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Dive into the research topics where Giuseppe Aliberti is active.

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Featured researches published by Giuseppe Aliberti.


Journal of Internal Medicine | 1990

Platelet count, mean platelet volume and their relation to prognosis in cerebral infarction

Emilio D'Erasmo; Giuseppe Aliberti; Francesco S. Celi; Elisabetta Romagnoli; E. Vecci; G. F. Mazzuoli

Abstract. The study was performed on patients with ischaemic cerebral infarction in order to obtain information on serial changes of some platelet parameters and to test their prognostic significance.


Annals of Medicine | 2010

Inflammation and immune response in acute aortic dissection.

Flavia Del Porto; Maria Proietta; Luigi Tritapepe; Fabio Miraldi; Angela Koverech; Patrizia Cardelli; Fabio Tabacco; Vincenzo De Santis; Andrea Vecchione; Anna Paola Mitterhofer; Italo Nofroni; Rachele Amodeo; Trappolini M; Giuseppe Aliberti

Abstract Objective. The aim of our study was to evaluate the lymphocyte subpopulations and the cytokines in the peripheral blood of patients with type-A Stanford acute aortic dissection (AAD group) and to determine whether inflammatory cells are present at the site of aortic dissection. Methods. Thirty-five consecutive patients with type-A Stanford dissection were evaluated for haemochrome and lymphocyte subpopulations (CD3+, CD4+, CD8+, CD19+, CD4+CD25+, CD16+CD56+, CD4+CD28−, CD8+CD28−) by flow cytometry. C-reactive protein (CRP), tumour necrosis factor (TNF)-α, interleukin (IL)-2, IL-4, IL-6, IL-8, IL-10, interferon-gamma (IFN-γ), and monocyte chemoattractant protein (MCP)-1 were measured by ELISA. In addition, immunohistochemical staining with cell type-specific antibodies was performed to study the inflammatory cells detected inside the aortic wall. Results. In the AAD group, a significant increase in natural killer (NK) (P = 0.032), B cells (P = 0.022), and CD8+CD28− (P = 0.045) subpopulations was observed, whereas there was a significant decrease in total T lymphocytes (P = 0.004) and T helper fractions (P = 0.005). Moreover, a significant increase in CRP (P < 0.0001), IL-6 (P < 0.0001), IL-8 (P < 0.0001), IL-10 (P < 0.0001), TNF-α (P < 0.0001), and MCP-1 (P < 0.001) was observed; macrophages represented the main population detected inside the media. Conclusions. Our results strongly support the hypothesis of a pivotal role of innate immunity in type-A Stanford AAD.


Journal of Internal Medicine | 2003

Bone metabolism in ochronotic patients

Giuseppe Aliberti; Isabella Pulignano; Angelo Schiappoli; S. Minisola; Elisabetta Romagnoli; Maria Proietta

Abstract. Aliberti G, Pulignano I, Schiappoli A, Minisola S, Romagnoli E, Proietta M (Università di Roma ‘La Sapienza’, Rome, Italy). Bone metabolism in ochronotic patients (Case report). J Intern Med 2003; 254: 296–300.


Hip International | 2010

Transient osteoporosis of the hip

Massimiliano Rocchietti March; Venceslao Tovaglia; Antonella Meo; Daniela Pisani; Priscilla Tovaglia; Giuseppe Aliberti

Transient osteoporosis of the hip (TOH) is not an uncommon condition, usually with a benign course. The syndrome classically affects women during the last trimester of pregnancy, but also middle aged men. Recently, TOH has been described in non pregnant women. The pathophysiology of the disease is uncertain, though several hypotheses have been suggested. Joint pain is the main symptom. TOH is a self-limited condition, which resolves spontaneously with complete recovery within several months in most cases.


Clinical Chemistry and Laboratory Medicine | 1998

Assessment of Serum Total and Bone Alkaline Phosphatase Measurement in Clinical Practice

Elisabetta Romagnoli; Giovanni Minisola; Vincenzo Carnevale; Alfredo Scillitani; Vincenzo Frusciante; Giuseppe Aliberti; Salvatore Minisola

Abstract The aim of the study was to measure serum levels of the bone-specific isoenzyme of alkaline phosphatase in normal subjects and patients with metabolic bone disease by using an immunoadsorption assay. We studied 140 healthy adults, 122 patients affected by metabolic bone disease and 15 patients with cholestatic liver disease. Mean values of the bone-specific isoenzyme of alkaline phosphatase in healthy men were significantly higher than those found in premenopausal women (17.8 ± 4.2 U/l vs 15.6 ± 4.6 U/l, p<0.02); postmenopausal women had significantly higher levels of bone-specific isoenzyme of alkaline phosphatase (22.6 ± 6.4 U/l) than premenopausal women (p<0.0001). After the menopause total alkaline phosphatase increased by 46 %, while the increase in bone-specific isoenzyme of alkaline phosphatase was 39 %. No significant correlations were found between bone-specific isoenzyme of alkaline phosphatase and either age or years since menopause, in postmenopausal subjects. In patients with bone-specific isoenzyme of alkaline phosphatase above the upper limit of normal, the assay had a sensitivity of 100 % only in patients with Pagets disease of bone. In patients with cholestatic liver disease we found no correlation between bone-specific isoenzyme of alkaline phosphatase and either total alkaline phosphatase and γ-glutamyl transpeptidase, while a positive correlation was found between total alkaline phosphatase and γ-glutamyl transpeptidase. Our results confirm the role of bone-specific isoenzyme of alkaline phosphatase assay in clinical research; however, its usefulness in clinical practice is unclear once liver involvement has been excluded.


Ultrastructural Pathology | 1994

Ochronotic arthropathy: structural and ultrastructural features.

Marco Melis; Paolo Onori; Giuseppe Aliberti; Emilio Vecci; Eugenio Gaudio

Fragments of articular cartilage and synovial membrane in a case of ochronosis were studied by light microscopy (LM), polarized light, and transmission electron microscopy (TEM). Granular and/or shard-shaped pigments were observed in the synovia, cartilage, and subchondral tissue, and dispersed pigment was also seen in the synovial fluid. Zones of the articular cartilage surface showed small erosions near shards, and sometimes, when the degenerative process was in an advanced stage, a substitutive fibrosis of the cartilage edge was demonstrated. LM and TEM observations of the samples studied revealed an alteration of collagen fibrils that appeared wavy and sometimes fragmented with loss of periodicity. They were always mixed with the dispersed pigment. A peculiar finding that characterized this ochronotic case was the complete absence of inflammatory infiltrates or signs of monocyte-macrophage activation. These structural and ultrastructural observations suggest that the pigment deposition in the articular surfaces was due to the synovial fluid circulation and partially to subchondral blood flow, which transports and stores the ochronotic pigments in the synovia and cartilage. These etiopathologic elements associated with the mechanical pathogenesis naturally present in the joints can contribute to the explanation of the pathogenesis and origin of ochronotic arthropathy.


Osteoporosis International | 2002

Uneven Deficits in Vertebral Bone Density in Postmenopausal Patients with Primary Hyperparathyroidism as Evaluated by Posterior–Anterior and Lateral Dual-Energy Absorptiometry

Salvatore Minisola; R. Rosso; Elisabetta Romagnoli; Jessica Pepe; S. De Geronimo; S. Dionisi; Federica Paglia; N. Raejntroph; Giuseppe Aliberti; G. F. Mazzuoli

Abstract: This investigation was undertaken to determine whether the preservation of bone mass in patients with mild primary hyperparathyroidism (PHPT) could be detected when measuring spine density in the lateral projection. We compared the bone mineral density (BMD) of L2–L4 utilizing the posterior–anterior (PA) and lateral projections in postmenopausal patients with PHPT and in a group of 27 postmenopausal normal women. Thirty-three consecutive postmenopausal patients with PHPT were studied; 25 were asymptomatic whereas the remaining 8 suffered complications related to the disease. Based upon the criteria established by the Consensus Conference on the Management of Asymptomatic PHPT, only 10 of the 25 asymptomatic patients could be considered affected by mild disease; the remaining patients were classified as having moderate disease. Patients with mild disease had mean lateral total BMD values (0.682 ± 0.113 g/cm2) significantly higher than normal women (0.588 ± 0.076, p<0.02) and patients with moderate disease (0.599 ± 0.077, p<0.05). There were significant differences among the three groups in both PA L2–L4 and L1–L4 levels: patients with mild disease had significantly higher mean BMD values than patients with moderate disease and normal women, when either three or four vertebrae were considered. Interestingly, at this latter site, patients with moderate disease had significantly (p<0.05) lower values than normal women. Our results indicate that patients with mild PHPT have a preservation of vertebral mass when compared with the other hyperparathyroid patients and normal women, when taking into account both the mainly trabecular portion and the whole vertebra. The finding that when the PA projection was assessed, BMD values of patients with moderate disease were significantly lower than those of normal women, might be attributed to the detrimental effect of raised parathyroid hormone levels on the cortical component of the vertebral body.


Lupus | 2011

Hypercalcaemia in systemic lupus erythematosus

F Del Porto; Maria Proietta; A. Koverech; Trappolini M; Giuseppe Aliberti

Hypercalcaemia is found in more than 90% of the cases of primitive hyperparathyroidism and malignancies. Rarely, D hypervitaminosis, sarcoidosis, other granulomatous diseases, some drugs, and endocrine diseases may be responsible. Nine patients with systemic lupus erythematosus (SLE) and hypercalcaemia, without evidence of primary hyperparathyroidism, have been previously described. Here we report the 10th patient with SLE and hypercalcaemia, along with a brief review of the literature.


Aging Clinical and Experimental Research | 2003

Impact of fractures on health care in a major university hospital in Rome

Elisabetta Romagnoli; Vincenzo Carnevale; Pierluigi Calandra; E. D’Erasmo; Simona De Geronimo; Jessica Pepe; Giuseppe Manfredi; Marianna Maranghi; Giuseppe Aliberti; Salvatore Minisola

Background and aims: The aim of the study was to investigate the impact of fractures (i.e., hip, Colles, humeral and vertebral fractures), compared with that of other common diseases requiring hospitalization, on health care in the main hospital in Rome (Italy). Methods: Hospital discharge forms, filled in according to the 9th International Classification of Diseases, were examined from 1996 to 1999. Data on fractures were compared with those related to other diseases which occupy a considerable proportion of hospital operating time in Italy: coronary heart disease (CHD), cerebrovascular disorders (CVD), diabetes mellitus (DM), chronic obstructive pulmonary disease (COPD) and breast cancer (BC). Results: In all groups of patients, the mean age of females was significantly higher (p<0.0001) than that of males. Male patients with hip fractures had hospital stays significantly longer than females (p<0.0001), whereas women with Colles fractures had significantly (p<0.02) longer stays. When patients were divided according to age (i.e., over or under 60 years), mean hospital stays did not differ between younger and older patients in all groups except Colles fractures (p<0.001). Hip fractures in older patients showed striking in-hospital mortality. Throughout the study period, hip fractures accounted for the highest overall and per-patient costs. The number of female patients with fractures (and, obviously, breast cancer) was higher, while the opposite applied to the other disorders. Male patients with fractures, CHD and CVD were significantly younger than females (p<0.0001). When the percentage of deaths was added to that of patients discharged to other institutions, fractures showed the poorest outcome of any hospitalization event. Per-patient costs were remarkably higher for CHD, followed by fractures. Conclusions: Fractures represent a growing but often underestimated burden for hospital care in Italy; further studies are needed on this issue.


Lupus | 2009

Renal limited Wegener's granulomatosis.

F Del Porto; Maria Proietta; A Stoppacciaro; Trappolini M; P Menè; Giuseppe Aliberti

Differential diagnosis in patients presenting with fever of unknown origin (FUO) is often difficult because infectious diseases, neoplasms, infective endocarditis or systemic autoimmune diseases may all be responsible for the condition. Furthermore, vasculitis may generate typical, atypical or limited syndromes depending on the extent of vascular involvement. Here, we report the case of a 73-year-old man with FUO and renal failure due to a rare variant of Wegener’s granulomatosis, limited to the kidneys.

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Maria Proietta

Sapienza University of Rome

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Isabella Pulignano

Sapienza University of Rome

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Flavia Del Porto

Sapienza University of Rome

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Luigi Tritapepe

Sapienza University of Rome

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Trappolini M

Sapienza University of Rome

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Angelo Schiappoli

Sapienza University of Rome

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Emilio D'Erasmo

Sapienza University of Rome

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G. F. Mazzuoli

Sapienza University of Rome

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