Serena Barozzi
Overview
Explore the profile of Serena Barozzi including associated specialties, affiliations and a list of published articles.
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Articles
26
Citations
377
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Recent Articles
1.
Freddi G, Parimbelli E, Vai F, Quaglini S, Bozzi V, Barozzi S, et al.
EJHaem
. 2024 Dec;
5(6):1125-1132.
PMID: 39691250
Thrombocytopenia during pregnancy is often thought to be associated with severe bleeding manifestations. Three are the main disorders associated with this condition: gestational thrombocytopenia (GT), immune thrombocytopenia (ITP), and inherited...
2.
Kamiya L, Barozzi S, Isidori F, Ganiewich D, De Luca G, Bozzi V, et al.
Br J Haematol
. 2024 Oct;
205(6):2315-2320.
PMID: 39375928
Correct interpretation of the pathogenicity of germline RUNX1 variants is essential for FPD/AML diagnosis, clinical management and leukaemia surveillance. We report two families with clear FPD/AML phenotypic features harbouring missense...
3.
Marzollo A, Zampieri S, Barozzi S, Yousaf M, Quartararo J, De Rocco D, et al.
Br J Haematol
. 2024 May;
205(1):306-315.
PMID: 38815995
Thrombocytopenia 4 (THC4) is an autosomal-dominant thrombocytopenia caused by mutations in CYCS, the gene encoding cytochrome c (CYCS), a small haeme protein essential for electron transport in mitochondria and cell...
4.
ACTN1-related thrombocytopenia: Homozygosity for an ACTN1 variant results in a more severe phenotype
Zanchetta M, Barozzi S, Isidori F, Marconi C, Farinasso L, Bottega R, et al.
Br J Haematol
. 2024 Apr;
204(6):2453-2457.
PMID: 38594875
ACTN1-related thrombocytopenia is a rare disorder caused by heterozygous variants in the ACTN1 gene characterized by macrothrombocytopenia and mild bleeding tendency. We describe for the first time two patients affected...
5.
Barozzi S, Pecci A, Marinoni M, Fontana G, Zanchetta M, Noris P, et al.
Ann Hematol
. 2022 Dec;
102(3):677-679.
PMID: 36539614
No abstract available.
6.
Marconi C, Pecci A, Palombo F, Melazzini F, Bottega R, Nardi E, et al.
Haematologica
. 2022 Dec;
108(7):1909-1919.
PMID: 36519321
Inherited thrombocytopenias (IT) are genetic diseases characterized by low platelet count, sometimes associated with congenital defects or a predisposition to develop additional conditions. Next-generation sequencing has substantially improved our knowledge...
7.
Barozzi S, Bozzi V, De Rocco D, Giangregorio T, Noris P, Savoia A, et al.
Int J Mol Sci
. 2021 Oct;
22(19).
PMID: 34638529
Bernard-Soulier syndrome (BSS) is an autosomal-recessive bleeding disorder caused by biallelic variants in the , , and genes encoding the subunits GPIbα, GPIbβ, and GPIX of the GPIb-IX complex. Pathogenic...
8.
Di Buduo C, Laurent P, Zaninetti C, Lordier L, Soprano P, Ntai A, et al.
Elife
. 2021 Jun;
10.
PMID: 34059198
Thrombocytopenic disorders have been treated with the Thrombopoietin-receptor agonist Eltrombopag. Patients with the same apparent form of thrombocytopenia may respond differently to the treatment. We describe a miniaturized bone marrow...
9.
Zaninetti C, Sacco C, Rahal D, Barozzi S, Balduini C, Lodigiani C, et al.
Blood Transfus
. 2020 Dec;
19(3):257-260.
PMID: 33263523
No abstract available.
10.
Barozzi S, Di Buduo C, Marconi C, Bozzi V, Seri M, Romano F, et al.
Haematologica
. 2020 Oct;
106(3):918-922.
PMID: 33054137
No abstract available.