Bone histomorphometry in acromegaly patients with fragility vertebral fractures von Carbonare, L. Dalle, Micheletti, V., Cosaro, E., Valenti, M. T., Mottes, M., Francia, G., Davì, M. V.

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Increased Gene Expression of RUNX2 and SOX9 in Mesenchymal Circulating Progenitors Is Associated with Autophagy during Physical Activity von Valenti, M. T., Lippi, Giuseppe, Schena, Federico, Gabbiani, D., Zamboni, F., Deiana, M., Cheri, S., Mottes, M., Dalle Carbonare, L., Salvagno, Gian Luca

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Diffuse pancreatic serous cystic neoplasm: A rare cause of pancreatic insufficiency von Bellocchi, M.C. Conti, Mottes, M. Cattani, Crino', S., Amodio, A., Frulloni, L.

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The clinical impact of autoimmune pancreatitis and ulcerative colitis association: A third-level, single-center italian experience von Conti Bellocchi, M.C., Crino', S., La Monaca, L., Marconato, E., Mottes, M. Cattani, Gabbrielli, A., Frulloni, L.

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Deficiency of CRTAP in non-lethal recessive osteogenesis imperfecta reduces collagen deposition into matrix von Valli, M, Barnes, AM, Gallanti, A, Cabral, WA, Viglio, S, Weis, MA, Makareeva, E, Eyre, D, Leikin, S, Antoniazzi, F, Marini, JC, Mottes, M

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Osteogenesis imperfecta: clinical, biochemical and molecular findings von Venturi, G, Tedeschi, E, Mottes, M, Valli, M, Camilot, M, Viglio, S, Antoniazzi, F, Tatò, L

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Osteoporosis in β-Thalassemia: Clinical and Genetic Aspects von ORIGA, R., FIUMANA, E., GAMBERINI, M. R., ARMARI, S., MOTTES, M., SANGALLI, A., PAGLIETTI, E., GALANELLO, R., BORGNA-PIGNATTI, C.

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Null CRTAP mutation associated with non-lethal OI and minimal collagen deposition in culture von Valli, M, Barnes, A, Cabral, W.A, Gallanti, A, Viglio, S, Weis, M, Eyre, D, Antoniazzi, F, Mottes, M, Marini, J.C

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BOC.01.11: IMMUNOLOGICAL EFFECTS OF EXTRACELLULAR VESICLES FROM BONE MARROW-DERIVED MESENCHYMAL STEM CELLS ON A CELIAC DISEASE'S EXPERIMENTAL MODEL von Cattani Mottes, M., Gianfrani, C., Mottola, I., Zuliani, V., Adamo, A., Krampera, M., Vitale, S., Picascia, S., Del Pozzo, G., Frulloni, L., Ciccocioppo, R.

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T01.01.1 ROLE OF MIRNAS IN GASTRIC ATROPHY, AUTOIMMUNITY AND DISEASE PROGRESSION von Maddalo, G., Cattani Mottes, M., Fassan, M., Orlando, C., Rugge, M., Pilotto, V., Farinati, F.

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Lack of expression of SERPINF1, the gene coding for pigment epithelium-derived factor, causes progressively deforming osteogenesis imperfecta with normal type I collagen von Venturi, Giacomo, Gandini, Alberto, Monti, Elena, Carbonare, Luca Dalle, Corradi, Massimiliano, Vincenzi, Monica, Valenti, Maria Teresa, Valli, Maurizia, Pelilli, Enrico, Boner, Attilio, Mottes, Monica, Antoniazzi, Franco

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Osteogenesis imperfecta: practical treatment guidelines von Antoniazzi, F, Mottes, M, Fraschini, P, Brunelli, P C, Tatò, L

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Relationship among VDR (BsmI and FokI), COLIA1, and CTR polymorphisms with bone mass, bone turnover markers, and sex hormones in men von Braga, V, Sangalli, A, Malerba, G, Mottes, M, Mirandola, S, Gatti, D, Rossini, M, Zamboni, M, Adami, S

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Growth hormone treatment in osteogenesis imperfecta with quantitative defect of type I collagen synthesis von Antoniazzi, Franco, Bertoldo, Francesco, Mottes, Monica, Valli, Maurizia, Sirpresi, Stefania, Zamboni, Giorgio, Valentini, Roberta, Tatò, Luciano

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Association of CTR and COLIA1 alleles with BMD values in peri- and postmenopausal women von Braga, V, Mottes, M, Mirandola, S, Lisi, V, Malerba, G, Sartori, L, Bianchi, G, Gatti, D, Rossini, M, Bianchini, D, Adami, S

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Osteogenesis imperfecta at the beginning of bone and joint decade von Primorac, D, Rowe, D W, Mottes, M, Barisić, I, Anticević, D, Mirandola, S, Gomez Lira, M, Kalajzić, I, Kusec, V, Glorieux, F H

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Type VI Osteogenesis Imperfecta: effect of plasma transfusion on bone metabolism von Antoniazzi, F., Pietrobelli, A., Gandini, A., Cavarzere, P., Ramaroli, D., Mottes, M., Guzzo, A., De Gironcoli, M., Genesini, S., Zaffanello, M., Gaudino, R., Carbonare, L. Dalle, Valenti, M. T., Gatti, D., Fassio, A., Bertoldo, F., Tardivo, S., Piacentini, G.

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Characterization and functional analysis of cis-acting elements of the human farnesyl diphosphate synthetase (FDPS) gene 5′ flanking region von Romanelli, Maria Grazia, Lorenzi, Pamela, Sangalli, Antonella, Diani, Erica, Mottes, Monica

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Rapid and efficient genotype analysis of the COL1A1 Sp1 binding site dimorphism, a genetic marker for bone mineral density von Mirandola, S., Sangalli, A., Mottes, M.

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Detection of mutations in the ALD gene (ABCD1) in seven Italian families: Description of four novel mutations von Lira, M. Gomez, Mottes, M., Pignatti, P.F., Medica, I., Uziel, G., Cappa, M., Bertini, E., Rizzuto, N., Salviati, A.

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