C Angelini
Overview
Explore the profile of C Angelini 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
537
Citations
5262
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Crous P, Osieck E, Jurjevic Z, Boers J, van Iperen A, Starink-Willemse M, et al.
Persoonia
. 2023 Sep;
47:178-374.
PMID: 37693795
Novel species of fungi described in this study include those from various countries as follows: , from coastal sea sand. , on soil, on dead wood, from roots and leaves...
2.
Giunco S, Padovan M, Angelini C, Cavallin F, Cerretti G, Morello M, et al.
ESMO Open
. 2023 May;
8(3):101570.
PMID: 37230028
Background: The clinical relevance of promoter mutations and single nucleotide polymorphism rs2853669 of telomerase reverse transcriptase (TERT) and telomere length in patients with isocitrate dehydrogenase (IDH) wild-type glioblastoma (GBM) patients...
3.
Di Stadio A, Bernitsas E, Ralli M, Severini C, Brenner M, Angelini C
Eur Rev Med Pharmacol Sci
. 2022 Feb;
26(2):347-349.
PMID: 35113409
No abstract available.
4.
Crous P, Cowan D, Maggs-Kolling G, Yilmaz N, Larsson E, Angelini C, et al.
Persoonia
. 2021 Aug;
45:251-409.
PMID: 34456379
Novel species of fungi described in this study include those from various countries as follows: , on soil, on leaves of on leaves of on leaves of sp., on soil,...
5.
Percivale G, Angelini C, Falugi C, Picco C, Prestipino G
Zygote
. 2021 Jul;
30(2):213-216.
PMID: 34315559
In this work, the presence of calcium-dependent calcium channels and their receptors (RyR) has been investigated in Paracentrotus lividus eggs and early embryos, from unfertilized egg to four-blastomere stages. Electrophysiological...
6.
Farid A, Gelardi M, Angelini C, Franck A, Costanzo F, Kaminsky L, et al.
Fungal Syst Evol
. 2020 May;
2:341-359.
PMID: 32467893
The monotypic genus is described as new to science based on This species occurs widely in eastern North America and Central America. It is reported for the first time from...
7.
Cenacchi G, Papa V, Pegoraro V, Marozzo R, Fanin M, Angelini C
Neuropathol Appl Neurobiol
. 2019 Nov;
46(4):303-322.
PMID: 31698507
Danon disease is a severe multisystem disorder clinically characterized by hypertrophic cardiomyopathy, skeletal myopathy and mental retardation in male patients, and by a milder phenotype (predominantly involving cardiac muscle) in...
8.
Cenacchi G, Papa V, Costa R, Pegoraro V, Marozzo R, Fanin M, et al.
Virchows Arch
. 2019 Aug;
475(6):671-686.
PMID: 31363843
An abnormal structural form of glycogen (with less branching points or amylopectin-like polysaccharide) called polyglucosan (PG) may accumulate in various tissues such as striated and smooth muscles, brain, nerve, liver...
9.
Orsucci D, Angelini C, Bertini E, Carelli V, Comi G, Federico A, et al.
J Neurol
. 2017 Jul;
264(8):1777-1784.
PMID: 28695364
Ocular myopathy, typically manifesting as progressive external ophthalmoplegia (PEO), is among the most common mitochondrial phenotypes. The purpose of this study is to better define the clinical phenotypes associated with...
10.
Ripolone M, Violano R, Ronchi D, Mondello S, Nascimbeni A, Colombo I, et al.
Neuropathol Appl Neurobiol
. 2017 Jun;
44(5):449-462.
PMID: 28574618
Aims: Pompe disease is an autosomal recessive lysosomal storage disorder resulting from deficiency of acid α-glucosidase (GAA) enzyme. Histopathological hallmarks in skeletal muscle tissue are fibre vacuolization and autophagy. Since...