Search Results - "Sanges, G"

Cognitive impairment in systemic lupus erythematosus : a follow-up study by CARLOMAGNO, S, MIGLIARESI, S, AMBROSONE, L, SANNINO, M, SANGES, G, DI IORIO, G

“…We evaluated outcome and the clinical value of cognitive impairment in systemic lupus erythematosus (SLE). Fifty-one consecutive SLE subjects with or without…”
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Peripheral nervous system involvement in HCV-related mixed cryoglobulinemia by Migliaresi, S., Di Iorio, G., Ammendola, A., Ambrosone, L., Sanges, G., Ugolini, G., Sampaolo, S., Bravaccio, F., Tirri, G.

“…In HCV-related mixed cryoglobulinemia (MC) a peripheral neuropathy (PN) may occur. To evaluate the prevalence and the characteristics of PN, 133 consecutive…”
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One-stop surgery in pediatric surgery. Aspects of anesthesia. Preliminary report by Astuto, M, Disma, N, Sentina, P, Sanges, G

“…One-Stop Surgery (OSS) is a new day surgery combining preoperative evaluation and subsequent operation in one medical examination. This paper reports the…”
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Peripheral nervous system involvement in Klippel-Trenaunay syndrome by Di Iorio, G, Sanges, G, Sannino, V, De Cristofaro, M, D'Ambrosio, M R, Budillon, A, Sampaolo, S

“…Klippel-Trenaunay syndrome (KTS) is a rare congenital malformation of unknown etiology characterized by cutaneous hemangiomas, venous varicosities and bony and…”
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Craniofacial pain followed by scalp necrosis and stroke. An unusual presentation of the primary antiphospholipid syndrome by Sanges, G, Sampaolo, S, Di Iorio, G

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Lack of sodium channel mutation in an italian family with paramyotonia congenita by SAMPAOLO, S, PUCA, A. A, NIGRO, V, CAPPA, V, SANNINO, V, SANGES, G, BONAVITA, V, DI IORIO, G

“…To conduct the genotype-phenotype correlation in a family in which several individuals share clinical and electrophysiologic features of paramyotonia congenita…”
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A comment on: ‘Molecular diagnosis of transthyretin Met30 mutation in an Italian family with familial amyloidotic polyneuropathy’ by Paola Strocchi et al., FEBS Letters 359 (1995) 203–205 by lorio, G.Di, Sanges, G., Sampaolo, S., Bonavita, V.

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A new de novo mutation of the connexin-32 gene in a patient with X-linked Charcot-Marie-Tooth type 1 disease by Di Iorio, G, Cappa, V, Ciccodicola, A, Sampaolo, S, Ammendola, A, Sanges, G, Giugliano, R, D'Urso, M

“…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…”
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Mapping of a Gene for Parkinson's Disease to Chromosome 4q21-q23 by Polymeropoulos, Mihael H., Higgins, Joseph J., Golbe, Lawrence I., Johnson, William G., Ide, Susan E., Di Iorio, Giuseppe, Sanges, Giuseppe, Stenroos, Edward S., Pho, Lana T., Schaffer, Alejandro A., Lazzarini, Alice M., Nussbaum, Robert L., Duvoisin, Roger C.

“…Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting approximately 1 percent of the population…”
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Rhabdomyomatous mesenchymal hamartoma of oral cavity: an unusual location for such a rare lesion by Magro, Gaetano, Di Benedetto, Aurelio, Sanges, Giuseppe, Scalisi, Filippo, Alaggio, Rita

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Clinical genetic analysis of Parkinson's disease in the Contursi kindred by Golbe, L I, Di Iorio, G, Sanges, G, Lazzarini, A M, La Sala, S, Bonavita, V, Duvoisin, R C

“…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…”
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Familial amyloidotic polyneuropathy: description of an Italian kindred by Di Iorio, G, Sanges, G, Cerracchio, A, Sampaolo, S, Sannino, V, Bonavita, V

“…Familial amyloidotic polyneuropathy (FAP) is a heterogeneous group of genetic disorders characterized by progressive systemic deposition of extracellular…”
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Prophylaxis and therapy by mezlocillin in pediatric surgery by Di Benedetto, A, Abela, M, Sanges, G, Randazzo, G, Bagnara, V, Di Benedetto, A G, Cacciaguerra, S, Vasta, G, Speciale, A, Caccamo, F, Nicoletti, G

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PERIPHERAL NEUROPATHY IN HCV-RELATED MIXED CRYOGLOBULINEMIA by Sanges, G., Ammendola, A., Ambrosone, L., Sampaolo, S., Cesarano, M., Migliaresi, S., Di Iorio, G.

“…Objective: To evaluate the prevalence and features of peripheral neuropathy in HCV‐related mixed cryoglobulinemia (MC). Methods: 133 consecutive patients (23…”
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One stop surgery in pediatric surgery. Preliminary report by Sanges, G, Astuto, M, Sentina, P, Morinello, E, Di Benedetto, A

“…The One-Stop Surgery (OSS) is a new method of Day Surgery, which combines preoperative evaluation and subsequent operation into one visit. This report…”
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Prevalence of autonomic neuropathy in HCV-related mixed cryoglobulinemia by Ambrosone, L., Cantillo, A., Sanges, G., Ugolini, G., Mennella, M., Ammendola, A., Di Iorio, G., Migliaresi, S.

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CHARGE association: report of a clinical case with anal atresia and rectovaginal fistula by Rodonò, A, Romeo, M G, Sanges, G, Distefano, G

“…CHARGE association is a non-random constellation of Coloboma, Heart Disease, Atresia of the choana, Retarded mental development and growth, Genital hypoplasia,…”
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Cerebral hemodynamics and major surgery by Romeo, D M M, Betta, P, Sanges, G, Di Benedetto, V, Astuto, M, Romeo, M G

“…Near infrared spectroscopy (NIRS) is a non invasive optical technique to assess the monitoring of oxygenation and cerebral hemodynamics. Aim of our study was…”
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The VACTERL association: a report of a clinical case with hepatic cystic lymphangiectasis by Distefano, G, Rodonò, A, Smilari, P, Saporito, A, Di Bella, D, Magro, G, Sanges, G, Romeo, M G

“…VACTERL association includes three or more of the following six anomalies: V (vertebral anomalies), A (anal atresia), C (cardiac abnormalities), TE…”
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Esophageal atresia and malformative association. Clinical contribution by Smilari, P, La Spina, M, Salvo, V, Romeo, M G, Sanges, G

“…Esophageal atresia (EA) is a congenital malformation with an incidence of 1/3,000-3,500 live birth, due to anomalies of the foregut. Although an interstitial…”
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