Universitą degli studi di Pavia
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Giagnacovo pubblicazioni
Pubblicazioni in extenso
Perdoni F, Cardani R, Giagnacovo M, Veneroni P, Meola G, Pellicciari C, Malatesta M. Ultrastructural characterization of the MBNL1-containing foci occurring in myoblast and myotube nuclei from patients affected by myotonic dystrophy type 2. Microscopie 2009, n. 2 (12): 60-64.
Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Meola G. Ribonuclear inclusions as biomarker of myotonic distrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies. European Journal of Histochemistry 2009, vol. 53 (2): 107-112.
Perdoni F, Malatesta M, Cardani R, Giagnacovo M, Mancinelli E, Meola G, Pellicciari C. RNA/MBNL1-containing foci in myoblast nuclei form patients affected by myotonic dystrophy type 2: an immunocytochemical study. European Journal of Histochemistry 2009, vol. 53 (3): 151-158.
Giagnacovo M, Cardani R, Meola G, Pellicciari C, Malatesta M. Routinely frozen biopsies of human muscle are suitable for morphological and immunocytochemical analyses at trasmission electron microscopy. European Journal of Histochemistry 2010, vol. 54:e31: 137-142.
Giagnacovo M, Malatesta M, Veneroni P, Wang E, Pellicciari C. Ultrastructural immunolocalization of the senescence related protein terminin in human fibroblast. Microscopie 2010, n.2 (14): 32-37.
Malatesta M, Giagnacovo M, Cardani R, Meola G, Pellicciari C. RNA processing is altered in skeletal muscle nuclei of patients affected by miotonic dystrophy. Histochemistry and Cell Biology 2011, vol. 153 (4): 419-425.
Giagnacovo M, Costanzo M, Cardani R, Veneroni P, Pellicciari C, Meola G. In vitro senescence of myotube derived from myoblasts of patient affected by myotonic dystrophy type 2 (DM2): ultrastructural evidence. Microscopie 2011, n.1 (16): 60-67.
Malatesta M, Fattoretti P, Giagnacovo M, Pellicciari C, Zancanaro C. Physical training modulates structural and functional features of skeletal muscle nuclei in old mice. Rejuvenation Research 2011, , vol. 14 (5): 543-552.
Manuela M, Giagnacovo M, Cardani R, Meola G, Pellicciari C. Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features. (sottoposto)
Cardani R, Giagnacovo M, Botta A, Rinaldi F, Morgante A, Udd B, Raheem O, Penttila S, Suominen T, Renna LV, Sansone V, Bugiardini E, Novelli G, Meola G. Clinical and biomolecular findings in a juvenile inset case of myotonic dystrophy tipe 2. Journal of Neurology, Neurosurgery and Psychiatry (submitted)
Giagnacovo M, Malatesta M, Cardani R, Meola G, Pellicciari C Nuclear ribonucleoprotein-containing foci increase in size upon cell cycle exit in myotonic dystrophy type 2. Histochemistry and Cell Biology (Submitted)
Malatesta M, Giagnacovo M, Cardani R, Meola G, Pellicciari C Human myoblasts from skeletal muscle biopsies: in vitro culture preparations for morphological and cytochemical analyses at light and electron microscopy. Aging and stem cells. Methods and Protocols; Humana Press (in press)
Comunicazioni a congresso
Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Dragoni G, Meola G. Ribonuclear inclusions as biomarker of DM2 even in improperly frozen or defrost skeletal muscle biopsies. “XXXIII congresso della societą italiana di istochimica” Roma, 8-10 giugno 2009
Meola G, Piras R, Cardani R, Giagnacovo M, Lucchiari S, Comi GP, Mancinelli E, Marrosu G. Double genetic trouble (DM2/FSHD) in a Sardinian DM2/PROMM family. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Giagnacovo M, Cardani R, Botta A, Rinaldi F, Morgante A, Novelli G, Meola G. Clinical and biomolecular findings in a juvenile onset case of myotonic dystrophy type 2. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Cardani R, Giagnacovo M, Mancinelli E, Dragoni G, Sansone V, Meola G. Clinical, muscle pathology and FISH biomolecular findings correlation in 42 Italian patients with myotonic dystrophy type 2. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Renna LV, Cardani R, Giagnacovo M, Malatesta M, Pellicciari C, Meola G. Invecchiamento precoce delle cellule satelliti: suo possibile ruolo nell’atrofia muscolare dei pazienti affetti da distrofia miotonica. “10° congresso nazionale dell’associazione italiana di miologia” Milano, 3-5 giugno 2010
Giagnacovo M, Cardani R, Meola G, Pellicciari C, Malatesta M. Campioni bioptici congelati di muscolo scheletrico umano sono utlizzati per analisi morfologiche ed immunocitochimiche in microscopia elettronica a trasmissione. “10° congresso nazionale dell’associazione italiana di miologia” Milano, 3-5 giugno 2010
Giagnacovo M, Malatesta M, Cardani R, Pellicciari C, Meola G. RNA processing is altered in the nuclei of skeletal muscles from patients affected by myotonic dystrophy type 1 and 2. “Myology 2011” Lille (France), 9-13 maggio 2011
Renna LV, Cardani R, Giagnacovo M, Malatesta M, Pellicciari C, Meola G. Abnormalities of proliferative and differentiative properties in DM1 and DM2 senescent myoblasts “in vitro”. “Myology 2011” Lille (France), 9-13 maggio 2011
Giagnacovo M, Malatesta M, Veneroni P, Pellicciari C. Immunolocalization at electron microscopy of the senescence-related protein, terminin in human fibroblast. “10th Multinational Congress on Microscopy” Urbino (Italy), 04-09 settembre 2011
Giagnacovo M, Costanzo M, Malatesta M, Cardani R, Meola G, Pellicciari C. Ultrastructural study of the ageing in vitro of myotubes derived from myoblasts of patients affected by myotonic dystrophy type 2. “10th Multinational Congress on Microscopy” Urbino (Italy), 04-09 settembre 2011
Giagnacovo M, Malatesta M, Cardani R, Meola G, Pellicciari C. Ribonucleoprotein-containing foci increase in size upon cell-cycle exit in cell nuclei from patients affected by myotonic dystrophy type 2. “53rd Symposium of the Society for Histochemistry: current role of histochemistry in preclinical and clinical research”, Munich (Germany), 12-15 ottobre 2011
Perdoni F, Cardani R, Giagnacovo M, Veneroni P, Meola G, Pellicciari C, Malatesta M. Ultrastructural characterization of the MBNL1-containing foci occurring in myoblast and myotube nuclei from patients affected by myotonic dystrophy type 2. Microscopie 2009, n. 2 (12): 60-64.
Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Meola G. Ribonuclear inclusions as biomarker of myotonic distrophy type 2, even in improperly frozen or defrozen skeletal muscle biopsies. European Journal of Histochemistry 2009, vol. 53 (2): 107-112.
Perdoni F, Malatesta M, Cardani R, Giagnacovo M, Mancinelli E, Meola G, Pellicciari C. RNA/MBNL1-containing foci in myoblast nuclei form patients affected by myotonic dystrophy type 2: an immunocytochemical study. European Journal of Histochemistry 2009, vol. 53 (3): 151-158.
Giagnacovo M, Cardani R, Meola G, Pellicciari C, Malatesta M. Routinely frozen biopsies of human muscle are suitable for morphological and immunocytochemical analyses at trasmission electron microscopy. European Journal of Histochemistry 2010, vol. 54:e31: 137-142.
Giagnacovo M, Malatesta M, Veneroni P, Wang E, Pellicciari C. Ultrastructural immunolocalization of the senescence related protein terminin in human fibroblast. Microscopie 2010, n.2 (14): 32-37.
Malatesta M, Giagnacovo M, Cardani R, Meola G, Pellicciari C. RNA processing is altered in skeletal muscle nuclei of patients affected by miotonic dystrophy. Histochemistry and Cell Biology 2011, vol. 153 (4): 419-425.
Giagnacovo M, Costanzo M, Cardani R, Veneroni P, Pellicciari C, Meola G. In vitro senescence of myotube derived from myoblasts of patient affected by myotonic dystrophy type 2 (DM2): ultrastructural evidence. Microscopie 2011, n.1 (16): 60-67.
Malatesta M, Fattoretti P, Giagnacovo M, Pellicciari C, Zancanaro C. Physical training modulates structural and functional features of skeletal muscle nuclei in old mice. Rejuvenation Research 2011, , vol. 14 (5): 543-552.
Manuela M, Giagnacovo M, Cardani R, Meola G, Pellicciari C. Cultured myoblasts from patients affected by myotonic dystrophy type 2 exhibit senescence-related features. (sottoposto)
Cardani R, Giagnacovo M, Botta A, Rinaldi F, Morgante A, Udd B, Raheem O, Penttila S, Suominen T, Renna LV, Sansone V, Bugiardini E, Novelli G, Meola G. Clinical and biomolecular findings in a juvenile inset case of myotonic dystrophy tipe 2. Journal of Neurology, Neurosurgery and Psychiatry (submitted)
Giagnacovo M, Malatesta M, Cardani R, Meola G, Pellicciari C Nuclear ribonucleoprotein-containing foci increase in size upon cell cycle exit in myotonic dystrophy type 2. Histochemistry and Cell Biology (Submitted)
Malatesta M, Giagnacovo M, Cardani R, Meola G, Pellicciari C Human myoblasts from skeletal muscle biopsies: in vitro culture preparations for morphological and cytochemical analyses at light and electron microscopy. Aging and stem cells. Methods and Protocols; Humana Press (in press)
Comunicazioni a congresso
Cardani R, Mancinelli E, Giagnacovo M, Sansone V, Dragoni G, Meola G. Ribonuclear inclusions as biomarker of DM2 even in improperly frozen or defrost skeletal muscle biopsies. “XXXIII congresso della societą italiana di istochimica” Roma, 8-10 giugno 2009
Meola G, Piras R, Cardani R, Giagnacovo M, Lucchiari S, Comi GP, Mancinelli E, Marrosu G. Double genetic trouble (DM2/FSHD) in a Sardinian DM2/PROMM family. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Giagnacovo M, Cardani R, Botta A, Rinaldi F, Morgante A, Novelli G, Meola G. Clinical and biomolecular findings in a juvenile onset case of myotonic dystrophy type 2. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Cardani R, Giagnacovo M, Mancinelli E, Dragoni G, Sansone V, Meola G. Clinical, muscle pathology and FISH biomolecular findings correlation in 42 Italian patients with myotonic dystrophy type 2. “IDMC-7: 7th International Myotonic Dystrophy Consortium Meeting” Wurzburg (Germany), 9-12 settembre 2009
Renna LV, Cardani R, Giagnacovo M, Malatesta M, Pellicciari C, Meola G. Invecchiamento precoce delle cellule satelliti: suo possibile ruolo nell’atrofia muscolare dei pazienti affetti da distrofia miotonica. “10° congresso nazionale dell’associazione italiana di miologia” Milano, 3-5 giugno 2010
Giagnacovo M, Cardani R, Meola G, Pellicciari C, Malatesta M. Campioni bioptici congelati di muscolo scheletrico umano sono utlizzati per analisi morfologiche ed immunocitochimiche in microscopia elettronica a trasmissione. “10° congresso nazionale dell’associazione italiana di miologia” Milano, 3-5 giugno 2010
Giagnacovo M, Malatesta M, Cardani R, Pellicciari C, Meola G. RNA processing is altered in the nuclei of skeletal muscles from patients affected by myotonic dystrophy type 1 and 2. “Myology 2011” Lille (France), 9-13 maggio 2011
Renna LV, Cardani R, Giagnacovo M, Malatesta M, Pellicciari C, Meola G. Abnormalities of proliferative and differentiative properties in DM1 and DM2 senescent myoblasts “in vitro”. “Myology 2011” Lille (France), 9-13 maggio 2011
Giagnacovo M, Malatesta M, Veneroni P, Pellicciari C. Immunolocalization at electron microscopy of the senescence-related protein, terminin in human fibroblast. “10th Multinational Congress on Microscopy” Urbino (Italy), 04-09 settembre 2011
Giagnacovo M, Costanzo M, Malatesta M, Cardani R, Meola G, Pellicciari C. Ultrastructural study of the ageing in vitro of myotubes derived from myoblasts of patients affected by myotonic dystrophy type 2. “10th Multinational Congress on Microscopy” Urbino (Italy), 04-09 settembre 2011
Giagnacovo M, Malatesta M, Cardani R, Meola G, Pellicciari C. Ribonucleoprotein-containing foci increase in size upon cell-cycle exit in cell nuclei from patients affected by myotonic dystrophy type 2. “53rd Symposium of the Society for Histochemistry: current role of histochemistry in preclinical and clinical research”, Munich (Germany), 12-15 ottobre 2011
