Results 31 to 40 of about 2,738,400 (241)

The Effect of Iron on Cognitive Development and Function in Infants, Children and Adolescents: A Systematic Review [PDF]

open access: yes, 2011
A systematic review was conducted to summarize the evidence currently available from randomized controlled trials (RCTs) concerning the effect of iron intake of infants, children and adolescents on measures of cognitive development and function.
Vesna Vucic   +24 more
core   +1 more source

The Psychomotor Vigilance Test: Sources of State and Trait Variance [PDF]

open access: yes, 2013
Within the context of pilot and air traffic controller selection tests the Psychomotor Vigilance Test (PVT, Dinges & Powell, 1985) was evaluated for its underlying sources of variance.
Hörmann, Hans-Jürgen   +1 more
core  

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu   +21 more
wiley   +1 more source

What factors influence learning of psychomotor skills by dental students? [PDF]

open access: yes, 2010
Several key factors have been identified that relate to skill acquisition: a) ability, b) motivation, c) thinking processes and d) learning environments.
Suksudaj, Nattira
core  

The feasibility of psychomotor therapy in acute mental health services for adults with intellectual disability [PDF]

open access: yes, 2015
Background. Psychomotor therapy enables people to reflect on the relationship between experiences and feelings by starting from awareness of bodily responses rather than from awareness of emotion.
Emck, Claudia   +8 more
core   +1 more source

Posterior Disconnection Syndrome in Early‐Stage Adult‐Onset Cerebral Adrenoleukodystrophy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Adult‐onset cerebral adrenoleukodystrophy is potentially treatable but often difficult to recognize before advanced cerebral involvement. Herein, we describe three men with early‐stage disease who initially presented with subtle visual complaints rather than subcortical dementia. Targeted neuropsychological testing revealed higher‐order visual
Kazuto Katsuse   +13 more
wiley   +1 more source

Validity of the Musculoskeletal Tumor Society Score for lower extremity in patients with bone sarcoma or giant cell tumour of bone undergoing bone resection and reconstruction surgery in hip and knee

open access: yesBMC Cancer
Background The Musculoskeletal Tumor Society Score (MSTS) is widely used to evaluate functioning following surgery for bone and soft-tissue sarcoma. However, concerns have been raised about its content validity due to the lack of patient involvement ...
Nikolai Sherling   +4 more
doaj   +1 more source

The influence on daily occupations of Danish adolescents experiencing stress

open access: yesScandinavian Journal of Occupational Therapy
Background Stress, particularly prevalent during adolescence, is linked to negative outcomes like anxiety and depression. Without support, it can impact education, employability, and social relations as it is closely associated with resilience and ...
Christina Jessen-Winge   +2 more
doaj   +1 more source

Teaching Psychomotor Skills in a Virtual Environment: An Educational Case Study

open access: yesEducation Sciences, 2021
In March 2020, most physical therapy schools across the globe transitioned to online learning in response to the COVID-19 pandemic. This change posed unique challenges not only because it required adapting to new technology in a short period but, more ...
Laura Plummer   +3 more
doaj   +1 more source

A Rare Form of Microcephalic Primordial Dwarfism due to NSMCE2 Deficiency (Seckel Syndrome Type 10): A Report of Macular Involvement

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Biallelic variants in NSMCE2 (MMS21), which encodes the SUMO E3 ligase subunit of the SMC5/6 chromatin‐maintenance complex, have recently been implicated in microcephalic primordial dwarfism (MPD), corresponding to Seckel syndrome type 10 (OMIM #617246).
Cristina Peduto   +5 more
wiley   +1 more source

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