Massimo Carella
Overview
Explore the profile of Massimo Carella including associated specialties, affiliations and a list of published articles.
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Articles
205
Citations
3142
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Recent Articles
11.
dOrsi G, Farolfi A, Muccioli L, Palumbo O, Palumbo P, Modoni S, et al.
Front Neurol
. 2023 Jul;
14:1202971.
PMID: 37448753
Purpose: To evaluate the electro-clinical features in association with laboratory and instrumental correlates of neurodegeneration to detect the progression of Lafora disease (LD). Methods: We investigated the electro-clinical longitudinal data...
12.
Quarato C, Dama E, Maggi M, Feragalli B, Borelli C, Del Colle A, et al.
Front Med (Lausanne)
. 2023 Jun;
10:1146807.
PMID: 37261121
Objectives: We validated a screening protocol in which thoracic ultrasound (TUS) acts as a first-line complementary imaging technique in selecting patients which may deserve a second-line low-dose high resolution computed...
13.
De Summa S, Traversa D, Daniele A, Palumbo O, Carella M, Stallone R, et al.
Front Oncol
. 2023 Apr;
13:1147190.
PMID: 37081976
Background: Breast cancer onset is determined by a genetics-environment interaction. BRCA1/2 gene alterations are often genetically shared in familial context, but also food intake and hormonal assessment seem to influence...
14.
Cecere F, Pignata L, Mele B, Saadat A, DAngelo E, Palumbo O, et al.
Cancers (Basel)
. 2023 Apr;
15(7).
PMID: 37046605
CRC is an adult-onset carcinoma representing the third most common cancer and the second leading cause of cancer-related deaths in the world. EO-CRC (<45 years of age) accounts for 5%...
15.
Tolomeo D, Agostini A, Solimando A, Cunsolo C, Cimarosto L, Palumbo O, et al.
Cancer Genet
. 2023 Jan;
272-273:16-22.
PMID: 36641997
13q14 deletion is the most recurrent chromosomal aberration reported in B-CLL, having a favorable prognostic significance when occurring as the sole cytogenetic alteration. However, its clinical outcome is also related...
16.
dOrsi G, Di Claudio M, Palumbo O, Carella M
Front Neurol
. 2022 Oct;
13:969297.
PMID: 36277909
Purpose: The aim of this study was to elucidate the electro-clinical features and management of the late stage of Lafora disease (LD). Methods: We investigated the electro-clinical data and medical...
17.
Innella G, Scarano E, Palumbo P, Carella M, Severi G
Am J Med Genet A
. 2022 Oct;
191(1):306-309.
PMID: 36269129
No abstract available.
18.
Russo E, Russo G, Cassese M, Braccio M, Carella M, Compagnucci P, et al.
Cells
. 2022 Aug;
11(15).
PMID: 35954250
Valve leaflets and chordae structurally normal characterize functional mitral regurgitation (FMR), which in heart failure (HF) setting results from an imbalance between closing and tethering forces secondary to alterations in...
19.
Biagini T, Petrizzelli F, Bianco S, Liorni N, Napoli A, Castellana S, et al.
Comput Struct Biotechnol J
. 2022 Jul;
20:3151-3160.
PMID: 35782738
KDM6A is the disease causative gene of type 2 Kabuki Syndrome, a rare multisystem disease; it is also a known cancer driver gene, with multiple somatic mutations found in a...
20.
Pignata L, Cecere F, Verma A, Mele B, Monticelli M, Acurzio B, et al.
Clin Epigenetics
. 2022 Jun;
14(1):71.
PMID: 35643636
Background: Beckwith-Wiedemann syndrome (BWS) and Pseudohypoparathyroidism type 1B (PHP1B) are imprinting disorders (ID) caused by deregulation of the imprinted gene clusters located at 11p15.5 and 20q13.32, respectively. In both of...