Large-scale geomorphology of the Entella River floodplain (Italy) for coastal urban areas management

This research presents a geomorphological map of the Entella River floodplain (scale 1:10,000), one of the largest and urbanized Ligurian Tyrrhenian flat area. The coastal floodplain suffered substantial modifications due to human activities since the latter half of the nineteenth century, which transformed the natural landscape into an anthropogenic environment. Fluvial, marine and anthropogenic geomorphological features have been investigated through a multi-temporal analysis and the reviewing, re-elaboration and summarization of previous geographical and geomorphological materials. An historical analysis has been performed to reconstruct morphological modifications and their correlation with anthropogenic interventions. The main geomorphological map includes a multi-temporal analysis of shoreline and major anthropogenic landforms. Small sketch maps on the geographical, geological and land use settings are also provided. The detailed geomorphological map can be used for urban and land planning, including the mitigation of the meteo- and geo-hydrological risk, which historically has dramatically influenced the Entella coastal floodplain

Serum human epididymis protein 4 vs. carbohydrate antigen 125 in ovarian cancer follow-up

The addition of human epididymis protein 4 (HE4) to carbohydrate antigen 125 (CA125) in ovarian cancer (OC) assessment has been proposed. We compared the clinical value of biomarker changes in a prospective series of patients undergoing OC monitoring

Engineering geological map of the Chiavari city area (Liguria, Italy)

An engineering geological map at a scale of 1:10,000 of the Chiavari city area (Northern Italy) – a major tourist and economic attraction of the Ligurian East Riviera – is presented in this paper. The municipality land shows an excellent geomorphological case-study of the well-known Ligurian coast: a floodplain, fairly wide and inhabited, formed by several floods of the two main rivers, a hill hinterland, reasonably inhabited, developed in marly limestones and sandy shales flysch and the coast – featuring cliffs and narrow pebbly beaches – deeply modified. This map was compiled by combining available geological data with a new engineering geomorphological field survey and including geotechnical data which were obtained from studies carried out for town planning and building purposes. On the basis of the critical review of the available lithostratigraphic data from drilling, as well as geotechnical and geophysical analyses carried out between 1981 and 2010 on the municipality land, an engineering geologica..

PRRT2 Mutations Are the Major Cause of Benign Familial Infantile Seizures

Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and infantile convulsions with choreoathetosis (PKD with infantile seizures), and recently also in some families with benign familial infantile seizures (BFIS) alone. We analyzed PRRT2 in 49 families and three sporadic cases with BFIS only of Italian, German, Turkish, and Japanese origin and identified the previously described mutation c.649dupC in an unstable series of nine cytosines to occur in 39 of our families and one sporadic case (77% of index cases). Furthermore, three novel mutations were found in three other families, whereas 17% of our index cases did not show PRRT2 mutations, including a large family with late-onset BFIS and febrile seizures. Our study further establishes PRRT2 as the major gene for BFIS alone. Hum Mutat 33:1439-1443, 2012. (C) 2012 Wiley Periodicals, Inc

PRRT2 Mutations are the major cause of benign familial infantile seizures

Mutations in PRRT2 have been described in paroxysmal kinesigenic dyskinesia (PKD) and infantile convulsions with choreoathetosis (PKD with infantile seizures), and recently also in some families with benign familial infantile seizures (BFIS) alone. We analyzed PRRT2 in 49 families and three sporadic cases with BFIS only of Italian, German, Turkish, and Japanese origin and identified the previously described mutation c.649dupC in an unstable series of nine cytosines to occur in 39 of our families and one sporadic case (77% of index cases). Furthermore, three novel mutations were found in three other families, whereas 17% of our index cases did not show PRRT2 mutations, including a large family with late-onset BFIS and febrile seizures. Our study further establishes PRRT2 as the major gene for BFIS alone. Hum Mutat 33:1439-1443, 2012. (C) 2012 Wiley Periodicals, Inc