A rarely seen syndrome in rehabilitation of hemiplegia: antiphospholipid antibody-negative Sneddon’s syndrome-Reference-Cited by-同舟云学术

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A rarely seen syndrome in rehabilitation of hemiplegia: antiphospholipid antibody-negative Sneddon’s syndrome

Published:2009-08-21 Issue:11 Volume:30 Page:1489-1491
ISSN:0172-8172
Container-title:Rheumatology International
language:en
Short-container-title:Rheumatol Int

Author:

Akbal Ayla,Kurtaran Aydan,Selçuk Barın,Ersöz Murat,Akyüz Müfit

Publisher

Springer Science and Business Media LLC

Subject

Immunology,Immunology and Allergy,Rheumatology

Link

http://link.springer.com/content/pdf/10.1007/s00296-009-1093-2.pdf

Reference15 articles.

1. Champion RH, Rook A (1960) Livedo reticularis. Proc R Soc Med 53:961–962

2. Sneddon IB (1965) Cerebro-vasküler lesions and livedo retikülaris. Br J Dermatol 77:180–185. doi: 10.1111/j.1365-2133.1965.tb14628.x

3. Zelger B, Sepp N, Stockhammer G et al (1993) Sneddon’s syndrome: a long-term follow-up of 21 patients. Arch Dermatol 129:437–447. doi: 10.1001/archderm.129.4.437

4. Wright RA, Kokmen E (1999) Gradually progressive dementia without discrete cerebrovascular events in a patient with Sneddon’s syndrome. Mayo Clin Proc 74:57–61. doi: 10.4065/74.1.57

5. Karagülle AT, Karadağ D, Erden A, Erden I (2002) Sneddon’s syndrome: MR imaging findings. Eur Radiol 12:144–146. doi: 10.1007/s003300100876

Cited by 10 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Sneddon’s Syndrome: clinical case;Journal of Health Care and Research;2020-03-24

2. Zerebrovaskuläre Ereignisse, Kopfschmerzen und Livedo racemosa – Blickdiagnose?;Fortschritte der Neurologie · Psychiatrie;2019-12-18

3. The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review;Journal of the Neurological Sciences;2016-05

4. Cardiac valve degeneration in a patient with Sneddon syndrome;Clinical Research in Cardiology;2014-12-06

5. Sneddon’s syndrome: a comprehensive review of the literature;Orphanet Journal of Rare Diseases;2014-12

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