Dieker syndrome.
Mizuguchi M; Takashima S; Kakita A; Yamada M; Ikeda K
Am J Pathol; 1995 Oct; 147(4):1142-51. PubMed ID: 7573359
[TBL] [Abstract][Full Text] [Related]
2. Isolation of a Miller-Dieker lissencephaly gene containing G protein beta-subunit-like repeats.
Reiner O; Carrozzo R; Shen Y; Wehnert M; Faustinella F; Dobyns WB; Caskey CT; Ledbetter DH
Nature; 1993 Aug; 364(6439):717-21. PubMed ID: 8355785
[TBL] [Abstract][Full Text] [Related]
3. Interneuron deficits in patients with the Miller-Dieker syndrome.
Pancoast M; Dobyns W; Golden JA
Acta Neuropathol; 2005 Apr; 109(4):400-4. PubMed ID: 15739099
[TBL] [Abstract][Full Text] [Related]
4. [Lissencephalia syndromes].
Bode H; Bubl R
Schweiz Rundsch Med Prax; 1992 Dec; 81(51):1529-33. PubMed ID: 1470795
[TBL] [Abstract][Full Text] [Related]
5. Syndromes with lissencephaly. I: Miller-Dieker and Norman-Roberts syndromes and isolated lissencephaly.
Dobyns WB; Stratton RF; Greenberg F
Am J Med Genet; 1984 Jul; 18(3):509-26. PubMed ID: 6476009
[TBL] [Abstract][Full Text] [Related]
6. The MIller-Dieker syndrome.
Jones KL; Gilbert EF; Kaveggia EG; Opitz JM
Pediatrics; 1980 Aug; 66(2):277-81. PubMed ID: 7402813
[TBL] [Abstract][Full Text] [Related]
7. A new microduplication syndrome encompassing the region of the Miller-Dieker (17p13 deletion) syndrome.
Roos L; Jønch AE; Kjaergaard S; Taudorf K; Simonsen H; Hamborg-Petersen B; Brøndum-Nielsen K; Kirchhoff M
J Med Genet; 2009 Oct; 46(10):703-10. PubMed ID: 19520700
[TBL] [Abstract][Full Text] [Related]
8. Fukutin protein is expressed in neurons of the normal developing human brain but is reduced in Fukuyama-type congenital muscular dystrophy brain.
Saito Y; Mizuguchi M; Oka A; Takashima S
Ann Neurol; 2000 Jun; 47(6):756-64. PubMed ID: 10852541
[TBL] [Abstract][Full Text] [Related]
9. Molecular analysis of the lissencephaly gene 1 (LIS-1) in medulloblastomas.
Koch A; Tonn J; Kraus JA; Sorensen N; Albrecht NS; Wiestler OD; Pietsch T
Neuropathol Appl Neurobiol; 1996 Jun; 22(3):233-42. PubMed ID: 8804025
[TBL] [Abstract][Full Text] [Related]
10. Expression of the LIS-1 gene product in brain anomalies with a migration disorder.
Isumi H; Takashima S; Kakita A; Yamada M; Ikeda K; Mizuguchi M
Pediatr Neurol; 1997 Jan; 16(1):42-4. PubMed ID: 9044400
[TBL] [Abstract][Full Text] [Related]
11. [Miller-Dieker syndrome: a new case with cerebral echographic study].
Vaquerizo-Madrid J; Gómez-Martín H; Rincón-Rodera P; Alonso-Luengo O
Rev Neurol; 2000 Jan 1-15; 30(1):48-50. PubMed ID: 10742996
[TBL] [Abstract][Full Text] [Related]
12. DNA analysis in patients with lissencephaly type I and other cortical dysplasias.
Oostra BA; de Rijk-van Andel JF; Eussen HJ; van Hemel JO; Halley DJ; Niermeijer MF
Am J Med Genet; 1991 Sep; 40(3):383-6. PubMed ID: 1951447
[TBL] [Abstract][Full Text] [Related]
13. Stathmin: cellular localization of a major phosphoprotein in the adult rat and human CNS.
Peschanski M; Hirsch E; Dusart I; Doye V; Marty S; Manceau V; Sobel A
J Comp Neurol; 1993 Nov; 337(4):655-68. PubMed ID: 8288776
[TBL] [Abstract][Full Text] [Related]
14. Report of two Turkish infants with Norman-Roberts syndrome.
Caksen H; Tuncer O; Kirimi E; Fryns JP; Uner A; Unal O; Cinal A; Odabaş D
Genet Couns; 2004; 15(1):9-17. PubMed ID: 15083694
[TBL] [Abstract][Full Text] [Related]
15. Deletion of 17p13 and LIS1 gene mutation in isolated lissencephaly sequence.
Elias RC; Galera MF; Schnabel B; Briones MR; Borri ML; Lipay M; Carvalheira G; Brunoni D; Melaragno MI
Pediatr Neurol; 2006 Jul; 35(1):42-6. PubMed ID: 16814084
[TBL] [Abstract][Full Text] [Related]
16. [A case of Miller-Dieker syndrome associated with satellite on chromosome 17p].
Obara Y; Koseki N; Fujiwara J; Kikuchi M; Miura T; Funato T; Kaku M
Rinsho Byori; 2001 Feb; 49(2):189-92. PubMed ID: 11307315
[TBL] [Abstract][Full Text] [Related]
17. Partial deletion of LIS1: a pitfall in molecular diagnosis of Miller-Dieker syndrome.
Izumi K; Kuratsuji G; Ikeda K; Takahashi T; Kosaki K
Pediatr Neurol; 2007 Apr; 36(4):258-60. PubMed ID: 17437911
[TBL] [Abstract][Full Text] [Related]
18. Predominant localization of the LIS family of gene products to Cajal-Retzius cells and ventricular neuroepithelium in the developing human cortex.
Clark GD; Mizuguchi M; Antalffy B; Barnes J; Armstrong D
J Neuropathol Exp Neurol; 1997 Sep; 56(9):1044-52. PubMed ID: 9291945
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. MLPA analysis for a panel of syndromes with mental retardation reveals imbalances in 5.8% of patients with mental retardation and dysmorphic features, including duplications of the Sotos syndrome and Williams-Beuren syndrome regions.
Kirchhoff M; Bisgaard AM; Bryndorf T; Gerdes T
Eur J Med Genet; 2007; 50(1):33-42. PubMed ID: 17090394
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]