Antozzi C - Search Results

1

Experience with immunomodulatory treatments in Rasmussen's encephalitis.

Granata T, Fusco L, Gobbi G, Freri E, Ragona F, Broggi G, Mantegazza R, Giordano L, Villani F, Capovilla G, Vigevano F, Bernardina BD, Spreafico R, Antozzi C. Granata T, et al. Among authors: antozzi c. Neurology. 2003 Dec 23;61(12):1807-10. doi: 10.1212/01.wnl.0000099074.04539.e0. Neurology. 2003. PMID: 14694056

2

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNA(Leu)(UUR).

Zeviani M, Gellera C, Antozzi C, Rimoldi M, Morandi L, Villani F, Tiranti V, DiDonato S. Zeviani M, et al. Among authors: antozzi c. Lancet. 1991 Jul 20;338(8760):143-7. doi: 10.1016/0140-6736(91)90136-d. Lancet. 1991. PMID: 1677065

3

Prognosis of myasthenia gravis: a multicenter follow-up study of 844 patients.

Beghi E, Antozzi C, Batocchi AP, Cornelio F, Cosi V, Evoli A, Lombardi M, Mantegazza R, Monticelli ML, Piccolo G, et al. Beghi E, et al. Among authors: antozzi c. J Neurol Sci. 1991 Dec;106(2):213-20. doi: 10.1016/0022-510x(91)90260-e. J Neurol Sci. 1991. PMID: 1802969 Clinical Trial.

4

A short plasma exchange protocol is effective in severe myasthenia gravis.

Antozzi C, Gemma M, Regi B, Berta E, Confalonieri P, Peluchetti D, Mantegazza R, Baggi F, Marconi M, Fiacchino F, et al. Antozzi C, et al. J Neurol. 1991 Apr;238(2):103-7. doi: 10.1007/BF00315690. J Neurol. 1991. PMID: 1856735

5

A multicentre follow-up study of 1152 patients with myasthenia gravis in Italy.

Mantegazza R, Beghi E, Pareyson D, Antozzi C, Peluchetti D, Sghirlanzoni A, Cosi V, Lombardi M, Piccolo G, Tonali P, et al. Mantegazza R, et al. Among authors: antozzi c. J Neurol. 1990 Oct;237(6):339-44. doi: 10.1007/BF00315656. J Neurol. 1990. PMID: 2277266 Clinical Trial.

6

Azathioprine as a single drug or in combination with steroids in the treatment of myasthenia gravis.

Mantegazza R, Antozzi C, Peluchetti D, Sghirlanzoni A, Cornelio F. Mantegazza R, et al. Among authors: antozzi c. J Neurol. 1988 Nov;235(8):449-53. doi: 10.1007/BF00314245. J Neurol. 1988. PMID: 3062134 Clinical Trial.

7

Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA.

Mariotti C, Savarese N, Suomalainen A, Rimoldi M, Comi G, Prelle A, Antozzi C, Servidei S, Jarre L, DiDonato S, Zeviani M. Mariotti C, et al. Among authors: antozzi c. J Neurol. 1995 May;242(5):304-12. doi: 10.1007/BF00878873. J Neurol. 1995. PMID: 7643139

8

Removal of antiacetylcholine receptor antibodies by protein-A immunoadsorption in myasthenia gravis.

Berta E, Confalonieri P, Simoncini O, Bernardi G, Busnach G, Mantegazza R, Cornelio F, Antozzi C. Berta E, et al. Among authors: antozzi c. Int J Artif Organs. 1994 Nov;17(11):603-8. Int J Artif Organs. 1994. PMID: 7744521 Clinical Trial.

9

Protein-A immunoadsorption in immunosuppression-resistant myasthenia gravis.

Antozzi C, Berta E, Confalonieri P, Zuffi M, Cornelio F, Mantegazza R. Antozzi C, et al. Lancet. 1994 Jan 8;343(8889):124. Lancet. 1994. PMID: 7903764 No abstract available.

10

Late-onset riboflavin-responsive myopathy with combined multiple acyl coenzyme A dehydrogenase and respiratory chain deficiency.

Antozzi C, Garavaglia B, Mora M, Rimoldi M, Morandi L, Ursino E, DiDonato S. Antozzi C, et al. Neurology. 1994 Nov;44(11):2153-8. doi: 10.1212/wnl.44.11.2153. Neurology. 1994. PMID: 7969976

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