Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs

By Norgren Nina   Olsson Malin   Nyström Hanna   Ericzon Bo Göran   de Tayrac Marie   Genin Emmanuelle   Planté-Bordeneuve Violaine   Suhr Ole B  

Amyloid: The Journal of Protein Folding Disorders, Vol. 21, Iss. 2, 2014-06 ,pp. : 113-119

Informa Healthcare

Access to resources Recommend Favorite

Variation in the Uric Acid Transporter Gene SLC2A9 and Its Association with AAO of Parkinson’s Disease

By Facheris Maurizio   Hicks Andrew   Minelli Cosetta   Hagenah Johann   Kostic Vladimir   Campbell Susan   Hayward Caroline   Volpato Claudia   Pattaro Cristian   Vitart Veronique   Wright Alan   Campbell Harry   Klein Christine   Pramstaller Peter  

Journal of Molecular Neuroscience, Vol. 43, Iss. 3, 2011-03 ,pp. : 246-250

Humana Press, Inc

Access to resources Recommend Favorite

Pathogenesis of transthyretin amyloidosis

By Benson Merrill D.  

Amyloid: The Journal of Protein Folding Disorders, Vol. 19, Iss. 1, 2012-06 ,pp. : 14-15

Informa Healthcare

Access to resources Recommend Favorite

A compound T60A and V122I heterozygosity in the transthyretin gene causing early onset severe cardiac amyloidosis

By Liu Yi-Chang   Reddi Honey Vodur   Waheed Sarah   Alapat Daisy   Highsmith W. Edward   Edmondson Ricky D.   Barlogie Bart   van Rhee Frits  

Amyloid: The Journal of Protein Folding Disorders, Vol. 21, Iss. 2, 2014-06 ,pp. : 134-135

Informa Healthcare

Access to resources Recommend Favorite

A case of biopsy-proven leptomeningeal amyloidosis and intravenous Ig-responsive polyneuropathy associated with the Ala25Thr transthyretin gene mutation

By Shimizu Yuko   Takeuchi Megumi   Matsumura Miyuki   Tokuda Takahiko   Iwata Makoto  

Amyloid: The Journal of Protein Folding Disorders, Vol. 13, Iss. 1, 2006-03 ,pp. : 37-41

Informa Healthcare

Access to resources Recommend Favorite