Results 321 to 330 of about 714,652 (372)
Sliding Guide System Concept for 3D Motion of the Hip Joint in Walking Assist Robots
The human hip joint has three degrees of freedom. However, most current walking assist robots only support flexion–extension. As the human femoral head is almost a perfect sphere, the sliding guide system employs two guide plates that contour spherical surfaces.
Naoto Saito+2 more
wiley +1 more source
Topology Optimization of Exo‐Glove Poly II for Enhancing Functionality and Wearability
This study proposes a topology optimization method for Exo‐Glove Poly II to enhance functionality and wearability. By modeling its finger body as a longitudinally periodic structure, a unit cell‐level optimization—aimed at minimizing distortion and achieving user‐preferred stretchability—is established. Experimental validation shows reduced distortion,
Soomin Choi+4 more
wiley +1 more source
Developing transcranial direct current stimulation as a treatment for phantom limb pain: from pilot mechanistic studies to large clinical studies. [PDF]
Zhang XC, Pacheco-Barrios K, Fregni F.
europepmc +1 more source
ABSTRACT This exploratory cross‐sectional study aimed to estimate the family quality of life (FQoL) among 70 Brazilian families with children with Cornelia de Lange syndrome (CdLS). Data were collected using sociodemographic and clinical data forms, the Barthel index for activities of daily living, and the Beach Center FQoL Scale, a 5‐point Likert tool
Aline Apis+8 more
wiley +1 more source
ABSTRACT Uniparental disomy (UPD) is a rare phenomenon in which both copies of a chromosome are inherited from a single parent. This can lead to genomic imprinting disorders and recessive disorders due to the presence of recessive pathogenic variants in both alleles. Additionally, depending on the mechanisms by which UPD occurs, mosaic aneuploidies may
Marta Carreño‐Hidalgo+4 more
wiley +1 more source
Visuo-Vestibular and Cardiovascular Contributions to Vertical Ego-motion Representation [PDF]
Giannopulu, I
core
Long‐Read Whole‐Genome Sequencing Uncovers a Deletion Upstream to HOXD13 Causing Synpolydactyly
ABSTRACT Synpolydactyly (SPD) is a heterogeneous distal‐limb malformation syndrome, characterized by webbing and duplication of adjacent digits. SPD1, the most common type, is attributed to disease‐causing variants in HOXD13, a transcription factor in the HOXD cluster that is essential for limb development. Here, we present a challenging exome‐negative
Jonathan Rips+9 more
wiley +1 more source
ABSTRACT Wisconsin syndrome is a very rare genetic condition characterized by coarse facies, prominent nasal tip, bushy high arched/upsweeping eyebrows, and a full/everted lower lip. Deletion of chromosome 3q24q25 region is considered critical for its manifestation.
Pankaj Prasun+2 more
wiley +1 more source
Physiotherapy: A potential and novel treatment approach for phantom limb pain in post-amputee patients - A systematic review. [PDF]
Gautam S, Srivastav AK, Sharma D.
europepmc +1 more source