Bianca Maria Goffredo
Overview
Explore the profile of Bianca Maria Goffredo including associated specialties, affiliations and a list of published articles.
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Articles
51
Citations
487
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Recent Articles
1.
Berlingerio S, Bondue T, Tassinari S, Siegerist F, Ferrulli A, Lismont C, et al.
J Transl Med
. 2025 Feb;
23(1):206.
PMID: 39980044
Background: Cystinosis is a rare, incurable lysosomal storage disease caused by mutations in the CTNS gene encoding the cystine transporter cystinosin, which leads to lysosomal cystine accumulation in all cells...
2.
Cascone A, De Luca M, Simeoli R, Goffredo B, Cursi L, Tripiciano C, et al.
Pathogens
. 2025 Jan;
14(1).
PMID: 39860965
Brain abscesses are invasive infections of the central nervous system with a high level of treatment complexity especially in pediatric patients. Here, we describe a 3-month-old infant with multiple brain...
3.
Volpicelli L, Cairoli S, Al Ismail D, Baisi F, Sacco F, Goffredo B, et al.
J Glob Antimicrob Resist
. 2025 Jan;
41:20.
PMID: 39787673
No abstract available.
4.
De Leo E, Taranta A, Raso R, Pezzullo M, Piccione M, Matteo V, et al.
Biomed Pharmacother
. 2024 Aug;
178:117236.
PMID: 39096619
In infantile nephropathic cystinosis, variants of the CTNS gene cause accumulation of cystine in lysosomes, causing progressive damage to most organs. Patients usually present before 1 year of age with...
5.
Simeoli R, Lava S, Di Deo A, Roversi M, Cairoli S, Tambucci R, et al.
Pharmaceutics
. 2024 Jul;
16(7).
PMID: 39065569
Eosinophilic oesophagitis is a long-term complication of oesophageal atresia (EA), an uncommon condition that affects approximately 1 in 3500 infants. An exploratory, open-label phase 2 clinical trial was conducted in...
6.
Bellomo F, Pugliese S, Cairoli S, Krohn P, De Stefanis C, Raso R, et al.
J Am Soc Nephrol
. 2024 Jul;
35(11):1493-1506.
PMID: 38995697
No abstract available.
7.
Simeoli R, Cairoli S, Greco M, Bellomo F, Mancini A, Rossi C, et al.
Pharmaceuticals (Basel)
. 2024 May;
17(5).
PMID: 38794219
Cystinosis is a rare lysosomal storage disorder caused by autosomal recessive mutations in the gene that encodes for the cystine transporter cystinosin, which is expressed on the lysosomal membrane mediating...
8.
Bondue T, Khodaparast L, Khodaparast L, Cairoli S, Goffredo B, Gijsbers R, et al.
Am J Physiol Renal Physiol
. 2024 Mar;
326(6):F981-F987.
PMID: 38545650
Cystinosis is an autosomal recessive lysosomal storage disorder, caused by mutations in the gene, resulting in an absent or altered cystinosin (CTNS) protein. Cystinosin exports cystine out of the lysosome,...
9.
Volpicelli L, Cairoli S, Al Ismail D, Baisi F, Sacco F, Goffredo B, et al.
J Glob Antimicrob Resist
. 2024 Mar;
37():86-90.
PMID: 38519025
Objective: A case of post-neurosurgical ventriculitis caused by a KPC-producing Klebsiella pneumoniae (KPC-Kp) with a ceftazidime/avibactam-resistant, meropenem-susceptible phenotype is reported. Methods And Results: The patient had a concomitant bloodstream infection...
10.
Mercadante S, Tripiciano C, Romani L, Di Nardo M, Bottari G, Goffredo B, et al.
Antibiotics (Basel)
. 2024 Jan;
13(1).
PMID: 38247596
Background: Infections caused by antimicrobial-resistant (AMR) pathogens are increasing worldwide, representing a serious global public health issue with high morbidity and mortality rates The treatment of (PA) infections has become...