Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Relationship between non-alcoholic steatohepatitis, PNPLA3 I148M genotype and bone mineral density in adolescents.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers.

Genomic-based multiple-trait evaluation in Eucalyptus grandis using dominant DArT markers.

CXCR4 involvement in neurodegenerative diseases.

Immune-related genetic enrichment in frontotemporal dementia: An analysis of genome-wide association studies.

Combined Socio-Behavioral Evaluation Improves the Differential Diagnosis Between the Behavioral Variant of Frontotemporal Dementia and Alzheimer's Disease: In Search of Neuropsychological Markers.

Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH).

[Metabolism of Inula cappa extract by rat intestinal bacteria in vitro].

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS.

Estimating the number of children in formal alternative care: Challenges and results.

Type 2 diabetes is associated with an increased prevalence of respiratory symptoms as compared to the general population.

Subjective well-being among young people in five Eastern European countries.

WAKE-Up Exoskeleton to Assist Children With Cerebral Palsy: Design and Preliminary Evaluation in Level Walking.

Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency.