Zobrazeno 1 - 10
of 70
pro vyhledávání: '"Salvati AM"'
Autor:
Maria Pia Cappabianca, Maria Pia Caforio, Maria Teresa Pasquino, Francesco Sorrentino, Patrizia Caprari, Salvati Am, Paolo Cianciulli, Donatella Maffi
Publikováno v:
Clinica Chimica Acta. 321:43-47
Background: Glucose-6-phosphate dehydrogenase (G6PD) deficiency is a common X chromosome-linked hereditary enzymopathy in humans. The authors have developed an amplification refractory mutation system (ARMS) to detect the G6PD Mediterranean mutation
Autor:
S. Amadori, Anna Tarzia, Paolo Cianciulli, Patrizia Caprari, Donatella Maffi, Salvati Am, Maria Pia Caforio, Maria Teresa Pasquino
Publikováno v:
Annals of Hematology. 80:41-44
A rare case of hereditary erythrocyte enzymopathy, namely 6-phosphogluconate dehydrogenase (6PGD) deficiency, was found in an Italian family. The activity of the enzyme was reduced to 35% in the propositus and her mother, but was normal in the other
Autor:
Barbara Furciniti La Chiusa, Patrizia Caprari, Argante Bozzi, Roberto Strom, Salvati Am, Anna Giuliani, Lucietta Ferroni
Publikováno v:
Biochemical Medicine and Metabolic Biology. 45:16-27
After in vitro treatment of normal, glucose-6-phosphate dehydrogenase-deficient or pyruvate kinase-deficient human erythrocytes with three different oxidizing agents, the extent of lipid peroxidative degradation and the alterations of membrane protei
Autor:
Anna Tarzia, Alessandro Stefani, Toshitaka Kawarai, Salvati Am, Antonio Pisani, Giorgio Bernardi, Adriana Rum, Antonio Orlacchio, Paolo Cianciulli, Paolo Calabresi, Patrizia Caprari
Publikováno v:
BMC Neurology, Vol 7, Iss 1, p 4 (2007)
BMC Neurology
BMC Neurology
Background Neuroacanthocytosis (NA) denotes a heterogeneous group of diseases that are characterized by nervous system abnormalities in association with acanthocytosis in the patients' blood. The 4.1R protein of the erythrocyte membrane is critical f
Autor:
Salvati Am, Anna Tarzia, Vincenzo Marigliano, Patrizia Caprari, Angelo Scuteri, D. Modesti, Alfredo Cantafora, Roberta Masella, C. Bauco
Publikováno v:
Experimental gerontology. 34(1)
Successful aging, characterized by little or no loss in physiological functions, should be the usual aging process in centenarians. It is known that well-preserved physiological functions depend on the proper functioning of cell systems. In this arti
Autor:
Alessandra Bottini, Maria Teresa Santini, Salvati Am, Argante Bozzi, Walter Malorni, Patrizia Caprari, Francesca Iosi
Publikováno v:
Chemico-biological interactions. 94(3)
The oxidative denaturation of the erythrocyte membrane, which is considered a major cause of the haemolytic process, 'was evaluated upon ‘in vitro’ oxidative stress with tert -butylhydroperoxide. Biochemical and ultrastructural analyses were perf
Autor:
Lucietta Ferroni, Anna Giuliani, Maria Teresa Ramacci, Bruno Giardina, Saverio C. Condò, Patrizia Caprari, Stefano Marini, Salvati Am
Publikováno v:
Advances in Experimental Medicine and Biology ISBN: 9781468459876
The appearance of band 3 structural modifications related to aging could be evidenced by means of monoclonal antibodies against senescence antigen. Hence in the attempt to provide an immunological marker of erythrocyte aging, we raised a monoclonal a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b7da5fbe305d1de3ee19b806166382a2
https://doi.org/10.1007/978-1-4684-5985-2_31
https://doi.org/10.1007/978-1-4684-5985-2_31
Autor:
M. Quarantelli, G. Zini, G. Marsili, Salvati Am, P. Berti, Mango G, C. Casini, M. P. Cappabianca, C. De Philippis, Pierluigi Rossi Ferrini, Giuseppe d'Onofrio
Publikováno v:
Clinical and laboratory haematology. 13(1)
In two institutions at Rome and Florence we evaluated the clinical sensitivity of two Coulter STKR systems using the NCCLS standard H20-T for leucocyte differential count in a patient population with high prevalence of haematologic abnormalities. Ref
Autor:
P Cianciulli, Salvati Am, Francesca Iosi, Walter Malorni, Patrizia Caprari, Gianfranco Donelli
Publikováno v:
Blood. 81:2821-2822
Akademický článek
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