Search Results - "Reni, Lizia"

COVID-19-related and not related Guillain-Barré syndromes share the same management pitfalls during lock down: The experience of Liguria region in Italy by Garnero, Martina, Del Sette, Massimo, Assini, Andrea, Beronio, Alessandro, Capello, Elisabetta, Cabona, Corrado, Reni, Lizia, Serrati, Carlo, Bandini, Fabio, Granata, Alfredo, Pesce, Giampaola, Mancardi, Giovanni L., Uccelli, Antonio, Schenone, Angelo, Benedetti, Luana

“…Recently, during the pandemic infection of the novel SARS-CoV-2, some cases of Guillan-Barré Syndrome (GBS) have been reported. The aim of this work is to…”
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Isolated musculocutaneous nerve involvement in COVID-19 related Neuralgic amyotrophy. Comment on: “Neuralgic amyotrophy and COVID-19 infection: 2 cases of spinal accessory nerve palsy” by Coll et al. Joint Bone Spine 2021;88:105196 by Cabona, Corrado, Zaottini, Federico, Pistoia, Federico, Grisanti, Stefano, Schenone, Cristina, Villani, Flavio, Schenone, Angelo, Aloé, Teresita, Reni, Lizia, Benedetti, Luana

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Contribution of ultrasound in the assessment of patients with suspect idiopathic pudendal nerve disease by Tagliafico, Alberto, Bignotti, Bianca, Miguel Perez, Maribel, Reni, Lizia, Bodner, Gerd, Martinoli, Carlo

“…Highlights • Diagnosis of pudendal neuralgia is difficult and classical diagnostic criteria are not sufficient for all clinical situations. • High-resolution…”
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Dysimmune mononeuropathies: A diagnosis not to be missed by Garnero, Martina, Martinoli, Carlo, Tagliafico, Alberto, Bignotti, Bianca, Benedetti, Luana, Beronio, Alessandro, Reni, Lizia, Grandis, Marina, Mancardi, Giovanni Luigi, Schenone, Angelo

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Influence of comorbidities on the phenotype of patients affected by Charcot–Marie–Tooth neuropathy type 1A by Ursino, Giulia, Alberti, M. Antonia, Grandis, Marina, Reni, Lizia, Pareyson, Davide, Bellone, Emilia, Gemelli, Chiara, Sabatelli, Mario, Pisciotta, Chiara, Luigetti, Marco, Santoro, Lucio, Massollo, Laura, Schenone, Angelo

“…Abstract Charcot–Marie–Tooth type 1A (CMT1A) is the most common inherited neuropathy. The phenotype of patients affected by CMT1A is highly variable and may be…”
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Outcome measures and rehabilitation treatment in patients affected by Charcot-Marie-Tooth neuropathy: a pilot study by Maggi, Giovanni, Monti Bragadin, Margherita, Padua, Luca, Fiorina, Elisabetta, Bellone, Emilia, Grandis, Marina, Reni, Lizia, Bennicelli, Alessandra, Grosso, Manuela, Saporiti, Riccardo, Scorsone, Debora, Zuccarino, Riccardo, Crimi, Emanuele, Schenone, Angelo

“…: We evaluated the sensitivity of various rehabilitation and lung function scales to detect differences between people with Charcot-Marie-Tooth (CMT) disease…”
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Innovative quantitative testing of hand function in Charcot‐Marie‐Tooth neuropathy by Alberti, Maria A., Mori, Laura, Francini, Luca, Poggi, Ilaria, Monti Bragadin, Margherita, Bellone, Emilia, Grandis, Marina, Maggi, Giovanni, Reni, Lizia, Sormani, Maria P., Tacchino, Andrea, Padua, Luca, Prada, Valeria, Bove, Marco, Schenone, Angelo

“…To describe a new test to quantitatively evaluate hand function in patients affected by Charcot‐Marie‐Tooth neuropathy (CMT). The sensor‐engineered glove test…”
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Brown-Vialetto-Van Laere syndrome: Clinical and neuroradiological findings of a genetically proven patient by Bandettini Di Poggio, Monica, Monti Bragadin, Margherita, Reni, Lizia, Doria-Lamba, Laura, Cereda, Cristina, Pardini, Matteo, Roccatagliata, Luca, Rossi, Andrea, Schenone, Angelo

“…Abstract The Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare neurological disorder characterized by progressive pontobulbar palsy, sensorineural deafness…”
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Influence of comorbidities on the phenotype of patients affected by CharcotaMarieaTooth neuropathy type 1A by Ursino, Giulia, Alberti, M, Grandis, Marina, Reni, Lizia, Pareyson, Davide, Bellone, Emilia, Gemelli, Chiara, Sabatelli, Mario, Pisciotta, Chiara, Luigetti, Marco, Santoro, Lucio, Massollo, Laura, Schenone, Angelo

“…CharcotaMarieaTooth type 1A (CMT1A) is the most common inherited neuropathy. The phenotype of patients affected by CMT1A is highly variable and may be…”
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The spectrum of GNE mutations: allelic heterogeneity for a common phenotype by Grandis, Marina, Gulli, Rossella, Cassandrini, Denise, Gazzerro, Elisabetta, Benedetti, Luana, Narciso, Eleonora, Nobbio, Lucilla, Bruno, Claudio, Minetti, Carlo, Bellone, Emilia, Reni, Lizia, Mancardi, Giovanni Luigi, Mandich, Paola, Schenone, Angelo

“…Hereditary inclusion body myopathy (IBM2) was mainly reported in Middle Eastern Jewish patients. Distal myopathy with rimmed vacuoles has been described as a…”
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PREVALENCE OF DIABETIC NEUROPATHIC PAIN IN A POPULATION OF PATIENTS OBSERVED IN THE SETTING OF AN INTERDISCIPLINARY TEAM FOR DIABETIC NEUROPATHY by Torti, Roberta, Reni, Lizia, Schenone, Angelo, Viviani, Giorgio, Mostarda, Federica

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Thalidomide in agnogenic and secondary myelofibrosis by Canepa, Letizia, Ballerini, Filippo, Varaldo, Riccardo, Quintino, Sabrina, Reni, Lizia, Clavio, Marino, Miglino, Maurizio, Pierri, Ivana, Gobbi, Marco

“…Myelofibrosis with myeloid metaplasia (MMM) is a clonal disorder involving disregulation of angiogenesis and immunomodulatory mechanisms. Thalidomide (Thal)…”
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Postvibration Depression of the H-Reflex as a Result of a Dual Mechanism: An Experimental Study in Humans by Abbruzzese, Michele, Minatel, Cinzia, Reni, Lizia, Favale, Emilio

“…SUMMARY Changes in amplitude of the soleus H (SH)-reflex and its neurographic correlates (P1 and P2 waves) after vibration of the soleus muscle have been…”
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Presynaptic and postsynaptic mechanisms underlying H-reflex changes produced by a selective voluntary contraction by Abbruzzese, Michele, Reni, Lizia, Minatel, Cinzia, Favale, Emilio

“…Concurrent recordings of (i) the soleus H reflex and (ii) the underlying afferent (P1) and efferent (P2) neural volleys were performed during a protracted,…”
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Interindividual variability of central delay changes in the soleus H reflex pathway by Abbruzzese, M, Reni, L, Favale, E

“…Central delay (CD) changes in the soleus H reflex pathway, as demonstrated by variations in the time interval between afferent (P1) and efferent (P2)…”
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Brown-Vialetto-Van Laere syndrome: Clinical and neuroradiological findings of a genetically proven patient by Bandettini Di Poggio, Monica, Monti Bragadin, Margherita, Reni, Lizia, Doria-Lamba, Laura, Cereda, Cristina, Pardini, Matteo, Roccatagliata, Luca, Rossi, Andrea, Schenone, Angelo

“…The Brown-Vialetto-Van Laere syndrome (BVVLS) is a rare neurological disorder characterized by progressive pontobulbar palsy, sensorineural deafness and mixed…”
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