Transillumination Assisted Cricopharyngeal Myotomy

Author:

Avior Galit,Noy RoeeORCID,Blumen Sergiu C.,Guily Jean Lacau St,Braverman Itzhak

Publisher

Springer Science and Business Media LLC

Subject

Otorhinolaryngology,Surgery

Reference24 articles.

1. Trollet C, Gidaro T, Klein P et al (2001) Oculopharyngeal Muscular Dystrophy. In: Adam MP, Ardinger HH, Pagon RA et al (eds) GeneReviews® [Internet]. University of Washington, Seattle, Seattle (WA), pp 1993–2020. https://www.ncbi.nlm.nih.gov/books/NBK1126/

2. Brais B, Bouchard JP, Xie YG et al (1998) Short GCG expansions in the PABPN2 gene cause oculopharyngeal muscular dystrophy. Nat Genet 18:164–167

3. Blumen SC, Nisipeanu P, Sadeh M et al (1997) Epidemiology and inheritance of oculopharyngeal muscular dystrophy in Israel. NeuromusculDisord 7(Suppl. 1):S38-40

4. Blumen SC, Korczyn AD, Lavoie H et al (2000) Oculopharyngeal MD among Bukhara Jews is due to a founder (GCG)9 mutation in the PABP2 gene. Neurology 55:1267–1270

5. Blumen SC, Brais B, Korczyn AD et al (1994) Homozygotes for Oculopharyngeal muscular dystrophy have a severe form of the disease. Ann Neurol 46:115–118

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