(Q33594663)

28 July 2017

Intestinal pseudo-obstruction in myotonic dystrophy (English)

1 reference

intestinal pseudo-obstruction

28 July 2017

1 reference

1 reference

Brunner HG

1

1 reference

28 July 2017

Hamel BC

2

1 reference

28 July 2017

Rieu P

3

1 reference

28 July 2017

Höweler CJ

4

1 reference

28 July 2017

Peters FT

5

1 reference

28 July 2017

language of work or name

English

0 references

publication date

1 November 1992

1 reference

Journal of Medical Genetics

28 July 2017

1 reference

28 July 2017

29

1 reference

28 July 2017

11

1 reference

28 July 2017

791-793

1 reference

Gastrointestinal manifestations of the muscular dystrophies

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Calcifying epithelioma of Malherbe. Association with myotonic muscular dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Focal myocarditis in familial dystrophia myotonica

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Mitral valve prolapse in myotonic dystrophy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Cardiac involvement in myotonic muscular dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Anaesthetic problems in myotonic dystrophy. A case report and review of the Aberdeen experience comprising 48 general anaesthetics in a further 16 patients

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Myotonic dystrophy associated with hereditary motor and sensory neuropathy.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Childhood neurofibromatosis: risk factors for malignant disease.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Optic atrophy in Leber hereditary optic neuroretinopathy is probably determined by an X-chromosomal gene closely linked to DXS7.

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Independent genetic determinants of pancreatic and pulmonary status in cystic fibrosis

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

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

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Familial mitral valve prolapse and myotonic dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Pilomatricomas associated with myotonic dystrophy

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

Myotonic dystrophy (urological features and histochemical findings in muscle) (author's transl)

14 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016174

UNUSUAL MANIFESTATIONS DUE TO INVOLVEMENT OF INVOLUNTARY MUSCLE IN DYSTROPHIA MYOTONICA

14 July 2018

1 reference

12 December 2020

Genetic linkage with chromosome 19 but not chromosome 17 in a family with myotonic dystrophy associated with hereditary motor and sensory neuropathy

1 reference

12 December 2020

Variability of pulmonary function in alpha-1-antitrypsin deficiency: residual family resemblance beyond the effect of the Pi locus

1 reference

12 December 2020

Congenital hepatic fibrosis in autosomal-dominant polycystic kidney disease

1 reference

12 December 2020

Smooth Muscle Involvement in Congenital Myotonic Dystrophy

1 reference

12 December 2020

Megacolon in myotonic dystrophy caused by a degenerative neuropathy of the myenteric plexus

1 reference

12 December 2020

Normal pressure hydrocephalus in myotonic dystrophy

1 reference

12 December 2020

Intestinal pseudo-obstruction in a patient with myotonic dystrophy

1 reference

12 December 2020

Multiple familial pilomatricomas: a cutaneous marker for myotonic dystrophy

1 reference

12 December 2020

Smooth muscle involvement in primary muscle disease. I. Myotonic dystrophy

1 reference

12 December 2020

Families with myotonic dystrophy with and without cardiac involvement

1 reference

12 December 2020

Identifiers

DOI

10.1136/JMG.29.11.791

1 reference

28 July 2017

1 reference

28 July 2017

1 reference