Results 161 to 168 of about 141,957 (168)

Role of 99mTc-DPD Scintigraphy in Diagnosis and Prognosis of Hereditary Transthyretin-Related Cardiac Amyloidosis

JACC: Cardiovascular Imaging, 2011
Ornella Leone, Christian Gagliardi, Massimiliano Lorenzini   +2 more
exaly  

Inotersen for the treatment of adults with polyneuropathy caused by hereditary transthyretin-mediated amyloidosis

Expert Review of Clinical Pharmacology, 2019
Laura Obici, Morton Aaron Scheinberg, Morie A Gertz   +2 more
exaly  

An indirect treatment comparison of the efficacy of patisiran and tafamidis for the treatment of hereditary transthyretin-mediated amyloidosis with polyneuropathy

Expert Opinion on Pharmacotherapy, 2019
Violaine Planté-Bordeneuve, Jared Gollob   +1 more
exaly  

Loss of gastric interstitial cells of Cajal in patients with hereditary transthyretin amyloidosis

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2013
Yukio Andō, Konen Obayashi, Jonas Wixner   +2 more
exaly  

Molecular strategies in genetic diagnosis of transthyretin-related hereditary amyloidosis

FASEB Journal, 1992
Fabrizio Salvi, S Fini
exaly  

An evaluation of patisiran: a viable treatment option for transthyretin-related hereditary amyloidosis

Expert Opinion on Pharmacotherapy, 2019
Giovanni Palladini, Laura Obici, Stefano Perlini   +2 more
exaly  

Long-term outcome of patients with hereditary transthyretin V30M amyloidosis with polyneuropathy after liver transplantation

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis, 2016
Satoshi Yamashita, Mitsuharu Ueda, Yukihiro Inomata   +2 more
exaly  

Comparison of cardiac involvement, extracardiac manifestations and outcomes between homozygote and heterozygote transthyretin p.Val142Ile (V122I) variant in patients with hereditary transthyretin amyloidosis: a cohort study

Amyloid: the International Journal of Experimental and Clinical Investigation: the Official Journal of the International Society of Amyloidosis
Zaroui Amira
exaly