Francesco O Logullo
Overview
Explore the profile of Francesco O Logullo including associated specialties, affiliations and a list of published articles.
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Articles
7
Citations
437
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0
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Recent Articles
1.
Scendoni R, Petrelli C, Giustozzi M, Logullo F
Int J Immunopathol Pharmacol
. 2022 Sep;
36:3946320221128534.
PMID: 36123789
In the current international scientific panorama, rare cases of venous thrombotic complications following mRNA vaccine administration have been reported, consisting mainly of cerebral sinus thromboses and acute venous thromboembolism. The...
2.
Portaccio E, Fonderico M, Iaffaldano P, Pasto L, Razzolini L, Bellinvia A, et al.
JAMA Neurol
. 2022 Jul;
79(9):869-878.
PMID: 35877104
Importance: Except for ocrelizumab, treatment options in primary progressive multiple sclerosis (PPMS) are lacking. Objective: To investigate the effectiveness of DMTs on the risk of becoming wheelchair dependent in a...
3.
Johnson J, Miller D, Li R, Kumaran R, Alahmady N, Cookson M, et al.
JAMA Neurol
. 2021 Aug;
78(10):1236-1248.
PMID: 34459874
Importance: Juvenile amyotrophic lateral sclerosis (ALS) is a rare form of ALS characterized by age of symptom onset less than 25 years and a variable presentation. Objective: To identify the...
4.
Nicolas A, Kenna K, Renton A, Ticozzi N, Faghri F, Chia R, et al.
Neuron
. 2018 Mar;
97(6):1267-1288.
PMID: 29566793
To identify novel genes associated with ALS, we undertook two lines of investigation. We carried out a genome-wide association study comparing 20,806 ALS cases and 59,804 controls. Independently, we performed...
5.
Chio A, Mora G, Sabatelli M, Caponnetto C, Lunetta C, Traynor B, et al.
Neurobiol Aging
. 2016 Jan;
39:218.e5-8.
PMID: 26733254
There are indications that both familial amyotrophic lateral sclerosis (ALS) and sporadic ALS phenotype and prognosis are partly regulated by genetic and environmental factors, supporting the theory that ALS is...
6.
Chio A, Mora G, Sabatelli M, Caponnetto C, Lunetta C, Traynor B, et al.
Neurobiol Aging
. 2015 Jul;
36(10):2906.e7-11.
PMID: 26174855
It has been recently reported that the p.His63Asp polymorphism of the HFE gene accelerates disease progression both in the SOD1 transgenic mouse and in amyotrophic lateral sclerosis (ALS) patients. We...
7.
Chio A, Mora G, Sabatelli M, Caponnetto C, Traynor B, Johnson J, et al.
Neurobiol Aging
. 2015 Mar;
36(4):1767.e3-1767.e6.
PMID: 25726362
Mutations in CHCHD10 have recently been described as a cause of frontotemporal dementia (FTD) comorbid with amyotrophic lateral sclerosis (ALS). The aim of this study was to assess the frequency...