Mignogna T - Search Results

1

Pure motor chronic inflammatory demyelinating polyneuropathy.

Sabatelli M, Madia F, Mignogna T, Lippi G, Quaranta L, Tonali P. Sabatelli M, et al. Among authors: mignogna t. J Neurol. 2001 Sep;248(9):772-7. doi: 10.1007/s004150170093. J Neurol. 2001. PMID: 11596782

2

Interferon-alpha may benefit steroid unresponsive chronic inflammatory demyelinating polyneuropathy.

Sabatelli M, Mignogna T, Lippi G, Milone M, Di Lazzaro V, Tonali P, Bertini E. Sabatelli M, et al. Among authors: mignogna t. J Neurol Neurosurg Psychiatry. 1995 May;58(5):638-9. doi: 10.1136/jnnp.58.5.638. J Neurol Neurosurg Psychiatry. 1995. PMID: 7745420 Free PMC article. No abstract available.

3

Intramyelinic edema in chronic inflammatory demyelinating polyneuropathy.

Sabatelli M, Mignogna T, Lippi G, Porcu C, Tonali P. Sabatelli M, et al. Among authors: mignogna t. Clin Neuropathol. 1996 Jan-Feb;15(1):17-21. Clin Neuropathol. 1996. PMID: 8998850

4

Acute axonal idiopathic polyneuropathy: a Guillain-Barré syndrome variant?

Magi S, Sabatelli M, Mignogna T, Porcu C, Tonali P. Magi S, et al. Among authors: mignogna t. Ital J Neurol Sci. 1992 Sep;13(6):481-6. doi: 10.1007/BF02230868. Ital J Neurol Sci. 1992. PMID: 1428785

5

Chronic progressive steroid responsive axonal polyneuropathy: a CIDP vaariant or a primary axonal disorder?

Uncini A, Sabatelli M, Mignogna T, Lugaresi A, Liguori R, Montagna P. Uncini A, et al. Among authors: mignogna t. Muscle Nerve. 1996 Mar;19(3):365-71. doi: 10.1002/(SICI)1097-4598(199603)19:3<365::AID-MUS14>3.0.CO;2-R. Muscle Nerve. 1996. PMID: 8606703

6

Hereditary motor and sensory neuropathy with deafness, mental retardation, and absence of sensory large myelinated fibers: confirmation of a new entity.

Sabatelli M, Mignogna T, Lippi G, Servidei S, Zollino M, Padua L, Lo Monaco M, De Armas L, Mereu ML, Tonali P. Sabatelli M, et al. Among authors: mignogna t. Am J Med Genet. 1998 Jan 23;75(3):309-13. Am J Med Genet. 1998. PMID: 9475604

7

Familial spastic paraplegia, axonal sensory-motor polyneuropathy and bulbar amyotrophy with facial dysmorphia: new cases of Troyer-like syndrome.

Bertini E, Sabatelli M, Di Capua M, Cilio MR, Mignogna T, Federico A, Tonali P. Bertini E, et al. Among authors: mignogna t. Eur J Paediatr Neurol. 1998;2(5):245-54. doi: 10.1016/s1090-3798(98)80038-x. Eur J Paediatr Neurol. 1998. PMID: 10726827 Review.

8

Autosomal recessive hypermyelinating neuropathy.

Sabatelli M, Mignogna T, Lippi G, Servidei S, Manfredi G, Ricci E, Bertini E, Lo Monaco M, Tonali P. Sabatelli M, et al. Among authors: mignogna t. Acta Neuropathol. 1994;87(4):337-42. doi: 10.1007/BF00313601. Acta Neuropathol. 1994. PMID: 8017168

9

Gliomatosis cerebri: report of an atypical case.

di Trapani G, Sabatelli M, Carnevale A, Colosimo C, Mignogna T, Tonali P. di Trapani G, et al. Among authors: mignogna t. Clin Neuropathol. 1995 Jan-Feb;14(1):13-8. Clin Neuropathol. 1995. PMID: 7729074

10

Differential electrophysiological features of neuropathies associated with 17p11.2 deletion and duplication.

Uncini A, Di Guglielmo G, Di Muzio A, Gambi D, Sabatelli M, Mignogna T, Tonali P, Marzella R, Finelli P, Archidiacono N, et al. Uncini A, et al. Among authors: mignogna t. Muscle Nerve. 1995 Jun;18(6):628-35. doi: 10.1002/mus.880180610. Muscle Nerve. 1995. PMID: 7753126

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