Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study (Q48224285)

9 February 2018

title

Merosin-deficient congenital muscular dystrophy associated with abnormal cerebral cortical gyration: an autopsy study (English)

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9 February 2018

congenital muscular dystrophy

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Taratuto AL

1

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Lubieniecki F

2

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Díaz D

3

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Schultz M

4

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Ruggieri V

5

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Saccoliti M

6

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Dubrovsky A

7

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publication date

1 March 1999

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9 February 2018

published in

Neuromuscular Disorders

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volume

9

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issue

2

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page(s)

86-94

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9 February 2018

Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping

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Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

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Merosin-negative congenital muscular dystrophy, occipital epilepsy with periodic spasms and focal cortical dysplasia. Report of three Italian cases in two families.

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Presence of Laminin 5 Chain and Lack of Laminin 1 Chain during Human Muscle Development and in Muscular Dystrophies

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Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophy

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Localization of laminin alpha 2 chain in normal human central nervous system: an immunofluorescence and ultrastructural study

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

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

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Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsy

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Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophy

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Immunohistochemical study of merosin-negative congenital muscular dystrophy: laminin alpha 2 deficiency in skin biopsy

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Intracellular detection of laminin alpha 2 chain in skin by electron microscopy immunocytochemistry: comparison between normal and laminin alpha 2 chain deficient subjects

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Basement membrane abnormality in merosin-negative congenital muscular dystrophy

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Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency

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Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy

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Peripheral nerve involvement in merosin-deficient congenital muscular dystrophy and dy mouse

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Localization of the laminin alpha 2 chain in normal human skeletal muscle and peripheral nerve: an ultrastructural immunolabeling study

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7 January 2021

10.1016/S0960-8966(98)00112-6

Identifiers

DOI

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9 February 2018

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9 February 2018