about
Reliability of quadriceps surface electromyography measurements is improved by two vs. single site recordingsReduced firing rates of high threshold motor units in response to eccentric overload.Muscle size and strength: debunking the "completely separate phenomena" suggestion.Tendinous tissue properties after short- and long-term functional overload: Differences between controls, 12 weeks and 4 years of resistance training.The influence of patellar tendon and muscle-tendon unit stiffness on quadriceps explosive strength in man.Do changes in neuromuscular activation contribute to the knee extensor angle-torque relationship?Training-specific functional, neural, and hypertrophic adaptations to explosive- vs. sustained-contraction strength training.Changes in agonist neural drive, hypertrophy and pre-training strength all contribute to the individual strength gains after resistance training.Neural adaptations after 4 years vs. 12 weeks of resistance training vs. untrainedTendinous Tissue Adaptation to Explosive- vs. Sustained-Contraction Strength TrainingEvaluation of electromyography normalisation methods for the back squatComparison of acute countermovement jump responses after functional isometric and dynamic half squatsIs the joint-angle specificity of isometric resistance training real? And if so, does it have a neural basis?Does normalization of voluntary EMG amplitude to MMAX account for the influence of electrode location and adiposity?Biceps femoris long head muscle fascicle length does not differ between sexesExplosive strength: effect of knee-joint angle on functional, neural, and intrinsic contractile propertiesWhat makes long-term resistance-trained individuals so strong? A comparison of skeletal muscle morphology, architecture, and joint mechanics
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Q33665809-76DFC384-C0F4-47B1-AB82-4C381633C9EAQ37609059-87F25436-23C0-4028-AA6B-5F96E3301D28Q47218820-CD048BD9-911A-43EA-96C5-ACA74888A2DAQ48046075-21C54BA7-8D30-4749-877E-2512DEDE1F8BQ48047142-F512FFDB-F33A-4332-87DF-2FA94B570B7AQ48306763-A8EC261D-0388-4149-882B-803048301676Q53726882-F4B75D12-3056-4C76-8580-6C9E12D99B14Q53749552-B243D7BA-56A1-4A1A-8770-B1BC88B381A6Q58577246-684AE12D-598E-47A5-B8E5-A33B5AFFF150Q58764820-A5BC2C38-D6F5-4826-961B-769770856AA5Q82877828-5AE53F45-9B4F-45C0-A276-3D8B13D2A7D0Q88057673-D20C9AF4-8D7E-4F79-A9FE-E4791A10A193Q90111612-EB192BF1-1774-40FD-98BF-C0B35356C41AQ90379430-8E7F23E9-7AA3-409D-A517-518D0F5407C8Q91860493-E2AF808D-9BB0-4AC2-9A5C-AD27B245A35EQ92209203-A7988E82-1537-4F6A-95BD-476BC19BF5EBQ92228732-17133A0D-6DA2-49AA-A4EE-03F7915E63B4
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Thomas G Balshaw
@en
Thomas G Balshaw
@nl
type
label
Thomas G Balshaw
@en
Thomas G Balshaw
@nl
prefLabel
Thomas G Balshaw
@en
Thomas G Balshaw
@nl
P31
P496
0000-0001-6935-8228