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Nature Structural & Molecular Biology|June 9, 2015
The pilus usher controls protein interactions via domain masking and is functional as an oligomerGlenn T Werneburg, Nadine S Henderson, Erica B Portnoy, et al.
The American Journal of Cardiology|February 8, 2005
Comparison of the strain Doppler echocardiographic features of familial amyloid polyneuropathy (FAP) and light-chain amyloidosisFumiaki Ogiwara, Jun Koyama, Shu-Ichi Ikeda, et al.
The New England Journal of Medicine|January 2, 1975
Vinyl-chloride-induced liver disease. From idiopathic portal hypertension (Banti's syndrome) to AngiosarcomasL B Thomas, H Popper, P D Berk, et al.
Dermatology Online Journal|February 4, 2012
Hidradenitis suppurativa resulting in systemic amyloid A amyloidosis: a case report and review of the literatureSasha D Girouard, Rodney H Falk, Helmut G Rennke, et al.
The Journal of Infectious Diseases|August 1, 1976
Rapid intravenous injection of tobramycin: suggested dosage schedule and concentrations in serumA P Gillett, R H Falk, J Andrews, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|December 8, 2009
Reference-free automatic quality assessment of tracheoesophageal speechAndy Huang, Tiago H Falk, Wai-Yip Chan, et al.
The Journal of the Acoustical Society of America|September 20, 2014
A model that predicts the binaural advantage to speech intelligibility from the mixed target and interferer signalsStefano Cosentino, Torsten Marquardt, David McAlpine, et al.
Heart (British Cardiac Society)|July 1, 1997
Familial and primary (AL) cardiac amyloidosis: echocardiographically similar diseases with distinctly different clinical outcomesS W Dubrey, K Cha, M Skinner, et al.
The American Journal of Cardiology|November 14, 1997
Features and prognosis of exertional syncope in light-chain associated AL cardiac amyloidosisB Chamarthi, S W Dubrey, K Cha, et al.
The Journal of Gene Medicine|March 4, 2005
Solid tissues can be manipulated ex vivo and used as vehicles for gene therapyE Hasson, Y Slovatizky, Y Shimoni, et al.
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