Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Paola, Di Biagio"'
Publikováno v:
Professioni infermieristiche. 73(3)
Web and social networks play a crucial role in health information seeking and health literacy levels. In the last ten years people are able to access a wide range of health information from a plethora of sources. People who live in the city experienc
Autor:
Antonio Amato, Enrico Dainese, Annalaura Sabatucci, Alessia Colosimo, Roberta Piscitelli, Daniela Zei, Maria Pia Cappabianca, Paola Di Biagio, Ofelia Sarra
Publikováno v:
Hemoglobin. 41:53-55
We report a clinical update of the hemoglobin (Hb) variant [β27(B9)Ala→Gly; HBB: c.83C>G], named Hb Siirt, that was previously described as a silent variant in a 23-year-old Kurdish female. The patient was also a carrier of the codon 5 (–CT) (HB
Autor:
Silvana Rinaldi, Antonio Amato, Maria Pia Cappabianca, Paola Grisanti, Enrica Foglietta, Paola Di Biagio, Fabrizio Mastropietro, D Ponzini
Publikováno v:
Hemoglobin. 31:375-378
A new beta-globin variant at codon 106 (CTG-->GTG), and which we named Hb L'Aquila [beta106(G8)Leu-->Val], was detected by DNA analysis. The proband and her father presented with the features of a mild beta(+)-thalassemia (thal), confirmed by their a
Autor:
Silvana Rinaldi, Antonio Amato, Lerone M, Maria Pia Cappabianca, Maria Perri, Debora Gianni, Roberta Piscitelli, Paola Grisanti, D Ponzini, Paola Di Biagio, Alessia Colosimo
Publikováno v:
Journal of community genetics. 5(3)
To reduce the incidence of β-thalassaemia major and other severe haemoglobin-related disorders by the early identification of healthy carriers, the Centro Studi Microcitemie Roma has been organising since 1975 a prevention programme in Latium, an It
Autor:
Roberta Piscitelli, Ivo Zaghis, Maria Pia Cappabianca, Paola Di Biagio, Fabrizio Mastropietro, Antonio Amato, Maria Perri, D Ponzini
Publikováno v:
Hemoglobin. 36(5)
We report a novel frameshift mutation in exon 3 of the β-globin gene, that, in the heterozygous state, leads to a β-thalassemia intermedia (β-TI) phenotype (marked anemia, splenomegaly, hyperbilirubinemia, jaundice, unbalanced synthesis of α/non-
Autor:
Antonio, Amato, Maria, Lerone, Paola, Grisanti, Maria Pia, Cappabianca, Donatella, Ponzini, Debora, Gianni, Paola, Di Biagio, Silvana, Rinaldi, Nadia, D'Arcangeli, Brunella, Sidorini, Roberta, Piscitelli
Publikováno v:
Igiene e sanita pubblica. 67(1)
Autor:
Antonio Amato, I Bianco, Enrica Foglietta, Fabrizio Mastropietro, Paola Di Biagio, Maria Pia Cappabianca, D Ponzini, Silvana Rinaldi, Paola Grisanti, Bruno Dallapiccola, Alessia Colosimo, Valentina Guida
Publikováno v:
Hemoglobin. 30(3)
In this study we report on the hematological and molecular findings of a family from Central Italy, whose 33-year-old male proband presented with a beta0-thalassemia (thal) trait associated to a relevant Hb F level. The proband and his family (parent
Autor:
Guido Modiano, I Bianco, Mauro Mezzabotta, Paola Di Biagio, Laura Maffei, Lerone M, Enrica Foglietta, D Ponzini, Antonio Amato, Maria Pia Cappabianca, Silvana Rinaldi, Paola Grisanti, Carmelo D'asero, Fabrizio Mastropietro
Publikováno v:
BMC Blood Disorders
BMC Blood Disorders, Vol 2, Iss 1, p 2 (2002)
BMC Blood Disorders, Vol 2, Iss 1, p 2 (2002)
Background The thalassemic syndromes originate from mutations of the globin genes that cause, besides the characteristic clinical picture, also an increased Hb F amount. It is not yet clear if there are more factors, besides the beta globin genotype,
Publikováno v:
Journal of hepatology. 27(1)
Background/Aims: In chronic active liver diseases (CALD) with viral aetiology, a population of plasma cells localised in the piecemeal necrosis areas was previously detected by means of autoradiography after in vitro 3 H-proline incorporation, a meth