Papacci M - Search Results

1

Manifesting heterozygotes in McArdle's disease: clinical, morphological and biochemical studies in a family.

Manfredi G, Silvestri G, Servidei S, Ricci E, Mirabella M, Bertini E, Papacci M, Rana M, Tonali P. Manfredi G, et al. Among authors: papacci m. J Neurol Sci. 1993 Mar;115(1):91-4. doi: 10.1016/0022-510x(93)90071-6. J Neurol Sci. 1993. PMID: 8468596

2

Peripheral neuropathy with giant axons and cardiomyopathy associated with desmin type intermediate filaments in skeletal muscle.

Sabatelli M, Bertini E, Ricci E, Salviati G, Magi S, Papacci M, Tonali P. Sabatelli M, et al. Among authors: papacci m. J Neurol Sci. 1992 May;109(1):1-10. doi: 10.1016/0022-510x(92)90086-z. J Neurol Sci. 1992. PMID: 1517757 Review.

3

Reducing body myopathy and desmin storage in skeletal muscle: morphological and biochemical findings.

Bertini E, Salviati G, Apollo F, Ricci E, Servidei S, Broccolini A, Papacci M, Tonali P. Bertini E, et al. Among authors: papacci m. Acta Neuropathol. 1994;87(1):106-12. doi: 10.1007/BF00386261. Acta Neuropathol. 1994. PMID: 8140891

4

Single-fiber PCR in MELAS(3243) patients: correlations between intratissue distribution and phenotypic expression of the mtDNA(A3243G) genotype.

Silvestri G, Rana M, Odoardi F, Modoni A, Paris E, Papacci M, Tonali P, Servidei S. Silvestri G, et al. Among authors: papacci m. Am J Med Genet. 2000 Sep 18;94(3):201-6. doi: 10.1002/1096-8628(20000918)94:3<201::aid-ajmg5>3.0.co;2-2. Am J Med Genet. 2000. PMID: 10995506

5

Apoptosis and ROS detoxification enzymes correlate with cytochrome c oxidase deficiency in mitochondrial encephalomyopathies.

Di Giovanni S, Mirabella M, Papacci M, Odoardi F, Silvestri G, Servidei S. Di Giovanni S, et al. Among authors: papacci m. Mol Cell Neurosci. 2001 Apr;17(4):696-705. doi: 10.1006/mcne.2001.0970. Mol Cell Neurosci. 2001. PMID: 11312605

6

Pathogenic role of mtDNA duplications in mitochondrial diseases associated with mtDNA deletions.

Odoardi F, Rana M, Broccolini A, Mirabella M, Modoni A, D'Amico A, Papacci M, Tonali P, Servidei S, Silvestri G. Odoardi F, et al. Among authors: papacci m. Am J Med Genet A. 2003 Apr 30;118A(3):247-54. doi: 10.1002/ajmg.a.20006. Am J Med Genet A. 2003. PMID: 12673655

7

Insulin-like growth factor I in inclusion-body myositis and human muscle cultures.

Broccolini A, Ricci E, Pescatori M, Papacci M, Gliubizzi C, D'Amico A, Servidei S, Tonali P, Mirabella M. Broccolini A, et al. Among authors: papacci m. J Neuropathol Exp Neurol. 2004 Jun;63(6):650-9. doi: 10.1093/jnen/63.6.650. J Neuropathol Exp Neurol. 2004. PMID: 15217093

8

MyoD expression restores defective myogenic differentiation of human mesoangioblasts from inclusion-body myositis muscle.

Morosetti R, Mirabella M, Gliubizzi C, Broccolini A, De Angelis L, Tagliafico E, Sampaolesi M, Gidaro T, Papacci M, Roncaglia E, Rutella S, Ferrari S, Tonali PA, Ricci E, Cossu G. Morosetti R, et al. Among authors: papacci m. Proc Natl Acad Sci U S A. 2006 Nov 7;103(45):16995-7000. doi: 10.1073/pnas.0603386103. Epub 2006 Oct 31. Proc Natl Acad Sci U S A. 2006. PMID: 17077152 Free PMC article.

9

A case of CMT 1B due to Val 102/fs null mutation of the MPZ gene presenting as hyperCKemia.

Luigetti M, Modoni A, Renna R, Silvestri G, Ricci E, Montano N, Tasca G, Papacci M, Monforte M, Conte A, Pomponi MG, Sabatelli M. Luigetti M, et al. Among authors: papacci m. Clin Neurol Neurosurg. 2010 Nov;112(9):794-7. doi: 10.1016/j.clineuro.2010.05.001. Epub 2010 May 26. Clin Neurol Neurosurg. 2010. PMID: 20537790

10

Long-term Follow-up and Muscle Imaging Findings in Brachio-Cervical Inflammatory Myopathy.

Lucchini M, Bortolani S, Monforte M, Papacci M, Ricci E, Mirabella M, Tasca G. Lucchini M, et al. Among authors: papacci m. Neurol Neuroimmunol Neuroinflamm. 2021 May 19;8(4):e1016. doi: 10.1212/NXI.0000000000001016. Print 2021 Jul. Neurol Neuroimmunol Neuroinflamm. 2021. PMID: 34011678 Free PMC article.

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