(Q33595768)

English

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

muscular dystrophy

1 reference

based on heuristic

inferred from title

author name string

L V Nicholson

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

M A Johnson

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

K M Bushby

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D Gardner-Medwin

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

A Curtis

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

I B Ginjaar

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

J T den Dunnen

7

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

J L Welch

8

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

T J Butler

9

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

E Bakker

10

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 September 1993

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

30

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

745-751

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Cosegregation of schizophrenia with Becker muscular dystrophy: susceptibility locus for schizophrenia at Xp21 or an effect of the dystrophin gene in the brain?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Dystrophin expression in Duchenne patients with "in-frame" gene deletions.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Familial X-linked myalgia and cramps: a nonprogressive myopathy associated with a deletion in the dystrophin gene

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Molecular deletion patterns in Duchenne muscular dystrophy patients.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Very mild muscular dystrophy associated with the deletion of 46% of dystrophin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Molecular genetics of Duchenne and Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Preservation of the C-terminus of dystrophin molecule in the skeletal muscle from Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Differentiation of Duchenne and Becker muscular dystrophy phenotypes with amino- and carboxy-terminal antisera specific for dystrophin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

A convenient multiplex PCR system for the detection of dystrophin gene deletions: a comparative analysis with cDNA hybridisation shows mistypings by both methods

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Dystrophin abnormalities in polymyositis and dermatomyositis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Is the carboxyl-terminus of dystrophin required for membrane association? A novel, severe case of duchenne muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Possible influences on the expression of X chromosome-linked dystrophin abnormalities by heterozygosity for autosomal recessive Fukuyama congenital muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Somatic reversion/suppression in Duchenne muscular dystrophy (DMD): evidence supporting a frame-restoring mechanism in rare dystrophin-positive fibers

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Genetic and clinical correlations of Xp21 muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Prevalence of dystrophin-positive fibers in 85 Duchenne muscular dystrophy patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

In vitro digestion of dystrophin by calcium-dependent proteases, calpains I and II

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Dystrophin or a "related protein" in Duchenne muscular dystrophy?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Investigation of a female manifesting Becker muscular dystrophy

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016531

21 June 2018

Becker muscular dystrophy: detection of unusual disease courses by combined approach to dystrophin analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Becker muscular dystrophy or spinal muscular atrophy?—Dystrophin studies resolve conflicting results of electromyography and muscle biopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variable dystrophin expression in different muscles of a Duchenne muscular dystrophy carrier

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Becker muscular dystrophy: demonstration of the carrier status of a female by immunoblotting and immunostaining

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

X inactivation and dystrophin studies in a t(X;12) female: evidence for biochemical normalization in Duchenne muscular dystrophy carriers

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The clinical, genetic and dystrophin characteristics of Becker muscular dystrophy. II. Correlation of phenotype with genetic and protein abnormalities

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mosaic expression of dystrophin in symptomatic carriers of Duchenne's muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Estimates of conditional heterozygosity risks for young females in Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An unusual variant of Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin analysis in duchenne and becker muscular dystrophy carriers: Correlation with intracellular calcium and albumin

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and incidence of Becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunofluorescence dystrophin study in Duchenne dystrophy through the concomitant use of two antibodies directed against the carboxy-terminal and the amino-terminal region of the protein

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serum creatine-kinase (CK) and pyruvate-kinase (PK) activities in Duchenne (DMD) as compared with Becker (BMD) muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterisation of dystrophin in carriers of Duchenne muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Muscle histology in becker muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Immunocytochemical analysis of dystrophin in congenital muscular dystrophy

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dystrophin immunofluorescence pattern in manifesting and asymptomatic carriers of Duchenne's and Becker muscular dystrophies of different ages

1 reference

https://pubmed.ncbi.nlm.nih.gov/8411069

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.30.9.745

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

0 references

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=Q33595768&oldid=1535362793"