Výsledky vyhledávání - "Rocca Cingari"

Akademický článek

Bone turnover markers in patients with type 1 Gaucher disease

Autor: Gaetano Giuffrida, Maria Rocca Cingari, Nunziatina Parrinello, Alessandra Romano, Anna Triolo, Magda Franceschino, Francesco Di Raimondo

Publikováno v: Hematology Reports, Vol 4, Iss 4, Pp e21-e21 (2012)

Bone complications occur frequently in Gaucher disease (GD) and reduce the quality of life of these patients. Skeletal involvement is an important indication for treatment to ameliorate symptoms and reduce the risk of irreversible and debilitating di

Externí odkaz: https://doaj.org/article/542e6395e09f46da9201ef8c482313f4

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Preliminary Results of a Prospective Observational Study to Assess the Prevalence of Gaucher Disease in an Adult Population Affected By MGUS

Autor: Giuseppe Longo, Caterina Musolino, Concetta Conticello, Vanessa Innao, Daniela Nicolosi, Cinzia Maugeri, Ugo Consoli, Francesco Di Raimondo, Maria Rocca Cingari, Flavia Fiorenza, Valeria Calafiore, Gaetano Giuffrida, Alessandra Romano

Publikováno v: Blood. 134:4868-4868

INTRODUCTION: Gaucher disease (GD) is a rare, autosomal recessive genetic disorder. It is due to a deficiency of the lysosomal enzyme, glucocerebrosidase, which leads to an accumulation of its substrate, glucosylceramide, in tissue macrophage with da

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b7ab5f782b8493fbfd6d2100c96ff22
https://doi.org/10.1182/blood-2019-129944

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Bone Turnover Markers In Gaucher Disease Patients

Autor: Nunziatina Laura Parrinello, Maria Rocca Cingari, Gaetano Giuffrida, Francesco Di Raimondo, Magda Franceschino, Alessandra Romano, Anna Triolo

Abstract 3780 Background: Gaucher Disease (GD) is an autosomal recessive hereditary disorder of glycosphingolipid metabolism, characterized by accumulation of glucosylceramide in cells of the reticulo-endothelial system, due to the deficient activity

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b8c2ecee20ee698332ff498f431dec9
http://hdl.handle.net/20.500.11769/97935

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Improving survival with deferiprone treatment in patients with thalassemia major: A prospective multicenter randomised clinical trial under the auspices of the Italian Society for Thalassemia and Hemoglobinopathies

The prognosis for thalassemia major has dramatically improved in the last two decades. However, many transfusion-dependent patients continue to develop progressive accumulation of iron. This can lead to tissue damage and eventually death, particularl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c528499eeaa1c4acab63f412e90b29eb
http://hdl.handle.net/10447/62337

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Long-Term Use of Deferiprone Enhances Significantly the Left Ventricular Ejection Function in Thalassemia Major

Publikováno v: Blood. 118:5302-5302

Abstract 5302 Background: A multicentre randomized controlled trial (RCT) was designed to assess the effectiveness of long-term sequential deferiprone-deferoxamine (DFO-DFP) versus DFP alone to treat thalassaemia major (TM) (Maggio et al.,2009). Effe

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::4df26054fb082163631d85a967c15307
https://doi.org/10.1182/blood.v118.21.5302.5302

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The Hydroxyurea Effects on Plasma Levels and Surface Expression of Adhesion Molecules ICAM-1 VCAM-1, E-SELECTIN and on Plasma Levels of Protein C and Protein S in Patients with Sickle Cell Disease and β-Thalassemia Intermedia

Autor: Gaetano Giuffrida, Maria Rocca Cingari, Nunziatina Laura Parrinello, Amalia Figuera

Publikováno v: Blood. 112:5468-5468

The pathophysiological mechanism of vaso-occlusion in Sickle Cell disease (SCA) is complex, involving adhesive processes between sickle red blood, leukocyte, and the activated endothelium. Reduced activity of the protein C and protein S may contribut

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::dba07b3824e1ff9787fc6843b945b13a
https://doi.org/10.1182/blood.v112.11.5468.5468

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Rituximab in Chronic Relapsing Acquired Thrombotic Thrombocytopenic Purpura

Autor: Santo Maccarone, Ernesto Di Francesco, Amalia Figuera, Rosario Giustolisi, Rocca Cingari, Gaetano Giuffrida

Publikováno v: Blood. 106:3997-3997

Thrombotic thrombocytopenic purpura (TTP) is a rare syndrome characterized by microangiopathic hemolytic anemia, thrombocytopenia, fever, renal failure and neurological manifestation. It is caused by a severe decreased of Von Willebrand factor cleavi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::b4bf528c0e9c5209d3dac4abeac0b980
https://doi.org/10.1182/blood.v106.11.3997.3997

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Repeated Echocardiographic Left Ventricular Ejection Fraction Measurements: A Strong and Accessible Tool for Detecting At High Risk of Heart Failure Thalassemia Major Population

Publikováno v: Publons

Abstract 3197 Background: The prognosis for thalassemia major (TM) has dramatically improved in the last two decades. However, many transfusion-dependent patients continue to develop secondary iron overloading, and eventually death, particularly from

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf5580d9acb2fcb9373516adabd90cc0
https://publons.com/publon/34078116/

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Bone turnover markers in patients with type 1 Gaucher disease

Autor: Anna Triolo, Gaetano Giuffrida, Alessandra Romano, Nunziatina Laura Parrinello, Francesco Di Raimondo, Maria Rocca Cingari, Magda Franceschino

Publikováno v: Scopus-Elsevier
Hematology Reports
Hematology Reports, Vol 4, Iss 4, Pp e21-e21 (2012)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b619b3692be4af84b73dd604919094e9
http://www.scopus.com/inward/record.url?eid=2-s2.0-84875392024&partnerID=MN8TOARS

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