Prevalence of congenital muscular dystrophy in Italy: a population study (Q28256516)

From Wikidata

Jump to navigation Jump to search

scientific article

edit

Language	Label	Description	Also known as
English	Prevalence of congenital muscular dystrophy in Italy: a population study	scientific article

Statements

instance of

scholarly article

0 references

title

Prevalence of congenital muscular dystrophy in Italy: a population study (English)

0 references

main subject

congenital disorder

0 references

Italy

0 references

congenital muscular dystrophy

1 reference

based on heuristic

inferred from title

author

Eugenio Mercuri

series ordinal

32

0 references

Adele D'Amico

series ordinal

3

0 references

Francesco Muntoni

series ordinal

28

0 references

Angela Berardinelli

series ordinal

12

0 references

Francesca Magri

series ordinal

10

0 references

Sonia Messina

series ordinal

5

object named as

Sonia Messina

0 references

Mauro Monforte

object named as

Mauro Monforte

series ordinal

18

0 references

Giorgio Tasca

object named as

Giorgio Tasca

series ordinal

17

0 references

Enzo Ricci

object named as

Enzo Ricci

series ordinal

21

0 references

Marina Mora

object named as

Marina Mora

series ordinal

8

0 references

Roberta Battini

object named as

Roberta Battini

series ordinal

23

0 references

Giacomo P Comi

object named as

Giacomo P Comi

series ordinal

11

0 references

Enrico Bertini

object named as

Enrico Bertini

series ordinal

30

0 references

Isabella Moroni

series ordinal

4

object named as

Isabella Moroni

0 references

Maurizio Moggio

series ordinal

13

object named as

Maurizio Moggio

0 references

Tiziana Mongini

series ordinal

20

object named as

Tiziana Mongini

0 references

Isabella Moroni

1 reference

stated in

ORCID Public Data File 2021

Filippo Maria Santorelli

object named as

Filippo Maria Santorelli

series ordinal

29

1 reference

stated in

ORCID Public Data File 2021

author name string

Alessandra Graziano

series ordinal

1

0 references

Flaviana Bianco

series ordinal

2

0 references

Claudio Bruno

series ordinal

6

0 references

Elena Pegoraro

series ordinal

7

0 references

Guja Astrea

series ordinal

9

0 references

Lucia Morandi

series ordinal

14

0 references

Antonella Pini

series ordinal

15

0 references

Roberta Petillo

series ordinal

16

0 references

Carlo Minetti

series ordinal

19

0 references

Ksenija Gorni

series ordinal

22

0 references

Marcello Villanova

series ordinal

24

0 references

Luisa Politano

series ordinal

25

0 references

Francesca Gualandi

series ordinal

26

0 references

Alessandra Ferlini

series ordinal

27

0 references

Marika Pane

series ordinal

31

0 references

language of work or name

English

0 references

publication date

3 March 2015

0 references

published in

Neurology

0 references

volume

84

0 references

issue

9

0 references

page(s)

904-11

0 references

cites work

Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

20 March 2017

Refining genotype phenotype correlations in muscular dystrophies with defective glycosylation of dystroglycan

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

20 March 2017

Mutations of the selenoprotein N gene, which is implicated in rigid spine muscular dystrophy, cause the classical phenotype of multiminicore disease: reassessing the nosology of early-onset myopathies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

20 March 2017

Diagnostic approach to the congenital muscular dystrophies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Natural history of pulmonary function in collagen VI-related myopathies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

The ever-expanding spectrum of congenital muscular dystrophies

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Relative frequency of congenital muscular dystrophy subtypes: analysis of the UK diagnostic service 2001-2008.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

SEPN1-related myopathies: clinical course in a large cohort of patients

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Dystroglycanopathies: coming into focus

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Brain involvement in muscular dystrophies with defective dystroglycan glycosylation

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

29 September 2017

Congenital muscular dystrophy associated with calf hypertrophy, microcephaly and severe mental retardation in three Italian families: evidence for a novel CMD syndrome.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

2 June 2018

Congenital muscular dystrophies with cognitive impairment. A population study.

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

27 November 2018

Congenital muscular dystrophy with merosin deficiency

1 reference

stated in

PubMed Central

reference URL

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4351663

retrieved

27 November 2018

Congenital muscular dystrophy with rigid spine syndrome: a clinical, pathological, radiological, and genetic study

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

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

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Diagnosis and etiology of congenital muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Skin changes in Ullrich congenital muscular dystrophy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neuromuscular disorders in childhood: a descriptive epidemiological study from western Sweden

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/25653289

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1212/WNL.0000000000001303

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3805327

OpenCitations bibliographic resource ID

3805327

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3805327

PMC publication ID

4351663

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3805327

PubMed publication ID

25653289

1 reference

stated in

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

3805327

 

Sitelinks

Wikipedia(0 entries)

edit

Wikibooks(0 entries)

edit

Wikinews(0 entries)

edit

Wikiquote(0 entries)

edit

Wikisource(0 entries)

edit

Wikiversity(0 entries)

edit

Wikivoyage(0 entries)

edit

Wiktionary(0 entries)

edit

Multilingual sites(0 entries)

edit

Retrieved from "https://www.wikidata.org/w/index.php?title=Q28256516&oldid=1612924486"