(Q48277389)

10 February 2018

title

Immature astrocytes in Fukuyama congenital muscular dystrophy: an immunohistochemical study. (English)

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10 February 2018

Fukuyama congenital muscular dystrophy

main subject

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0 references

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Yamamoto T

1

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10 February 2018

Armstrong D

2

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10 February 2018

Shibata N

3

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10 February 2018

Kanazawa M

4

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10 February 2018

Kobayashi M

5

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10 February 2018

publication date

1 January 1999

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10 February 2018

published in

Pediatric Neurology

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10 February 2018

volume

20

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10 February 2018

issue

1

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10 February 2018

page(s)

31-37

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10 February 2018

Congenital progressive muscular dystrophy of the Fukuyama type - clinical, genetic and pathological considerations

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7 January 2021

Congenital muscular dystrophy as a disease of the central nervous system

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Ocular manifestations in Fukuyama type congenital muscular dystrophy.

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Electron microscopic examination of basal lamina in Fukuyama congenital muscular dystrophy

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7 January 2021

Abnormal localization of laminin subunits in muscular dystrophies

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Dystrophin-glycoprotein complex: its role in the molecular pathogenesis of muscular dystrophies.

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Molecular heterogeneity of basal laminae: isoforms of laminin and collagen IV at the neuromuscular junction and elsewhere

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Early ultrastructural changes in the central nervous system in Fukuyama congenital muscular dystrophy.

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7 January 2021

Localization of laminin subunits in the central nervous system in Fukuyama congenital muscular dystrophy: an immunohistochemical investigation.

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Role of the basement membrane in neurogenesis and repair of injury in the central nervous system

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Developmental events during the early stages of cerebral cortical neurogenesis in man. A correlative light, electron microscopic, immunohistochemical and Golgi study

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Pial-glial barrier abnormalities in fetuses with Fukuyama congenital muscular dystrophy

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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

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Histopathological study of alobar holoprosencephaly. 1. Abnormal laminar architecture of the telencephalic cortex

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Regressive changes of astroglia in white matter lesions in cerebrovascular disease and Alzheimer's disease patients.

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The role of swollen astrocytes in human brain lesions after edema--an immunohistochemical study using formalin-fixed paraffin-embedded sections

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7 January 2021

Changes in glial cell markers in recent and old demyelinated lesions in central pontine myelinolysis

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7 January 2021

Transition between immature radial glia and mature astrocytes studied with a monoclonal antibody to vimentin.

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Developmental changes revealed by immunohistochemical markers in human cerebral cortex.

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Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement

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7 January 2021

Prenatal development of fibrous (white matter), protoplasmic (gray matter), and layer I astrocytes in the human cerebral cortex: a Golgi study.

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7 January 2021

The topographical distribution of S-100 and GFA proteins in the adult rat brain: An immunohistochemical study using horseradish peroxidase-labelled antibodies

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7 January 2021

MAP 1A and MAP 1B are structurally related microtubule associated proteins with distinct developmental patterns in the CNS

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7 January 2021

Cortical dysplasia in Fukuyama congenital muscular dystrophy (FCMD): a Golgi and angioarchitectonic analysis

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7 January 2021

Meningeal cells are involved in foliation, lamination, and neurogenesis of the cerebellum: evidence from 6-hydroxydopamine-induced destruction of meningeal cells

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7 January 2021

Destruction of meningeal cells over the newborn hamster cerebellum with 6-hydroxydopamine prevents foliation and lamination in the rostral cerebellum

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7 January 2021

Epithelial membrane antigen and cytokeratin expression by meningiomas: an immunohistological study

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7 January 2021

Fibronectin-like immunoreactivity in the developing cerebral cortex.

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7 January 2021

Expression of small heat-shock protein hsp 27 in reactive gliosis in Alzheimer disease and other types of dementia.

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7 January 2021

Induction of heat shock (stress) genes in the mammalian brain by hyperthermia and other traumatic events: a current perspective

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7 January 2021

10.1016/S0887-8994(98)00089-7

Identifiers

DOI

1 reference

10 February 2018

1 reference

10 February 2018