Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Cristina Curcio"'
Autor:
Rawand P. Shamoon, Amir Charkaneh, Elena Di Pierro, Milena Irrera, Cristina Curcio, Ahmed Yassin, Rozhgar A. Khailany
Publikováno v:
Hematology, Vol 29, Iss 1 (2024)
Background Thalassemias are genetic disorders of globin chain synthesis. In Iraq, β-thalassemia is more prevalent than α-thalassemia. This study identifies two unpredicted globin gene mutations, a rare α-globin gene mutation (Hb SKMC) and a novel
Externí odkaz:
https://doaj.org/article/cb6c7b1af1674f8286969f500083ff2d
Autor:
Silvio Marchesani, Margherita Di Mauro, Giulia Ceglie, Ginevra Grassia, Michaela Carletti, Rosa Carmela Cristofaro, Matilde Cossutta, Cristina Curcio, Giuseppe Palumbo
Publikováno v:
Frontiers in Pediatrics, Vol 11 (2023)
IntroductionApproximately 7% of the worldwide population exhibits variations in the globin genes. The recent migration of populations from countries where hemoglobin disorders are endemic has resulted in important epidemiological changes with the dif
Externí odkaz:
https://doaj.org/article/a30a1d96e6f74badbd4144dfe52fb269
Autor:
Francesco Amati, Andrea Gramegna, Martina Contarini, Anna Stainer, Cristina Curcio, Stefano Aliberti, Angelo Guido Corsico, Francesco Blasi
Publikováno v:
Biomedicines, Vol 10, Iss 12, p 3248 (2022)
Cystic fibrosis (CF) and alpha-1 antitrypsin (AAT) deficiency are two of the commonest genetic diseases affecting the Caucasian population. Neutrophil-mediated inflammation due to protease–antiprotease imbalance leads to progressive pulmonary invol
Externí odkaz:
https://doaj.org/article/46ebe9124035413bbce98e98c7cf895f
Autor:
Elisa Fermo, Cristina Vercellati, Anna Paola Marcello, Anna Zaninoni, Richard van Wijk, Nadia Mirra, Cristina Curcio, Agostino Cortelezzi, Alberto Zanella, Wilma Barcellini, Paola Bianchi
Publikováno v:
Case Reports in Hematology, Vol 2017 (2017)
Hereditary xerocytosis (HX) is a rare disorder caused by defects of RBC permeability, associated with haemolytic anaemia of variable degree and iron overload. It is sometimes misdiagnosed as hereditary spherocytosis or other congenital haemolytic ana
Externí odkaz:
https://doaj.org/article/8b7f8c63ed534579880dfe03212bca26
Autor:
Silvia Galbiati, Barbara Foglieni, Maurizio Travi, Cristina Curcio, Gabriella Restagno, Luca Sbaiz, Maddalena Smid, Federica Pasi, Augusto Ferrari, Maurizio Ferrari, Laura Cremonesi
Publikováno v:
Haematologica, Vol 93, Iss 4 (2008)
The presence of fetal DNA in maternal plasma can be exploited to develop new procedures for non-invasive prenatal diagnosis. Tests to detect 7 frequent β-globin gene mutations in people of Mediterranean origin were applied to the analysis of materna
Externí odkaz:
https://doaj.org/article/dcd6f08a94ff44c280f56ddc8d224466
Publikováno v:
PSICOLOGIA DELLA SALUTE. :76-99
L'emergenza da COVID-19 pone le organizzazioni sanitarie di fronte ad una sfida e com-porta un sovraccarico lavorativo degli operatori senza precedenti. Medici e infermieri non solo sono stati sovraesposti al rischio contagio, ma si sono ritrovati an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7f11b95ff95fa9528cbde7b6ed8b879
https://doi.org/10.3280/pds2021-002006
https://doi.org/10.3280/pds2021-002006
Autor:
Elena Cassinerio, Manuela Seia, Giovanna Graziadei, Claudia Cesaretti, Valentina Giannone, Cristina Curcio, Elena Benzoni
Publikováno v:
Journal of Medical Cases
Non-transfusion dependent thalassemia (NTDT) is an inherited hemoglobin disorder characterized by an ?/non-? globin chain imbalance of variable severity, resulting in a wide spectrum of clinical manifestations. The coinheritance of additional ? genes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88e23d2ea665b36664360ea879a572f4
http://europepmc.org/articles/PMC8383574
http://europepmc.org/articles/PMC8383574
Autor:
Giovanni Antonello, Carlo Lo Monaco, Patrizia Napoli, Daniela Solimando, Cristina Curcio, Giuseppina Barberio, Sauro Maoggi, Giovanni Ivaldi, Marco Nigra
Publikováno v:
Clinical chemistry and laboratory medicineReferences. 60(6)
Objectives The observation of numerous new structural defects in hemoglobin (Hb) has often been linked to the evolution and development of device technologies used for the separation and quantification of hemoglobin components. However, the increased
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6a207764fcb54ec1e0803009f84da6b
https://pubmed.ncbi.nlm.nih.gov/35218178
https://pubmed.ncbi.nlm.nih.gov/35218178
Autor:
Mariarosa Carta, Francesco Zanolli, Antonella Maffè, Noraesah Mahmud, Gian Luca Forni, Domenico Coviello, Silvana Ungari, Massimo Mogni, Giovanni Ivaldi, Valeria Pinto, Raffaella Paventa, Giuseppina Barberio, Sauro Maoggi, Cristina Curcio, Mariella Mercadanti, Alberta Caleffi, Massimo Maffei
Publikováno v:
Genes, Vol 12, Iss 1821, p 1821 (2021)
Genes
Volume 12
Issue 11
Genes
Volume 12
Issue 11
Background: Hemoglobin A (Hb A) (α2β2) in the normal adult subject constitutes 96–98% of hemoglobin, and Hb F is normally less than 1%, while for hemoglobin A2 (Hb A2) (α2δ2), the normal reference values are between 2.0 and 3.3%. It is importan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2688ad0334ca800131de2bb08ff85486
https://www.mdpi.com/2073-4425/12/11/1821
https://www.mdpi.com/2073-4425/12/11/1821
Autor:
Chiara Giulietti, Massimo Mogni, Vittoria Monaco, Cornelis L. Harteveld, Massimo Maffei, Sauro Maoggi, Piero Pucci, Cristina Curcio, Giuseppina Barberio, Giovanni Ivaldi, Iacopo Iacomelli
Publikováno v:
Clinical Chemistry and Laboratory Medicine (CCLM), 59(10), 1670-1679. WALTER DE GRUYTER GMBH
Objectives Artifactually altered glycated hemoglobin (HbA1c) concentrations are frequently linked to hemoglobin (Hb) variants. Their expression and detection require in-depth analysis. Methods Cation exchange high performance liquid chromatography (H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d553f2ca79c560cd0ebd06a5643512cb
https://hdl.handle.net/1887/3249334
https://hdl.handle.net/1887/3249334
