(Q34332191)

1 August 2017

title

Arachnodactyly--a key to diagnosing heritable disorders of connective tissue (English)

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1 August 2017

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1

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author name string

Alan J Hakim

series ordinal

2

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1 August 2017

language of work or name

English

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publication date

12 March 2013

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Nature Reviews Rheumatology

1 August 2017

published in

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1 August 2017

volume

9

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1 August 2017

issue

6

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1 August 2017

page(s)

358-364

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THE METACARPAL INDEX. A USEFUL AID IN THE DIAGNOSIS OF THE MARFAN SYNDROME.

1 August 2017

cites work

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Articular mobility in an African population

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Physical properties of the skin in the Ehlers-Danlos syndrome

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A novel in vivo skin extensibility test for joint hypermobility.

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The lack of clinical distinction between the hypermobility type of Ehlers-Danlos syndrome and the joint hypermobility syndrome (a.k.a. hypermobility syndrome).

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Joint hypermobility syndrome

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Unexplained gastrointestinal symptoms and joint hypermobility: is connective tissue the missing link?

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Anxiety disorders in the joint hypermobility syndrome.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

The genetic basis of the joint hypermobility syndromes.

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Aneurysm syndromes caused by mutations in the TGF-beta receptor

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

The Loeys-Dietz syndrome: an update for the clinician

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Fibrillin-2 (FBN2) mutations result in the Marfan-like disorder, congenital contractural arachnodactyly

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literature

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Lujan-Fryns syndrome (mental retardation, X-linked, marfanoid habitus)

21 January 2018

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Clinical features of hereditary progressive arthro-ophthalmopathy (Stickler syndrome): a survey

21 January 2018

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The revised Ghent nosology for the Marfan syndrome

21 January 2018

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A simple screening test for the Marfan syndrome

21 January 2018

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The Harpenden skinfold caliper

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Revised diagnostic criteria for the Marfan syndrome

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Non-musculoskeletal symptoms in joint hypermobility syndrome. Indirect evidence for autonomic dysfunction?

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Stickler syndrome: clinical characteristics and diagnostic criteria

31 March 2020

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https://api.crossref.org/works/10.1038%2FNRRHEUM.2013.24

Revised diagnostic criteria for the Marfan syndrome

31 March 2020

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12 December 2020

Association of mitral valve prolapse and systemic abnormalities of connective tissue. A phenotypic continuum

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12 December 2020

Shprintzen-Goldberg syndrome: a clinical analysis

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12 December 2020

The wrist sign. A useful physical finding in the Marfan syndrome

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The revised (Brighton 1998) criteria for the diagnosis of benign joint hypermobility syndrome (BJHS)

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12 December 2020

Identifiers

DOI

10.1038/NRRHEUM.2013.24

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Dimensions Publication ID

1 August 2017

1004187487

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