Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency (Q48774323)

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scientific article

Language	Label	Description	Also known as
English	Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency	scientific article

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

muscular dystrophy

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based on heuristic

inferred from title

Francesco Muntoni

8

object named as

Muntoni F

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

author name string

Tan E

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Topaloglu H

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Sewry C

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Zorlu Y

4

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Naom I

5

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Erdem S

6

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

D'Alessandro M

7

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Dubowitz V

9

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

publication date

1 March 1997

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Neuromuscular Disorders

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

7

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

2

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

85-89

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Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

Expression of laminin subunits in congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900421-X

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%2FS0960-8966%2896%2900421-X

7 January 2021

based on heuristic

inferred from DOI database lookup

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

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https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900421-X

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%2FS0960-8966%2896%2900421-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900421-X

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%2FS0960-8966%2896%2900421-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial adult-onset muscular dystrophy with leukoencephalopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900421-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Congenital muscular dystrophy with laminin alpha 2 chain deficiency: identification of a new intermediate phenotype and correlation of clinical findings to muscle immunohistochemistry

1 reference

https://api.crossref.org/works/10.1016%2FS0960-8966%2896%2900421-X

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0960-8966(96)00421-X

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/9131648

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