Francesca Gualandi
Overview
Explore the profile of Francesca Gualandi 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
161
Citations
4025
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.
Carigi S, Olivucci G, Cristalli C, Marzo F, Isidori F, Palmieri S, et al.
Int J Cardiol
. 2025 Jan;
423:132999.
PMID: 39855353
Background: non-syndromic dilated cardiomyopathy (DCM) is found to correlate with a genetic cause in 30-40 % of cases. The identification of a causative gene variant can guide treatment options and...
2.
Bottillo I, Ciccone M, Magliozzi M, Pilichou K, Girotto G, Girolami F, et al.
J Mol Cell Cardiol
. 2024 Dec;
199:46-50.
PMID: 39674365
No abstract available.
3.
Benati D, Cattin E, Corradi F, Ferrari T, Pedrazzoli E, Patrizi C, et al.
Biomolecules
. 2024 Nov;
14(11).
PMID: 39595588
Collagen VI is an essential component of the extracellular matrix (ECM) composed by α1, α2 and α3 chains and encoded by , and genes. Dominant negative pathogenic variants in genes...
4.
Mikulska M, Gualandi F, Anserini P
Handb Clin Neurol
. 2024 Aug;
202:135-151.
PMID: 39111905
As autologous stem cell transplantation (ASCT) is increasingly frequent in some patients with multiple sclerosis (MS), the knowledge of its adverse effects is paramount. Early complications (within 30 from transplantation)...
5.
Foley A, Bolduc V, Guirguis F, Donkervoort S, Hu Y, Orbach R, et al.
medRxiv
. 2024 Apr;
PMID: 38585825
Collagen VI-related dystrophies (COL6-RDs) manifest with a spectrum of clinical phenotypes, ranging from Ullrich congenital muscular dystrophy (UCMD), presenting with prominent congenital symptoms and characterised by progressive muscle weakness, joint...
6.
Balla C, Margutti A, De Carolis B, Canovi L, Di Domenico A, Vivaldi I, et al.
Heart Rhythm
. 2024 Mar;
21(8):1363-1369.
PMID: 38467355
Background: Cardiac conduction disorder (CCD) in patients <50 years old is a rare and mostly unknown condition. Objective: We aimed to assess clinical characteristics and genetic background of patients <50...
7.
Gemignani F, Percesepe A, Gualandi F, Allegri I, Bellanova M, Nuredini A, et al.
Int J Mol Sci
. 2024 Feb;
25(3).
PMID: 38338934
Charcot-Marie-Tooth disease (CMT) rarely presents with painful symptoms, which mainly occur in association with myelin protein zero () gene mutations. We aimed to further characterize the features of painful neuropathic...
8.
Di Francesco A, Raiola A, Dominietto A, di Grazia C, Gualandi F, Van Lint M, et al.
Front Med (Lausanne)
. 2024 Feb;
10:1320692.
PMID: 38327272
We studied the incidence of acute graft versus host disease (GvHD) and its outcome in three consecutive time frames (year <2000; 2000-2010; >2010), in 3,120 patients allografted in two transplant...
9.
Tonelli L, Balla C, Farne M, Margutti A, Maniscalchi E, De Feo G, et al.
J Cardiovasc Med (Hagerstown)
. 2023 Nov;
24(12):864-870.
PMID: 37942788
Aims: Brugada syndrome (BrS) is an inherited arrhythmic disease characterized by a coved ST-segment elevation in the right precordial electrocardiogram leads (type 1 ECG pattern) and is associated with a...
10.
Liantonio A, Bertini M, Mele A, Balla C, Dinoi G, Selvatici R, et al.
Biomedicines
. 2023 Aug;
11(8).
PMID: 37626795
Brugada syndrome (BrS) is an inherited cardiac channelopathy first diagnosed in 1992 but still considered a challenging disease in terms of diagnosis, arrhythmia risk prediction, pathophysiology and management. Despite about...