Camptocormia as an unusual manifestation of myofibrillar myopathy

No abstract is available for this paper.

• Publication year

  2010

• Venue

  Pathology

• Publication date

  Unknown publication date

• Fields of study

  Medicine

• Identifiers
  DOI 10.1097/01268031-201042001-00158
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar

• No claims are published for this paper.

• No concepts are published for this paper.

• Personal History

  2021cited by this paper
• Voltage-gated potassium channel antibody-associated encephalitis with basal ganglia lesions

  2006cited by this paper
• Camptocormia

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• Myofibrillar myopathy: clinical, morphological and genetic studies in 63 patients.

  2004cited by this paper
• Is Camptocormia a Primary Muscular Disease?

  1995cited by this paper

• No citing papers are available for this paper.