Spatial analyses of archaeobotanical record reveal site uses and activities at Early to Middle Holocene Takarkori (Libya, Central Sahara).

This study investigates botanical remains from the Takarkori site in the Tadrart Acacus region (SW Libya) to reconstruct socio-economic and cultural characteristics of human groups during the Holocene. By analyzing micro- and macrofossils of plant origin, we aim to understand the availability and management of environmental resources and how plant taxa were used by humans. The exceptional preservation of archaeobotanical material across all occupation levels, facilitated by the region's geomorphological and environmental conditions, provides a unique opportunity to study pre-Pastoral and Pastoral Neolithic activities within a comprehensive diachronic framework.

Recent developments in tornado theory and observations.

This article critically reviews research on tornado theory and observations over the last decade. From the theoretical standpoint, the major advances have come through improved numerical-simulation models of supercell convective storms, which contain the tornado's parent circulation. These simulations are carried out on a large domain (to capture the supercell's circulation system), but with high grid resolution and improved representations of sub-grid physics (to capture the tornado).

Clinical and Molecular Spectrum of Sporadic Vascular Malformations: A Single-Center Study.

Sporadic vascular malformations (VMs) are a large group of disorders of the blood and lymphatic vessels caused by somatic mutations in several genes-mainly regulating the RAS/MAPK/ERK and PI3K/AKT/mTOR pathways. We performed a cross-sectional study of 43 patients affected with sporadic VMs, who had received molecular diagnosis by high-depth targeted next-generation sequencing in our center. Clinical and imaging features were correlated with the sequence variants identified in lesional tissues.

PIK3CA-related overgrowth with an uncommon phenotype: case report.

Background: Megalencephaly-capillary malformation syndrome is a rare multiple-malformation syndrome secondary to somatic activating mutations in the PI3K-AKT-MTOR pathway. This is included in a heterogeneous group of disorders, now defined "PIK3CA-related overgrowth spectrum".

Case Presentation: We report a 22-months-old female presenting an uncommon phenotype associated with a genetic mosaicism in the PIK3CA gene, detected on DNA extracted from blood peripheral and tissue biopsy.