4 results match your criteria: "Mahatma Gandhi Mission School of Physiotherapy[Affiliation]"
Indian J Orthop
June 2024
Children's Orthopaedic Centre, 2nd Floor, Bobby Apartments, 143 L.J. Road, Mahim (West), Mumbai, 400016 India.
Background: Optimal management and surgical planning of severe bony deformities and muscle tendon unit contractures demands comprehensive evaluation of all structures including the dynamic muscle tendon length of all muscles around the joint during gait.
Objectives: Present study aimed to explore dynamic muscle-tendon length for all muscles around the knee joint along with pelvis, hip, and ankle joint kinematics among adolescent children with varying crouch angle.
Methods: Muscle-tendon length of 29 adolescent children with cerebral palsy with varying crouch angles was computed using a full-body musculo-skeletal model and expressed as a percentage of muscle-tendon length during walking compared to resting condition.
Bull World Health Organ
November 2022
Department of Community Medicine, Mahatma Gandhi Mission Institute of Health Sciences, Navi Mumbai, India.
Objective: To implement rehabilitation services in a rural area of Raigad district, Maharashtra, India.
Methods: We piloted a rehabilitation service delivery model through the Mahatma Gandhi Mission Institute of Health Sciences, in five villages. The institute performed participatory rural appraisal and focus group discussions with stakeholders to identify general issues in village life that could affect delivery.
Pan Afr Med J
February 2022
Mahatma Gandhi Mission School of Physiotherapy, Aurangabad Campus, Mahatma Gandhi Institute of Health Sciences, Navi Mumbai, India.
Cureus
July 2021
Community Physiotherapy, Mahatma Gandhi Mission School of Physiotherapy, Aurangabad, IND.
Goyal-Naqvi syndrome (GNS) is a newly documented clinical entity that comprises trisomy 10p and terminal 14q deletion, though trisomy 10p and terminal 14q deletion have been discovered as distinct conditions in 1974 and 1997, respectively. Nevertheless, to date, the total number of reported cases of each of these conditions is estimated to be in double digits. Both manifest as a constellation of features like craniofacial dysmorphism, hypotonia, intellectual impairment and global developmental delay.
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