Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Trebini, F."'
Autor:
Bouillon, Céline, Cane, Stéphanie, Trebini, F., Derudas, A., Fernandez Ramiro, M.M., Sirca, C., García, B.F., Casula, F., Long-Fournel, M., Pellizzaro, G., Arca, B., Tedim, F.
Publikováno v:
AF3 Forest fires models workshops
AF3 Forest fires models workshops, Jun 2017, Rome, Italy. pp.2
AF3 Forest fires models workshops, Jun 2017, Rome, Italy. pp.2
[Departement_IRSTEA]Territoires [TR1_IRSTEA]SEDYVIN [ADD1_IRSTEA]Dynamiques spatiales d'anthropisation; International audience; This presentation shows different situations of the use of interfaces mapping which contribute to improve the Rural Urban
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4a44607773f816d3c38cf1b73d7a3c72
https://hal.inrae.fr/hal-02607379
https://hal.inrae.fr/hal-02607379
Autor:
Bouillon, Christophe, Fernandez Ramiro, M. M., Sirca, C., Fierro Garcia, B., Casula, F., Vila, B., Long Fournel, M., Pellizzaro, G., Arca, B., Tedim, Fantina, Trebini, F., Derudas, A., Cane, S.
The aim of this paper is to present the methodologies, a software and results developed in the European FUME program to map the rural-urban interfaces (RUI). Three methodologies were set up for RUI mapping: two on the local scale (the community scale
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1406::3bc9c63a046420c1fdf0df8c2fb48d60
https://repositorio-aberto.up.pt/handle/10216/78075
https://repositorio-aberto.up.pt/handle/10216/78075
Publikováno v:
The Italian Journal of Neurological Sciences. 12:479-484
Vogt-Koyanagi-Harada syndrome is a rare disease, which probably has a cell-mediated autoimmune pathogenesis, marked by ocular (anterior and/or posterior uveitis), dermatological (poliosis, canities, vitiligo) and neurological (meningo-encephalitis) d
Autor:
Giordani, G., Viaroli, P., Murray, N., Zaldivar, J. M., Guerzoni, S., Bergamasco, A., Solidoro, C., Rabitti, S., Castaldelli, G., Abbiati, M., Ponti, M., Manini, E., Danovaro, R., Basset, A., Azzaro, M., Mazzola, A., Maugeri, T. L., Porrello, S., Lenzi, M., Innamorati, M., Melillo, C., Fabiano, M., Povero, Paolo, Trebini, F., Sechi, N.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3710::c88813809ac85db405c687f4804d7bb1
http://hdl.handle.net/11567/391931
http://hdl.handle.net/11567/391931
A late onset variant of ataxia-telangiectasia with a compound heterozygous genotype, A8030G/7481insA
Autor:
Saviozzi, S, Saluto, A, Taylor, A, Last, J, Trebini, F, Paradiso, M, Grosso, E, Funaro, A, Ponzio, G, Migone, N, Brusco, A
A taxia-telangiectasia (A-T) is a multisystem autosomal recessive disorder, with an estimated frequency of 1/40 000-1/100 000 live births.1 The ataxia-telangiectasia mutated gene ( ATM ), located on chromosome 11q22-23,2 encodes a nuclear 370 kDa pho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1a047b68b9c23474f09a39a2f293440
https://europepmc.org/articles/PMC1734960/
https://europepmc.org/articles/PMC1734960/
Publikováno v:
Italian journal of neurological sciences. 13(4)
The Miller Fisher syndrome (MFS) is generally considered to be a disease of the peripheral nervous system. In some cases contemporary involvement of the central nervous system has been described (CNS). We report a case in which it was possible to pro
Akademický článek
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Akademický článek
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Autor:
Saviozzi, S., Saluto, A., Taylor, A.M.R., Last, J.I.L., Trebini, F., Paradiso, M.C., Grosso, E., Funaro, A., Ponzio, G., Migone, N., Brusco, A.
Publikováno v:
Journal of Medical Genetics; Jan2002, Vol. 39 Issue 1, p57, 5p, 3 Diagrams, 1 Chart, 1 Graph
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry; Jan1980, Vol. 43 Issue 1, p91-94, 4p