Fiore Manganelli
Overview
Explore the profile of Fiore Manganelli including associated specialties, affiliations and a list of published articles.
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Articles
230
Citations
2134
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Recent Articles
1.
Cassano E, Iodice R, Di Sarno I, Bencivenga R, Manganelli F, Tozza S
Neurol Sci
. 2025 Mar;
PMID: 40053180
Background And Aim: Anti-myelin-associated glycoprotein (anti-MAG) neuropathy is typically a chronic, progressive, predominantly sensory distal and demyelinating neuropathy, with ataxia and postural tremor METHODS AND RESULTS: Herein we describe an...
2.
Patisiran in ATTRv amyloidosis with polyneuropathy: "PatisiranItaly" multicenter observational study
Di Stefano V, Guaraldi P, Romano A, Antonini G, Barilaro A, Briani C, et al.
J Neurol
. 2025 Feb;
272(3):209.
PMID: 39954098
Background: Hereditary amyloid transthyretin amyloidosis with polyneuropathy (ATTRv-PN) is a rare, inherited, multisystemic, progressive adult-onset disease, affecting sensorimotor nerves, and various organs. It is caused by mutations in the TTR...
3.
Bertini A, Reilly M, Pisciotta C, Previtali S, Parman Y, Battaloglu E, et al.
Eur J Neurol
. 2025 Feb;
32(2):e70084.
PMID: 39943887
Background And Aims: In 2019, we conducted a cross-sectional study, collecting information on 50 patients with CMT4B, an ultrarare CMT subtype, to better define the clinical phenotype. We now aimed...
4.
Cortese A, Dohrn M, Curro R, Negri S, Lassuthova P, Pisciotta C, et al.
Brain
. 2025 Feb;
PMID: 39938083
Biallelic loss-of-function mutations in the sorbitol dehydrogenase (SORD) gene cause the most common recessive type of Charcot-Marie-Tooth disease (CMT), CMT-SORD. However, the full genotype-phenotype spectrum and progression of the disease...
5.
Wang Y, Ciampi Q, Cortigiani L, Zagatina A, Padang R, Kane G, et al.
J Am Soc Echocardiogr
. 2025 Jan;
PMID: 39818322
Background: Heart failure with preserved ejection fraction (HFpEF) is a heterogeneous entity including different phenotypes of near normal, normal, and supernormal left ventricular (LV) function. The aim of this study...
6.
Nobile-Orazio E, Cocito D, Manganelli F, Fazio R, Pinter G, Benedetti L, et al.
Brain
. 2024 Dec;
PMID: 39658326
Chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) often requires prolonged ongoing treatment to prevent worsening. The efficacy of rituximab in preventing worsening after the discontinuation of immunoglobulin therapy in CIDP patients was...
7.
Canciello G, Tozza S, Todde G, Nolano M, Borrelli F, Palumbo G, et al.
Orphanet J Rare Dis
. 2024 Dec;
19(1):458.
PMID: 39639351
Background: Hereditary transthyretin (ATTRv) amyloidosis is rare, autosomal dominant disease with a fatal outcome if left untreated. Early stages detection is crucial for intervention. We aimed identifying early indexes of...
8.
Geroldi A, La Barbera A, Mammi A, Origone P, Gaudio A, Ponti C, et al.
J Peripher Nerv Syst
. 2024 Sep;
29(4):472-486.
PMID: 39251209
Background And Aims: Since 2016, biallelic mutations in the membrane metalloendopeptidase (MME) gene have been associated with late-onset recessive CMT2 (CMT2T). More recently, heterozygous mutations have also been identified in...
9.
Di Sarno I, Tozza S, Santorelli F, Cassano E, Natale G, Dubbioso R, et al.
Neurol Sci
. 2024 Sep;
45(12):5933-5937.
PMID: 39223423
Background And Aims: Charcot-Marie-Tooth (CMT) is a heterogeneous group of genetic neuropathies and is typically characterized by distal muscle weakness, sensory loss, pes cavus and areflexia. Herein we describe a...
10.
Salvalaggio A, Cacciavillani M, Tierro B, Coraci D, Curro R, Ferrarini M, et al.
J Peripher Nerv Syst
. 2024 Sep;
29(4):464-471.
PMID: 39219417
Background And Aims: Ultrasound nerve cross-sectional area (CSA) of patients affected with axonal neuropathy usually shows normal value. Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) seems to represent an...