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pro vyhledávání: '"G. Sanges"'
Autor:
S. Migliaresi, G. Di Iorio, A. Ammendola, L. Ambrosone, G. Sanges, G. Ugolini, S. Sampaolo, F. Bravaccio, G. Tirri
Publikováno v:
Reumatismo, Vol 53, Iss 1 (2001)
In HCV-related mixed cryoglobulinemia (MC) a peripheral neuropathy (PN) may occur. To evaluate the prevalence and the characteristics of PN, 133 consecutive patients with HCV-MC (117 type II, 16 type III) were studied. Neurologic evaluation was perfo
Externí odkaz:
https://doaj.org/article/5c76d2689a604fa99e02364dddbe436d
Akademický článek
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Publikováno v:
International Journal of Grid and Utility Computing. 8:330
Within the Cloud application life cycle, Cloud monitoring takes an important role since the fulfilment of the requirements has to be continuously controlled in order to avoid saturation or under-utilisation of Cloud resources and to check the complia
Autor:
G. Sanges, Alfredo Ciccodicola, Simone Sampaolo, G. Di Iorio, A. Ammendola, R. Giugliano, Vittorio Cappa, Michele D'Urso
Publikováno v:
Neurological Sciences. 21:109-112
We report a 26-year-old Italian man with X-linked Charcot-Marie-Tooth (CMT) disease type 1 (CMT-X1) and a negative family history for neuromuscular diseases. Clinical and electrophysiological examinations of the patient's mother and siblings were nor
Autor:
G. Sanges, Lawrence I. Golbe, Salvatore la Sala, Roger C. Duvoisin, Vincenzo Bonavita, Giuseppe Di Iorio, Alice M. Lazzarini
Publikováno v:
Annals of Neurology. 40:767-775
We performed a clinical genetic analysis of a kindred originating in the town of Contursi in Salerno province, Italy, in which 60 individuals in 5 generations are known to have had Parkinson's disease (PD). Two previously reported autopsy cases showe
Autor:
Vincenzo Di Benedetto, Francesco Arena, G. Sanges, C. Arena, Maria Grazia Scuderi, Salvatore Arena
Urethral duplication is a rare congenital anomaly, affecting mainly boys. Clinical presentation varies because of the different anatomical patterns of this abnormality. We report our experience in ten males affected by urethral duplication. We retros
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df2c38ce84aef3ac74d49d48e13cfaaf
http://hdl.handle.net/20.500.11769/6534
http://hdl.handle.net/20.500.11769/6534
Autor:
G, Di Iorio, G, Sanges, V, Sannino, M, De Cristofaro, M R, D'Ambrosio, A, Budillon, S, Sampaolo
Publikováno v:
Clinical neuropathology. 24(1)
Klippel-Trenaunay syndrome (KTS) is a rare congenital malformation of unknown etiology characterized by cutaneous hemangiomas, venous varicosities and bony and soft tissues hypertrophy usually affecting one limb. Several complex anomalies involving v
Sir, Rhabdomyomatous mesenchymal hamartoma (RMH) is a rare congenital lesion occurring in the skin, particularly of the face and neck [4]. The term hamartoma has been histologically proven as a lesion composed of a disordered mixture of mature adipos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41e1077fa23dd4cd7732285960a0410f
http://hdl.handle.net/20.500.11769/7481
http://hdl.handle.net/20.500.11769/7481
Autor:
G. Sanges, Roger C. Duvoisin, Lana T. Pho, Alejandro A. Schäffer, Giuseppe Di Iorio, Lawrence I. Golbe, William G. Johnson, Edward S. Stenroos, Robert L. Nussbaum, Alice M. Lazzarini, J. J. Higgins, Susan E. Ide, Mihael H. Polymeropoulos
Publikováno v:
Science. 274:1197-1199
Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting approximately 1 percent of the population over age 50. Recent studies have confirmed significant familial aggregation of PD and a large
Publikováno v:
La Pediatria medica e chirurgica : Medical and surgical pediatrics. 24(4)
The One-Stop Surgery (OSS) is a new method of Day Surgery, which combines preoperative evaluation and subsequent operation into one visit. This report describes the initial experience of the authors. Referring physicians were informed by fax about me