Results 331 to 340 of about 121,688 (385)

Clinical Phenotype and Neuroimaging Findings in Siblings with COX15 Deficiency: Case Report and Review of Previously Reported Cases

open access: yes
Movement Disorders Clinical Practice, EarlyView.
Haya S. AlFaris   +8 more
wiley   +1 more source

Reply to “Neurophysiological Testing to Diagnose Stiff‐Person Spectrum Disorder”

open access: yes
Movement Disorders Clinical Practice, EarlyView.
João Moura   +5 more
wiley   +1 more source

Progressive Muscular Atrophy

Neurologic Clinics, 2015
Progressive muscular atrophy (PMA) is a rare, sporadic, adult-onset motor neuron disease, clinically characterized by isolated lower motor neuron features; however, clinically evident upper motor neuron signs may emerge in some patients. Subclinical upper motor neuron involvement is identified pathologically, radiologically, and neurophysiologically in
Teerin Liewluck   +2 more
openaire   +4 more sources

Tetrahedral Framework Nucleic Acids Inhibit Muscular Mitochondria-Mediated Apoptosis and Ameliorate Muscle Atrophy in Sarcopenia.

Nano letters (Print), 2023
Sarcopenia is known as age-related muscle atrophy, which influences over a quarter of the elderly population worldwide. It is characterized by a progressive decline in muscle mass, strength, and performance. To date, clinical treatments in sarcopenia are
Xi Yu   +19 more
semanticscholar   +1 more source

Progressive Muscular Atrophy

2017
Progressive muscular atrophy is a chronic, sporadic, slowly progressive degeneration of the anterior horn cells and cranial nerve nuclei. It differs from amyotrophic lateral sclerosis in that there are no pyramidal signs. However, it has links and overlaps with amyotrophic lateral sclerosis. The condition needs to be considered in the wide differential
Bhagyadhan A. Patel   +2 more
openaire   +2 more sources

Progressive Muscular Atrophy in an Infant

The American Journal of Nursing, 1963
D ON IS A TWO-MONTH-OLD boy with the infantile form of progressive muscular atrophy who was admitted to the pediatric service of a U.S. Air Force Hospital in England. In infants the condition is known as Werdnig-Hoffmann disease. This is primarily a disease of the anterior horn cells of the spinal cord, resulting in degeneration of the peripheral motor
openaire   +3 more sources

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