检索结果 - Gennari, C

Letter: Diphosphonate therapy in deafness associated with Paget's disease. 由 Gennari, C, Sensini, I

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Intestinal Absorption of 45Ca in Stone-forming Patients 由 Caniggia, A., Gennari, C., Cesari, L.

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Urinary cyclic adenosine monophosphate in young adults and elderly subjects. 由 Gennari, C, Galli, M, Montagnani, M

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Urinary excretion of cyclic adenosine 3',5'-monophosphate and cyclic guanosine 3',5'-monophosphate in malignancy. 由 Gennari, C, Francini, G, Galli, M, Lore, F

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2,3-Dihydroxybenzoate pathway in Pseudomonas putida. 1H n.m.r. study on the ring-cleavage site. 由 Andreoni, V, Canonica, L, Galli, E, Gennari, C, Treccani, V

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A study of the maloalcoholic fermentation pathway in Schizosaccharomyces pombe. 由 Maconi, E, Manachini, P L, Aragozzini, F, Gennari, C, Ricca, G S

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Paget's disease of bone: diagnosis and management. 由 Hosking, D., Meunier, P. J., Ringe, J. D., Reginster, J. Y., Gennari, C.

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Bone turnover in postmenopausal osteoporosis. Effect of calcitonin treatment. 由 Civitelli, R, Gonnelli, S, Zacchei, F, Bigazzi, S, Vattimo, A, Avioli, L V, Gennari, C

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Activity of omeprazole on Helicobacter pylori and relation to toxicity of strains. 由 Figura, N, Armellini, D, Bugnoli, M, Bayeli, P F, Gennari, C, Crabtree, J E

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Data on chloroquine/hydroxychloroquine content in compounded oral suspension after filtration and centrifugation 由 Musazzi, U.M., Zanon, D., Gennari, C.M.G., Fortini, M., Maximova, N., Cilurzo, F., Minghetti, P.

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cagA positive and negative Helicobacter pylori strains are simultaneously present in the stomach of most patients with non-ulcer dyspepsia: relevance to histological damage 由 Figura, N, Vindigni, C, Covacci, A, Presenti, L, Burroni, D, Vernillo, R, Banducci, T, Roviello, F, Marrelli, D, Biscontri, M, Kristodhullu, S, Gennari, C, Vaira, D

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Evidence for efficacy of drugs affecting bone metabolism in preventing hip fracture. 由 Kanis, J. A., Johnell, O., Gullberg, B., Allander, E., Dilşen, G., Gennari, C., Lopes Vaz, A. A., Lyritis, G. P., Mazzuoli, G., Miravet, L.

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Mild brachydactyly type A1 maps to chromosome 2q35-q36 and is caused by a novel IHH mutation in a three generation family 由 Giordano, N, Gennari, L, Bruttini, M, Mari, F, Meloni, I, Baldi, C, Capoccia, S, Geraci, S, Merlotti, D, Amendola, A, Martini, G, Nuti, R, Gennari, C, Renieri, A

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