Results 171 to 180 of about 51,348 (353)
This study presents a tendon‐driven compliant snake robot that uses globally applied vertical bending and axial twisting along its body to enable various gaits. Body deflection from compliance and weight passively generates the ground contact patterns required for locomotion.
Serdar Incekara +3 more
wiley +1 more source
Aerospace medicine and biology: A continuing bibliography with indexes (supplement 331) [PDF]
This bibliography lists 129 reports, articles and other documents introduced into the NASA Scientific and Technical Information System during December, 1989.
core +1 more source
Neuromuscular blockade in infants following intramuscular succinylcholine in two or five per cent concentration [PDF]
Gordon Sutherland +2 more
openalex +1 more source
Neuromuscular blockade for cardiac arrest patients treated with targeted temperature management: A protocol of systematic review and meta-analysis [PDF]
Tong Lin +3 more
openalex +1 more source
Respiratory Involvement in HIST1H1E‐Related Rahman Syndrome: A Case of Severe Mixed Apnea
ABSTRACT Rahman syndrome (HIST1H1E‐related neurodevelopmental syndrome, OMIM #617537) is a rare autosomal‐dominant condition caused by truncating variants in the C‐terminal domain of the HIST1H1E gene. It is characterized by macrocephaly, hypotonia, craniofacial anomalies, and multisystem anomalies.
Nada Barakat +4 more
wiley +1 more source
PATTERN OF CHANGE OF BRONCHOMOTOR TONE FOLLOWING REVERSAL OF NEUROMUSCULAR BLOCKADE
Judith Hammond +2 more
openalex +1 more source
STING deficiency promotes motor recovery in mice following brachial plexus root avulsion
STING deficiency can increase the body weight, promote motor recovery, decrease MN death, inhibit pyroptosis and neuroinflammation, increase remyelination, and reduce the atrophy of the biceps brachii in mice with BPRA. Abstract Background Brachial plexus root avulsion (BPRA), a well‐known form of peripheral nerve injury, results in motor function loss
Yu Peng +4 more
wiley +1 more source
Objective Mutations in TARDBP (encoding TDP‐43) are associated with the neurodegenerative disease amyotrophic lateral sclerosis (ALS) and include familial missense mutations where there are a lack of models and mechanisms examining how they are pathogenic.
Ziyaan A. Harji +10 more
wiley +1 more source
Sugammadex for reversing neuromuscular blockade in infants and children. [PDF]
Raphael CK +9 more
europepmc +1 more source
Objective Myotonic dystrophy type 1 (DM1) is a highly variable, multisystemic genetic disorder caused by a CTG repeat expansion in the 3′ untranslated region of DMPK. Toxicity is exerted by repeat‐containing DMPK transcripts that sequester muscleblind‐like (MBNL) proteins and lead to deleterious yet predictable changes in alternative splicing.
Samuel T. Carrell +3 more
wiley +1 more source

