C Terracciano
Overview
Explore the profile of C Terracciano including associated specialties, affiliations and a list of published articles.
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12
Citations
100
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Recent Articles
1.
Reilly-ODonnell B, Ferraro E, Tikhomirov R, Nunez-Toldra R, Shchendrygina A, Patel L, et al.
Front Cardiovasc Med
. 2024 Dec;
11:1430772.
PMID: 39691494
Introduction: Cardiac fibrosis occurs in a wide range of cardiac diseases and is characterised by the transdifferentiation of cardiac fibroblasts into myofibroblasts these cells produce large quantities of extracellular matrix,...
2.
Frezza E, Terracciano C, Giacanelli M, Rastelli E, Greco G, Massa R
Case Rep Neurol Med
. 2018 Oct;
2018:4127213.
PMID: 30363678
Pompe disease is an autosomal recessive disorder characterized by deficiency of alpha-glucosidase, a lysosomal enzyme, which can lead to glycogen accumulation in skeletal muscle, heart, and nervous system. Clinical presentation...
3.
Romigi A, Albanese M, Placidi F, Izzi F, Liguori C, Marciani M, et al.
Eur J Neurol
. 2013 Jul;
21(6):929-34.
PMID: 23837695
Background And Purpose: There is a paucity of data available regarding the occurrence of sleep disorders in myotonic dystrophy type 2 (DM2). In this study the sleep-wake cycle and daytime...
4.
Terracciano C, Celi M, Lecce D, Baldi J, Rastelli E, Lena E, et al.
Osteoporos Int
. 2012 Apr;
24(3):1095-100.
PMID: 22535191
Unlabelled: We demonstrated that osteoporosis is associated with a preferential type II muscle fiber atrophy, which correlates with bone mineral density and reduced levels of Akt, a major regulator of...
5.
Rinaldi F, Terracciano C, Pisani V, Massa R, Loro E, Vergani L, et al.
Neurobiol Dis
. 2011 Aug;
45(1):264-71.
PMID: 21872659
Myotonic dystrophy type 1 (DM1) is a complex multisystemic disorder caused by an expansion of a CTG repeat located at the 3' untranslated region (UTR) of DMPK on chromosome 19q13.3....
6.
Pisani V, Tirabasso A, Mazzone S, Terracciano C, Botta A, Novelli G, et al.
Eur J Neurol
. 2011 Jul;
18(12):1412-6.
PMID: 21777352
Background: Myotonic dystrophy type 1 (DM1) is an autosomal-dominant inherited disorder clinically characterized by variable systemic manifestations. Among clinical features of the disease, 'precocious presbyacusis' has been previously reported. The...
7.
Massa R, Panico M, Caldarola S, Fusco F, Sabatelli P, Terracciano C, et al.
Neuropathol Appl Neurobiol
. 2010 Jan;
36(4):275-84.
PMID: 20102514
Aims: Myotonic dystrophy type 2 (DM2) is caused by a [CCTG]n intronic expansion in the zinc finger protein 9 (ZNF9) gene. As for DM1, sharing with DM2 a similar phenotype,...
8.
Cacciatore F, Gallo C, Ferrara N, Abete P, Paolisso G, Canonico S, et al.
Arch Gerontol Geriatr
. 2008 Jul;
26(3):201-13.
PMID: 18653137
The goal of the study was to investigated the prevalence of disability, cognitive impairment, depressive symptomatology and chronic diseases in a sample of the elderly population. A cross-sectional study was...
9.
Pachatz C, Terracciano C, Desiato M, Orlacchio A, Mori F, Rocchi C, et al.
Clin Neurophysiol
. 2006 Dec;
118(2):262-8.
PMID: 17137837
Objective: Clinicopathological findings of X-linked recessive bulbospinal muscular atrophy (SBMA) are indicative of lower motor neuron and primary sensory neuron involvement. The aim of our study was to investigate the...
10.
Subacute demyelinating polyneuropathy in B-cell lymphoma with IgM antibodies against glycolipid GD1b
Marfia G, Pachatz C, Terracciano C, Leone G, Bernardini S, Bernardi G, et al.
Neurol Sci
. 2006 Jan;
26(5):355-7.
PMID: 16388373
Peripheral neuropathy associated with IgM monoclonal gammopathy of unknown significance is a common disorder, while the association of paraproteinaemic neuropathies with haematological malignancies is far less frequent. We report a...