Familial amyloid polyneuropathy associated with TTRSer50Arg mutation in two Iberian families presenting a novel single base change in the mutant gene

By Munar-Qués Miguel   Masjuan Jaime   Coelho Teresa   Moreira Paul   Viader-Farré Carlos   Saraiva María J. M.  

Amyloid: The Journal of Protein Folding Disorders, Vol. 14, Iss. 2, 2007-01 ,pp. : 147-152

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Chinese familial transthyretin amyloidosis with vitreous involvement is associated with the transthyretin mutation Gly83Arg: a case report and literature review

By Yin Jie   Xia Xinyi   Shi Yao   Lu Yan   Zhao Changlin   Huang Zhenping   Tian Nong  

Amyloid: The Journal of Protein Folding Disorders, Vol. 21, Iss. 2, 2014-06 ,pp. : 140-142

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Familial amyloid polyneuropathy associated with the novel transthyretin variant Arg34Gly

By Levy Jaime  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 4, 2012-12 ,pp. : 201-203

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An unusual transthyretin gene missense mutation (TTR Phe33Val) linked to familial amyloidotic polyneuropathy

By Frigerio Roberta   Fabrizi Gian Maria   Ferrarini Moreno   Cavallaro Tiziana   Brighina Laura   Santoro Patrizia   Agostoni Elio   Cavaletti Guido   Rizzuto Nicolò   Ferrarese Carlo  

Amyloid: The Journal of Protein Folding Disorders, Vol. 11, Iss. 2, 2004-06 ,pp. : 121-124

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TTR-familial amyloid polyneuropathy – neurological aspects

By Said Gérard   Planté-Bordeneuve Violaine  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 1, 2012-06 ,pp. : 25-27

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