muscular atrophy


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Translations

muscular atrophy

nMuskelatrophie f, → Muskelschwund m
References in periodicals archive ?
The absence of true ankylosis permits surgery for arytenoid mobilization and VC medialization, but with protracted paralysis, muscular atrophy and fibrosis may be limiting factors to medialization.
Brionni Alexander is the only child in Scotland with type one Spinal Muscular Atrophy, an incurable genetic condition.
Designed to address the needs of patients suffering from numerous respiratory complications, including chronic obstructive pulmonary disease, pneumonia, severe asthma, pleurisy, muscular atrophy, respiratory failure, neuromuscular disease and other diseases or injuries that impair respiration.
Spinal muscular atrophy (SMA) has plagued humanity for generations.
Such enlarged genetic segments have also been discovered in spinal-bulbar muscular atrophy, a rare inherited muscle-wasting syndrome.
com/research/8r4rv5/spinal_muscular) has announced the addition of Global Markets Direct's new report "Spinal Muscular Atrophy (SMA) - Pipeline Review, H2 2012" to their offering.
Further, the analyst sees the potential for upside from additional Phase 2 data on spinal muscular atrophy agent RG7916 and from a trial design update on plans to generate dystrophin production data for Translarna in pursuit of accelerated approval.
M2 PHARMA-October 6, 2017-Earlier Treatment Initiation with Spinraza (nusinersen) May Lead to Improved Motor Function in Spinal Muscular Atrophy
Global Markets Direct's, 'Spinal Muscular Atrophy (SMA) - Pipeline Review, H2 2015', provides an overview of the Spinal Muscular Atrophy (SMA)'s therapeutic pipeline.
4,5) Specific genetic tests are available for X-linked bulbospinal neuronopathy (Kennedy's disease), which causes a slowly progressive lower motor neurone syndrome, sensory neuropathy, and partial androgen insensitivity leading to gynaecomastia and the recessive form of proximal spinal muscular atrophy which can occasionally come on in adult life.
M2 EQUITYBITES-June 25, 2015-AveXis receives orphan drug designation from European Medicines Agency for gene therapy treatment for spinal muscular atrophy
New research on how motor-neuron cell-death occurs in patients with spinal muscular atrophy offers an important clue in identifying potential medicines to treat this leading genetic cause of death in infants and toddlers.