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15. Early suppression of immune response in Heliothis virescens larvae by the endophagous parasitoid Toxoneuron nigriceps

Author

Ferrarese, R., MAURIZIO FRANCESCO BRIVIO, Congiu, T., Falabella, P., Grimaldi, A., Mastore, M., Perletti, G., Pennacchio, F., Sciacca, L., Tettamanti, G., Valvassori, R., Eguileor, M., Ferrarese, P., Brivio, M., Congiu, T., Falabella, P., Grimaldi, A., Mastoie, M., Perletti, G., Pennacchio, Francesco, Sciacca, L., Tettamanti, G., Valvassori, R., and DE EGUILEOR, M.

Subjects
Insects, lcsh:Biology (General), Immune defenses, fungi, insect, Parasitoid, lcsh:QH301-705.5
Abstract

Toxoneuron nigriceps is an endophagous parasitoid of larval stages of the noctuid moth Heliothis virescens. As all parasitoids, this wasp avoid host immune reaction by a combination of several passive and active mechanisms. Secretions injected by ovipositing females, which contain venom, calyx fluid and polydnaviruses, are the most probably factors actively disrupting Heliothis virescens immune system. This paper describes the main alterations of the host immune response observed shortly after oviposition by T. nigriceps. A transient block of prophenoloxidase activity is registered along with changes in hemocyte number, adhesion and structure, which suggest the occurrence of apoptosis. In contrast, the host plasmatocytes appear structurally unaltered, but unable to produce a capsule in vitro.

Published
2005

16. Functional amyloid formation in LPS activated cells from invertebrates to vertebrates

Author

Grimaldi, A., Gianluca Tettamanti, Girardello, R., Pulze, L., Valvassori, R., Malagoli, D., Ottaviani, E., and Eguileor, M.

Subjects
amyloid fibrils, LPS, lcsh:Biology (General), ACTH axis, Amyloid fibrils, ROS, lcsh:QH301-705.5
Abstract

LPS stimulation provokes serious cellular stress with an increase of cytoplasmic reactive oxygen species (ROS). We have investigated, among the different cellular defenses, amyloidogenesis as common physiological response to attenuate oxidative stress. Optical and electron microscopic observations of the following LPS activated cell lines [insect (larval hemocytes, IPLB-LdFB and Drosophila Schneider’s S2 cells); mouse (NIH3T3 embryonic fibroblasts); Human (Human Umbilical Vein Endothelial Cells (HUVEC), neutrophils, and mesenchymal stem cells] reveal that, all are characterized by irregular profiles, cytoplasmic empty vacuoles or by cisternae containing fibrillar material. The compartmentalized fibrillar material shows staining properties typical of amyloid fibrils. LPS activation leads to ROS generation, resulting in pH acidification. Stimulated cells show pink cytoplasm in May-Grünwald Giemsa differential staining, giving a gross indication of a lower intracellular pH. Moreover the activation of amyloidogenesis is also linked with an extensive production of ACTH and α-MSH in all cultured cell types. We suggest that amyloidogenesis is a common, physiological cellular response to weak ROS, starting when other anti-stress cellular systems failed to restore homeostasis. The morphological evidence and/or functional characterization of synthesized amyloid fibrils could be an early indicator of oxidative stress that may lead to a general inflammatory process.

Published
2014

20. Ras activation in Hirudo medicinalis angiogenic process

Author

Grimaldi, A., Roberto Ferrarese, Tettamanti, G., Valvassori, R., and Eguileor, M.

Subjects
angiogenesis, lcsh:Biology (General), leech, cytoskeleton, lcsh:QH301-705.5, Ras
Abstract

In some leeches like Hirudo medicinalis, any kind of stimulation (surgical wound or growth factor injection) provokes the botryoidal tissue response. This peculiar tissue, localized in the loose connective tissue between gut and body wall, is formed by granular botryoidal cells and flattened endothelial-like cells. Under stimulation, the botryoidal tissue changes its shape to form new capillaries. In mammals, the molecular regulation of the angiogenic phenotype requires coordinated input from a number of signalling molecules: among them the GTPase Ras is one of the major actor. In our current study, we determine whether Ras activation alone would be sufficient to drive vessels formation from leech botryoidal tissue. Our findings indicate that assembly and disassembly of actin filaments regulated by Ras protein is involved in morphological modification of botryoidal tissue cells during leech angiogenic process.

Published
2013

22. Amyloid/Melanin distinctive mark in invertebrate immunity

Author

Grimaldi, A., Girardello, R., Malagoli, D., Falabella, P., Gianluca Tettamanti, Valvassori, R., Ottaviani, E., and Eguileor, M.

Subjects
amyloid fibrils, invertebrate immunity, amyloid fibrils, melanin, ACTH, α-MSH, neutral endopeptidase, invertebrate immunity, lcsh:Biology (General), ACTH, Amyloid fibrils, Invertebrate immunity, Melanin, Neutral endopeptidase, α-MSH, neutral endopeptidase, lcsh:QH301-705.5, melanin
Abstract

Protostomes and Deuterostomes show the same nexus between melanin production, and amyloid fibril production, i.e., the presence of melanin is indissolubly linked to amyloid scaffold that, in turn, is conditioned by the redox status/cytoplasmic pH modification, pro-protein cleavage presence, adrenocorticotropin hormone (ACTH), melanocyte-stimulating hormone (α-MSH), and neutral endopeptidase (NEP) overexpressions. These events represent the crucial component of immune response in invertebrates, while in vertebrates these series of occurrences could be interpreted as a modest and very restricted innate immune response. On the whole, it emerges that the mechanisms involving amyloid fibrils/pigment synthesis in phylogenetically distant metazoan (viz, cnidaria, molluscs, annelids, insects, ascidians and vertebrates) are evolutionary conserved. Furthermore, our data show the relationship between immune and neuroendocrine systems in amyloid/melanin synthesis. Indeed the process is closely associated to ACTH-α-MSH production, and their role in stress responses leading to pigment production reflects and confirms again their ancient phylogeny.

Published
2012

23. Effects of carbon nanotube environmental dispersion on an aquatic invertebrate, Hirudo medicinalis

Author

Girardello, R, Tasselli, S, Baranzini, N, Valvassori, R, De Eguileor, M, Grimaldi, A, Girardello, R, Tasselli, S, Baranzini, N, Valvassori, R, De Eguileor, M, and Grimaldi, A

Abstract

The recent widespread applications of nanomaterials, because of their properties, opens new scenarios that affect their dispersal in the environment. In particular multiwall carbon nanotubes (MWCNTs), despite their qualities, seem to be harmful for animals and humans. To evaluate possible toxic effects caused by carbon nanotube environmental dispersion, with regard to aquatic compartment, we proposed as experimental model a freshwater invertebrate: Hirudo medicinalis. In the present study we analyse acute and chronic immune responses over a short (1, 3, 6 and 12 hours) and long time (from 1 to 5 weeks) exposure to MWCNTs by optical, electron and immunohistochemical approaches. In the exposed leeches angiogenesis and fibroplasia accompanied by massive cellular migration occur. Immunocytochemical characterization using specific markers shows that in these inflammatory processes the monocyte-macrophages (CD45+, CD68+) are the most involved cells. These immunocompetent cells are characterized by sequence of events starting from the expression of pro-inflammatory cytokines (in particular IL-18), and amyloidogenensis. Our combined experimental approaches, basing on high sensitive inflammatory response can highlight adverse effects of nanomaterials on aquatic organisms and could be useful to assess the MWCNTs impact on aquatic, terrestrial animal and human health.

Published
2015

24. NET amyloidogenic backbone in human activated neutrophils

Author

Pulze, L, primary, Bassani, B, additional, Gini, E, additional, D'Antona, P, additional, Grimaldi, A, additional, Luini, A, additional, Marino, F, additional, Noonan, D M, additional, Tettamanti, G, additional, Valvassori, R, additional, and de Eguileor, M, additional

Published
2015
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35. Integumental amino acid uptake in a carnivorous predator mollusc (Sepia officinalis, Cephalopoda)

Author

de Eguileor, M, Leonardi, M, Grimaldi, A, Tettamanti, G, Fiandra, L, Giordana, B, Valvassori, R, Lanzavecchia, G, Leonardi, M G, de Eguileor, M, Leonardi, M, Grimaldi, A, Tettamanti, G, Fiandra, L, Giordana, B, Valvassori, R, Lanzavecchia, G, and Leonardi, M G

Abstract

The epithelial cells of the integument of body, arms and tentacles of Sepia officinalis present on their apical membrane a well-organised brush border and show the morphological and histochemical characteristics of a typical absorptive epithelium. The ability of the integument to absorb amino acids was investigated both in the arms incubated in vitro and in a purified preparation of brush border membrane vesicles (BBMV). Autoradiographic pictures of the integument after incubation of the arms in sea-water with or without sodium, showed that proline intake was Na+-dependent, whereas leucine intake appeared to be a largely cation-independent process. Time course experiments of labelled leucine, proline and lysine uptakes in BBMV evidenced that these amino acids are accumulated within the vesicles in the presence of an inwardly directed sodium gradient. The sodium-driven accumulation proves that cationic and neutral amino acids are taken up by the apical membrane of the epithelium of Sepia integument through a secondary active mechanism. For leucine, a 90% inhibition of the uptake was recorded in the presence of a large excess of the substrate. In agreement with the autoradiography results, an analysis of the cation specificity transport in BBMV showed that leucine uptake had a low cation specificity, whereas lysine and proline uptakes were Na+-dependent. An excess of lysine and proline, which share with alanine two different transport systems in the gill epithelium of marine bivalves, reduced eucine uptake. The possible role of the absorptive ability of the integument in a carnivorous mollusc is discussed

Published
2000

38. Structural and biochemical analysis of the parasite Gordius villoti(Nematomorpha, Gordiacea) cuticle.

Author

Brivio, M.F., Eguileor, M.de, Grimaldi, A., Vigetti, D., Valvassori, R., and Lanzavecchia, G.

Abstract

The cuticle of the nematomorpha Gordius villotiis a proteinaceous extracellular structure that covers the body during the endoparasitic life in the hemocoelic cavity of insect hosts, and of the free-living adult animals. The ultrastructure of the cuticle has a complex spatial organization with several parallel layers of large diameter fibers, interposed thinner fibrous elements and honeycomb-shaped matrix surrounding the fibers. When adult isolated cuticles were partially solubilized by several compounds, the structure revealed a strong insolubility and the main fibers were always observable. HPLC and spectrophotometric assays carried out to investigate the presence of tyrosine cross-linking, indicated such a mechanism as a key-element in the hardening process of the cuticle. Such data strongly suggest that the Gordiuscuticle contains dityrosine compounds, whose formation is probably mediated by endogenous peroxidase activity.

Published
2000
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39. T-system in muscles of microdriles

Author

Eguileor, M., Valvassori, R., Lanzavecchia, G., and Lernia, L.

Abstract

Ribbon-like longitudinal fibers of the body wall of enchytraeids and lumbriculids are grouped in fuctional units. The organization of subsarcolemmal cisternae, membrane foldings and extracellular spaces between fibers is described. The data seem to indicate that the spaces between fibers within each functional unit are interpretable as T-tubules of a cross-striated fiber.

Published
1989
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40. Taxonomy and phylogenetic inference

Author

Avanzati, A. M., Bernini, F., Petrucci, R., Baccetti, B., Benazzi, M., Nascetti, G., Bullini, L., Bianco, P. G., Capanna, E., Civitelli, M. V., Maggini, L., Manzella, L., Cervella, P., Ramella, L., Robotti, C., Sella, G., Cobror, O., Odierna, G., Olmo, E., Agata, M. Dell', Pannunzio, G., Pantant, C., Teichner, A., Ferracin, A., Filippucci, M. G., Lettini, T., Vacca, E., Potente, F., Delfino, V. Pesce, Mantovani, B., Mazzini, M., Scali, V., Bullini, L., Mazzini, M., Gaino, E., Nardi, I., Ahdromico, F., de Lucchini, S., Batistoni, R., Capula, M., Lanza, B., Ortenzi, C., Valbonesi, A., Luporini, P., Pesce, G. L., Galassi, D. P., Ricco, R., Picariello, O., Scillitani, G., Randi, E., Ragni, B., Randi, E., Spina, F., Rossaro, B., Simonetta, A. M., Magnoni, M. L., Valvassori, R., de Eguileor, M., Lernia, L. di, Melone, G., Scari, G., Zerunian, S., Rossi, V., Franzini, G., and Gibertini, G.

Published
1986
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41. Cytology, Histology and Histochemistry

Author

Accordi, F., Albanese, M. P., Cannata, F., Calabho, C., Ponar, L. Acosta, Alfei, L., Bertoncello, G., Pace, C., Gelosi, E., Parvopassu, F., Baccetti, B., Gibbons, B., Gibbons, J., Bairati, A., Cheli, F., de Biasi, S., Vitellaro-Zuccarello, L., Bianchi, S., Cosmo, A. di, Brizzi, R., Delfino, G., Calloni, C., Cheli, F., Vitellaro-Zuccarello, L., Cetta, G., Bairati, A., Civinini, A., Castrucci, B., Facciola, C., Zerunian, S., Mastrolia, L., Conti-Devirgiliis, L., Dini, L., Russo-Caia, S., Coppellotti, O., Trito, P., Guidolin, L., Piccinni, E., Corso, G., Pala, M., Casu, S., Dallai, R., Yin, Wen-Ying, Xue, Luxen, de Eguileor, M., Lernia, L. di, Lanzavecchia, G., Paoletti, A., Valvassori, R., Faraldi, G., Borgiani, L., Farina, L., Tagliafierro, G., Ferri, D., Liquori, G. E., Fratello, B., Sabatini, M. A., Bianchi, F., Sonetti, D., Giambruni, A., Verni, F., Grandi, G., Barbieri, R., Colombo, G., Grigolo, A., Sacchi, L., Polver, P. de Piceis, Cima, L., Dealessi, F., Laudani, U., Guarnieri, P., Irato, P., Longo, G., Viscuso, R., de Luca, V., Sottile, L., Margotta, V., Gibertini, G., Bevilacqua, P., Orticelli, G., Martinucci, G. B., Zaniolo, G., Burighel, P., Mastrolia, L., Gallo, V. P., de Pascalis, M., Ventola, F., Zerunian, S., Mezzasalma, V., Stefano, L. di, Tognon, G., Ghiretti-Magaldi, A., Milanesi, C., Zatta, P., Nano, P., Bernocchi, G., Gerzeli, G., Nigro, M., Gremigni, V., Ottaviani, E., Vergine, C., Parrinello, N., Arizza, V., Canicatti, C., Pascolini, R., Rosa, I. di, Pica, A., Della Corte, F., Pigini, E., Miceli, C., Luporini, P., Raffioni, S., Ravera, F., Pestarino, M., Rivola, V., Miyake, A., Mazzini, M., Bigliardi, E., Saita, A., Comazzi, M., Vallesi, A., Raffioni, S., Loporini, P., Viseuso, R., Giuffrida, A., Vitellaro-Zuccarello, L., de Biasi, S., Zaccone, G., Fasulo, S., Lioata, A., Locascio, P., and Ainis, L.

Published
1986
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42. Ecology and ethology of protozoans and invertebrates

Author

Balsamo, M., Picciafuoco, L., Barbera, C., Basset, A., Rossi, L., Boato, A., Rasotto, M. B., Brandmayr, P., Pizzolotto, R., Paoletti, A. Di Chiara, Moli, F. Le, Mori, A., Lorenzi, K., Utzeri, C., Manca, M., de Bernardi, R., Palestrini, C., Piazza, R., Zunino, M., Paoletti, M. G., Paoletti, M. G., Iovane, E., Cortese, M., Canova, F., Caravello, G. U., Baroni, A., Pessani, D., Palomba, I., Petrahca, V., Robert, V., Carnevale, P., Coluzzi, H., Lucarelli, M., Caridi, F., Basset, A., Massini, G., Tella, E. Scotto di, Scapini, F., Scari, G., Lernia, L. di, Magnetti, P., Melone, G., Valvassori, R., Sciaky, R., Sella, G., Turillazzi, S., Utzeri, C., Valbonesi, A., Luporini, P., Vitagliano, G., Fano, E. A., Marchetti, E., and Colangelo, M. A.

Published
1986
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43. The allograft inflammatory factor-1 (AIF-1) homologous in hirudo medicinalis (medicinal leech) is involved in immune response during wound healing and graft rejection processes

Author

Schorn, T., Drago, F., Eguileor, M., Valvassori, R., Vizioli, J., Gianluca Tettamanti, and Grimaldi, A.

Subjects
leech, CD45, AIF-1, wounds, grafts, lcsh:Biology (General), lcsh:QH301-705.5
Abstract

Allograft inflammatory factor-1 (AIF-1) is a 17 kDa cytokine-inducible calcium-binding protein that in Vertebrates plays an important role in allografts immune response. Since its expression is mainly limited to the monocyte/macrophage lineage, it was recently suggested that it could play a key role during inflammatory responses, allograft rejection, as well as in the activation of macrophages. To clarify this point we have focused our research on the possible role of AIF-1 during the inflammatory response after injury in the leech Hirudo medicinalis (Annelida, Hirudinea). This invertebrate is an excellent animal model since the responses evoked during inflammation and tissue repair are clear and easily detectable and have a striking similarity with vertebrate responses. Moreover the analysis of an EST library from H. medicinalis CNS, revealed the presence of a gene, named Hmaif-1/alias Hmiba1, showing a high homology with vertebrate aif-1. Our data show that the related protein, named HmAIF-1, is constitutively expressed in unlesioned leeches and that dramatically increases 48 h after wounds and tissue transplants. Immunohistochemistry experiments, using a specific anti HmAIF-1 polyclonal antibody, shows that this factor is present in spread, CD68+ /CD45+ macrophage-like cells. A few days after experimental wounding of the body wall, the amount of these immunopositive cells increases at the lesion site. In conclusion here we propose that in leech HmAIF-1 factor is involved in inflammation events like its vertebrate counterparts.

44. A hedgehog-like signal is involved in slow muscle differentation in Sepia officinalis (Mollusca)

Author

Grimaldi, A., Gianluca Tettamanti, Guidali, M. L., Brivio, M. F., Valvassori, R., and Eguilor, M.

Subjects
animal structures, mollusc, lcsh:Biology (General), embryonic structures, Development, Helical and cross-striated fibres, Hh-like protein, Mollusc, Muscle differentiation, muscle differentiation, musculoskeletal system, helical and cross-striated fibres, tissues, development, lcsh:QH301-705.5
Abstract

In the tentacle of Sepia officinalis, smooth-like, helical and cross-striated fibres deriving from different populations of myoblasts are present. Myoblasts appear at different times during the development and express two muscle-specific transcription factors: Myf5-like and MyoD-like factors. Myoblasts expressing Myf5 give rise to slow fibres, whereas fast fibres derive from MyoD+ myoblasts. We found that a Hedgehog (Hh)-like signal was present in the central nerve cord of the tentacle from the early stages of development and in a specific population of myoblasts which are the precursors of slow muscle fibres. The model showed interesting similarities with vertebrates, in which Sonic hedgehog is a protein secreted by axial structures (the notochord and neurotube) and is involved in slow muscle differentiation and in survival of muscle precursors.

46. Cytology, Histology and Histochemistry

Author

Accordi, F., primary, Albanese, M. P., additional, Cannata, F., additional, Calabho', C., additional, Ponar, L. Acosta, additional, Alfei, L., additional, Bertoncello, G., additional, Pace, C., additional, Gelosi, E., additional, Parvopassu, F., additional, Baccetti, B., additional, Gibbons, B., additional, Gibbons, J., additional, Bairati, A., additional, Cheli, F., additional, de Biasi, S., additional, Vitellaro‐Zuccarello, L., additional, Bianchi, S., additional, di Cosmo, A., additional, Brizzi, R., additional, Delfino, G., additional, Calloni, C., additional, Cetta, G., additional, Civinini, A., additional, Castrucci, B., additional, Facciola, C., additional, Zerunian, S., additional, Mastrolia, L., additional, Conti‐Devirgiliis, L., additional, Dini, L., additional, Russo‐Caia, S., additional, Coppellotti, O., additional, Trito, P., additional, Guidolin, L., additional, Piccinni, E., additional, Corso, G., additional, Pala, M., additional, Casu, S., additional, Dallai, R., additional, Yin, Wen‐Ying, additional, Xue', Luxen, additional, de Eguileor, M., additional, di Lernia, L., additional, Lanzavecchia, G., additional, Paoletti, A., additional, Valvassori, R., additional, Faraldi, G., additional, Borgiani, L., additional, Farina, L., additional, Tagliafierro, G., additional, Ferri, D., additional, Liquori, G. E., additional, Fratello, B., additional, Sabatini, M. A., additional, Bianchi, F., additional, Sonetti, D., additional, Giambruni, A., additional, Verni, F., additional, Grandi, G., additional, Barbieri, R., additional, Colombo, G., additional, Grigolo, A., additional, Sacchi, L., additional, de Piceis Polver, P., additional, Cima, L., additional, Dealessi, F., additional, Laudani, U., additional, Guarnieri, P., additional, Irato, P., additional, Longo, G., additional, Viscuso, R., additional, de Luca, V., additional, Sottile, L., additional, Margotta, V., additional, Gibertini, G., additional, Bevilacqua, P., additional, Orticelli, G., additional, Martinucci, G. B., additional, Zaniolo, G., additional, Burighel, P., additional, Gallo, V. P., additional, de Pascalis, M., additional, Ventola, F., additional, Mezzasalma, V., additional, di Stefano, L., additional, Tognon, G., additional, Ghiretti‐Magaldi, A., additional, Milanesi, C., additional, Zatta, P., additional, Nano, P., additional, Bernocchi, G., additional, Gerzeli, G., additional, Nigro, M., additional, Gremigni, V., additional, Ottaviani, E., additional, Vergine, C., additional, Parrinello, N., additional, Arizza, V., additional, Canicatti', C., additional, Pascolini, R., additional, di Rosa, I., additional, Pica, A., additional, Corte, F. Della, additional, Pigini, E., additional, Miceli, C., additional, Luporini, P., additional, Raffioni, S., additional, Ravera, F., additional, Pestarino, M., additional, Rivola, V., additional, Miyake, A., additional, Mazzini, M., additional, Bigliardi, E., additional, Saita, A., additional, Comazzi, M., additional, Vallesi, A., additional, Loporini, P., additional, Viseuso, R., additional, Giuffrida, A., additional, Zaccone, G., additional, Fasulo, S., additional, Lioata, A., additional, Locascio, P., additional, and Ainis, L., additional

Published
1986
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47. Taxonomy and phylogenetic inference

Author

Avanzati, A. M., primary, Bernini, F., additional, Petrucci, R., additional, Baccetti, B., additional, Benazzi, M., additional, Nascetti, G., additional, Bullini, L., additional, Bianco, P. G., additional, Capanna, E., additional, Civitelli, M. V., additional, Maggini, L., additional, Manzella, L., additional, Cervella, P., additional, Ramella, L., additional, Robotti, C., additional, Sella, G., additional, Cobror, O., additional, Odierna, G., additional, Olmo, E., additional, Agata, M. Dell', additional, Pannunzio, G., additional, Pantant, C., additional, Teichner, A., additional, Ferracin, A., additional, Filippucci, M. G., additional, Lettini, T., additional, Vacca, E., additional, Potente, F., additional, Delfino, V. Pesce, additional, Mantovani, B., additional, Mazzini, M., additional, Scali, V., additional, Gaino, E., additional, Nardi, I., additional, Ahdromico, F., additional, de Lucchini, S., additional, Batistoni, R., additional, Capula, M., additional, Lanza, B., additional, Ortenzi, C., additional, Valbonesi, A., additional, Luporini, P., additional, Pesce, G. L., additional, Galassi, D. P., additional, Ricco, R., additional, Picariello, O., additional, Scillitani, G., additional, Randi, E., additional, Ragni, B., additional, Spina, F., additional, Rossaro, B., additional, Simonetta, A. M., additional, Magnoni, M. L., additional, Valvassori, R., additional, de Eguileor, M., additional, di Lernia, L., additional, Melone, G., additional, Scari', G., additional, Zerunian, S., additional, Rossi, V., additional, Franzini, G., additional, and Gibertini, G., additional

Published
1986
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49. Ecology and ethology of protozoans and invertebrates

Author

Balsamo, M., primary, Picciafuoco, L., additional, Barbera, C., additional, Basset, A., additional, Rossi, L., additional, Boato, A., additional, Rasotto, M. B., additional, Brandmayr, P., additional, Pizzolotto, R., additional, Di Chiara Paoletti, A., additional, Le Moli, F., additional, Mori, A., additional, Lorenzi, K., additional, Utzeri, C., additional, Manca, M., additional, de Bernardi, R., additional, Palestrini, C., additional, Piazza, R., additional, Zunino, M., additional, Paoletti, M. G., additional, Iovane, E., additional, Cortese, M., additional, Canova, F., additional, Caravello, G. U., additional, Baroni, A., additional, Pessani, D., additional, Palomba, I., additional, Petrahca, V., additional, Robert, V., additional, Carnevale, P., additional, Coluzzi, H., additional, Lucarelli, M., additional, Caridi, F., additional, Massini, G., additional, di Tella, E. Scotto, additional, Şcapini, F., additional, Scari, G., additional, di Lernia, L., additional, Magnetti, P., additional, Melone, G., additional, Valvassori, R., additional, Sciaky, R., additional, Sella, G., additional, Turillazzi, S., additional, Valbonesi, A., additional, Luporini, P., additional, Vitagliano, G., additional, Fano, E. A., additional, Marchetti, E., additional, and Colangelo, M. A., additional

Published
1986
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