Results 221 to 230 of about 245,637 (381)
SYSTEMATIC REVIEWS TO HELP GUIDE CLINICAL PRACTICE IN NEUROMUSCULAR DISEASE [PDF]
Kate Jewitt, Richard AC Hughes
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Arthrogryposis Multiplex Congenita (AMC) is characterized by the presence of multiple joint contractures in the fetus' body. The diagnosis of arthrogryposis is complex and often missed prenatally. This comprehensive review of the literature published over the last 20 years, with an emphasis on the role of prenatal ultrasound in predicting postnatal ...
Mario Brock Leao+7 more
wiley +1 more source
Mechanical insufflation-exsufflation use in neuromuscular disease: a single centre cohort study. [PDF]
Shah NM+12 more
europepmc +1 more source
Respiratory muscle training in neuromuscular disease: a systematic review and meta-analysis. [PDF]
Watson K+7 more
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Pressure Support Versus Assisted Controlled Noninvasive Ventilation in Neuromuscular Disease [PDF]
Karim Chadda+5 more
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Abstract Venous blood gases (VBGs) are safe and effective at screening for hypercarbic respiratory failure. Multiple studies have validated that a VBG with a PvCO2 less than 45 reliably rules out hypercarbia. The use of VBGs for the initial screening of hypercarbia when hypercarbic respiratory failure is suspected can reduce the overall use of arterial
Mary E. Lacy+3 more
wiley +1 more source
Therapeutic targeting of RNA for neurological and neuromuscular disease. [PDF]
Bubenik JL, Scotti MM, Swanson MS.
europepmc +1 more source
Optically pumped magnetometers detect altered maximal muscle activity in neuromuscular disease. [PDF]
Semeia L+13 more
europepmc +1 more source
Genetically‐targeted control of the spinal cord and peripheral nervous system
Application of genetically‐targeted stimulation for treating diseases or injuries outside the brain. Optogenetic and chemogenetic systems have been developed for dysfunction in the cochlea, spinal cord, dorsal root ganglia (DRGs), peripheral nerves, lower urinary tract, and enteric nervous system (ENS). Created with Biorender.com.
Anakaren Romero Lozano+3 more
wiley +1 more source
Charcot-Marie-Tooth disease (CMT) is a genetic peripheral neuropathy caused by mutations in many functionally diverse genes. The aminoacyl-tRNA synthetase (ARS) enzymes, which transfer amino acids to partner tRNAs for protein synthesis, represent the ...
Elena R. Rhymes+10 more
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