One repetition maximum prediction models for children using the OMNI RPE Scale.

This investigation developed statistical models to estimate one repetition maximum (1 RM) muscular strength using submaximal ratings of perceived exertion (RPE) as predictor variables. Ten- to 14-year-old girls (n = 35) and boys (n = 35) performed two sets (10 repetitions) of biceps curl (BC) and knee extension (KE) exercise using weights approximating 30% and 50% 1 RM. RPE was assessed during the final repetition of each set using the children's OMNI Resistance Exercise Scale (0-10).

Physiological responses during graded treadmill exercise in chemical-resistant personal protective equipment.

Background: As the likelihood of terrorist acts increases, prehospital personnel have been forced to train in the proper use of chemical-resistant personal protective equipment (PPE). This protective ensemble has been reported to be physiologically taxing for the wearer, imposing an additional thermal load resulting in hypohydration, hyperthermia, and reduced work time. Victim extrication, the rescue-the-rescuer role of the rapid intervention team and rapid self-extrication, typically requires high-intensity work that can be maintained only for short time intervals.

The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance.

The combination of pulmonary agenesis/dysgenesis/hypoplasia, microphthalmia/anophthalmia, and a diaphragmatic defect (agenesis or eventration) is a rare syndrome presumed to have an autosomal recessive mode of inheritance based on a report of affected siblings born to unaffected parents [Seller et al., 1996]. The condition is known as Spear syndrome and Matthew-Wood syndrome, although genetic heterogeneity cannot be ruled out.

Frequency of genomic rearrangements involving the SHFM3 locus at chromosome 10q24 in syndromic and non-syndromic split-hand/foot malformation.

Split-hand/foot malformation (SHFM), or ectrodactyly, is characterized by underdeveloped or absent central digital rays, clefts of the hands and feet, and variable syndactyly of the remaining digits. SHFM occurs as both an isolated finding and a component of many syndromes. SHFM is a heterogeneous condition caused by multiple loci, including SHFM1 (chromosome region 7q21-q22), SHFM2 (Xq26), SHFM3 (10q24), SHFM4 (3q27), and SHFM5 (2q31).

Observation of perceived exertion in children using the OMNI pictorial scale.

Purpose: Concurrent and construct validity of a kinematic exertional observation procedure was examined for 10- to 14-yr-old female (N = 22) and male (N = 22) healthy children.

Methods: A load-incremented treadmill test protocol employing speed/grade changes every 3 min was used. RPE for the overall body (RPE-Overall), legs (RPE-Legs), and chest (RPE-Chest) were simultaneously estimated by an independent observer and self-rated by a subject during each treadmill stage using the Children's OMNI-Walk/Run Scale.

Evaluation of the SenseWear Pro Armband to assess energy expenditure during exercise.

Purpose: To assess the accuracy of the SenseWear Pro Armband for estimating energy expenditure during exercise.

Methods: : Forty subjects (age = 23.2 +/- 3.

Is Jaffe-Campanacci syndrome just a manifestation of neurofibromatosis type 1?

This article describes four patients with non-ossifying fibromas (NOFs) and multiple café-au-lait spots. Two of the patients were diagnosed with NOFs when they presented with a femur fracture. The other two patients were diagnosed with NOFs because of complaints of leg problems.