Laura Sainati
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Explore the profile of Laura Sainati including associated specialties, affiliations and a list of published articles.
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74
Citations
673
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Recent Articles
1.
Reggiani G, Boaro M, Menzato F, De Bon E, Bertomoro A, Casonato A, et al.
Pediatr Blood Cancer
. 2024 Mar;
71(6):e30971.
PMID: 38553897
Adults with sickle cell trait (SCT) have a procoagulant state with increased risk of thromboembolism, but limited data are available for children. We compared the coagulation profile of children with...
2.
Bugarin C, Antolini L, Buracchi C, Matarraz S, Coliva T, Van der Velden V, et al.
Haematologica
. 2023 Aug;
109(2):521-532.
PMID: 37534527
Diagnostic criteria for juvenile myelomonocytic leukemia (JMML) are currently well defined, however in some patients diagnosis still remains a challenge. Flow cytometry is a well established tool for diagnosis and...
3.
Reggiani G, Coppadoro B, Munaretto V, Pieroni A, Viaro F, Manara R, et al.
Eur J Haematol
. 2023 Jun;
111(3):414-422.
PMID: 37282348
Background: Stroke and cerebral vasculopathy are leading causes of morbidity and mortality in patients with sickle cell disease (SCD). Transcranial Doppler (TCD) is a reliable and validated predictor of stroke...
4.
Pinto V, De Franceschi L, Gianesin B, Gigante A, Graziadei G, Lombardini L, et al.
J Clin Med
. 2023 May;
12(10).
PMID: 37240547
The number of individuals with the sickle cell trait exceeds 300 million worldwide, making sickle cell disease one of the most common monogenetic diseases globally. Because of the high frequency...
5.
Severe hemolytic anemia in a newborn: Look out for rare Gardos channelopathies due to KCNN4 mutation
Munaretto V, Martella M, Francescato S, Reggiani G, Boaro M, Bianchi P, et al.
Pediatr Blood Cancer
. 2023 May;
70(8):e30325.
PMID: 37132095
No abstract available.
6.
Guerzoni M, Marchesi S, Palazzi G, Lodi M, Pinelli M, Venturelli D, et al.
Children (Basel)
. 2022 Oct;
9(10).
PMID: 36291415
Background: Environmental factors seem to influence clinical manifestations of sickle cell disease (SCD), but few studies have shown consistent findings. We conducted a retrospective multicentric observational study to investigate the...
7.
Cani A, Tretti Parenzan C, Frasson C, Rampazzo E, Scarparo P, Francescato S, et al.
Blood Adv
. 2022 Sep;
7(8):1513-1524.
PMID: 36053787
Juvenile myelomonocytic leukemia (JMML) is a rare clonal stem cell disorder that occurs in early childhood and is characterized by the hyperactivation of the RAS pathway in 95% of the...
8.
Po C, Nosadini M, Zedde M, Pascarella R, Mirone G, Cicala D, et al.
Front Pediatr
. 2022 May;
10:892445.
PMID: 35601411
Background: Moyamoya is a rare progressive cerebral arteriopathy, occurring as an isolated phenomenon (moyamoya disease, MMD) or associated with other conditions (moyamoya syndrome, MMS), responsible for 6-10% of all childhood...
9.
Martella M, Campeggio M, Pule G, Wonkam A, Menzato F, Munaretto V, et al.
Front Pediatr
. 2022 Apr;
10:826262.
PMID: 35463879
Background: Sickle Cell Disease (SCD) is an inherited condition that is widespread globally and especially in malaria-endemic West African countries. Limited epidemiological data on SCD are available for Guinea Bissau,...
10.
Graziadei G, De Franceschi L, Sainati L, Venturelli D, Masera N, Bonomo P, et al.
Front Med (Lausanne)
. 2022 Apr;
9:832154.
PMID: 35372393
Clinical Trial Registration: ClinicalTrials.gov, identifier: NCT03397017.