Co-nonsolvency of PNiPAM at the transition between solvation mechanisms von Bischofberger, I, Calzolari, D C E, Trappe, V

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Hydrophobic hydration of poly-N-isopropyl acrylamide: a matter of the mean energetic state of water von Bischofberger, I., Calzolari, D. C. E., De Los Rios, P., Jelezarov, I., Trappe, V.

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Anorectal malformations and pregnancy‐related disorders: a registry‐based case–control study in 17 European regions von Wijers, CHW, Rooij, IALM, Bakker, MK, Marcelis, CLM, Addor, MC, Barisic, I, Béres, J, Bianca, S, Bianchi, F, Calzolari, E, Greenlees, R, Lelong, N, Latos‐Bielenska, A, Dias, CM, McDonnell, R, Mullaney, C, Nelen, V, O'Mahony, M, Queisser‐Luft, A, Rankin, J, Zymak‐Zakutnia, N, Blaauw, I, Roeleveld, N, Walle, HEK

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An epidemiological survey of Mycoplasma hominis and Ureaplasma urealyticum in gynaecological outpatients, Rome, Italy von VERTERAMO, R., PATELLA, A., CALZOLARI, E., RECINE, N., MARCONE, V., OSBORN, J., CHIARINI, F., DEGENER, A. M.

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An X-ray chamber for in situ structural studies of solvent-mediated nanoparticle self-assembly von Calzolari, Davide C. E., Pontoni, Diego, Daillant, Jean, Reichert, Harald

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Evidence of kinesin heavy chain (KIF5A) involvement in pure hereditary spastic paraplegia von FICHERA, M, LO GIUDICE, M, FALCO, M, STURNIO, M, AMATA, S, CALABRESE, O, BIGONI, S, CALZOLARI, E, NERI, M

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Prenatal genetic counseling referrals for advanced maternal age: still room for improvement von Pompilii, E., Astolfi, G., Calabrese, O., Calzolari, E., Ferlini, A., Lucci, M., Parmeggiani, G., Seri, M., Baroncini, A.

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Bacterial vaginosis and contraceptive methods von Calzolari, E, Masciangelo, R, Milite, V, Verteramo, R

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Congenital Heart Defects: 15 Years of Experience of the Emilia-Romagna Registry (Italy) von Calzolari, E., Garani, G., Cocchi, G., Magnani, C., Rivieri, F., Neville, A., Astolfi, G., Baroncini, A., Garavelli, L., Gualandi, F., Scorrano, M., Bosi, G., IMER Working Group

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Nanoscale structure of surfactant-induced nanoparticle monolayers at the oil-water interface von Calzolari, Davide CE, Pontoni, Diego, Deutsch, Moshe, Reichert, Harald, Daillant, Jean

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Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene von Gualandi, F., Rimessi, P., Trabanelli, C., Spitali, P., Neri, M., Patarnello, T., Angelini, C., Yau, S.C., Abbs, S., Muntoni, F., Calzolari, E., Ferlini, A.

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The human brain networks mediating the vestibular sensation of self-motion von Hadi, Z, Mahmud, M, Pondeca, Y, Calzolari, E, Chepisheva, M, Smith, RM, Rust, HM, Sharp, DJ, Seemungal, BM

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Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion von Gualandi, F, Trabanelli, C, Rimessi, P, Calzolari, E, Toffolatti, L, Patarnello, T, Kunz, G, Muntoni, F, Ferlini, A

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Core–shell nanoparticle monolayers at planar liquid–liquid interfaces: effects of polymer architecture on the interface microstructure von Isa, Lucio, Calzolari, Davide C. E., Pontoni, Diego, Gillich, Torben, Nelson, Adrienne, Zirbs, Ronald, Sánchez-Ferrer, Antoni, Mezzenga, Raffaele, Reimhult, Erik

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Maternal Occupational Risk Factors for Oral Clefts von Lorente, Christine, Cordier, Sylvaine, Bergeret, Alain, De Walle, Hermien EK, Goujard, Janine, Aymé, Ségolène, Knill-Jones, Robin, Calzolari, Elisa, Bianchi, Fabrizio

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Vestibular agnosia in traumatic brain injury and its link to imbalance von Calzolari, E, Chepisheva, M, Smith, RM, Hellyer, PJ, Tahtis, V, Arshad, Q, Jolly, A, Mahmud, M, Wilson, M, Rust, H, Sharp, DJ, Seemungal, BM

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Correction: Co-nonsolvency of PNiPAM at the transition between solvation mechanisms von Bischofberger, I, Calzolari, D. C. E, Trappe, V

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Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report von Bovicelli, L., Ghi, T., Pilu, G., Farina, A, Savelli, L., Simonazzi, G., Calzolari, E., Ferlini, A., Santini, D., Valeri, B.

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International Cooperation and Networking in Genetic Health Care Provision: Issues Arising from the Genetic Services Plan for the Emilia-Romagna Region, Italy von Calzolari, E., Baroncini, A.

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Occurrence of del( GIB6 -D13S1830) mutation in italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele von Gualandi, F., Ravani, A., Berto, A., Burdo, S., Trevisi, P., Ferlini, A., Martini, A., Calzolari, E.

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