Raffaella Tanel
Overview
Explore the profile of Raffaella Tanel including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
18
Citations
267
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Saez-Atienzar S, Souza C, Chia R, Beal S, Lorenzini I, Huang R, et al.
Cell Genom
. 2024 Oct;
4(11):100679.
PMID: 39437787
Repeat expansions in the C9orf72 gene are the most common genetic cause of (ALS) and frontotemporal dementia (FTD). Like other genetic forms of neurodegeneration, pinpointing the precise mechanism(s) by which...
2.
Govoni A, Ricci G, Bonanno S, Bello L, Magri F, Meneri M, et al.
Muscle Nerve
. 2024 Aug;
70(4):816-823.
PMID: 39096012
Introduction/aims: Fatigue (subjective perception) and fatigability (objective motor performance worsening) are relevant aspects of disability in individuals with spinal muscular atrophy (SMA). The effect of nusinersen on fatigability in SMA...
3.
Sabatelli M, Cerri F, Zuccarino R, Patanella A, Bernardo D, Bisogni G, et al.
J Neurol
. 2024 Jun;
271(8):5177-5186.
PMID: 38829431
Background: In Amyotrophic Lateral Sclerosis (ALS) patients with SOD1 mutation the intrathecal administration of tofersen slowed down the progression of disease in a controlled clinical study, but results were not...
4.
Donini L, Tanel R, Zuccarino R, Basso M
Neurosci Res
. 2023 Sep;
197:31-41.
PMID: 37689321
Amyotrophic Lateral Sclerosis (ALS) is the most common motor neuron disease, still incurable. The disease is highly heterogenous both genetically and phenotypically. Therefore, developing efficacious treatments is challenging in many...
5.
Canosa A, Calvo A, Mora G, Moglia C, Brunetti M, Barberis M, et al.
Biomedicines
. 2023 Mar;
11(3).
PMID: 36979682
: Data from published studies about the effect of HFE polymorphisms on ALS risk, phenotype, and survival are still inconclusive. We aimed at evaluating whether the p.H63D polymorphism is a...
6.
Maggi L, Bello L, Bonanno S, Govoni A, Caponnetto C, Passamano L, et al.
J Neurol Neurosurg Psychiatry
. 2022 Oct;
93(12):1253-1261.
PMID: 36220341
Background: Natural history of spinal muscular atrophy (SMA) in adult age has not been fully elucidated yet, including factors predicting disease progression and response to treatments. Aim of this retrospective,...
7.
Bonanno S, Zanin R, Bello L, Tramacere I, Bozzoni V, Caumo L, et al.
J Neurol
. 2022 Jan;
269(6):3264-3275.
PMID: 34978620
Objective: To retrospectively evaluate quality of life (QoL) in a large multicenter cohort of adult patients affected by spinal muscular atrophy (SMA) during nusinersen treatment. Methods: We included adult (≥ ...
8.
Piffer S, Cantalupo G, Filipponi S, Poretto V, Pellegrini M, Tanel R, et al.
Eur J Neurol
. 2021 Oct;
29(3):890-894.
PMID: 34679240
Background And Purpose: The core manifestations of leucine-rich glioma-inactivated 1 (LGI1) autoantibody-mediated encephalitis are limbic encephalitis and faciobrachial dystonic seizures. Agrypnia excitata (AE) is a rare syndrome characterized by sleep-wake...
9.
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...
10.
Maggi L, Bello L, Bonanno S, Govoni A, Caponnetto C, Passamano L, et al.
J Neurol Neurosurg Psychiatry
. 2020 Sep;
91(11):1166-1174.
PMID: 32917822
Objective: To retrospectively investigate safety and efficacy of nusinersen in a large cohort of adult Italian patients with spinal muscular atrophy (SMA). Methods: Inclusion criteria were: (1) clinical and molecular...