Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal ...

Three patients with spinal muscular atrophy had improved muscle strength and could walk farther after a month of daily spinal stimulation.

From February 12, all newborn babies will be offered screening for spinal muscular atrophy (SMA), a rare progressive neuromuscular disease. SMA will be one of more than 20 other rare disorders ...

A new drug-free, minimally invasive intervention targets the root cause of progressive loss of neural function in spinal muscle atrophy (SMA), an inherited neuromuscular disease.

Symptoms of SMA can vary widely depending ... strategies to enhance mobility and daily living skills. Spinal Muscular Atrophy (SMA) is a significant, life-changing condition, yet advancements ...

Is a very rare form of Spinal Muscular Atrophy caused by mutations in the gene. Symptoms appear during infancy, between ages 6 weeks and 6 months. Children with SMARD1 suddenly may be unable to ...

Spinal muscular atrophy (SMA) is a rare hereditary neuromuscular ... treatment and support are available to manage the symptoms and help people with SMA obtain the best possible quality of life.

From February 12, all newborn babies will be offered screening for spinal muscular atrophy (SMA), a rare progressive neuromuscular disease. SMA will be one of more than 20 other rare disorders ...

Background: Spinal and bulbar muscular atrophy (SBMA) or Kennedy disease [OMIM ... 21 healthy male controls without known neurological disease or neurologic symptoms were enrolled in this study as a ...