Publications by authors named "Michela Morbin"

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Kufs disease due to mutation of CLN6: clinical, pathological and molecular genetic features.
Samuel F Berkovic, Karen L Oliver, Laura Canafoglia, Penina Krieger, John A Damiano, Michela Morbin

Brain· January 2019

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A Novel Focal Seizure Pattern Generated in Superficial Layers of the Olfactory Cortex.
Laura Uva, Stefania Saccucci, Maia Chikhladze, Laura Tassi, Vadym Gnatkovsky, Michela Morbin

J Neurosci· March 2017

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Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot-Marie-Tooth disease (CMT4).
Giuseppe Piscosquito, Paola Saveri, Stefania Magri, Claudia Ciano, Claudia Gandioli, Michela Morbin

J Peripher Nerv Syst· September 2016

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Measles Inclusion-Body Encephalitis: Neuronal Phosphorylated Tau Protein is Present in the Biopsy but not in the Autoptic Specimens of the Same Patient.
Emanuela Maderna, Valeria Fugnanesi, Michela Morbin, Francesca Cacciatore, Sonia Spinello

Brain Pathol· July 2016

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The diagnostic challenge of Divry van Bogaert and Sneddon Syndrome: Report of three cases and literature review.
Anna Bersano, Michela Morbin, Elisa Ciceri, Gloria Bedini, Peter Berlit

J Neurol Sci· May 2016

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Loss of exosomes in progranulin-associated frontotemporal dementia.
Luisa Benussi, Miriam Ciani, Elisa Tonoli, Michela Morbin, Luisa Palamara

Neurobiol Aging· April 2016

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A 52-Year-Old Man with Myoclonic Jerks.
Giorgio Giaccone, Francesco Carella, Carlo Parravicini, Erika Longhi, Luisa Chiapparini, Michela Morbin

Brain Pathol· March 2016

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Tackling amyloidogenesis in Alzheimer's disease with A2V variants of Amyloid-β.
Giuseppe Di Fede, Marcella Catania, Emanuela Maderna, Michela Morbin, Fabio Moda

Sci Rep· February 2016

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Type II focal cortical dysplasia: Ex vivo 7T magnetic resonance imaging abnormalities and histopathological comparisons.
Ileana Zucca, Gloria Milesi, Valentina Medici, Laura Tassi, Giuseppe Didato, Michela Morbin

Ann Neurol· January 2016

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Stem cell salvage of injured peripheral nerve.
Nadia Grimoldi, Federica Colleoni, Francesca Tiberio, Ignazio G Vetrano, Alberto Cappellari, Michela Morbin

Cell Transplant· November 2015

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NO-donor thiacarbocyanines as multifunctional agents for Alzheimer's disease.
Konstantin Chegaev, Antonella Federico, Elisabetta Marini, Barbara Rolando, Roberta Fruttero, Michela Morbin

Bioorg Med Chem· August 2015

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Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations.
Laura Canafoglia, Isabella Gilioli, Federica Invernizzi, Vito Sofia, Valeria Fugnanesi, Michela Morbin

Neurology· July 2015

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Presynaptic c-Jun N-terminal Kinase 2 regulates NMDA receptor-dependent glutamate release.
Robert Nisticò, Fulvio Florenzano, Dalila Mango, Caterina Ferraina, Massimo Grilli, Michela Morbin

Sci Rep· March 2015

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Pentraxin-3 and VEGF in POEMS syndrome: a 2-year longitudinal study.
Chiara Briani, Chiara Dalla Torre, Federica Lessi, Tiziana Cavallaro, Marina Scarlato, Michela Morbin

J Neuroimmunol· December 2014

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Therapy in prion diseases.
Gianluigi Forloni, Vladimiro Artuso, Ignazio Roiter, Michela Morbin, Fabrizio Tagliavini

Curr Top Med Chem· November 2014

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Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis.
Eleonora Dalla Bella, Andrea Rigamonti, Vittorio Mantero, Michela Morbin, Stefania Saccucci

J Neurol Neurosurg Psychiatry· September 2014

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The peculiar role of the A2V mutation in amyloid-β (Aβ) 1-42 molecular assembly.
Massimo Messa, Laura Colombo, Elena del Favero, Laura Cantù, Tatiana Stoilova, Michela Morbin

J Biol Chem· August 2014

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Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation.
Laura Canafoglia, Michela Morbin, Vidmer Scaioli, Davide Pareyson, Ludovico D'Incerti

Epilepsia· June 2014

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Different mutations at V363 MAPT codon are associated with atypical clinical phenotypes and show unusual structural and functional features.
Giacomina Rossi, Antonio Bastone, Elena Piccoli, Michela Morbin, Giulia Mazzoleni

Neurobiol Aging· February 2014

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Pantethine treatment is effective in recovering the disease phenotype induced by ketogenic diet in a pantothenate kinase-associated neurodegeneration mouse model.
Dario Brunetti, Sabrina Dusi, Carla Giordano, Costanza Lamperti, Michela Morbin

Brain· January 2014

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Coexistence of Charcot-Marie-Tooth disease type 1A and anti-MAG neuropathy.
Giuseppe Piscosquito, Ettore Salsano, Claudia Ciano, Luisa Palamara, Michela Morbin

J Peripher Nerv Syst· June 2013

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Loss of prohibitin membrane scaffolds impairs mitochondrial architecture and leads to tau hyperphosphorylation and neurodegeneration.
Carsten Merkwirth, Paola Martinelli, Anne Korwitz, Michela Morbin, Hella S Brönneke

PLoS Genet· May 2013

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Adult-onset Alexander disease, associated with a mutation in an alternative GFAP transcript, may be phenotypically modulated by a non-neutral HDAC6 variant.
Laura Melchionda, Mingyan Fang, Hairong Wang, Valeria Fugnanesi, Michela Morbin

Orphanet J Rare Dis· May 2013

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Cathepsin F mutations cause Type B Kufs disease, an adult-onset neuronal ceroid lipofuscinosis.
Katherine R Smith, Hans-Henrik M Dahl, Laura Canafoglia, Eva Andermann, John Damiano, Michela Morbin

Hum Mol Genet· April 2013

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Myelin protein zero Arg36Gly mutation with very late onset and rapidly progressive painful neuropathy.
Patrizia Dacci, Franco Taroni, Eleonora Dalla Bella, Micaela Milani, Davide Pareyson, Michela Morbin

J Peripher Nerv Syst· December 2012

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