... INTEND, HMFSE) for People With SMA and How They Are Used To Monitor Treatment Outcomes — Spinal Muscular Atrophy UK Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy — The New England Journal of Medicine ...
... INTEND, HMFSE) for People With SMA and How They Are Used To Monitor Treatment Outcomes — Spinal Muscular Atrophy UK Nusinersen Versus Sham Control in Infantile-Onset Spinal Muscular Atrophy — The New England Journal of Medicine ...
... — SMA Reach UK The Hammersmith Functional Motor Scale for Children With Spinal Muscular Atrophy: A Scale To Test Ability and Monitor Progress in Children With Limited Ambulation — European Journal of Paediatric Neurology Hammersmith Functional Motor Scale and Motor Function Measure-20 in Non Ambulant SMA Patients — Neuromuscular Disorders Spinal Muscular ...
... — SMA Reach UK The Hammersmith Functional Motor Scale for Children With Spinal Muscular Atrophy: A Scale To Test Ability and Monitor Progress in Children With Limited Ambulation — European Journal of Paediatric Neurology Hammersmith Functional Motor Scale and Motor Function Measure-20 in Non Ambulant SMA Patients — Neuromuscular Disorders Spinal Muscular ...
... References Therapeutic Approaches — Cure SMA Spinal Muscular Atrophy: The Use of Functional Motor Scales in the Era of Disease-Modifying Treatment — Child Neurology Open Motor Neuron Diseases Fact Sheet — National Institute of Neurological Disorders and Stroke The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOPINTEND ...
... References Therapeutic Approaches — Cure SMA Spinal Muscular Atrophy: The Use of Functional Motor Scales in the Era of Disease-Modifying Treatment — Child Neurology Open Motor Neuron Diseases Fact Sheet — National Institute of Neurological Disorders and Stroke The Children’s Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOPINTEND ...
... Motor neurons affected by SMA-LED, however, only extend from the lower spinal cord to the thigh muscles. When intracellular transport along these nerves is impaired (i.e., due to a genetic mutation), the nerve cannot signal to the muscle to move. Eventually, both the nerve and muscle die. ...
... Motor neurons affected by SMA-LED, however, only extend from the lower spinal cord to the thigh muscles. When intracellular transport along these nerves is impaired (i.e., due to a genetic mutation), the nerve cannot signal to the muscle to move. Eventually, both the nerve and muscle die. ...
... People who have this mutation have it in all cells in their body, and it is not known why degeneration is seen more in motor neurons than in other cells.Pattern of InheritanceThe most common types of SMA are due to the autosomal recessive inheritance of a gene mutation, meaning that the mutated gene that causes the disease must be inherited from both ...
... People who have this mutation have it in all cells in their body, and it is not known why degeneration is seen more in motor neurons than in other cells.Pattern of InheritanceThe most common types of SMA are due to the autosomal recessive inheritance of a gene mutation, meaning that the mutated gene that causes the disease must be inherited from both ...
... References Breathing Basics: Respiratory Care for Children with Spinal Muscular Atrophy — CureSMA Spinal Muscular Atrophy (SMA): Signs and Symptoms — Muscular Dystrophy Association Breathing Risks and Care — CureSMA Spinal Muscular Atrophy (SMA): Medical Management — Muscular Dystrophy Association What is BiPAP? ...
... References Breathing Basics: Respiratory Care for Children with Spinal Muscular Atrophy — CureSMA Spinal Muscular Atrophy (SMA): Signs and Symptoms — Muscular Dystrophy Association Breathing Risks and Care — CureSMA Spinal Muscular Atrophy (SMA): Medical Management — Muscular Dystrophy Association What is BiPAP? ...
... Find Your TeamOn mySMAteam, the social network for people with SMA, more than 1,500 members come together to ask questions, give advice, and share their stories with others who understand life with SMA.Have you been diagnosed with SMA later in life? ...
... Find Your TeamOn mySMAteam, the social network for people with SMA, more than 1,500 members come together to ask questions, give advice, and share their stories with others who understand life with SMA.Have you been diagnosed with SMA later in life? ...
... Because SMA is a rare disease, there’s a good chance you may not already know people who can relate to what you and your family are going through. Meeting others who are also dealing with this condition can provide insight and inspiration for living with SMA. ...
... Because SMA is a rare disease, there’s a good chance you may not already know people who can relate to what you and your family are going through. Meeting others who are also dealing with this condition can provide insight and inspiration for living with SMA. ...
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