Results 221 to 230 of about 346,964 (351)
The rib cage stiffens the thoracic spine in a cadaveric model with body weight load under dynamic moments. [PDF]
Mannen EM +5 more
europepmc +1 more source
Rib Cage IMU and sEMG Dataset: Kinematics and Respiratory Muscle Activation
SILVIA SANTOS +3 more
openalex +1 more source
Unifying microorganisms and macrograzers in intertidal rocky shore ecological networks
Abstract Over the past decades, our understanding of the vital role microbes play in ecosystem processes has greatly expanded. However, we still have limited knowledge about how microbial communities interact with larger organisms. Many existing representations of microbial interactions are based on co‐occurrence patterns, which do not provide clear ...
Clara Arboleda‐Baena +7 more
wiley +1 more source
Re: bone: an acute buffer of plasma sodium during exhaustive exercise? [PDF]
Hind, K, Jones, B, King, RF
core +1 more source
Response of oxygen saturation in preterm infants receiving rib cage stabilization with an elastic band in two body positions: a randomized clinical trial [PDF]
Marisa Afonso Andrade Brunherotti +1 more
openalex +1 more source
ABSTRACT Background and Aims Children with cerebral palsy (CP) are vulnerable to respiratory infections and chronic airway inflammation, which leads to diminished respiratory function. This decline is exacerbated by muscle tone abnormalities and reduced strength, worsening as CP progresses.
Dolors Casellas‐Vidal +8 more
wiley +1 more source
An Approach to the Girth Problem in Cubic Graphs
ABSTRACT We offer a new, gradual approach to the largest girth problem for cubic graphs. It is easily observed that the largest possible girth of all n‐vertex cubic graphs is attained by a 2‐connected graph G = ( V , E ). By Petersen's graph theorem, E is the disjoint union of a 2‐factor and a perfect matching M.
Aya Bernstine, Nati Linial
wiley +1 more source
ABSTRACT Cytosolic phosphoenolpyruvate carboxykinase (PEPCK‐C) deficiency is a rare autosomal recessive gluconeogenesis disorder caused by variants in the PCK1 gene. Clinically, PEPCK‐C deficiency is characterized by recurrent episodes of fasting‐induced hypoglycemia, liver dysfunction, and seizures, with the first hypoglycemic episode typically ...
Lauma Vasiļevska +6 more
wiley +1 more source

