Effects of short‐to‐long term enzyme replacement therapy (ERT) on skeletal muscle tissue in late onset Pompe disease (LOPD) von Ripolone, M., Violano, R., Ronchi, D., Mondello, S., Nascimbeni, A., Colombo, I., Fagiolari, G., Bordoni, A., Fortunato, F., Lucchini, V., Saredi, S., Filosto, M., Musumeci, O., Tonin, P., Mongini, T., Previtali, S., Morandi, L., Angelini, C., Mora, M., Sandri, M., Sciacco, M., Toscano, A., Comi, G. P., Moggio, M.

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Congenital muscular dystrophies with defective glycosylation of dystroglycan: A population study von MERCURI, E, MESSINA, S, BOFFI, P, CASSANDRINI, D, LAVERDA, A, MOGGIO, M, MORANDI, L, MORONI, I, PANE, M, PEZZANI, R, PICHIECCHIO, A, PINI, A, BRUNO, C, MINETTI, C, MONGINI, T, MOTTARELLI, E, RICCI, E, RUGGIERI, A, SAREDI, S, SCUDERI, C, TESSA, A, TOSCANO, A, TORTORELLA, G, MORA, M, TREVISAN, C. P, UGGETTI, C, VASCO, G, SANTORELLI, F. M, BERTINI, E, PEGORARO, E, COMI, G. P, D'AMICO, A, AIELLO, C, BIANCHERI, R, BERARDINELLI, A

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Protein O-mannosylation is crucial for human mesencyhmal stem cells fate von Ragni, E, Lommel, M, Moro, M, Crosti, M, Lavazza, C, Parazzi, V, Saredi, S, Strahl, S, Lazzari, L

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Altered extracellular matrix transcript expression and protein modulation in primary Duchenne muscular dystrophy myotubes von Zanotti, S., Saredi, S., Ruggieri, A., Fabbri, M., Blasevich, F., Romaggi, S., Morandi, L., Mora, M.

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Novel POMGNT1 point mutations and intragenic rearrangements associated with muscle-eye-brain disease von Saredi, S, Ardissone, A, Ruggieri, A, Mottarelli, E, Farina, L, Rinaldi, R, Silvestri, E, Gandioli, C, D'Arrigo, S, Salerno, F, Morandi, L, Grammatico, P, Pantaleoni, C, Moroni, I, Mora, M

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A fourth case of POMT2-related limb girdle muscle dystrophy with mild reduction of α-dystroglycan glycosylation von Saredi, S, Gibertini, S, Ardissone, A, Fusco, I, Zanotti, S, Blasevich, F, Morandi, L, Moroni, I, Mora, M

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Congenital muscular dystrophies with cognitive impairment: A population study von MESSINA, S, BRUNO, C, MINETTI, C, MOGGIO, M, MONGINI, T, MOTTARELLI, E, PANE, M, PANTALEONI, C, PICHIECCHIO, A, PINI, A, RICCI, E, SAREDI, S, MORONI, I, SFRAMELI, M, TORTORELLA, G, TOSCANO, A, TREVISAN, C. P, UGGETTI, C, VASCO, G, COMI, G. P, SANTORELLI, F. M, BERTINI, E, MERCURI, E, PEGORARO, E, D'AMICO, A, BIANCHERI, R, BERARDINELLI, A, BOFFI, P, CASSANDRINI, D, FARINA, L

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G.P.311 von Baranello, G, Morandi, L, Sansanelli, S, Savadori, P, Saredi, S, Pantaleoni, C, Balestri, P, Malandrini, A, Arnoldi, M.T, Chiapparini, L, Mora, M

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POMT1 and POMT2 mutations in CMD patients: A multicentric Italian study von Messina, S, Mora, M, Pegoraro, E, Pini, A, Mongini, T, D’Amico, A, Pane, M, Aiello, C, Bruno, C, Biancheri, R, Berardinelli, A, Boito, C, Farina, L, Morandi, L, Moroni, I, Pezzani, R, Pichiecchio, A, Ricci, E, Ruggieri, A, Saredi, S, Scuderi, C, Tessa, A, Toscano, A, Tortorella, G, Trevisan, C.P, Uggetti, C, Santorelli, F.M, Bertini, E, Mercuri, E

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Effect of streptozotocin-induced diabetes on the gene expression and biological activity of 3β-hydroxysteroid dehydrogenase in the rat spinal cord von Saredi, S., Patte-Mensah, C., Melcangi, R.C., Mensah-Nyagan, A.G.

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EM.P.3.04 Muscle-derived Duchenne muscular dystrophy fibroblasts show altered production of extra-cellular matrix components von Zanotti, S, Gibertini, S, Saredi, S, Blasevich, F, Mantegazza, R, Morandi, L, Mora, M

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G.P.2.03 Clinical and molecular characterization of 12 patients with defective α-dystroglycan glycosylation von Moroni, I, Saredi, S, Ruggieri, A, Pantaleoni, C, Morandi, L, Mora, M

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EM.P.2.08 Fukutin gene mutations in an Italian patient with early onset muscular dystrophy but no central nervous system involvement von Saredi, S, Mottarelli, E, Ruggieri, A, Ardissone, A, Zanotti, S, Farina, L, Morandi, L, Moroni, I, Mora, M

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Smad Proteins are Targets of Transforming Growth Factor β1 in Immortalised Gonadotrophin-Releasing Hormone Releasing Neurones von Galbiati, M., Saredi, S., Romanò, N., Martini, L., Motta, M., Melcangi, R. C.

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G.P.7.07 In vitro dissection of the pathogenic mechanisms of muscle fibrosis in Duchenne muscular dystrophy von Zanotti, S, Saredi, S, Cappelletti, C, Ruggieri, A, Blasevich, F, Bernasconi, P, Morandi, L, Mora, M

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G.P.2.07 Alpha-dystroglycanopathy in an Italian patient due to large intragenic and single nucleotide deletions in the POMGnT1 gene von Saredi, S, Ruggieri, A, Pantaleoni, C, D’Arrigo, S, Mottarelli, E, Blasevich, F, Morandi, L, Moroni, I, Mora, M

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G.P.16.09 Altered expression and modulation of extracellular matrix transcripts and proteins in primary DMD muscle cultures von Zanotti, S, Saredi, S, Ruggieri, A, Blasevich, F, Romaggi, S, Morandi, L, Mora, M

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P.245 - Potential role of exosomes in skeletal muscle fibrosis von Zanotti, S., Gibertini, S., Blasevich, F., Saredi, S., Bragato, C., Ruggieri, A., Mantegazza, R., Maggi, L., Mora, M.

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Potential role of exosomes in skeletal muscle fibrosis von Zanotti, S., Gibertini, S., Blasevich, F., Saredi, S., Bragato, C., Ruggieri, A., Mantegazza, R., Maggi, L., Mora, M.

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Neurogenic pain and steroid synthesis in the spinal cord von Patte-Mensah, Christine, Kibaly, Cherkaouia, Boudard, Domitille, Schaeffer, Véronique, Béglé, Aurélie, Saredi, Simona, Meyer, Laurence, Mensah-Nyagan, Ayikoe G

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