Related Experiment Videos

[Gas gangrene. Apropos of 23 cases]

S Grosbuis, P Gajdos, A Barois

Revue Medicale De La Suisse Romande

|November 1, 1971

Abstract

No abstract available in PubMed .

Related Concept Videos

Articles linked to this work by shared authors, journal, and citation graph.

The CHRNE 1293insG founder mutation is a frequent cause of congenital myasthenia in North Africa.

Neurology·2008

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

Neurology·2006

A gene for an autosomal recessive lower motor neuron disease with childhood onset maps to 1p36.

Neurology·2006

'Cap myopathy': case report of a family.

Neuromuscular disorders : NMD·2006

Congenital myasthenic syndrome due to rapsyn deficiency: three cases with arthrogryposis and bulbar symptoms.

Neuropediatrics·2004

[Congenital myasthenic syndromes due to mutations in the rapsyn gene].

Revue neurologique·2004

See all related articles