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Profil bibliographique

Carmela Marseglia

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

15Publications signalées
243Citations signalées
0Affiliations récentes

Les domaines associés

Hemoglobinopathies and Related DisordersErythrocyte Function and PathophysiologyDialysis and Renal Disease ManagementIron Metabolism and DisordersFolate and B Vitamins Research

Les publications récentes

2012 article OpenAlex

Extracorporeal dialysis: techniques and adequacy

C. Donadio, A. Kanaki, Adoración Martín-Gómez, S. Garcia et autres

formulas for spKt/V and urea reduction ratio (URR).Chart real-time Kt/V or URR is showing during HD session.Study S1: 34 uremic patients on chronic HD therapy three times/w were included (15 women, 19 men; mean age 57.5 years [26-85]; blood flow (Qb) ranged …

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1 citation Nephrology Dialysis Transplantation
Accès ouvert 2011 article OpenAlex

Effetti della sovraespressione di ferritina mitocondriale in precursori eritroidi normali

Serena Marra, Agnese Filocco, Erica Travaglino, Anna Gallì et autres

La ferritina mitocondriale (FtMt) è una isoforma ferritinica omopolimerica a localizzazione caratteristicamente mitocondriale. Nell’uomo è espressa a livello del sistema nervoso, miocardico, renale, testicolare, ossia tessuti ad elevato consumo di energia, ma anche nei sideroblasti ad anello in corso di anemia sideroblastica. …

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0 citations Università degli Studi di Pavia
2009 article OpenAlex

The Effects of Mitochondrial Ferritin Expression in Normal and Sideroblastic Erythropoiesis.

Matteo Giovanni Della Porta, Vittorio Rosti, Anna Gallì, Erica Travaglino et autres

Abstract Abstract 736 In erythroid cells from patients with refractory anemia with ringed sideroblasts (RARS), the expression of mitochondrial ferritin (MtF) - encoded by the nuclear FTMT gene located on chromosome 5q21.3 - occurs at a very early stage of differentiation and …

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2 citations Blood
2005 article OpenAlex

Mitochondrial Ferritin Expression and Clonality of Hematopoiesis in Patients with Refractory Anemia with Ringed Sideroblasts.

Matteo Giovanni Della Porta, Luca Malcovati, Anna Gallì, Sabrina Boggi et autres

Abstract Sideroblastic anemias are a heterogeneous group of disorders that have in common the presence of erythroblasts with iron-loaded mitochondria defined as ringed sideroblasts. We have previously demonstrated that mitochondrial iron deposition in these disorders is in the form of mitochondrial ferritin …

it (code pays fourni par la source)

8 citations Blood
2005 article OpenAlex

Evaluation of Progenitor Cells (CFU-GM, CFU-GEMM, BFU-E, CD34+ Cells) and White Blood Cells in Patients with Newly Diagnosed Diffuse Large B-Cell Lymphoma Treated with Rituximab-CHOP-14 and Supported with Pegfilgrastim.

Maurizio Bonfichi, Ercole Brusamolino, Carmela Marseglia, Chiara Rusconi et autres

Abstract Purpose: To investigate the behavior of CFU-GM, CFU-GEMM, BFU-E, CD34+ cells and white blood cells before and during six courses of dose-dense immune-chemotherapy (R-CHOP-14) supported by pegfilgrastim in eight patients affected with newly diagnosed diffuse large B cell lymphoma (3 men, …

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0 citations Blood
2005 article OpenAlex

Relationship between JAK2 V617F Mutation Status, Granulocyte CD177 mRNA Expression and CD177 Soluble Protein Level in Patients with Polycythemia Vera.

Daniela Pietra, Alessandra Balduini, Carmela Marseglia, Matteo Giovanni Della Porta et autres

Abstract A unique gain-of-function mutation of the Janus kinase 2 (JAK2) gene has been recently described in patients with polycythemia vera (PV), essential thrombocythemia and chronic idiopathic myelofibrosis [N Engl J Med. 2005 Apr 28;352(17):1779–90]. Although the currently available data clearly demonstrate …

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0 citations Blood
2005 article OpenAlex

Pathogenetic mechanisms of hematological abnormalities of patients with MYH9 mutations

Alessandro Pecci, Ilaria Canobbio, Alessandra Balduini, Lucia Stefanini et autres

Mutations of MYH9, the gene for non-muscle myosin heavy chain IIA (NMMHC-IIA), cause a complex clinical phenotype characterized by macrothrombocytopenia and granulocyte inclusion bodies, often associated with deafness, cataracts and/or glomerulonephritis. The pathogenetic mechanisms of these defects are either completely unknown or …

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56 citations Human Molecular Genetics

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