Cracking the Code: Genotype–Phenotype Correlation Models in Sarcoglycanopathies
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Sarcoglycanopathies are among the most severe limb‐girdle muscular dystrophies (LGMD), though milder presentations have been described. These diseases are primarily caused by missense variants, but the limited predictability of their effect on protein maturation, complex formation, and transport has hindered reliable genotype ...
Leonela Luce +72 more
wiley +1 more source
Equity, Diversity and Inclusion in Nursing Educational Institutions: A Scoping Review. [PDF]
J Adv NursLartey SA +3 more
europepmc +1 more source
Teaching Facilitation of Family Participation in Educational Institutions. [PDF]
Front Psychol, 2021 Gomariz MÁ +3 more
europepmc +1 more source
CSF Monoamine Metabolites and Cognitive Trajectory in Early Parkinson's Disease
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Background Imaging and postmortem studies indicate that abnormalities in monoaminergic neurotransmission contribute to cognitive impairment in Parkinson's disease (PD). However, it remains uncertain if cerebrospinal fluid (CSF) monoamine metabolites can serve as biomarkers of cognitive decline in early PD.
Jing‐Yu Shao +7 more
wiley +1 more source
GENDER VIOLENCE IN EDUCATIONAL INSTITUTIONS
, 2016 School violence is multifactorial. Social and cultural, family, personal, and institutional aspects, among others, influence educational institutions, in all academic levels.
Rosalva Ruiz-Ramírez +1 more
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Resilience and Work Stress in Educational Institutions of Chepén, 2024: Mediation of Motivation and Time Moderation. [PDF]
Behav Sci (Basel)Jara Cerdan AS +2 more
europepmc +1 more source
Chiropractic techniques and treatment modalities included in academic programs: A survey of chiropractic educational institutions. [PDF]
J Chiropr Educ, 2022 Dubuc É +5 more
europepmc +1 more source
SPG4 and Dementia: Expanding the Clinical Spectrum
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Hereditary spastic paraplegia (HSP) is a group of disorders characterized by progressive spasticity and lower limb weakness, with mutations in SPG4/SPAST being the most common cause. Detailed studies and clinical and molecular comparisons across different populations are missing.
Emanuele Panza +19 more
wiley +1 more source
Cross-sectional study on public health knowledge among first-year university students in Japan: Implications for educators and educational institutions. [PDF]
PLoS One, 2023 Sekine M +9 more
europepmc +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Considerable efforts have been dedicated to developing effective treatments for post‐stroke executive impairment (PSEI), among which repetitive transcranial magnetic stimulation (rTMS) has shown great potential. This study aimed to investigate the therapeutic effects of high‐frequency rTMS on working memory (WM) and response ...
Mengting Lao +6 more
wiley +1 more source