198,652 research outputs found
Molecular Genetics and Pathogenesis of Ehlers–Danlos Syndrome and Related Connective Tissue Disorders. Edited by Marina Colombi and Marco Ritelli
No full textThis is a reprint of articles from the Special Issue published online in the open access journal Genes
(ISSN 2073-4425) (available at: https://www.mdpi.com/journal/genes/special issues/Connective
Tissue Disorders)
Comparing Greek Colonies. Mobility and Settlement Consolidation from Southern Italy to the Black Sea (8th – 6th Century BC). Proceedings of the International Conference (Rome, 7.–9.11.2018)
No full textThe need for a "new" book on Greek colonization arose to analyse this phenomenon as a long-term process in a wide geographic area. The events related to individual cities and regions, although geographically very distant from each other, are linked through an articulated network of material and immaterial relations and have to be considered as part of a broader mobility process in a Mediterranean perspective. The intention of "Comparing Greek Colonies" is to bring geographically and culturally distant regions such as Southern Italy/Sicily and the Black Sea, closer together, not merely to find "similarities and differences", but to broaden the scholars’ perspective and overcome existing, generalizing, and biased models, that are often rooted in local scientific traditions.
The proceedings of the international conference "Comparing Greek Colonies. Mobility and Settlement Consolidation from Southern Italy to the Black Sea (8th – 6th century BC)", 7.–9.11.2018 in Rome, are structured around three core topics (economic system; relationships with the indigenous populations; social and territorial systems) that constitute the cornerstones of the political formation of the polis in the Archaic period and for its development during the Classical and Hellenistic Ages
The Madonna and Child with Saints Francis and Dominic and Angels by Giulio Cesare Procaccini: A masterpiece from the Archinto collection
No full textRecensione a Marchesa Colombi, "Un matrimonio in provincia", Einaudi
No full textRecensione a Marchesa Colombi, "Un matrimonio in provincia", Einaud
Milanese antique dealers and the international market: Giuseppe Baslini and the Grandi family company
No full textThis article provides two concrete examples of the opening of the Milanese art market to the international stage at the time of Gian Giacomo Poldi Pezzoli. The main focus is on the career of Giuseppe Baslini (1817-1887), the most important art dealer in nineteenth-century Milan. A true self-made man, Baslini entertained close relations with the most eminent Milanese collectors of the time, including Poldi Pezzoli and the Bagatti Valsecchi brothers; his success was secured by the international market on three major axes - London, Paris and Berlin. The second example concerns the family company of the Grandi art dealers, during the same years. In 1877 Baslini's brothers-in-law Carlo (1842-1914) and Antonio (1857-1923) Grandi inherited the company of their father, Antonio (1810-1877), which originally specialized in Old Master drawings and prints, but extended its interests to paintings and objets d'art soon after Baslini's death. The Grandi correspondence, preserved by the heirs and recently donated to the Fondo per l'Ambiente Italiano, has provided the opportunity to reconstruct their business, which had an international dimension from its inception
Bartolomeo Montagna (Bartolomeo Cincani) Vicenza (?), 1449 circa – Vicenza, 11 ottobre 1523, Madonna con il Bambino in trono tra i santi Sebastiano e Rocco
No full textScheda di catalog
Molecular genetics and pathogenesis of Ehlers–Danlos syndrome and related connective tissue disorders
No full textEhlers–Danlos syndromes (EDS) are a group of heritable connective tissue disorders (HCTDs) characterized by a variable degree of skin hyperextensibility, joint hypermobility and tissue fragility. The current EDS classification distinguishes 13 subtypes and 19 different causal genes mainly involved in collagen and extracellular matrix synthesis and maintenance. EDS need to be differentiated from other HCTDs with a variable clinical overlap including Marfan syndrome and related disorders, some types of skeletal dysplasia and cutis laxa. Clinical recognition of EDS is not always straightforward and for a definite diagnosis, molecular testing can be of great assistance, especially in patients with an uncertain phenotype. Currently, the major challenging task in EDS is to unravel the molecular basis of the hypermobile EDS that is the most frequent form, and for which the diagnosis is only clinical in the absence of any definite laboratory test. This EDS subtype, as well as other EDS-reminiscent phenotypes, are currently investigated worldwide to unravel the primary genetic defect and related pathomechanisms. The research articles, case report, and reviews published in this Special Issue focus on different clinical, genetic and molecular aspects of several EDS subtypes and some related disorders, offering novel findings and future research and nosological perspectives
La respuesta y sus vestidos : tipos discursivos y redes de poder en La respuesta a Sor Filotea
No full textFil: Colombi, Beatriz. Universidad de Buenos Aires. Facultad de Filosofía y Letras. Departamento de Letras; Argentina
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