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2021, Number 1

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Acta Med 2021; 19 (1)

Parsonage-Turner syndrome

Domínguez GLG, Magaña RJI, Domínguez CLG
Full text How to cite this article 10.35366/98585

DOI

DOI: 10.35366/98585
URL: https://dx.doi.org/10.35366/98585

Language: Spanish
References: 4
Page: 132-133
PDF size: 116.21 Kb.


Key words:

No keywords




REFERENCES

  1. Briceño PF, Rodríguez MS. Síndrome de Parsonage-Turner. Revisión bibliográfica. Sem Fund Esp Reumat. 2010; 11 (4): 144-151.

  2. Parsonage MJ, Turner JW. Neuralgic amyotrophy; the shoulder-girdle syndrome. Lancet. 1948; 1 (6513): 973-978.

  3. Kuhlenbäumer G, Meuleman J, De Jonghe P, Falck B, Young P, Hünermund G et al. Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneous. J Neurol. 2001; 248 (10): 861-865.

  4. Scalf RE, Wenger DE, Frick MA, Mandrekar JN, Adkins MC. MRI findings of 26 patients with Parsonage-Turner syndrome. AJR. 2007; 189: W39-W44.




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C?MO CITAR (Vancouver)

Acta Med. 2021;19