Results 231 to 240 of about 18,573,716 (306)
ABSTRACT Background Mitofusin 2 (MFN2) is a major causative gene for axonal Charcot – Marie – Tooth disease type 2A (CMT2A), with a wide phenotypic spectrum. Comprehensive large ‐ scale genotype – phenotype association studies are essential for understanding disease pathogenesis and improved clinical management.
Masahiro Ando +13 more
wiley +1 more source
Erratum: Attachment in Old Age: A Fundamental Pillar for Public Health and Wellbeing
Swiss School of Public Health Production Office
doaj +1 more source
Evaluating administrative measures of school quality as mediators of the relationship between attending a segregated school and cognitive function among older Black individuals: the STAR study. [PDF]
Gutierrez S +9 more
europepmc +1 more source
ABSTRACT Background Neurodegeneration with brain iron accumulation (NBIA) comprises a genetically and clinically heterogeneous group of rare neurological disorders characterized particularly by iron accumulation in the basal ganglia. To date, 15 genes have been associated with NBIA.
Seda Susgun +95 more
wiley +1 more source
Co-creating the COMMUNICATE toolkit to support the communication of physical activity messages with adolescents in schools. [PDF]
Grady CL +6 more
europepmc +1 more source
ABSTRACT Background Apolipoprotein ε4 (APOE ε4) is a potent genetic risk factor for Alzheimer's disease (AD). However, its role in cerebral small vessel disease (CSVD) remains unclear. Given the clinical and pathological similarities between CSVD and AD, this study aimed to investigate the associations of APOE ε4 gene dosage with cognitive function and
Tingru Jin +6 more
wiley +1 more source
Challenges in dietary management: a qualitative study on caregivers of preschool and school-age children with citrin deficiency. [PDF]
Zhang S, Cai L, Yang X, Gong N, Lin Q.
europepmc +1 more source

