Federico A - Search Results

1

A second MNGIE patient without typical mitochondrial skeletal muscle involvement.

Cardaioli E, Da Pozzo P, Malfatti E, Battisti C, Gallus GN, Gaudiano C, Macucci M, Malandrini A, Margollicci M, Rubegni A, Dotti MT, Federico A. Cardaioli E, et al. Among authors: federico a. Neurol Sci. 2010 Aug;31(4):491-4. doi: 10.1007/s10072-010-0225-5. Epub 2010 Mar 16. Neurol Sci. 2010. PMID: 20232099

2

A new missense mutation in caveolin-3 gene causes rippling muscle disease.

Dotti MT, Malandrini A, Gambelli S, Salvadori C, De Stefano N, Federico A. Dotti MT, et al. Among authors: federico a. J Neurol Sci. 2006 Apr 15;243(1-2):61-4. doi: 10.1016/j.jns.2005.11.032. Epub 2006 Feb 3. J Neurol Sci. 2006. PMID: 16458928

3

Occurrence of ankylosing spondylitis and multiple sclerosis-like syndrome in a HLA-B27 positive patient.

Mignarri A, Dotti MT, Battisti C, Vallone I, Federico A. Mignarri A, et al. Among authors: federico a. Neurol Sci. 2009 Aug;30(4):329-32. doi: 10.1007/s10072-009-0092-0. Epub 2009 May 15. Neurol Sci. 2009. PMID: 19444380

4

A novel point mutation in the mitochondrial tRNA((Trp)) gene produces late-onset encephalomyopathy, plus additional features.

Malfatti E, Cardaioli E, Battisti C, Da Pozzo P, Malandrini A, Rufa A, Rocchi R, Federico A. Malfatti E, et al. Among authors: federico a. J Neurol Sci. 2010 Oct 15;297(1-2):105-8. doi: 10.1016/j.jns.2010.06.009. Epub 2010 Aug 13. J Neurol Sci. 2010. PMID: 20708751

5

Progressive mitochondrial myopathy, deafness, and sporadic seizures associated with a novel mutation in the mitochondrial tRNASer(AGY) gene.

Cardaioli E, Malfatti E, Da Pozzo P, Gallus GN, Carluccio MA, Rufa A, Volpi N, Dotti MT, Federico A. Cardaioli E, et al. Among authors: federico a. J Neurol Sci. 2011 Apr 15;303(1-2):142-5. doi: 10.1016/j.jns.2010.12.020. Epub 2011 Jan 22. J Neurol Sci. 2011. PMID: 21257182

6

Mitochondria, oxidative stress and neurodegeneration.

Federico A, Cardaioli E, Da Pozzo P, Formichi P, Gallus GN, Radi E. Federico A, et al. J Neurol Sci. 2012 Nov 15;322(1-2):254-62. doi: 10.1016/j.jns.2012.05.030. Epub 2012 Jun 4. J Neurol Sci. 2012. PMID: 22669122 Review.

7

Effects of cerebrolysin administration on oxidative stress-induced apoptosis in lymphocytes from CADASIL patients.

Formichi P, Radi E, Battisti C, Di Maio G, Dotti MT, Muresanu D, Federico A. Formichi P, et al. Among authors: federico a. Neurol Sci. 2013 Apr;34(4):553-6. doi: 10.1007/s10072-012-1174-y. Epub 2012 Aug 10. Neurol Sci. 2013. PMID: 22878905

8

Sporadic myopathy, myoclonus, leukoencephalopathy, neurosensory deafness, hypertrophic cardiomyopathy and insulin resistance associated with the mitochondrial 8306 T>C MTTK mutation.

Cardaioli E, Malfatti E, Battisti C, Da Pozzo P, Rubegni A, Gallus GN, Malandrini A, Federico A. Cardaioli E, et al. Among authors: federico a. J Neurol Sci. 2012 Oct 15;321(1-2):92-5. doi: 10.1016/j.jns.2012.07.027. Epub 2012 Aug 24. J Neurol Sci. 2012. PMID: 22925535

9

Homozygosity and severity of phenotypic presentation in a CADASIL family.

Vinciguerra C, Rufa A, Bianchi S, Sperduto A, De Santis M, Malandrini A, Dotti MT, Federico A. Vinciguerra C, et al. Among authors: federico a. Neurol Sci. 2014 Jan;35(1):91-3. doi: 10.1007/s10072-013-1580-9. Epub 2013 Nov 26. Neurol Sci. 2014. PMID: 24277202

10

A case of 3243A>G mutation in mtDNA presenting as apparently idiopathic hyperCKemia.

Rubegni A, Cardaioli E, Chini E, Da Pozzo P, Battisti C, Malandrini A, Federico A. Rubegni A, et al. Among authors: federico a. J Neurol Sci. 2014 Mar 15;338(1-2):232-4. doi: 10.1016/j.jns.2014.01.010. Epub 2014 Jan 14. J Neurol Sci. 2014. PMID: 24468540

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