Viviana Palazzo
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Explore the profile of Viviana Palazzo including associated specialties, affiliations and a list of published articles.
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Articles
23
Citations
242
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Recent Articles
1.
Bacci G, Fortunato P, Cestaro S, Tiberi L, Dirupo E, Artuso R, et al.
Ophthalmic Genet
. 2025 Mar;
:1-9.
PMID: 40043730
Introduction: Monocentric retrospective case series to describe clinical and molecular peculiarities in a series of pediatric patients in attempting a possible genotype-phenotype correlation. Methods: We included 13 pediatric patients from...
2.
Daenen M, Hureaux M, Ashton E, Becherucci F, Barry I, Benz M, et al.
Nephrol Dial Transplant
. 2025 Jan;
PMID: 39837581
Background And Hypothesis: ATP6V1B1 encodes a subunit of the vacuolar H+-ATPase and pathogenic variants are associated with autosomal recessive distal renal tubular acidosis (dRTA) with deafness. Heterozygous variants predicted to...
3.
Raglianti V, Angelotti M, Cirillo L, Ravaglia F, Landini S, Palazzo V, et al.
Kidney Int
. 2024 Oct;
106(6):1124-1134.
PMID: 39368741
Podocytopathies represent a group of glomerular disorders associated with minimal changes (MC) or focal segmental glomerulosclerosis (FSGS) lesion patterns at biopsy and heterogeneous responses to steroids. Anti-nephrin antibodies were previously...
4.
Barbato A, Gori G, Sacchini M, Pochiero F, Bargiacchi S, Traficante G, et al.
Endocr Connect
. 2024 Aug;
13(10).
PMID: 39214134
Context: Cytochrome C oxidase (COX) is the fourth component of the respiratory chain and is located within the internal membrane of mitochondria. COX deficiency causes an inherited mitochondrial disease with...
5.
Bacci G, Marziali E, Bargiacchi S, Paques M, Virgili G, Fortunato P, et al.
Sci Rep
. 2024 Jul;
14(1):15454.
PMID: 38965328
Aim of the present study is to evaluate the relationship between genetic and phenotypic data in a series of patients affected by grade I and II of foveal hypoplasia with...
6.
Dodd D, Mechaussier S, Yeyati P, McPhie F, Anderson J, Khoo C, et al.
Science
. 2024 Apr;
384(6694):eadf5489.
PMID: 38662826
Tubulin, one of the most abundant cytoskeletal building blocks, has numerous isotypes in metazoans encoded by different conserved genes. Whether these distinct isotypes form cell type- and context-specific microtubule structures...
7.
Mazzierli T, Cirillo L, Palazzo V, Ravaglia F, Becherucci F
J Nephrol
. 2024 Jan;
37(2):539.
PMID: 38236476
No abstract available.
8.
Becherucci F, Landini S, Palazzo V, Cirillo L, Raglianti V, Lugli G, et al.
J Am Soc Nephrol
. 2023 Feb;
34(4):706-720.
PMID: 36753701
Significance Statement: To optimize the diagnosis of genetic kidney disorders in a cost-effective manner, we developed a workflow based on referral criteria for in-person evaluation at a tertiary center, whole-exome...
9.
Savige J, Storey H, Watson E, Hertz J, Deltas C, Renieri A, et al.
Eur J Hum Genet
. 2023 Jan;
32(1):132.
PMID: 36721056
No abstract available.
10.
Marziali E, Van den Broeck F, Bargiacchi S, Fortunato P, Caputo R, Sodi A, et al.
Ophthalmic Genet
. 2022 Dec;
44(2):152-162.
PMID: 36469668
Background: Congenital Stationary Night Blindness (CSNB) constitutes a group of non-progressive retinal disorders characterized by disturbances in scotopic vision and/or by a delay in adaptation to darkness, as well as...