(Q48897745)

English

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle.

scientific article published in October 1996

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

Brain alterations in the classical form of congenital muscular dystrophy. Clinical and neuroimaging follow-up of 12 cases and correlation with the expression of merosin in muscle. (English)

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

0 references

author name string

C P Trevisan

1

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

F Martinello

2

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

E Ferruzza

3

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

M Fanin

4

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

M Chevallay

5

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

F M Tomé

6

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

publication date

1 October 1996

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

Child's Nervous System

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

12

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

10

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

604-610

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

https://scigraph.springernature.com/pub.10.1007/bf00261655

0 references

Abnormal localization of laminin subunits in muscular dystrophies

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Involvement of the central nervous system in congenital muscular dystrophies.

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy with merosin deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy: brain alterations in an unselected series of Western patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Divergence of central nervous system involvement in 2 Italian sisters with congenital muscular dystrophy: a clinical and neuroradiological follow-up

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic epidemiology of congenital muscular dystrophy in a sample from north-east Italy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy and cerebral CT scan anomalies. Results of a collaborative study of the Société de Neurologie Infantile

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy with leukoencephalopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myoencephalopathy: cerebral hypomyelination revealed by CT scan of the head in a muscle disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/8934020

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF00261655

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

16 February 2018

http://europepmc.org/abstract/MED/8934020

ResearchGate publication ID

0 references

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