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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

120 related articles for article (PubMed ID: 8068155)

  • 1. Developmental study of leptomeningeal glioneuronal heterotopia.
    Iida K; Hirano S; Takashima S; Miyahara S
    Pediatr Neurol; 1994 Jun; 10(4):295-8. PubMed ID: 8068155
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Experimentally induced leptomeningeal glioneuronal heterotopia and underlying cortical dysplasia of the lateral limbic area in rats treated transplacentally with methylmercury.
    Kakita A; Wakabayashi K; Su M; Piao YS; Takahashi H
    J Neuropathol Exp Neurol; 2001 Aug; 60(8):768-77. PubMed ID: 11487051
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Distribution of leptomeningeal glioneuronal heterotopia in alobar holoprosencephaly.
    Mizuguchi M; Maekawa S; Kamoshita S
    Arch Neurol; 1994 Sep; 51(9):951-4. PubMed ID: 8080397
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Comparison of brain imaging and neuropathology in cases of trisomy 18 and 13.
    Inagaki M; Ando Y; Mito T; Ieshima A; Ohtani K; Takashima S; Takeshita K
    Neuroradiology; 1987; 29(5):474-9. PubMed ID: 3317111
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Pathophysiological analyses of leptomeningeal heterotopia using gyrencephalic mammals.
    Matsumoto N; Kobayashi N; Uda N; Hirota M; Kawasaki H
    Hum Mol Genet; 2018 Mar; 27(6):985-991. PubMed ID: 29325060
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Clinicopathologic studies on leptomeningeal glioneuronal heterotopia in congenital anomalies.
    Hirano S; Houdou S; Hasegawa M; Kamei A; Takashima S
    Pediatr Neurol; 1992; 8(6):441-4. PubMed ID: 1476573
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Partial distal 12q trisomy with arachnoid cyst.
    Masuno M; Fukushima Y; Sugio Y; Kuroki Y
    Jinrui Idengaku Zasshi; 1987 Mar; 32(1):39-43. PubMed ID: 3613245
    [No Abstract]   [Full Text] [Related]  

  • 8. Immunohistochemical expression of cell adhesion molecule L1 in hemimegalencephaly.
    Tsuru A; Mizuguchi M; Uyemura K; Becker LE; Takashima S
    Pediatr Neurol; 1997 Jan; 16(1):45-9. PubMed ID: 9044401
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Primary diffuse leptomeningeal oligodendroglioma. Case report.
    Chen R; Macdonald DR; Ramsay DA
    J Neurosurg; 1995 Oct; 83(4):724-8. PubMed ID: 7674024
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Trisomy (12p) with telocentric and pseudoisodicentric chromosome formation in a fetus.
    Plaja A; Mediano C; Farran I; Vendrell T; Toran N; Gili T; Sanchez MA; Sarret E
    Ann Genet; 1998; 41(1):52-5. PubMed ID: 9599652
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Mosaic 13 trisomy due to de novo 13/13 translocation with subsequent fission. Karyotype: 46,XX,-13, +t(13;13)(p11;q11)/46,XX,del(13)(p11). A second example.
    Fryns JP; Kleczkowska A; Jaeken J; Van Herck K; Van den Berghe MH
    Ann Genet; 1989; 32(3):177-9. PubMed ID: 2486064
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Periventricular heterotopia may result from radial glial fiber disruption.
    Santi MR; Golden JA
    J Neuropathol Exp Neurol; 2001 Sep; 60(9):856-62. PubMed ID: 11556542
    [TBL] [Abstract][Full Text] [Related]  

  • 13. In utero brain lesions in SIDS.
    Obonai T; Takashima S
    Pediatr Neurol; 1998 Jul; 19(1):23-5. PubMed ID: 9682880
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Intracranial extracerebral glioneuronal heterotopia. Case report and review of the literature.
    Oya S; Kawahara N; Aoki S; Hayashi N; Shibahara J; Izumi M; Kirino T
    J Neurosurg; 2005 Jan; 102(1 Suppl):105-12. PubMed ID: 16206744
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Discrete glioneuronal malformative lesions in the foetal and infantile cerebral cortex.
    Laure-Kamionowska M; Maślińska D; Raczkowska B
    Folia Neuropathol; 2002; 40(4):183-91. PubMed ID: 12572775
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Aberrant neuronal migration in the brainstem of fukuyama-type congenital muscular dystrophy.
    Saito Y; Kobayashi M; Itoh M; Saito K; Mizuguchi M; Sasaki H; Arima K; Yamamoto T; Takashima S; Sasaki M; Hayashi K; Osawa M
    J Neuropathol Exp Neurol; 2003 May; 62(5):497-508. PubMed ID: 12769189
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Trisomy 9p and tetrasomy 9p: a unique, clinically recognisable syndrome.
    Fryns JP
    Genet Couns; 1998; 9(3):229-30. PubMed ID: 9777347
    [No Abstract]   [Full Text] [Related]  

  • 18. An infant with double trisomy (48,XXX, + 18).
    Jaruratanasirikul S; Jinorose U
    Am J Med Genet; 1994 Jan; 49(2):207-10. PubMed ID: 8116670
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A case of mosaic trisomy 14 due to an isochromosome, i(14q).
    Ozawa N; Xu ZD; Soh K; Takabayashi T; Sato S; Yajima A; Suzuki M; Ikeuchi T; Tonomura A
    Jinrui Idengaku Zasshi; 1984 Mar; 29(1):69-76. PubMed ID: 6748330
    [No Abstract]   [Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 6.