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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 1
1988 1
1993 1
1996 1
2000 1
2014 2
2017 2
2018 7
2019 3
2020 7
2021 4
2022 5
2023 1
2024 0

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30 results

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Page 1
Vitamin D in Neurological Diseases.
Plantone D, Primiano G, Manco C, Locci S, Servidei S, De Stefano N. Plantone D, et al. Among authors: primiano g. Int J Mol Sci. 2022 Dec 21;24(1):87. doi: 10.3390/ijms24010087. Int J Mol Sci. 2022. PMID: 36613531 Free PMC article. Review.
Myoclonus in mitochondrial disorders.
Mancuso M, Orsucci D, Angelini C, Bertini E, Catteruccia M, Pegoraro E, Carelli V, Valentino ML, Comi GP, Minetti C, Bruno C, Moggio M, Ienco EC, Mongini T, Vercelli L, Primiano G, Servidei S, Tonin P, Scarpelli M, Toscano A, Musumeci O, Moroni I, Uziel G, Santorelli FM, Nesti C, Filosto M, Lamperti C, Zeviani M, Siciliano G. Mancuso M, et al. Among authors: primiano g. Mov Disord. 2014 May;29(6):722-8. doi: 10.1002/mds.25839. Epub 2014 Feb 7. Mov Disord. 2014. PMID: 24510442
It is not strictly linked to a specific genotype or phenotype, and only 1 of 3 patients with MERRF harbors the 8344A>G mutation (frequently labeled as "the MERRF mutation"). Finally, myoclonus is not inextricably linked to epilepsy in MERRF patients, but more to cerebel …
It is not strictly linked to a specific genotype or phenotype, and only 1 of 3 patients with MERRF harbors the 8344A>G mutation (f …
Mitochondrial epilepsy: a cross-sectional nationwide Italian survey.
Ticci C, Sicca F, Ardissone A, Bertini E, Carelli V, Diodato D, Di Vito L, Filosto M, La Morgia C, Lamperti C, Martinelli D, Moroni I, Musumeci O, Orsucci D, Pancheri E, Peverelli L, Primiano G, Rubegni A, Servidei S, Siciliano G, Simoncini C, Tonin P, Toscano A, Mancuso M, Santorelli FM. Ticci C, et al. Among authors: primiano g. Neurogenetics. 2020 Apr;21(2):87-96. doi: 10.1007/s10048-019-00601-5. Epub 2020 Jan 3. Neurogenetics. 2020. PMID: 31900734
Eighty of 90 patients (89%) displayed a 50-100% reduction of seizures on AEDs; levetiracetam was the most commonly used. Forty-one patients (42%) carried the m.3243A>G mutation, 16 (16%) the m.8344A>G, and 9 (9%) nuclear DNA (nDNA) mutations. ...
Eighty of 90 patients (89%) displayed a 50-100% reduction of seizures on AEDs; levetiracetam was the most commonly used. Forty-one patients …
Hearing Impairment and Neuroimaging Results in Mitochondrial Diseases.
Cadoni G, Primiano G, Picciotti PM, Calandrelli R, Galli J, Servidei S, Conti G. Cadoni G, et al. Among authors: primiano g. J Pers Med. 2023 Aug 29;13(9):1329. doi: 10.3390/jpm13091329. J Pers Med. 2023. PMID: 37763097 Free PMC article.
Neuroimaging evaluations considered global MRI abnormalities or structural brain changes. In total, 19/34 patients carried the m.3243A > G mutation (6 affected by MELAS, 12 affected by MIDD, and 1 affected by PEO); 11 had an mtDNA deletion (all affected by PEO); 3 had n …
Neuroimaging evaluations considered global MRI abnormalities or structural brain changes. In total, 19/34 patients carried the m.3243A > …
Purification and characterization of class mu glutathione S-transferase isozymes from rabbit hepatic tissue.
Primiano T, Novak RF. Primiano T, et al. Arch Biochem Biophys. 1993 Mar;301(2):404-10. doi: 10.1006/abbi.1993.1163. Arch Biochem Biophys. 1993. PMID: 8460949
Phenobarbital, 3-methylcholanthrene, and pyridine have failed to enhance the expression of class mu GST isozymes in rabbit hepatic tissue (T. Primiano, S. G. Kim, and R. F. Novak, Toxicol. Appl. Pharmacol., 113, 64-73, 1992). ...
Phenobarbital, 3-methylcholanthrene, and pyridine have failed to enhance the expression of class mu GST isozymes in rabbit hepatic tissue (T …
A Metabolic Signature of Hereditary Transthyretin Amyloidosis: A Pilot Study.
Luigetti M, Guglielmino V, Romano A, Sciarrone MA, Vitali F, Sabino A, Gervasoni J, Primiano A, Santucci L, Moroni R, Primiano G. Luigetti M, et al. Among authors: primiano g, primiano a. Int J Mol Sci. 2022 Dec 17;23(24):16133. doi: 10.3390/ijms232416133. Int J Mol Sci. 2022. PMID: 36555770 Free PMC article.
Biallelic SQSTM1 mutations in early-onset, variably progressive neurodegeneration.
Muto V, Flex E, Kupchinsky Z, Primiano G, Galehdari H, Dehghani M, Cecchetti S, Carpentieri G, Rizza T, Mazaheri N, Sedaghat A, Vahidi Mehrjardi MY, Traversa A, Di Nottia M, Kousi MM, Jamshidi Y, Ciolfi A, Caputo V, Malamiri RA, Pantaleoni F, Martinelli S, Jeffries AR, Zeighami J, Sherafat A, Di Giuda D, Shariati GR, Carrozzo R, Katsanis N, Maroofian R, Servidei S, Tartaglia M. Muto V, et al. Among authors: primiano g. Neurology. 2018 Jul 24;91(4):e319-e330. doi: 10.1212/WNL.0000000000005869. Epub 2018 Jun 29. Neurology. 2018. PMID: 29959261 Free PMC article.
Spinal Cord Involvement in Adult Mitochondrial Diseases: A Cohort Study.
Primiano G, Mariotti P, Turrini I, Sancricca C, Sabino A, Torraco A, Carrozzo R, Servidei S. Primiano G, et al. Life (Basel). 2021 Dec 21;12(1):5. doi: 10.3390/life12010005. Life (Basel). 2021. PMID: 35054398 Free PMC article.
While the clinical manifestations and the corresponding radiological findings of the brain involvement in mitochondrial diseases (e.g., stroke-like episodes, signal changes of the basal ganglia, cerebral and cerebellar atrophy) are well known, at present there are few data …
While the clinical manifestations and the corresponding radiological findings of the brain involvement in mitochondrial diseases (e.g …
Small fibre neuropathy in mitochondrial diseases explored with sudoscan.
Luigetti M, Primiano G, Cuccagna C, Bernardo D, Sauchelli D, Vollono C, Servidei S. Luigetti M, et al. Among authors: primiano g. Clin Neurophysiol. 2018 Aug;129(8):1618-1623. doi: 10.1016/j.clinph.2018.04.755. Epub 2018 Jun 1. Clin Neurophysiol. 2018. PMID: 29890373
METHODS: In order to investigate the involvement of small fibres in MDs we performed extensive neurophysiological test (nerve conduction studies; sympathetic skin response; sudoscan) in 27 patients with genetic diagnosis of MD (7 m.3243A > G; 4 m.8344A > G; 9 …
METHODS: In order to investigate the involvement of small fibres in MDs we performed extensive neurophysiological test (nerve conduction stu …
Choroid plexus recovery after transient forebrain ischemia: role of growth factors and other repair mechanisms.
Johanson CE, Palm DE, Primiano MJ, McMillan PN, Chan P, Knuckey NW, Stopa EG. Johanson CE, et al. Among authors: primiano mj. Cell Mol Neurobiol. 2000 Apr;20(2):197-216. doi: 10.1023/a:1007097622590. Cell Mol Neurobiol. 2000. PMID: 10696510 Review.
Moreover, growth factors secreted by choroid plexus into CSF are distributed by diffusion and convection into brain tissue near the ventricular system, e.g., hippocampus. By this endocrine-like mechanism, growth factors are conveyed throughout the choroid plexus-CSF-brain …
Moreover, growth factors secreted by choroid plexus into CSF are distributed by diffusion and convection into brain tissue near the ventricu …
30 results