(Q24632678)

1

0 references

Theodoros Kalampokas

2

0 references

Chrisostomos Sofoudis

3

0 references

Efthymios Deligeoroglou

4

0 references

Dimitrios Botsis

ISRN Obstetrics & Gynecology

5

0 references

language of work or name

English

0 references

publication date

2012

0 references

published in

1 reference

Creative Commons Attribution 3.0 Unported

volume

2012

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page(s)

264918

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copyright license

start time

23 September 2012

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

1 reference

April 2022 Public Data File from Crossref

cites work

Arthrogryposis: a review and update

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

A revised and extended classification of the distal arthrogryposes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis: a review and approach to prenatal diagnosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Review of perinatal management of arthrogryposis at a large UK teaching hospital serving a multiethnic population

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Early sonographic prenatal diagnosis of seizures.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis multiplex congenita (amyoplasia): an orthopaedic perspective

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Fetal arthrogryposis and maternal serum antibodies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Autopsy after termination of pregnancy for fetal anomaly: retrospective cohort study

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Multiple congenital contractures (congenital multiple arthrogryposis).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Teratogen update: maternal myasthenia gravis as a cause of congenital arthrogryposis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Antibodies affecting ion channel function in acquired neuromyotonia, in seropositive and seronegative myasthenia gravis, and in antibody-mediated arthrogryposis multiplex congenita

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis associated with unsuccessful attempts at termination of pregnancy

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Lethal arthrogryposis multiplex congenital (fetal akinesia deformation sequence, FADS).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Lethal congenital muscular dystrophy with arthrogryposis multiplex congenita: three new cases and review of the literature

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis multiplex congenita: a report of two cases

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Lethal arthrogryposis in Finland--a clinico-pathological study of 83 cases during thirteen years

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis multiplex congenita. Review with comment

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Congenital non-progressive peripheral neuropathy with arthrogryposis multiplex

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

A lethal autosomal recessive syndrome of multiple congenital contractures

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

The etiology of arthrogryposis (multiple congenital contracture).

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Analysis of Pena Shokeir phenotype

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Prenatal diagnosis of distal arthrogryposis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Cerebro-oculo-facio-skeletal syndrome: three additional cases with CSB mutations, new diagnostic criteria and an approach to investigation

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Fetal akinesia deformation sequence: a study of 30 consecutive in utero diagnoses.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis multiplex congenita: etiology, genetics, classification, diagnostic approach, and general aspects.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Lethal congenital muscular dystrophy in two sibs with arthrogryposis multiplex: new entity or variant of cobblestone lissencephaly syndrome?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Olivo-ponto-cerebellar atrophy with muscular atrophy, joint contractures and pulmonary hypoplasia of prenatal onset.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Congenital absence of peripheral myelin: abnormal Schwann cell development causes lethal arthrogryposis multiplex congenita

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Lethal arthrogryposis multiplex congenita: a pathological study of 21 cases.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Neurogenic arthrogryposis multiplex congenita: clinical and MRI findings.

30 May 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Maternal myasthenia gravis complicated by fetal arthrogryposis multiplex congenita

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Artrogryposis multiplex congenita -- a rare fetal condition caused by maternal myasthenia gravis

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Perioperative care of the child with arthrogryposis.

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Permanent neonatal diabetes with arthrogryposis multiplex congenita and neurogenic bladder - a new syndrome?

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Prenatal diagnosis of arthrogryposis multiplex congenita with increased nuchal translucency but without any underlying fetal neurogenic or myogenic pathology.

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Neonatal arthrogryposis and absent limb muscles: a muscle developmental gene defect?

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Arthrogryposis Multiplex Congenita

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Deficiency of a skeletal muscle isoform of α-actinin (α-actinin-3) in merosin-positive congenital muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Lethal congenital arthrogryposis presents with increased nuchal translucency at 10-14 weeks of gestation

21 January 2018

1 reference

https://api.crossref.org/works/10.5402%2F2012%2F264918

Misoprostol embryotoxicity: clinical evaluation of fifteen patients with arthrogryposis.

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3461621

Arthrogryposis multiplex congenita occurring with maternal multiple sclerosis

28 November 2018

1 reference

12 December 2020

Lipid storage myopathy associated with scoliosis and multiple joint contractures

1 reference

12 December 2020

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

1 reference

12 December 2020

Arthrogryposis multiplex congenita due to congenital myasthenic syndrome

1 reference

12 December 2020

Recurrent congenital arthrogryposis leading to a diagnosis of myasthenia gravis in an initially asymptomatic mother

1 reference

12 December 2020

Fetal akinesia and multiple perinatal fractures

1 reference

12 December 2020

Incidence of maxillofacial involvement in arthrogryposis multiplex congenita

1 reference

12 December 2020

Arthrogryposis due to infantile neuronal degeneration associated with deletion of the SMNT gene

1 reference

12 December 2020

Ragged-red fibers and complex I deficiency in a neonate With arthrogryposis congenita

1 reference

12 December 2020

Arthrogryposis multiplex congenita

1 reference

12 December 2020

Non-lethal arthrogryposis multiplex congenita presenting with cystic hygroma at 13 weeks gestational age

1 reference

12 December 2020

Multiple congenital contractures: birth prevalence, etiology, and outcome

1 reference

12 December 2020

Prenatal diagnosis: what does four-dimensional ultrasound add?

1 reference

12 December 2020

Congenital hypomyelination neuropathy with arthrogryposis multiplex congenita

1 reference

12 December 2020

Genetic aspects of arthrogryposis

1 reference

12 December 2020

Mitochondrial mutation in a child with distal arthrogryposis

1 reference

12 December 2020

Spectrum of features in pterygium syndrome

1 reference

12 December 2020

Prenatal diagnosis of Pena-Shokeir syndrome phenotype by ultrasonography and MR imaging

1 reference

12 December 2020

Endplate destruction due to maternal antibodies in arthrogryposis multiplex congenita

1 reference

12 December 2020

Arthrogryposis multiplex congenita

1 reference

12 December 2020

Identifiers

DOI

10.5402/2012/264918

1 reference

release_d3h34rqctvejdmllgo5ijxvrna

4182698

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/d3h34rqctvejdmllgo5ijxvrna

24 November 2022

mapped directly with Wikidata item

4182698

1 reference

1 reference

1 reference