These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
118 related articles for article (PubMed ID: 16456669)
41. Neocortical and cerebellar developmental abnormalities in conditions of selective elimination of peroxisomes from brain or from liver. Krysko O; Hulshagen L; Janssen A; Schütz G; Klein R; De Bruycker M; Espeel M; Gressens P; Baes M J Neurosci Res; 2007 Jan; 85(1):58-72. PubMed ID: 17075904 [TBL] [Abstract][Full Text] [Related]
42. Lissencephaly and LIS1: insights into the molecular mechanisms of neuronal migration and development. Wynshaw-Boris A Clin Genet; 2007 Oct; 72(4):296-304. PubMed ID: 17850624 [TBL] [Abstract][Full Text] [Related]
43. Cortical neuronal densities and lamination in focal cortical dysplasia. Thom M; Martinian L; Sen A; Cross JH; Harding BN; Sisodiya SM Acta Neuropathol; 2005 Oct; 110(4):383-92. PubMed ID: 16151726 [TBL] [Abstract][Full Text] [Related]
44. Rare Concurrence of Two Congenital Disorders: Miller-Dieker Syndrome and T-Cell Lymphopenia. Chee SY; Guo JW; Huang CJ; Chien YH; Lee YC; Feng WK Cytogenet Genome Res; 2019; 157(4):227-230. PubMed ID: 31030199 [TBL] [Abstract][Full Text] [Related]
46. Evidence for tangential migration disturbances in human lissencephaly resulting from a defect in LIS1, DCX and ARX genes. Marcorelles P; Laquerrière A; Adde-Michel C; Marret S; Saugier-Veber P; Beldjord C; Friocourt G Acta Neuropathol; 2010 Oct; 120(4):503-15. PubMed ID: 20461390 [TBL] [Abstract][Full Text] [Related]
47. 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]
49. Gallbladder cancer in a patient with Miller-Dieker syndrome. Ueda S; Kubota M; Kuroki S; Wada M Acta Paediatr; 2006 Jan; 95(1):113-4. PubMed ID: 16373307 [TBL] [Abstract][Full Text] [Related]
50. A Case of Concurrent Miller-Dieker Syndrome (17p13.3 Deletion) and 22q11.2 Deletion Syndrome. Atwal PS; Macmurdo C J Pediatr Genet; 2015 Dec; 4(4):201-3. PubMed ID: 27617133 [TBL] [Abstract][Full Text] [Related]
51. Isolated lissencephaly sequence associated with a microdeletion at chromosome 17p13. De Rijk-van Andel JF; Catsman-Berrevoets CE; Halley DJ; Wesby-van Swaay E; Niermeijer MF; Oostra BA Hum Genet; 1991 Aug; 87(4):509-10. PubMed ID: 1879837 [TBL] [Abstract][Full Text] [Related]
52. Neuronal production and precursor proliferation defects in the neocortex of mice with loss of function in the canonical Wnt signaling pathway. Zhou CJ; Borello U; Rubenstein JL; Pleasure SJ Neuroscience; 2006 Nov; 142(4):1119-31. PubMed ID: 16920270 [TBL] [Abstract][Full Text] [Related]
53. 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]
54. Familial Miller-Dieker syndrome associated with pericentric inversion of chromosome 17. Greenberg F; Stratton RF; Lockhart LH; Elder FF; Dobyns WB; Ledbetter DH Am J Med Genet; 1986 Apr; 23(4):853-9. PubMed ID: 3963054 [TBL] [Abstract][Full Text] [Related]
55. Miller-Dieker syndrome: a disorder affecting specific pathways of neuronal migration. Alvarez LA; Yamamoto T; Wong B; Resnick TJ; Llena JF; Moshé SL Neurology; 1986 Apr; 36(4):489-93. PubMed ID: 3960322 [TBL] [Abstract][Full Text] [Related]
56. Diagnostic features and clinical signs of 21 patients with lissencephaly type 1. de Rijk-van Andel JF; Arts WF; Barth PG; Loonen MC Dev Med Child Neurol; 1990 Aug; 32(8):707-17. PubMed ID: 2210085 [TBL] [Abstract][Full Text] [Related]
57. Further delineation of the 17p13.3 microdeletion involving YWHAE but distal to PAFAH1B1: four additional patients. Schiff M; Delahaye A; Andrieux J; Sanlaville D; Vincent-Delorme C; Aboura A; Benzacken B; Bouquillon S; Elmaleh-Berges M; Labalme A; Passemard S; Perrin L; Manouvrier-Hanu S; Edery P; Verloes A; Drunat S Eur J Med Genet; 2010; 53(5):303-8. PubMed ID: 20599530 [TBL] [Abstract][Full Text] [Related]
58. Pathogenesis of migration disorders. Gressens P Curr Opin Neurol; 2006 Apr; 19(2):135-40. PubMed ID: 16538086 [TBL] [Abstract][Full Text] [Related]
59. Neocortical layer formation of human developing brains and lissencephalies: consideration of layer-specific marker expression. Saito T; Hanai S; Takashima S; Nakagawa E; Okazaki S; Inoue T; Miyata R; Hoshino K; Akashi T; Sasaki M; Goto Y; Hayashi M; Itoh M Cereb Cortex; 2011 Mar; 21(3):588-96. PubMed ID: 20624841 [TBL] [Abstract][Full Text] [Related]