High Incidence of Later-Onset Fabry Disease Revealed by Newborn Screening von Spada, Marco, Pagliardini, Severo, Yasuda, Makiko, Tukel, Turgut, Thiagarajan, Geetha, Sakuraba, Hitoshi, Ponzone, Alberto, Desnick, Robert J.

Volltext

Transcriptomic landscape of TIMP3 oncosuppressor activity in thyroid carcinoma von Mazzoni, M, Todoerti, K, Agnelli, L, Minna, E, Pagliardini, S, Di Marco, T, Borrello, M G, Neri, A, Greco, A

Volltext

TIMP3 regulates migration, invasion and in vivo tumorigenicity of thyroid tumor cells von Anania, M C, Sensi, M, Radaelli, E, Miranda, C, Vizioli, M G, Pagliardini, S, Favini, E, Cleris, L, Supino, R, Formelli, F, Borrello, M G, Pierotti, M A, Greco, A

Volltext

Comparison of inhaled versus intravenous anesthesia for laryngoscopy and laryngeal electromyography in a rat model von Gazzaz, M, Saini, J, Pagliardini, S, Tsui, B, Jeffery, C, El-Hakim, H

Volltext

LOPED study: looking for an early diagnosis in a late-onset Pompe disease high-risk population von Musumeci, O, la Marca, G, Spada, M, Mondello, S, Danesino, C, Comi, G P, Pegoraro, E, Antonini, G, Marrosu, G, Liguori, R, Morandi, L, Moggio, M, Massa, R, Ravaglia, S, Di Muzio, A, Filosto, M, Tonin, P, Di Iorio, G, Servidei, S, Siciliano, G, Angelini, C, Mongini, T, Toscano, A

Volltext

Targeting COPZ1 in thyroid tumour cells von Anania, M.C, Cetti, E, Lecis, D, Cleris, L, Mazzoni, M, Pagliardini, S, Manenti, G, Greco, A

Volltext

Lysosomal enzyme activities in phenylketonuria von Porta, Francesco, Pagliardini, S., Pagliardini, V., Dotta, Anna, Mussa, Alessandro, Spada, Marco

Volltext

Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord von PAGLIARDINI, S, GIAVAZZI, A, SETOLA, V, LIZIER, C, DI LUCA, M, DEBIASI, S, BATTAGLIA, G

Volltext

Purinergic modulation of preBötzinger Complex inspiratory rhythm generating networks von Zwicker, J.D, Pagliardini, S, Kasparov, S, Gourine, A.V, Funk, G.D

Volltext

Presynaptic kainate receptors in primary afferents to the superficial laminae of the rat spinal cord von Hwang, Se Jin, Pagliardini, Silvia, Rustioni, Aldo, Valtschanoff, Juli G.

Volltext

The DNA rearrangement that generates the TRK-T3 oncogene involves a novel gene on chromosome 3 whose product has a potential coiled-coil domain von Greco, Angela, Mariani, Cristina, Miranda, Claudia, Lupas, Andrei, Pagliardini, Sonia, Pomati, Mauro, Pierotti, Marco A.

Volltext

Long-standing mild hypertransaminasaemia caused by congenital disorder of glycosylation (CDG) type IIx von Calvo, P. L., Pagliardini, S., Baldi, M., Pucci, A., Sturiale, L., Garozzo, D., Vinciguerra, T., Barbera, C., Jaeken, J.

Volltext

Congenital disorder of glycosylation (CDG) Ig: Report on a patient and review of the literature von Rocco, M. Di, Hennet, T., Grubenmann, C. E., Pagliardini, S., Allegri, A. E. M., Frank, C. G., Aebi, M., Vignola, S., Jaeken, J.

Volltext

NMDA receptor subunits are phosphorylated by activation of neurotrophin receptors in PSD of rat spinal cord von Di Luca, M, Gardoni, F, Finardi, A, Pagliardini, S, Cattabeni, F, Battaglia, G, Missale, C

Volltext

An adult patient with a 21-year-history of an unexplained increase in serum transaminases: A novel congenital glycosylation disorder CDG-IIx von Calvo, P.L, Pagliardini, S, Baldi, M, Pucci, A, Barbera, C, Jaeken, J

Volltext

Multiple Factors Influencing the Incidence of Congenital Hypothyroidism Detected by Neonatal Screening von Olivieri, Antonella, Fazzini, Cristina, Medda, Emanuela

Volltext

439 - Targeting COPZ1 in thyroid tumour cells von Anania, M.C., Cetti, E., Lecis, D., Cleris, L., Mazzoni, M., Pagliardini, S., Manenti, G., Greco, A.

Volltext

38 Reduction of activity of Arylsulfatasi B in patient with Cystic Fibrosis von Pagliardini, S, Veljkovic, A, Tardivo, I, Forneris, M.P, Bena, C, Ferrero, G.B, Bignamini, E

Volltext

Ontogeny of the Pre-Botzinger Complex in Perinatal Rats von Pagliardini, Silvia, Ren, Jun, Greer, John J

Volltext

Developmental Abnormalities of Neuronal Structure and Function in Prenatal Mice Lacking the Prader-Willi Syndrome Gene Necdin von Pagliardini, Silvia, Ren, Jun, Wevrick, Rachel, Greer, John J.

Volltext