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 *

54 related articles for article (PubMed ID: 1036064)

  • 1. [Congenital muscular dystrophy associated with micropolygyria of the cerebrum and cerebellum].
    Ogasawara Y; Ito K; Murofushi K
    No To Shinkei; 1976 May; 28(5):451-7. PubMed ID: 1036064
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Cerebellar micropolygyria in Fukuyama congenital muscular dystrophy: observations in fetal and pediatric cases.
    Takada K; Nakamura H
    Brain Dev; 1990; 12(6):774-8. PubMed ID: 2092587
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [2 autopsy cases of congenital muscular dystrophy of Fukuyama type--a typical and an atypical cases].
    Koga M; Abe M; Tateishi J; Antoku Y; Iwashita H; Miyoshino S
    No To Shinkei; 1984 Nov; 36(11):1103-8. PubMed ID: 6525323
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Are breaches in the glia limitans the primary cause of the micropolygyria in Fukuyama-type congenital muscular dystrophy (FCMD)? Pathological study of the cerebral cortex of an FCMD fetus.
    Nakano I; Funahashi M; Takada K; Toda T
    Acta Neuropathol; 1996; 91(3):313-21. PubMed ID: 8834545
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Magnetic resonance imaging in classification of congenital muscular dystrophies with brain abnormalities.
    van der Knaap MS; Smit LM; Barth PG; Catsman-Berrevoets CE; Brouwer OF; Begeer JH; de Coo IF; Valk J
    Ann Neurol; 1997 Jul; 42(1):50-9. PubMed ID: 9225685
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type).
    Takada K; Nakamura H; Tanaka J
    J Neuropathol Exp Neurol; 1984 Jul; 43(4):395-407. PubMed ID: 6737009
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Congenital muscular dystrophy associated with micropolygyria - report of two cases.
    Murakami T; Konishi Y; Rakamiya M; Tsukagoshi H
    Acta Pathol Jpn; 1975 Sep; 25(5):599-612. PubMed ID: 1199729
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Altered glycosylation of alpha-dystroglycan in neurons of Fukuyama congenital muscular dystrophy brains.
    Saito Y; Yamamoto T; Mizuguchi M; Kobayashi M; Saito K; Ohno K; Osawa M
    Brain Res; 2006 Feb; 1075(1):223-8. PubMed ID: 16466646
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Dysgenesis of CNS in dyscranio-pygo-phalangia (author's transl)].
    Hori A; Murofushi K; Iizuka R
    Acta Neuropathol; 1976 Aug; 35(4):327-32. PubMed ID: 822683
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Brain morphology in the Galloway syndrome.
    Kozlowski PB; Sher JH; Nicastri AD; Rudelli RD
    Clin Neuropathol; 1989; 8(2):85-91. PubMed ID: 2721045
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of cerebello-olivary degeneration in idiopathic late cortical cerebellar atrophy: clinicopathological study of four autopsy cases.
    Ota S; Tsuchiya K; Anno M; Niizato K; Akiyama H
    Neuropathology; 2008 Feb; 28(1):43-50. PubMed ID: 18181834
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Abnormality of cerebral gangliosides in Fukuyama type congenital muscular dystrophy.
    Izumi T; Hara K; Ogawa T; Osawa M; Saito K; Novo ML; Fukuyama Y; Takashima S
    Brain Dev; 1995; 17(1):33-7. PubMed ID: 7762760
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Congenital muscular dystrophy as a disease of the central nervous system.
    Kamoshita S; Konishi Y; Segawa M; Fukuyama Y
    Arch Neurol; 1976 Jul; 33(7):513-6. PubMed ID: 938276
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Lissencephaly with agenesis of corpus callosum and rudimentary dysplastic cerebellum: a subtype of lissencephaly with cerebellar hypoplasia.
    Miyata H; Chute DJ; Fink J; Villablanca P; Vinters HV
    Acta Neuropathol; 2004 Jan; 107(1):69-81. PubMed ID: 14566414
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Effects of lifelong ethanol consumption on cerebellar layer volumes in AA and ANA rats.
    Rintala J; Jaatinen P; Lu W; Sarviharju M; Eriksson CJ; Laippala P; Kiianmaa K; Hervonen A
    Alcohol Clin Exp Res; 1997 Apr; 21(2):311-7. PubMed ID: 9113269
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Cerebro-ocular dysplasia-muscular dystrophy (COD-MD) syndrome.
    Towfighi J; Sassani JW; Suzuki K; Ladda RL
    Acta Neuropathol; 1984; 65(2):110-23. PubMed ID: 6441438
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Congenital muscular dystrophy with cerebral white matter spongiosis.
    Echenne B; Pages M; Marty-Double C
    Brain Dev; 1984; 6(5):491-5. PubMed ID: 6517223
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [An autopsied case of idiopathic late cortical cerebellar atrophy--comparison with other cortical cerebellar atrophy].
    Iwabuchi K; Yagishita S
    Rinsho Shinkeigaku; 1990 Nov; 30(11):1190-6. PubMed ID: 2085923
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.