Psychiatric Emergency in Children and Adolescents: A Retrospective Study in Parma Local Health Unit von Deolmi, Michela, Turco, Emanuela Claudia, Pellegrini, Pietro, Marchesi, Carlo, Pisani, Francesco

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Age- and Gender-Based Differences in Nest-Building Behavior and Learning and Memory Performance Measured Using a Radial Six-Armed Water Maze in C57BL/6 Mice von Chen, Gui-Hai, Xiong, Shang-Shen, Xiong, Wei-Dong, Xiong, Xiang-Dong

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Prevalence and Associated Factors of Depressive Symptoms in Patients with Myasthenia Gravis: A Cross-Sectional Study of Two Tertiary Hospitals in Riyadh, Saudi Arabia von Alanazy, Mohammed H.

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Milestones and Timescale of Poststroke Recovery: A Cohort Study von Balbi, Pietro, Maestri, Roberto, Ferrari, Elena P., Abbamonte, Marta, Zaliani, Alberto, Loi, Marianna, Trojano, Luigi

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Cognitive-Enhancing Effect of a Hydroethanolic Extract of Crinum macowanii against Memory Impairment Induced by Aluminum Chloride in BALB/c Mice von Maponga, Charles Chiedza, Gadaga, Louis L., Tagwireyi, Dexter, Jilani, Mohammed S., Mutsimhu, Cosmas

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National survey to update the diagnostic reference levels in interventional radiology procedures in Italy: working methodology von D’Ercole, L, Rosi, A, Bernardi, G, Compagnone, G, Orlacchio, A, Padovani, R, Palma, A, Grande, S

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Patterns of Objective and Subjective Burden of Informal Caregivers in Multiple Sclerosis von Lubetzki, C., Pradat-Diehl, P., Papeix, C., Bayen, E., Joël, M. E.

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Carbon nanotubes and silver nanoparticles for multifunctional conductive biopolymer composites von Fortunati, E., D’Angelo, F., Martino, S., Orlacchio, A., Kenny, J.M., Armentano, I.

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Micropatterned hydrogenated amorphous carbon guides mesenchymal stem cells towards neuronal differentiation von D'Angelo, F, Armentano, I, Mattioli, S, Crispoltoni, L, Tiribuzi, R, Cerulli, G G, Palmerini, C A, Kenny, J M, Martino, S, Orlacchio, A

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Silver syndrome variant of hereditary spastic paraplegia : A locus to 4p and allelism with SPG4 von ORLACCHIO, A, PATRONO, C, GAUDIELLO, F, ROCCHI, C, MOSCHELLA, V, FLORIS, R, BERNARDI, G, KAWARAI, T

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Spastic paraplegia in Romania: high prevalence of SPG4 mutations von Orlacchio, A, Patrono, C, Borreca, A, Babalini, C, Bernardi, G, Kawarai, T

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A direct gene transfer strategy via brain internal capsule reverses the biochemical defect in Tay–Sachs disease von Martino, S., Marconi, P., Tancini, B., Dolcetta, D., De Angelis, M.G. Cusella, Montanucci, P., Bregola, G., Sandhoff, K., Bordignon, C., Emiliani, C., Manservigi, R., Orlacchio, A.

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Transarterial Chemoocclusion (Taco) With Degradable-Starch-Microsphere In Unresecable Hepatocellular Carcinoma: A Prospective Pilot-Study von Francioso, S, Orlacchio, A, Chegai, F, Santopaolo, F, Lenci, I, Milana, M, Brega, A, Angelico, M

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Accuracy of early and delayed FDG PET-CT and of contrast-enhanced CT in the evaluation of lung nodules: a preliminary study on 30 patients von Schillaci, O., Travascio, L., Bolacchi, F., Calabria, F., Bruni, C., Cicciò, C., Guazzaroni, M., Orlacchio, A., Simonetti, G.

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MicroRNA Implications across Neurodevelopment and Neuropathology von Martino, Sabata, di Girolamo, Ilaria, Orlacchio, Antonio, Datti, Alessandro, Orlacchio, Aldo

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Caspase 3 activation and PARP cleavage in lymphocytes from newborn babies of diabetic mothers with unbalanced glycaemic control von Tarquini, F., Tiribuzi, R., Crispoltoni, L., Porcellati, S., Del Pino, A. M., Orlacchio, A., Coata, G., Arnone, S., Torlone, E., Cappuccini, B., Di Renzo, G. C., Orlacchio, A.

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Acanthocytosis as a predisposing factor for non-ketotic hyperglycaemia induced chorea-ballism von Pisani, A, Diomedi, M, Rum, A, Cianciulli, P, Floris, R, Orlacchio, A, Bernardi, G, Calabresi, P

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Upper motor neuron involvement in X-linked recessive bulbospinal muscular atrophy von Pachatz, C, Terracciano, C, Desiato, M.T, Orlacchio, A, Mori, F, Rocchi, C, Bernardi, G, Massa, R

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Clinical validation of a link between TNF-α and the glycosylation enzyme core 2 GlcNAc-T and the relationship of this link to diabetic retinopathy von BEN-MAHMUD, B. M, CHAN, W. H, ABDULAHAD, R. M, DATTI, A, ORLACCHIO, A, KOHNER, E. M, CHIBBER, R

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Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity von Pippucci, T., Panza, E., Pompilii, E., Donadio, V., Borreca, A., Babalini, C., Patrono, C., Zuntini, R., Kawarai, T., Bernardi, G., Liguori, R., Romeo, G., Montagna, P., Orlacchio, A., Seri, M.

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