| ‘Autoimmune epilepsy’or exasperated search for the etiology of seizures of unknown origin? P Striano, C Minetti Epilepsy & Behavior 25 (3), 440-441, 2012 | 7 | 2012 |
| “Mitochondrial neuropathies”: A survey from the large cohort of the Italian Network M Mancuso, D Orsucci, C Angelini, E Bertini, V Carelli, GP Comi, ... Neuromuscular Disorders 26 (4-5), 272-276, 2016 | 42 | 2016 |
| 137P FROMThTEGRINS TO ENOS: THE ENDOTHELIAL CELL AS A MECHANORECEPTOR JA Engelman, XL Zhang, F Galbiati, D Volonte, F Sotgia, RG Pestell, ... | | |
| A case of annular lipoatrophy (Ferreira-Marques type) V Venzano, G Cavallero, C Minetti, M Lupi, E Rampini Giornale Italiano di Dermatologia e Venereologia: Organo Ufficiale, Societa …, 1983 | | 1983 |
| A case of congenital neuromuscular disease with uniform type I fibers, abnormal mitochondrial network and jagged Z-line G Pellegrini, S Barbieri, M Moggio, A Cheldi, G Scarlato, C Minetti Neuropediatrics 16 (03), 162-166, 1985 | 17 | 1985 |
| A case of Thomsen's disease associated with hypoparathyroidism G Cordone, A Iester, V Venzano, C Minetti Minerva pediatrica 30 (20), 1629-1634, 1978 | | 1978 |
| A clinical and genetic study of 33 new cases with early-onset absence epilepsy L Giordano, A Vignoli, P Accorsi, J Galli, M Pezzella, M Traverso, ... Epilepsy research 95 (3), 221-226, 2011 | 18 | 2011 |
| A new method for analysis of mitochondrial DNA point mutations and assess levels of heteroplasmy D Cassandrini, MG Calevo, A Tessa, G Manfredi, F Fattori, MC Meschini, ... Biochemical and biophysical research communications 342 (2), 387-393, 2006 | 43 | 2006 |
| A novel hepatocyte nuclear factor-1β (MODY-5) gene mutation in an Italian family with renal dysfunctions and early-onset diabetes. I Carbone, C Barella, C Minetti, GM Ghiggeri, G Caridi, F Perfumo, ... Diabetologia 45 (1), 2002 | 48 | 2002 |
| A novel missense mutation in the glycogen branching enzyme gene in a child with myopathy and hepatopathy C Bruno, M DiRocco, LD Lamba, M Bado, C Marino, S Tsujino, S Shanske, ... Neuromuscular Disorders 9 (6-7), 403-407, 1999 | 30 | 1999 |
| A novel mtDNA deletion associated with primary adrenal insufficiency.† 594 C Bruno, Y Tang, FM Santorelli, C Minetti, M Bado, G Cordone, ... Pediatric Research 41 (4), 101-101, 1997 | | 1997 |
| A NOVEL MUTATION IN THE SCO2 GENE IN A NEONATE WITH FATAL INFANTILE CARDIOENCEPHALOMYOPATHY AND COX DEFICIENCY C Bellini, D Cassandrini, C Savioli, D Massocco, M Marasini, S Stringara, ... Neuropediatrics 37 (S 1), MP75, 2006 | | 2006 |
| A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency C Bruno, R Biancheri, B Garavaglia, C Biedi, A Rossi, LD Lamba, M Bado, ... Journal of child neurology 17 (3), 233-236, 2002 | 45 | 2002 |
| A Novel SCN2A Mutation in Family with Benign Familial Infantile Seizures P Striano, L Bordo, ML Lispi, N Specchio, C Minetti, F Vigevano, F Zara Epilepsia 47 (1), 218-220, 2006 | 114 | 2006 |
| A NOVEL WHITE MATTER DISORDER WITH CEREBRAL HYPOMYELINATION AND CONGENITAL CATARACT R Biancheri, F Zara, A Rossi, C Bruno, L Bordo, S Gianotti, S Assereto, ... Neuropediatrics 37 (S 1), MP110, 2006 | | 2006 |
| A proof‐of‐concept trial of the whey protein alfa‐lactalbumin in chronic cortical myoclonus L Errichiello, M Pezzella, L Santulli, S Striano, F Zara, C Minetti, ... Movement disorders 26 (14), 2573-2575, 2011 | 19 | 2011 |
| A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus R Roberti, A Riva, G D’Onofrio, E Giacheri, E Amadori, MS Vari, ... Expert Review of Neurotherapeutics 24 (2), 133-138, 2024 | | 2024 |
| A proposed score tool with which to define abnormalities on muscle biopsy from children with juvenile dermatomyositis. LR Wedderburn, H Varsani, CK Li, AA Amato, B Banwell, KE Bove, ... WILEY-LISS 54 (9), S657-S658, 2006 | 1 | 2006 |
| Abnormal circadian rhythm in patients with GRIN1-related developmental epileptic encephalopathy M Scala, E Amadori, L Fusco, F Marchese, V Capra, C Minetti, MS Vari, ... European Journal of Paediatric Neurology 23 (4), 657-661, 2019 | 7 | 2019 |
| Abnormalities in the expression of β‐spectrin in Duchenne muscular dystrophy C Minetti, K Tanji, PG Rippa, G Morreale, G Cordone, E Bonilla Neurology 44 (6), 1149-1149, 1994 | 21 | 1994 |
Michael P. Lisanti, MD-PhD, FRSA, FR...Professor and Chair of Translational Medicine, University of Salford (Greater Manchester)Verified email at salford.ac.uk