Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Bill Martens"'
Autor:
Mamatha Pasnoor, Rabi Tawil, Bill Martens, Linda Greensmith, Omar Jawdat, Mazen M. Dimachkie, Michael P. McDermott, Melanie Glenn, Pedro Machado, Richard J. Barohn, J. Statland, April McVey, Laura Herbelin, Michael G. Hanna
Publikováno v:
RRNMF Neuromuscular Journal. 2
Autor:
Charles A. Thornton, Chad Heatwole, Bill Martens, Beilei Xu, Wencheng Wu, Trevor W. Richardson, Edgar A. Bernal, Lei Lin
Publikováno v:
2019 IEEE Healthcare Innovations and Point of Care Technologies, (HI-POCT).
Myotonia, which refers to delayed muscle relaxation after contraction, is the main symptom of myotonic dystrophy patients. The relaxation time after a hand squeeze has been used as a biomarker for diagnostic purposes and in clinical trials to quantif
Autor:
Dorcas Koenigsberger, Basil T. Darras, Douglas M. Sproule, Jayson Caracciolo, Maryjane Benton, Eugenio Mercuri, Mark Punyanitya, Wei Shen, Vanessa Battista, Jacqueline Montes, Sally Dunaway, Darryl C. De Vivo, Petra Kaufmann, Richard S. Finkel, Hailly Butler, Megan Montgomery, Bill Martens
Publikováno v:
Neuromuscular Disorders. 20:448-452
The relationship between body composition and function in spinal muscular atrophy (SMA) is poorly understood. 53 subjects with SMA were stratified by type and Hammersmith functional motor scale, expanded score into three cohorts: low-functioning non-
Autor:
Susan Riley, Wendy K. Chung, Maryjane Benton, Benjamin Koo, Jacqueline Montes, Peter B. Kang, Janet Quigley, Basil T. Darras, Christine Annis, Sally Dunaway, Petra Kaufmann, Jean Flickinger, A. Reghan Foley, Jayson Caracciolo, Michael P. McDermott, Hailly Butler, Jonathan Marra, Megan Montgomery, Bill Martens, Maryam Oskoui, Michele L. Yang, Douglas M. Sproule, Allan M. Glanzman, Rabi Tawil, Richard S. Finkel, Darryl C. De Vivo, Jessica O'Hagen, Patricia A. Ryan, Carrie Irvine, Andrei Constantinescu
Publikováno v:
Archives of neurology. 68(6)
To characterize the short-term course of spinal muscular atrophy (SMA) in a genetically and clinically well-defined cohort of patients with SMA.A comprehensive multicenter, longitudinal, observational study.The Pediatric Neuromuscular Clinical Resear
Autor:
Jacqueline Montes, Petra Kaufmann, Stephan Dashnaw, Vanessa Battista, Darryl C. De Vivo, Wei Shen, Richard S. Finkel, Basil T. Darras, Megan Montgomery, Bill Martens, Douglas M. Sproule, Mark Punyanitya
Publikováno v:
Journal of child neurology. 26(3)
Thigh muscle volume was assessed using magnetic resonance imaging in 16 subjects with spinal muscular atrophy. Scans were successful for 14 of 16 subjects (1 type 1, 6 type 2, and 7 type 3) as young as 5.7 years. Muscle volume with normal and abnorma
Publikováno v:
Archives of neurology. 63(8)
Background Myotonic dystrophy type 1 (DM1) is the most prevalent form of adult muscular dystrophy worldwide. Although well known for the classic manifestations of myotonia, weakness, and early cataracts, it has broad effects on multiple organ systems