muscular atrophy


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Related to muscular atrophy: progressive muscular atrophy, Spinal muscular atrophy
Translations

muscular atrophy

nMuskelatrophie f, → Muskelschwund m
References in periodicals archive ?
3, 2015 /PRNewswire/ -- Pipeline analysis of spinal muscular atrophy (SMA) market report provides with comprehensive analysis of drugs in clinical trials for treatment for spinal muscular atrophy.
com/research/xkbpfx/spinal_muscular) has announced the addition of the "Spinal Muscular Atrophy Market - Pipeline Assessment, Size, Growth, Trends, and Forecast 2015 - 2023" report to their offering.
MEMBERS of the Rotary Club of Warwick were given a presentation by Spinal Muscular Atrophy Support UK recently.
The family fun day, at the Sheraton Pub, Hardwick, from noon to 4pm, had already been organised after Bobby was diagnosed with Spinal Muscular Atrophy (SMA) Type 1 four weeks after his birth on May 16.
a biotechnology company focused on using gene therapy to transform the lives of patients with severe genetic and orphan diseases like Spinal Muscular Atrophy (SMA), today announced that the European Medicines Agency (EMA) has granted AveXis' wholly owned European subsidiary, AveXis EU Ltd.
It is reported that the children were suffering from spinal muscular atrophy (SMA) - a life-limiting illness.
Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disorder that affects approximately 1 in 10 000 newborns (4).
She is raising cash for two-year-old Junior Willoughby, who has Spinal Muscular Atrophy.
TIM suffers from a rare type of muscular dystrophy called spinal muscular atrophy.
CSC), Irvine, CA, and the Families of Spinal Muscular Atrophy and FSMA announced CSC is seeking FDA approval to start a Phase I Safety study on a jointly-developed stem-cell derived motor neuron transplantation therapy for Spinal Muscular Atrophy (SMA) Type 1.
SerVaas, In October 1994, you were so kind to publish my letter to raise awareness of spinal muscular atrophy (SMA).
Washington, July 28 (ANI): A team of researchers led by Indian origin scientist has come up with a potential new treatment for spinal muscular atrophy, the second-leading cause of infant mortality in the world.