Single-Step BLUP with Varying Genotyping Effort in Open-Pollinated Picea glauca.

Thieno[3,2-b]pyrrole-5-carboxamides as New Reversible Inhibitors of Histone Lysine Demethylase KDM1A/LSD1. Part 1: High-Throughput Screening and Preliminary Exploration.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases.

[Late life psychotic disorders : clinical aspects].

Rab3A, a possible marker of cortical granules, participates in cortical granule exocytosis in mouse eggs.

The Relationship between Intimate Partner Violence and Family Planning among Girls and Young Women in the Philippines.

Late Pleistocene echimyid rodents (Rodentia, Hystricognathi) from northern Brazil.

Efficacy and safety of growth hormone treatment in children with short stature: the Italian cohort of the GeNeSIS clinical study.

Length of Stay in the Emergency Department and Occurrence of Delirium in Older Medical Patients.

Development and Validation of a New Prognostic System for Patients with Hepatocellular Carcinoma.

A Multicenter Retrospective Survey regarding Diabetic Ketoacidosis Management in Italian Children with Type 1 Diabetes.

A Novel Mutation in RPL10 (Ribosomal Protein L10) Causes X-Linked Intellectual Disability, Cerebellar Hypoplasia, and Spondylo-Epiphyseal Dysplasia.

GH deficiency status combined with GH receptor polymorphism affects response to GH in children.

Interaction between Streptococcus pneumoniae and Staphylococcus aureus in paediatric patients suffering from an underlying chronic disease.