Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Jane Schneiderman‐Walker"'
Autor:
Carolyn E. Hutzal, Samantha K. Stephens, Jane Schneiderman-Walker, Brian M. Feldman, F. Virginia Wright
Publikováno v:
Physical & Occupational Therapy In Pediatrics. 29:409-425
Children with arthritis face challenges when they try to increase their physical activity. The study's objective was to identify elements of a successful community-based exercise program for children with arthritis by investigating the perspectives o
Autor:
Larry C. Lands, Felix Ratjen, Jane Schneiderman-Walker, Donna L. Wilkes, Maryam Elmi, Greg D. Wells, Elizabeth Tullis, Allan L. Coates
Publikováno v:
Pediatric Pulmonology. 43:345-353
Purpose To understand potential benefits of exercise in the cystic fibrosis (CF) population, there needs to be accurate methods to quantify it. The Habitual Activity Estimation Scale (HAES) questionnaire has been shown to be a feasible tool to measur
Publikováno v:
Pediatric Exercise Science. 18:30-52
The purpose of this research was to develop a comprehensive normative database of the physiological characteristics of elite swimmers. Data were obtained from 195 elite swimmers (89 males and 106 females) ages 12 to 18 years. Six protocols were used
Autor:
Hiran Selvadurai, Mary Corey, Richard Stein, Jane Schneiderman-Walker, Allan L. Coates, Donna L. Wilkes
Publikováno v:
Pediatric Pulmonology. 35:467-471
Maximal voluntary ventilation (MVV) may be determined directly by the sprint method or calculated from pulmonary function data, using the functions MVV = forced expired volume in 1 sec (FEV1) × 35 or MVV = FEV1 × 40. The purpose of this paper was t
Autor:
Mary Corey, Gerard J. Canny, Jane Schneiderman-Walker, Linda Pedder, Donna D. Wilkes, J. Reisman, Susan L. Pollock
Publikováno v:
The Journal of Pediatrics. 136:304-310
Objectives: To evaluate the effects of a 3-year home exercise program on pulmonary function and exercise tolerance in mildly to moderately impaired patients with cystic fibrosis (CF) and to assess whether regular aerobic exercise is a realistic treat
Autor:
Greg D, Wells, Donna L, Wilkes, Jane, Schneiderman-Walker, Maryam, Elmi, Elizabeth, Tullis, Larry C, Lands, Felix, Ratjen, Allan L, Coates
Publikováno v:
Pediatric pulmonology. 43(4)
To understand potential benefits of exercise in the cystic fibrosis (CF) population, there needs to be accurate methods to quantify it. The Habitual Activity Estimation Scale (HAES) questionnaire has been shown to be a feasible tool to measure physic
Autor:
Jane Schneiderman-Walker, Hiran Selvadurai, Shirley M. L. Tse, Samantha Stephens, Bonnie Cameron, Joseph Beyene, Oded Bar-Or, Davinder Singh-Grewal, Rayfel Schneider, Virginia Wright, Lynn Spiegel, Earl D. Silverman, Claire LeBlanc, Brian M. Feldman
Publikováno v:
Arthritis and rheumatism. 57(8)
Objective To determine the reliability of formal exercise testing and the reliability of functional and activity questionnaires in children with juvenile idiopathic arthritis (JIA). Methods Children with JIA of any subtype ages 8–16 years who were
Autor:
Samantha Stephens, Bonnie Cameron, Oded Bar-Or, Rayfel Schneider, Ronald M. Laxer, Jane Schneiderman-Walker, Shirley Ml Tse, Claire LeBlanc, Brian M. Feldman, Davinder Singh-Grewal, Janice Wong, Hiran Selvadurai, Joseph Beyene, Virginia Wright, Lynn Spiegel, Earl D. Silverman
Publikováno v:
Arthritis and rheumatism. 57(7)
Objective To examine the effectiveness of high-intensity aerobic training compared with low-intensity training in terms of energy cost of locomotion, peak oxygen uptake, peak power, and self-reported physical function in children with juvenile idiopa
Autor:
Desmond Bohn, Ian Adatia, Donna L. Wilkes, Jane Schneiderman-Walker, Allan L. Coates, Daniel Trachsel, Hiran Selvadurai
Publikováno v:
Pediatric pulmonology. 41(6)
Our objective was to study exercise capacity and cardiorespiratory response to exertion in survivors of congenital diaphragmatic hernia (CDH). This was a cross-sectional cohort study of 23 CDH survivors, aged 10-16 years, and 23 gender- and age-match
Publikováno v:
Archives of disease in childhood. 90(8)
Background: Carbon dioxide (CO 2 ) retention during exercise is uncommon in mild to moderate lung disease in cystic fibrosis (CF). The ability to deal with increased CO 2 is dependent on the degree of airflow limitation and inherent CO 2 sensitivity.