Rango M - Search Results

1

Familial mtDNA T8993C transition causing both the NARP and the MILS phenotype in the same generation. A morphological, genetic and spectroscopic study.

Sciacco M, Prelle A, D'Adda E, Lamperti C, Bordoni A, Rango M, Crimi M, Comi GP, Bresolin N, Moggio M. Sciacco M, et al. Among authors: rango m. J Neurol. 2003 Dec;250(12):1498-500. doi: 10.1007/s00415-003-0246-6. J Neurol. 2003. PMID: 14673588 No abstract available.

2

Mutated mitofusin 2 presents with intrafamilial variability and brain mitochondrial dysfunction.

Del Bo R, Moggio M, Rango M, Bonato S, D'Angelo MG, Ghezzi S, Airoldi G, Bassi MT, Guglieri M, Napoli L, Lamperti C, Corti S, Federico A, Bresolin N, Comi GP. Del Bo R, et al. Among authors: rango m. Neurology. 2008 Dec 9;71(24):1959-66. doi: 10.1212/01.wnl.0000327095.32005.a4. Epub 2008 Oct 22. Neurology. 2008. PMID: 18946002

3

Human fetal brain chemistry as detected by proton magnetic resonance spectroscopy.

Brighina E, Bresolin N, Pardi G, Rango M. Brighina E, et al. Among authors: rango m. Pediatr Neurol. 2009 May;40(5):327-42. doi: 10.1016/j.pediatrneurol.2008.11.001. Pediatr Neurol. 2009. PMID: 19380068 Review.

4

Magnetic resonance spectroscopy in Parkinson's disease and parkinsonian syndromes.

Rango M, Arighi A, Biondetti P, Barberis B, Bonifati C, Blandini F, Pacchetti C, Martignoni E, Bresolin N, Nappi G. Rango M, et al. Funct Neurol. 2007 Apr-Jun;22(2):75-9. Funct Neurol. 2007. PMID: 17637209 Review.

5

The brain is hypothermic in patients with mitochondrial diseases.

Rango M, Arighi A, Bonifati C, Del Bo R, Comi G, Bresolin N. Rango M, et al. J Cereb Blood Flow Metab. 2014 May;34(5):915-20. doi: 10.1038/jcbfm.2014.38. Epub 2014 Mar 12. J Cereb Blood Flow Metab. 2014. PMID: 24619278 Free PMC article.

6

Brain activation in normal subjects and in patients affected by mitochondrial disease without clinical central nervous system involvement: a phosphorus magnetic resonance spectroscopy study.

Rango M, Bozzali M, Prelle A, Scarlato G, Bresolin N. Rango M, et al. J Cereb Blood Flow Metab. 2001 Jan;21(1):85-91. doi: 10.1097/00004647-200101000-00011. J Cereb Blood Flow Metab. 2001. PMID: 11149672

7

Parkinson's disease and brain mitochondrial dysfunction: a functional phosphorus magnetic resonance spectroscopy study.

Rango M, Bonifati C, Bresolin N. Rango M, et al. J Cereb Blood Flow Metab. 2006 Feb;26(2):283-90. doi: 10.1038/sj.jcbfm.9600192. J Cereb Blood Flow Metab. 2006. PMID: 16094320

8

A 66-year-old patient with vanishing white matter disease due to the p.Ala87Val EIF2B3 mutation.

Ghezzi L, Scarpini E, Rango M, Arighi A, Bassi MT, Tenderini E, De Riz M, Jacini F, Fumagalli GG, Pietroboni AM, Galimberti D, Bresolin N. Ghezzi L, et al. Among authors: rango m. Neurology. 2012 Nov 13;79(20):2077-8. doi: 10.1212/WNL.0b013e3182749edc. Epub 2012 Oct 31. Neurology. 2012. PMID: 23115207

9

Increased brain temperature in Parkinson's disease.

Rango M, Arighi A, Bonifati C, Bresolin N. Rango M, et al. Neuroreport. 2012 Feb 15;23(3):129-33. doi: 10.1097/WNR.0b013e32834e8fac. Neuroreport. 2012. PMID: 22186803

10

Brain Mitochondria, Aging, and Parkinson's Disease.

Rango M, Bresolin N. Rango M, et al. Genes (Basel). 2018 May 11;9(5):250. doi: 10.3390/genes9050250. Genes (Basel). 2018. PMID: 29751692 Free PMC article. Review.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

41 results

Search Page

Filters