(Q74185143)

English

Alterations of the retino-cortical conduction in patients affected by classical congenital muscular dystrophy (CI-CMD) with merosin deficiency

scientific article published on 01 January 1999

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Alterations of the retino-cortical conduction in patients affected by classical congenital muscular dystrophy (CI-CMD) with merosin deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

congenital muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

A P Tormene

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

C Trevisan

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

F Martinello

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

C Riva

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

E Pastorello

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

publication date

1 January 1999

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

Documenta Ophthalmologica

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

98

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

127-138

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10946999%20AND%20SRC:MED&resulttype=core&format=json

9 November 2019

https://scigraph.springernature.com/pub.10.1023/a:1002093705611

0 references

Differential labelling of laminin alpha 2 in muscle and neural tissue of dy/dy mice: are there isoforms of the laminin alpha 2 chain?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy with partial merosin deficiency and late onset epilepsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

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/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Adhesion molecules and inherited diseases of the human nervous system

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID 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://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital muscular dystrophy with eye and brain malformations in six Dutch patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

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/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle-eye-brain disease (MEB)

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnostic criteria for Walker-Warburg syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/10946999

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q74185143&oldid=1946830618"