Search Results - "Terzoli, S"

Primer Note: A novel set of EST-SSR markers in Tamarix: a resource to characterize this genus by Terzoli, S., Cattan, E., Sabatti, M., Valentini, R., Zilberstain, A., Kuzminsky, E.

“…Both the negative and positive ecological impact of Tamarix plants is controversial, and thus a more comprehensive understanding is necessary. Tamarisks are…”
Get full text

Expression of Aux/IAA genes during development of sylleptic and proleptic buds in white poplar by Terzoli, S, Beritognolo, I, Giovannelli, A, Benelli, C, Migliaccio, F, Piconese, S, Sabatti, M, Kuzminsky, E, Scarascia Mugnozza, G

“…In this study, the genes of theAux/IAA family were used as functional markers to characterise bud break stages in a white poplar clone. In the first…”
Get full text

Growth and sexual maturation in thalassemia major by Borgna-Pignatti, C, De Stefano, P, Zonta, L, Vullo, C, De Sanctis, V, Melevendi, C, Naselli, A, Masera, G, Terzoli, S, Gabutti, V

“…Growth and sexual development were evaluated in 250 adolescents with beta-thalassemia major. Before transfusion hemoglobin concentration had not been less than…”
Get more information

Molecular recognition between cadherins studied by a coarse-grained model interacting with a coevolutionary potential by Terzoli, S, Tiana, G

“…Studying the conformations involved in the dimerization of cadherins is highly relevant to understand the development of tissue and its failure, which is…”
Get full text

Assessing genetic diversity of Tamarix spp. in three populations in Southern Italy by Terzoli, S., Abbruzzese, G., Beritognolo, I., Sabatti, M., Valentini, R., Kuzminsky, E.

Get full text

Congenital refractory anaemia with vacuolisation of bone marrow precursors, sideroblastosis and growth failure in a girl with normal endocrine pancreatic function by Sansone, G, Masera, G, Terzoli, S, Cantù-Rajnoldi, A

“…The case is described of an 8-years-old girl with consanguineous parents. She was apparently well, apart, from growth retardation, until 18 months of age when…”
Get more information

An unclassified case of congenital dyserythropoietic anaemia with a severe neonatal onset by Sansone, G, Masera, G, Cantù-Rajnoldi, A, Terzoli, S

“…The case of a 13-year-old child with a congenital dyserythropoietic anaemia (CDA) is reported. A severe anaemia associated with a slight increase in…”
Get more information

Cirrhosis associated with multiple transfusions in thalassaemia by Jean, G, Terzoli, S, Mauri, R, Borghetti, L, Di Palma, A, Piga, A, Magliano, M, Melevendi, M, Cattaneo, M

“…The study of surgical liver biopsy specimens obtained during splenectomy in 86 children with thalassaemia indicated that such patients may develop liver…”
Get full text

Hepatitis B or non-A, non-B virus infection in multitransfused thalassaemic patients by Moroni, G A, Piacentini, G, Terzoli, S, Jean, G, Masera, G

“…We undertook a four year study of 128 thalassaemic patients who had undergone several transfusions, to determine the incidence of hepatitis B virus markers and…”
Get full text

Feasibility of prenatal diagnosis of beta thalassaemia by DNA polymorphisms in an Italian population by Wainscoat, J S, Work, S, Sampietro, M, Cappellini, M D, Fiorelli, G, Terzoli, S, Weatherall, D J

“…A feasibility study of prenatal diagnosis of beta thalassaemia in a northern Italian population has been carried out. Twenty-five families have been studied,…”
Get more information

Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia by Camaschella, C, Serra, A, Saglio, G, Bertero, M T, Mazza, U, Terzoli, S, Brambati, B, Cremonesi, L, Travi, M, Ferrari, M

“…In the course of a prenatal diagnosis for beta thalassaemia by linkage analysis of restriction fragment length polymorphisms, a homozygous beta thalassaemia…”
Get full text

Sequential study of liver biopsy in thalassaemia by Masera, G, Jean, G, Conter, V, Terzoli, S, Mauri, R A, Cazzaniga, M

“…Liver biopsies were performed in 47 thalassaemic children. 33 of them had laboratory findings that suggested chronic hepatitis; the other 14 patients, without…”
Get full text

Phlebotomy to Reduce Iron Overload in Patients Cured of Thalassemia by Bone Marrow Transplantation by Angelucci, Emanuele, Muretto, Pietro, Lucarelli, Guido, Ripalti, Marta, Baronciani, Donatella, Erer, Buket, Galimberti, Maria, Giardini, Claudio, Gaziev, Djavid, Polchi, Paola

“…In thalassemia after successful bone marrow transplantation (BMT), iron overload remains an important cause of morbidity. After BMT, patients have normal…”
Get full text

Survival in thalassemia with conventional treatment by Borgna-Pignatti, C, Zurlo, M G, DeStefano, P, DiGregorio, F, Di Palma, A, Piga, A, Melevendi, C, Burattini, M G, Terzoli, S, Masera, G

Get more information

Intrauterine transfusion: the pediatric view by Marini, A, Cattaneo, F, Caccamo, M L, Barbarani, V, Terzoli, S, Dambrosio, F

Get more information

Treatment with biosynthetic growth hormone of short thalassaemic patients with impaired growth hormone secretion by Scacchi, M, Danesi, L, De Martin, M, Dubini, A, Forni, L, Masala, A, Gallisai, D, Burrai, C, Terzoli, S, Boffa, C

“…Impairment of linear growth is a common clinical feature in patients with beta-thalassaemia major. Although growth hormone secretion appears to be normal in…”
Get more information

Treatment of thalassemia by Terzoli, S, Fontanelli, G, Carnelli, V

“…The management of Cooley's anemia today is based on: a careful transfusional therapy using international schedules with standardized parameters for evaluating…”
Get more information

New therapeutic trends in thalassemia: oral chelating agents by Carnelli, V, Terzoli, S, Fossati, G, Careddu, G, Perri, M, Pedrotti, L, Mirra, N

“…The future therapeutic strategy for decreasing iron overload in poly-transfused patients will include oral chelation. The product currently undergoing the most…”
Get more information

Survival and causes of death in thalassaemia major by Zurlo, M G, De Stefano, P, Borgna-Pignatti, C, Di Palma, A, Piga, A, Melevendi, C, Di Gregorio, F, Burattini, M G, Terzoli, S

“…Survival and causes of death were studied in 1087 Italian patients with thalassaemia major who were born on or after Jan 1, 1960. At the age of 15 years, the…”
Get more information

Audiologic evaluation of patients with thalassemic syndromes treated with desferrioxamine B by Gaini, R M, Moretti, E, Boffa, C, Terzoli, S, Carnelli, V

“…Following various articles in literature which have appeared in the last 3 years regarding the neurotoxicity of desferrioxamine B we studied, from the auditory…”
Get more information