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(New York Stem Cell Foundation) The New York Stem Cell Foundation and Cbr Systems, Inc. DBA Cord Blood Registry® today announced a collaboration to customize the creation of high-quality stem cell li...
Voice therapy with a trained speech-language pathologist can assist patients with vocal cord paralysis.
By growing functional vocal cord tissue in the lab, scientists bring closer the day when people whose vocal cords have been lost to cancer or injury can get their voice back.
September 15, 2015 (Nanowerk News) Regenerative medicine using stem cells is an increasingly promising approach to treat many types of injury. Transplanted stem cells can differentiate into just about...
(University of Wisconsin-Madison) University of Wisconsin-Madison scientists have succeeded in growing functional vocal cord tissue in the laboratory, a major step toward restoring a voice to people w...
(Science Daily) – Scientists have succeeded in growing functional vocal cord tissue in the laboratory, a major step toward restoring a voice to people who have lost their vocal cords to cancer s...
University of Wisconsin-Madison scientists have succeeded in growing functional vocal cord tissue in the laboratory, a major step toward restoring a voice to people who have lost their vocal cords to ...
The Cbr Cord Blood Registry and the New York Stem Cell Foundation (NYSCR) are to collaborate on the creation of high-quality stem cell lines.
Anthracotic pigmentation in the bronchial mucosa is a bronchoscopic finding of pneumoconiosis, or evidence of heavy atmospheric soot. This pigmentation in the tracheobronchial mucosa is surrounded by ...
We report a patient with lung cancer. The first PET/CT imaging revealed hypermetabolic mass in the left aortopulmonary region and hypermetabolic nodule in the anterior segment of the upper lobe of the...
Needle electromyography is an important tool in the diagnosis of neuromuscular diseases and has also been applied successfully in the evaluation of the vocal cord paralysis. Laryngeal electromyography...
Williams-Beuren syndrome is a rare neurodevelopmental disorder caused by deletion of 1.5-1.8Mb genes on chromosome 7q11.23. The syndrome was first described as a triad of supra-valvular aortic stenosi...