Daniela De Rocco
Overview
Explore the profile of Daniela De Rocco including associated specialties, affiliations and a list of published articles.
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Articles
37
Citations
889
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Recent Articles
1.
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...
2.
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...
3.
Pascolo L, Zito G, Zupin L, Luppi S, Giolo E, Martinelli M, et al.
Microorganisms
. 2020 Oct;
8(10).
PMID: 32998451
The current knowledge concerning the connection between severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and the renin-angiotensin system (RAS) system in the male reproductive apparatus is still limited, so dedicated...
4.
Zaninetti C, De Rocco D, Giangregorio T, Bozzi V, Demeter J, Leoni P, et al.
Hamostaseologie
. 2018 Jul;
39(1):87-94.
PMID: 29996171
-related disease (-RD) is an autosomal-dominant thrombocytopenia caused by mutations in the gene for non-muscle myosin heavy chain IIA (NMMHC-IIA). Patients present congenital macrothrombocytopenia and inclusions of NMMHC-IIA in leukocytes,...
5.
Bottega R, Nicchia E, Cappelli E, Ravera S, De Rocco D, Faleschini M, et al.
Haematologica
. 2017 Dec;
103(3):417-426.
PMID: 29269525
Fanconi anemia is a rare disease characterized by congenital malformations, aplastic anemia, and predisposition to cancer. Despite the consolidated role of the Fanconi anemia proteins in DNA repair, their involvement...
6.
Pecci A, Ragab I, Bozzi V, De Rocco D, Barozzi S, Giangregorio T, et al.
EMBO Mol Med
. 2017 Dec;
10(1):63-75.
PMID: 29191945
Congenital amegakaryocytic thrombocytopenia (CAMT) is an inherited disorder characterized at birth by thrombocytopenia with reduced megakaryocytes, which evolves into generalized bone marrow aplasia during childhood. Although CAMT is genetically heterogeneous,...
7.
Noris P, Marconi C, De Rocco D, Melazzini F, Pippucci T, Loffredo G, et al.
Br J Haematol
. 2017 May;
181(5):698-701.
PMID: 28466964
No abstract available.
8.
Savoia A, De Rocco D, Pecci A
Platelets
. 2017 Apr;
28(3):312-315.
PMID: 28368695
No abstract available.
9.
De Rocco D, Melazzini F, Marconi C, Pecci A, Bottega R, Gnan C, et al.
Am J Hematol
. 2017 Feb;
92(6):E86-E88.
PMID: 28240786
No abstract available.
10.
Melazzini F, Palombo F, Balduini A, De Rocco D, Marconi C, Noris P, et al.
Haematologica
. 2016 Jul;
101(11):1333-1342.
PMID: 27365488
ETV6-related thrombocytopenia is an autosomal dominant thrombocytopenia that has been recently identified in a few families and has been suspected to predispose to hematologic malignancies. To gain further information on...