copy and paste this google map to your website or blog!
Press copy button and paste into your blog or website.
(Please switch to 'HTML' mode when posting into your blog. Examples: WordPress Example, Blogger Example)
MDA Community Support Groups - Muscular Dystrophy Association MDA offers four different Community Groups for you to choose from including: Adult Community Support Group Pediatric Community Support Group Pediatric Group for parents guardians with a child under the age of 18 (children are welcome) ALS Community Support Group
Quest - Article - Caution, Preparation and Teamwork Lead to the Best . . . Caution, Preparation and Teamwork Lead to the Best Pregnancy Outcomes in Women with Neuromuscular Diseases by Margaret Wahl, Amy Labbe and Miriam Davidson | Tuesday, June 29, 2010 When Emma Ciafaloni was preparing to become a neuromuscular disease specialist in the 1990s, and even when she directed the MDA neuromuscular disease clinic at Duke
Updates in Spinal-Bulbar Muscular Atrophy Learning Objectives: Recognize symptoms of and use genetic testing to differentially diagnose SBMA from other neuromuscular conditions that present similarly Explore evidence-based guidelines and best practices for managing SBMA
Time to Re-Evaluate Becker Muscular Dystrophy MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases
MDA Kickstart Program Launches for Ultra-Rare Neuromuscular Disease . . . The first MDA Kickstart project, developed by Ricardo A Maselli, MD, Professor, Neurology, Clinical Neuroscience, UC Davis, will focus on the development of a gene therapy for a form of Congenital Myasthenic Syndrome (CMS) caused by mutations in the CHAT gene, which encodes the enzyme Choline Acetyltransferase
Congenital Myopathies: Clinical Presentation, Diagnosis, and Management Learning Objectives: Upon completion of the educational activity, participants should be able to: Recognize the signs and symptoms of the different congenital myopathies Identify the testing modalities to utilize when encountering a patient with a suspected congenital myopathy