Formichi P - Search Results

1

Novel Biomarkers for Limb Girdle Muscular Dystrophy (LGMD).

Aguti S, Gallus GN, Bianchi S, Salvatore S, Rubegni A, Berti G, Formichi P, De Stefano N, Malandrini A, Lopergolo D. Aguti S, et al. Among authors: formichi p. Cells. 2024 Feb 10;13(4):329. doi: 10.3390/cells13040329. Cells. 2024. PMID: 38391941 Free PMC article.

2

Fibroblast growth factor 21 and grow differentiation factor 15 are sensitive biomarkers of mitochondrial diseases due to mitochondrial transfer-RNA mutations and mitochondrial DNA deletions.

Formichi P, Cardone N, Taglia I, Cardaioli E, Salvatore S, Gerfo AL, Simoncini C, Montano V, Siciliano G, Mancuso M, Malandrini A, Federico A, Dotti MT. Formichi P, et al. Neurol Sci. 2020 Dec;41(12):3653-3662. doi: 10.1007/s10072-020-04422-5. Epub 2020 Jun 6. Neurol Sci. 2020. PMID: 32504279

3

Analysis of opa1 isoforms expression and apoptosis regulation in autosomal dominant optic atrophy (ADOA) patients with mutations in the opa1 gene.

Formichi P, Radi E, Giorgi E, Gallus GN, Brunetti J, Battisti C, Rufa A, Dotti MT, Franceschini R, Bracci L, Federico A. Formichi P, et al. J Neurol Sci. 2015 Apr 15;351(1-2):99-108. doi: 10.1016/j.jns.2015.02.047. Epub 2015 Mar 6. J Neurol Sci. 2015. PMID: 25796301

4

Human peripheral blood lymphocytes and fibroblasts as Notch3 expression models.

Di Maio G, Formichi P, Radi E, Bianchi S, Onnis A, Tarquini E, Leoncini L, Federico A. Di Maio G, et al. Among authors: formichi p. J Cell Physiol. 2012 Apr;227(4):1771-5. doi: 10.1002/jcp.22901. J Cell Physiol. 2012. PMID: 21702048

5

HTRA1 expression profile and activity on TGF-β signaling in HTRA1 mutation carriers.

Fasano A, Formichi P, Taglia I, Bianchi S, Di Donato I, Battisti C, Federico A, Dotti MT. Fasano A, et al. Among authors: formichi p. J Cell Physiol. 2020 Oct;235(10):7120-7127. doi: 10.1002/jcp.29609. Epub 2020 Feb 4. J Cell Physiol. 2020. PMID: 32017060

6

DNA end labelling (TUNEL) in a 3 year old girl with Leigh syndrome and prevalent cortical involvement.

Formichi P, Malandrini A, Battisti C, Santorelli FM, Gambelli S, Tripodi SA, Berti G, Salvadori C, Tessa A, Federico A. Formichi P, et al. J Neurol Neurosurg Psychiatry. 2004 Jun;75(6):930-2. doi: 10.1136/jnnp.2003.016410. J Neurol Neurosurg Psychiatry. 2004. PMID: 15146020 Free PMC article.

7

Mitochondria, oxidative stress and neurodegeneration.

Federico A, Cardaioli E, Da Pozzo P, Formichi P, Gallus GN, Radi E. Federico A, et al. Among authors: formichi p. 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.

8

Hereditary diffuse leukoencephalopathy with axonal spheroids: three patients with stroke-like presentation carrying new mutations in the CSF1R gene.

Battisti C, Di Donato I, Bianchi S, Monti L, Formichi P, Rufa A, Taglia I, Cerase A, Dotti MT, Federico A. Battisti C, et al. Among authors: formichi p. J Neurol. 2014 Apr;261(4):768-72. doi: 10.1007/s00415-014-7257-3. Epub 2014 Feb 16. J Neurol. 2014. PMID: 24532199

9

Evidence of apoptosis via TUNEL staining in muscle biopsy from patients with mitochondrial encephaloneuromyopathies.

Formichi P, Battisti C, Bianchi S, Cardaioli E, Federico A. Formichi P, et al. J Submicrosc Cytol Pathol. 2003 Jan;35(1):29-34. J Submicrosc Cytol Pathol. 2003. PMID: 12762649

10

Genetic leukoencephalopathies with unknown metabolic pathogenesis.

Federico A, Rufa A, Battisti C, Bianchi S, Cardaioli E, Da Pozzo P, De Stefano N, Formichi P, Sicurelli F, Dotti MT. Federico A, et al. Among authors: formichi p. Neurol Sci. 2001 Nov;22 Suppl 2:S108-12. doi: 10.1007/s100720100046. Neurol Sci. 2001. PMID: 11794472 Review.

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