Andreetta F - Search Results

1

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.

Moraes CT, Shanske S, Tritschler HJ, Aprille JR, Andreetta F, Bonilla E, Schon EA, DiMauro S. Moraes CT, et al. Among authors: andreetta f. Am J Hum Genet. 1991 Mar;48(3):492-501. Am J Hum Genet. 1991. PMID: 1998336 Free PMC article.

2

Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.

Andreetta F, Tritschler HJ, Schon EA, DiMauro S, Bonilla E. Andreetta F, et al. J Neurol Sci. 1991 Sep;105(1):88-92. doi: 10.1016/0022-510x(91)90123-o. J Neurol Sci. 1991. PMID: 1665507 Free article.

3

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA.

Tritschler HJ, Andreetta F, Moraes CT, Bonilla E, Arnaudo E, Danon MJ, Glass S, Zelaya BM, Vamos E, Telerman-Toppet N, et al. Tritschler HJ, et al. Among authors: andreetta f. Neurology. 1992 Jan;42(1):209-17. doi: 10.1212/wnl.42.1.209. Neurology. 1992. PMID: 1734306

4

Replication-competent human mitochondrial DNA lacking the heavy-strand promoter region.

Moraes CT, Andreetta F, Bonilla E, Shanske S, DiMauro S, Schon EA. Moraes CT, et al. Among authors: andreetta f. Mol Cell Biol. 1991 Mar;11(3):1631-7. doi: 10.1128/mcb.11.3.1631-1637.1991. Mol Cell Biol. 1991. PMID: 1996112 Free PMC article.

5

Differential diagnosis of fatal and benign cytochrome c oxidase-deficient myopathies of infancy: an immunohistochemical approach.

Tritschler HJ, Bonilla E, Lombes A, Andreetta F, Servidei S, Schneyder B, Miranda AF, Schon EA, Kadenbach B, DiMauro S. Tritschler HJ, et al. Among authors: andreetta f. Neurology. 1991 Feb;41(2 ( Pt 1)):300-5. doi: 10.1212/wnl.41.2_part_1.300. Neurology. 1991. PMID: 1846953

6

Mitochondrial myopathy simulating spinal muscular atrophy.

Pons R, Andreetta F, Wang CH, Vu TH, Bonilla E, DiMauro S, De Vivo DC. Pons R, et al. Among authors: andreetta f. Pediatr Neurol. 1996 Sep;15(2):153-8. doi: 10.1016/0887-8994(96)00118-x. Pediatr Neurol. 1996. PMID: 8888051 Free article.

7

Sequential antibodies to potassium channels and glutamic acid decarboxylase in neuromyotonia.

Antozzi C, Frassoni C, Vincent A, Regondi MC, Andreetta F, Bernasconi P, Ciano C, Chang T, Cornelio F, Spreafico R, Mantegazza R. Antozzi C, et al. Among authors: andreetta f. Neurology. 2005 Apr 12;64(7):1290-3. doi: 10.1212/01.WNL.0000156945.39471.2C. Neurology. 2005. PMID: 15824370

8

Complete stable remission and autoantibody specificity in myasthenia gravis.

Baggi F, Andreetta F, Maggi L, Confalonieri P, Morandi L, Salerno F, Bernasconi P, Montomoli C, Barberis M, Mantegazza R, Antozzi C. Baggi F, et al. Among authors: andreetta f. Neurology. 2013 Jan 8;80(2):188-95. doi: 10.1212/WNL.0b013e31827b907b. Epub 2012 Dec 19. Neurology. 2013. PMID: 23255823

9

Non-paraneoplastic voltage-gated calcium channels antibody-mediated cerebellar ataxia responsive to IVIG treatment.

Rigamonti A, Lauria G, Stanzani L, Mantero V, Andreetta F, Salmaggi A. Rigamonti A, et al. Among authors: andreetta f. J Neurol Sci. 2014 Jan 15;336(1-2):169-70. doi: 10.1016/j.jns.2013.10.031. Epub 2013 Oct 29. J Neurol Sci. 2014. PMID: 24215945

10

Cognitive and neuropsychological evolution in children with anti-NMDAR encephalitis.

Matricardi S, Patrini M, Freri E, Ragona F, Zibordi F, Andreetta F, Nardocci N, Granata T. Matricardi S, et al. Among authors: andreetta f. J Neurol. 2016 Apr;263(4):765-71. doi: 10.1007/s00415-016-8056-9. Epub 2016 Feb 17. J Neurol. 2016. PMID: 26886205

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