Search Results - "Nunziata, V"

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  1. 1

    Pain Management in Nursing Home Residents: Results from the Incur Study by Nunziata, V., Proietti, Marco, Saporiti, E., Calcaterra, L., Rolland, Y., Vellas, B., Cesari, M.

    Published in The Journal of nutrition, health & aging (01-09-2020)
    “…Objectives Pain is very common among older persons living in nursing home, affecting 45% to 80% of residents, interfering with daily activities and quality of…”
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  2. 2

    Pain Management in Nursing Home Residents: Results from the INCUR Study by Nunziata, V, Proietti, M, Saporiti, E, Calcaterra, L, Rolland, Y, Vellas, B, Cesari, M

    Published in The Journal of nutrition, health & aging (13-07-2020)
    “…Pain is very common among older persons living in nursing home, affecting 45% to 80% of residents, interfering with daily activities and quality of life. Aims…”
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  3. 3

    Association between vitamin D receptor gene polymorphisms and tubular citrate handling in calcium nephrolithiasis by Mossetti, G., Vuotto, P., Rendina, D., Numis, F. G., Viceconti, R., Giordano, F., Cioffi, M., Scopacasa, F., Nunziata, V.

    Published in Journal of internal medicine (01-02-2003)
    “… Mossetti G, Vuotto P, Rendina D, Numis FG, Viceconti R, Giordano F, Cioffi M, Scopacasa F, Nunziata V (Federico II University Medical School, Naples, Italy)…”
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  4. 4
  5. 5

    Risedronate and pamidronate treatment in the clinical management of patients with severe Paget's disease of bone and acquired resistance to bisphosphonates by Rendina, D, Mossetti, G, Viceconti, R, Sorrentino, M, Nunziata, V

    Published in Calcified tissue international (01-09-2004)
    “…The aim of this study was to evaluate the efficacy and safety of risedronate and pamidronate in 30 patients (mean age = 57.86 +/- 8.90 years) with severe…”
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  6. 6

    Abnormalities of calcium metabolism in essential hypertension by Strazzullo, P, Nunziata, V, Cirillo, M, Giannattasio, R, Ferrara, L A, Mattioli, P L, Mancini, M

    Published in Clinical science (1979) (01-08-1983)
    “…Calcium metabolism has been investigated in patients with essential hypertension and normal renal function to evaluate the renal calcium handling and the…”
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  7. 7

    Frequent RET protooncogene mutations in multiple endocrine neoplasia type 2A by Quadro, L, Panariello, L, Salvatore, D, Carlomagno, F, Del Prete, M, Nunziata, V, Colantuoni, V, Di Giovanni, G, Brandi, M L, Mannelli, M

    “…The occurrence of mutations in the RET protooncogene has been investigated in 12 multiple endocrine neoplasia type 2A families and 18 cases of sporadic thyroid…”
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  8. 8

    The association between low skeletal muscle mass and delirium: results from the nationwide multi-centre Italian Delirium Day 2017 by Zucchelli, Alberto, Manzoni, F., Morandi, A., Di Santo, S., Rossi, E., Valsecchi, M. G., Inzitari, M., Cherubini, A., Bo, M., Mossello, E., Marengoni, A., Bellelli, G.

    Published in Aging clinical and experimental research (01-02-2022)
    “…Introduction Delirium and sarcopenia are common, although underdiagnosed, geriatric syndromes. Several pathological mechanisms can link delirium and low…”
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  9. 9

    Prevalence and features of delirium in older patients admitted to rehabilitation facilities: a multicenter study by Sidoli, Chiara, Zambon, Antonella, Tassistro, Elena, Rossi, Emanuela, Mossello, Enrico, Inzitari, Marco, Cherubini, Antonio, Marengoni, Alessandra, Morandi, Alessandro, Bellelli, Giuseppe

    Published in Aging clinical and experimental research (01-08-2022)
    “…Background Delirium is thought to be common across various settings of care; however, still little research has been conducted in rehabilitation. Aim We…”
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  10. 10

    Hereditary localized pruritus in affected members of a kindred with multiple endocrine neoplasia type 2A (Sipple's syndrome) by Nunziata, V, Giannattasio, R, Di Giovanni, G, D'Armiento, M R, Mancini, M

    Published in Clinical endocrinology (Oxford) (01-01-1989)
    “…We describe a kindred with medullary thyroid carcinoma and phaeochromocytoma (MEN 2A or Sipple's syndrome) in which a cutaneous manifestation is only present…”
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  11. 11

    High turnover osteoporosis in acro-osteolysis (hajdu-cheney syndrome) by NUNZIATA, V, DI GIOVANNI, G, BALLANTI, P, BONUCCI, E

    Published in Journal of endocrinological investigation (01-03-1990)
    “…Acro-osteolysis with diffuse osteoporosis in the absence of other associated diseases is named Hajdu-Cheney syndrome. Reduced bone formation rather than…”
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  12. 12

    Vitamin D status in Paget's bone disease. Effects of calcitonin therapy by Nunziata, V, Giannattasio, R, di Giovanni, G, Lettera, A M, Nunziata, C A

    Published in Clinical orthopaedics and related research (01-08-1993)
    “…In 15 patients suffering from Paget's disease, the serum levels of alkaline phosphatase (ALP), 25-hydroxycholecalciferol (25OHD3),…”
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  13. 13

    Altered extracellular calcium homoeostasis in essential hypertension: a consequence of abnormal cell calcium handling by Strazzullo, P, Galletti, F, Cirillo, M, Siani, A, Nunziata, V, Giannattasio, R, Mancini, M

    Published in Clinical science (1979) (01-09-1986)
    “…A number of abnormalities in the extracellular and intracellular handling of calcium in arterial hypertension, namely an increased urinary calcium excretion, a…”
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  14. 14

    The relationship between glycosylated haemoglobin levels and various degrees of glucose intolerance by Verrillo, A, de Teresa, A, Golia, R, Nunziata, V

    Published in Diabetologia (01-05-1983)
    “…To assess the use of glycosylated haemoglobin to discriminate between various degrees of glucose intolerance, glycosylated haemoglobin levels were determined…”
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  15. 15

    Altered kinetics of an intravenous calcium load in idiopathic hypercalciuria by Nunziata, V, Giannattasio, R, di Giovanni, G, Corrado, M F, Galletti, F, Mancini, M

    Published in Metabolism, clinical and experimental (01-09-1989)
    “…Increased gut calcium absorption or reduced renal tubular calcium reabsorption have been alternatively reported in idiopathic hypercalciuria with kidney…”
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  16. 16

    Characterization of the clinical features of five families with hereditary primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2 by Robinson, M F, Furst, E J, Nunziata, V, Brandi, M L, Ferrer, J P, Martins Bugalho, M J, di Giovanni, G, Smith, R J, Donovan, D T, Alford, B R

    “…The hereditary conditions of primary cutaneous lichen amyloidosis and multiple endocrine neoplasia type 2 (MEN 2) are rare clinical entities. The initial…”
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  17. 17

    Interleukin-6 and osteoprotegerin systems in Paget's disease of bone: relationship to risedronate treatment by Mossetti, Giuseppe, Rendina, Domenico, De Filippo, Gianpaolo, Viceconti, Roberto, Di Domenico, Gilda, Cioffi, Michele, Postiglione, Loredana, Nunziata, Vincenzo

    Published in Bone (New York, N.Y.) (01-03-2005)
    “…Serum concentrations of interleukin-6 (IL-6), IL-6-soluble receptor (sIL-6R), IL-6 gp130-soluble receptor (sgp130), ligand of receptor activator of nuclear…”
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  18. 18

    Raloxifene administration in post‐menopausal women with osteoporosis: effect of different BsmI vitamin D receptor genotypes by Palomba, Stefano, Numis, Fabio Giuliano, Mossetti, Giuseppe, Rendina, Domenico, Vuotto, Pietro, Russo, Tiziana, Zullo, Fulvio, Nappi, Carmine, Nunziata, Vincenzo

    Published in Human reproduction (Oxford) (01-01-2003)
    “…BACKGROUND: The vitamin D receptor (VDR) gene polymorphism has been considered a factor influencing the effectiveness of the anti‐osteoporotic treatments. The…”
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  19. 19

    Cutaneous lichen amyloidosis associated with multiple endocrine neoplasia type 2A by Nunziata, V, di Giovanni, G, Lettera, A M, D'Armiento, M, Mancini, M

    “…We have previously described a kindred with hereditary medullary thyroid carcinoma and pheochromocytoma (multiple endocrine neoplasia type 2A [MEN 2A]) with…”
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  20. 20

    Multiple endocrine neoplasia type 2 (Sipple's syndrome): clinical and cytogenetic analysis of a kindred by Zatterale, A, Stabile, M, Nunziata, V, Di Giovanni, G, Vecchione, R, Ventruto, V

    Published in Journal of medical genetics (01-04-1984)
    “…This report describes the clinical and cytogenetic analysis of a kindred with multiple endocrine neoplasia type 2 (MEN-2 or Sipple's syndrome) in two…”
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