1. A 52‐Year‐Old Man with Myoclonic Jerks. (March 2016) Authors: Giaccone, Giorgio; Carella, Francesco; Parravicini, Carlo; Longhi, Erika; Chiapparini, Luisa; Savoiardo, Mario; Montano, Nicola; Morbin, Michela; Albanese, Alberto; Tagliavini, Fabrizio Journal: Brain pathology Issue: Volume 26:Number 2(2016) Page Start: 291 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Coexistence of Charcot‐Marie‐Tooth disease type 1A and anti‐MAG neuropathy. Issue 2 (19th June 2013) Authors: Piscosquito, Giuseppe; Salsano, Ettore; Ciano, Claudia; Palamara, Luisa; Morbin, Michela; Pareyson, Davide Journal: Journal of the peripheral nervous system Issue: Volume 18:Issue 2(2013) Page Start: 185 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Electroclinical spectrum of the neuronal ceroid lipofuscinoses associated with CLN6 mutations. (28th July 2015) Authors: Canafoglia, Laura; Gilioli, Isabella; Invernizzi, Federica; Sofia, Vito; Fugnanesi, Valeria; Morbin, Michela; Chiapparini, Luisa; Granata, Tiziana; Binelli, Simona; Scaioli, Vidmer; Garavaglia, Barbara; Nardocci, Nardo; Berkovic, Samuel F.; Franceschetti, Silvana Journal: Neurology Issue: Volume 85:Number 4(2015) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Heterozygous D90A-SOD1 mutation in a patient with facial onset sensory motor neuronopathy (FOSMN) syndrome: a bridge to amyotrophic lateral sclerosis. Issue 9 (3rd March 2014) Authors: Dalla Bella, Eleonora; Rigamonti, Andrea; Mantero, Vittorio; Morbin, Michela; Saccucci, Stefania; Gellera, Cinzia; Mora, Gabriele; Lauria, Giuseppe Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 85:Issue 9(2014) Page Start: 1009 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Measles Inclusion‐Body Encephalitis: Neuronal Phosphorylated Tau Protein is Present in the Biopsy but not in the Autoptic Specimens of the Same Patient. (13th December 2015) Authors: Maderna, Emanuela; Fugnanesi, Valeria; Morbin, Michela; Cacciatore, Francesca; Spinello, Sonia; Godani, Massimiliano; Zoia, Riccardo; Tagliavini, Fabrizio; Giaccone, Giorgio Journal: Brain pathology Issue: Volume 26:Number 4(2016) Page Start: 542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. NO-donor thiacarbocyanines as multifunctional agents for Alzheimer's disease. Issue 15 (1st August 2015) Authors: Chegaev, Konstantin; Federico, Antonella; Marini, Elisabetta; Rolando, Barbara; Fruttero, Roberta; Morbin, Michela; Rossi, Giacomina; Fugnanesi, Valeria; Bastone, Antonio; Salmona, Mario; Badiola, Nahuai B.; Gasparini, Laura; Cocco, Sara; Ripoli, Cristian; Grassi, Claudio; Gasco, Alberto Journal: Bioorganic & medicinal chemistry Issue: Volume 23:Issue 15(2015) Page Start: 4688 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Novel mutation of the P0 extracellular domain causes a Déjérine-Sottas syndrome. Issue 3 (1st March 1999) Authors: Fabrizi, Gian Maria; Cavallaro, Tiziana; Morbin, Michela; Simonati, Alessandro; Taioli, Federica; Rizzuto, Nicolo' Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 66:Issue 3(1999) Page Start: 386 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Rapid progression of late onset axonal Charcot–Marie–Tooth disease associated with a novel MPZ mutation in the extracellular domain. Issue 11 (16th October 2007) Authors: Laurà, Matilde; Milani, Micaela; Morbin, Michela; Moggio, Maurizio; Ripolone, Michela; Jann, Stefano; Scaioli, Vidmer; Taroni, Franco; Pareyson, Davide Journal: Journal of neurology, neurosurgery and psychiatry Issue: Volume 78:Issue 11(2007) Page Start: 1263 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Recurrent generalized seizures, visual loss, and palinopsia as phenotypic features of neuronal ceroid lipofuscinosis due to progranulin gene mutation. Issue 6 (29th April 2014) Authors: Canafoglia, Laura; Morbin, Michela; Scaioli, Vidmer; Pareyson, Davide; D'Incerti, Ludovico; Fugnanesi, Valeria; Tagliavini, Fabrizio; Berkovic, Samuel F.; Franceschetti, Silvana Journal: Epilepsia Issue: Volume 55:Issue 6(2014:Jun.) Page Start: e56 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Screening for SH3TC2 gene mutations in a series of demyelinating recessive Charcot‐Marie‐Tooth disease (CMT4). Issue 3 (September 2016) Authors: Piscosquito, Giuseppe; Saveri, Paola; Magri, Stefania; Ciano, Claudia; Gandioli, Claudia; Morbin, Michela; Bella, Daniela D.; Moroni, Isabella; Taroni, Franco; Pareyson, Davide Journal: Journal of the peripheral nervous system Issue: Volume 21:Issue 3(2016) Page Start: 142 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗