(Q48261562)

English

A Golgi study of the cerebral cortex in Fukuyama-type congenital muscular dystrophy, Walker-type "lissencephaly," and classical lissencephaly.

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Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

A Golgi study of the cerebral cortex in Fukuyama-type congenital muscular dystrophy, Walker-type "lissencephaly," and classical lissencephaly (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

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congenital muscular dystrophy

1 reference

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author name string

S Takashima

1

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

L E Becker

2

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

F Chan

3

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

K Takada

4

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Europe PubMed Central

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29 September 2019

publication date

1 January 1987

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29 September 2019

Brain and Development

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

9

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29 September 2019

6

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29 September 2019

621-626

1 reference

Europe PubMed Central

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29 September 2019

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Lissencephaly and Pachygyria: an architectonic and topographical analysis

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Morphology of the developing visual cortex of the human infant: a quantitative and qualitative Golgi study.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital muscular dystrophy as a disease of the central nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Cortical dysplasia in congenital muscular dystrophy with central nervous system involvement (Fukuyama type).

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital hydrocephalus and eye abnormalities with severe developmental brain defects: Warburg's syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Cerebro-ocular dysgenesis (Walker-Warburg syndrome): neuropathologic and etiologic analysis.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Oculocerebral malformations. A reappraisal of Walker's 'lissencephaly'

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Miller-Dieker syndrome: a disorder affecting specific pathways of neuronal migration

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

LISSENCEPHALY IN 2 SIBLINGS.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Maple Syrup Urine Disease in an Infant with Microgyria

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Cerebro-hepato-renal syndrome of Zellweger: an inherited disorder of neuronal migration.

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Peroxisomal and mitochondrial defects in the cerebro-hepato-renal syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

[Disorders of neuronal migration in Zellwegers cerebrohepato-renal syndrome (author's transl)]

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

A Golgi study of the brain malformation in Zellweger's cerebro-hepato-renal disease

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Cerebral malformation associated with metabolic disorder. A report of 2 cases

1 reference

https://api.crossref.org/works/10.1016%2FS0387-7604%2887%2980097-9

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0387-7604(87)80097-9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2451446%20AND%20SRC:MED&resulttype=core&format=json

29 September 2019

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