(Q47938154)

English

Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study

scientific article published in March 1998

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Laminin-alpha2 (merosin), beta-dystroglycan, alpha-sarcoglycan (adhalin), and dystrophin expression in congenital muscular dystrophies: an immunohistochemical study (English)

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

immunohistochemistry

1 reference

based on heuristic

inferred from title

Fons John Marie Gabreëls

3

object named as

Gabreëls FJ

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

author name string

ter Laak HJ

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Leyten QH

2

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Kuppen H

4

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Renier WO

5

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Sengers RC

6

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

publication date

1 March 1998

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Clinical Neurology and Neurosurgery

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

100

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Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

5-10

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

Classification of the cerebro-oculo-muscular syndrome(s). Commentary to Kimura's paper (pp. 182-91)

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Lissencephaly and other malformations of cortical development: 1995 update

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

22nd ENMC sponsored workshop on congenital muscular dystrophy held in Baarn, The Netherlands, 14-16 May 1993

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Proceedings of the 27th ENMC sponsored workshop on congenital muscular dystrophy. 22-24 April 1994, The Netherlands

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal localization of laminin subunits in muscular dystrophies

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutations in the laminin alpha 2-chain gene (LAMA2) cause merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Primary structure of dystrophin-associated glycoproteins linking dystrophin to the extracellular matrix

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital muscular dystrophy. A histochemical study with morphometric analysis on biopsied muscles

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscle histochemistry in congenital muscular dystrophy with central nervous system involvement

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Abnormal expression of dystrophin-associated proteins in Fukuyama-type congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Deficiency of the 50K dystrophin-associated glycoprotein in severe childhood autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

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

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Muscle-eye-brain disease and Fukuyama type congenital muscular dystrophy are not allelic

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Missense mutations in the adhalin gene linked to autosomal recessive muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Merosin-negative congenital muscular dystrophy associated with extensive brain abnormalities

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of a gene for Fukuyama type congenital muscular dystrophy to chromosome 9q31-33

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Preserved merosin M-chain (or laminin-alpha 2) expression in skeletal muscle distinguishes Walker-Warburg syndrome from Fukuyama muscular dystrophy and merosin-deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Laminin 2 chain and adhalin deficiency in the skeletal muscle of Walker-Warburg syndrome (cerebroocular dysplasia-muscular dystrophy)

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Clinical variation within sibships in Fukuyama-type congenital muscular dystrophy.

1 reference

https://api.crossref.org/works/10.1016%2FS0303-8467%2897%2900109-1

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0303-8467(97)00109-1

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

6 February 2018

http://europepmc.org/abstract/MED/9637197

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