Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Sandra Bosio"'
Autor:
Frédéric Blanc, François Peters, Jurriaan J. J. Gillissen, Michael E. Cates, Sandra Bosio, Camille Benarroche, Romain Mari
Publikováno v:
Physical Review Letters. 130
Dense non-Brownian suspensions exhibit a spectacular and abrupt drop in viscosity under change of shear direction, as revealed by shear inversions (reversals) or orthogonal superposition. Here, we introduce an experimental setup to systematically exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49cc3b7864710a1b9d7ba8d487e9461d
https://doi.org/10.1103/physrevlett.130.118202
https://doi.org/10.1103/physrevlett.130.118202
Autor:
Christophe Den Auwer, Simon Bayle, Maria Rosa Beccia, Sandra Bosio, Gaëlle Creff, Aurélie Jeanson, Hervé Michel, Christophe Pitiot, Cyril Zurita
Publikováno v:
Journal of Chemical Education. 99:646-653
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d15de92d8520c6f7c7d1a9bfcd6126f
https://doi.org/10.1021/acs.jchemed.1c00734
https://doi.org/10.1021/acs.jchemed.1c00734
Autor:
Clara Camaschella, Marta M. Cravino, P. Ghio, Giorgio V. Scagliotti, Sandra Bosio, Gabriella Zecchina
Publikováno v:
Clinical Lung Cancer. 8:264-267
Thrombotic risk is increased in patients with cancer and further potentiated by chemotherapy. We assessed whether early hemostatic alterations could represent a risk factor for thrombosis in patients undergoing chemotherapy for lung cancer.Forty-nine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a6a3654fd93370a9f1b35aac21329b4
https://doi.org/10.3816/clc.2007.n.004
https://doi.org/10.3816/clc.2007.n.004
Autor:
Maria Francesca Campagnoli, Bruno Oldani, Roberta Pimazzoni, Gabriella Zecchina, Sandra Bosio, Marco DeGobbi, Paola Bosso, Ugo Ramenghi
Publikováno v:
European Journal of Pediatrics. 161:499-502
We describe the onset of cataract in early infancy in a family with hereditary hyperferritinaemia-cataract syndrome. The two probands presented with isolated hyperferritinaemia and had developed cataracts at the age of 18 months. Two members of their
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0acd434b0d3744d2ae3f6973b579251c
https://doi.org/10.1007/s00431-002-1019-4
https://doi.org/10.1007/s00431-002-1019-4
Autor:
Domenico Girelli, Ugo Ramenghi, Sandra Bosio, Clara Camaschella, Sonia Levi, Roberto Corrocher, Claudia Bozzini, Gabriella Zecchina, Elisa Tinazzi, Jutta Peters, Alberto Piperno
Publikováno v:
British Journal of Haematology. 115:334-340
Summary. Hereditary hyperferritinaemia‐cataract syndrome (HHCS) is an autosomal dominant disease caused by mutations in the iron responsive element (IRE) of the lferritin gene. Despite the elucidation of the genetic basis, the overall clinical spec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ceeab4e03b318bf478b9c578861c694a
https://doi.org/10.1046/j.1365-2141.2001.03116.x
https://doi.org/10.1046/j.1365-2141.2001.03116.x
Autor:
Sandra Bosio, Silvia Fargion, Anna Vergani, Domenico Girelli, Alberto Piperno, Maurizio Sampietro, Gemino Fiorelli, Clara Camaschella, Dario Conte, Mirella Fraquelli, Raffaella Mariani, Cristina Arosio
Publikováno v:
British Journal of Haematology. 111:908-914
Severe iron overload has been reported in patients with the beta-thalassaemia trait. Studies performed before the discovery of the haemochromatosis gene (HFE) have yielded conflicting results: some suggest that iron overload might arise from the inte
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bf86d665c50b7044f5033cf25d4ad09
https://doi.org/10.1111/j.1365-2141.2000.02436.x
https://doi.org/10.1111/j.1365-2141.2000.02436.x
Autor:
Alberto Piperno, Raffaella Mariani, Cristina Arosio, Anna Vergani, Sandra Bosio, Silvia Fargion, Maurizio Sampietro, Domenico Girelli, Mirella Fraquelli, Dario Conte, Gemino Fiorelli, Clara Camaschella
Publikováno v:
British Journal of Haematology. 111:908-914
Severe iron overload has been reported in patients with the beta -thalassaemia trait. Studies performed before the discovery of the haemochromatosis gene (HFE) have yielded conflicting results: some suggest that iron overload might arise from the int
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35e19e05c734a9c333cc38a5d7759f7a
https://doi.org/10.1046/j.1365-2141.2000.02436.x
https://doi.org/10.1046/j.1365-2141.2000.02436.x
Autor:
Sonia Levi, Alessandro Campanella, Paolo E. Porporato, Laura Cremonesi, Sandra Bosio, Clara Camaschella, Enrico Gramaglia, Filomena Longo
Hyperferritinemia-cataract syndrome (HHCS) is a dominant disorder characterized by high serum ferritin and early onset of bilateral cataract. The disorder is caused by mutations in the iron-responsive element (IRE) of l-ferritin, which disrupt the po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9ab401a4402475e11da5bf3c2cca2e3
Autor:
Sandra Bosio, Massimo Terzolo, Clara Camaschella, Alberto Angeli, Fulvia Daffara, Barbara Allasino, Elena Brusa, Gianna Sacchetto, M. Ventura, Giuseppe Reimondo, Emiliano Aroasio
We evaluated serum homocysteine concentrations and the C677T polymorphism of the gene encoding for methylene tetrahydrofolate reductase, a key enzyme for homocysteine metabolism, in 57 patients with Cushing's syndrome, 41 with active disease, and 16
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6808c97813f3163412e209cba362f5e3
http://hdl.handle.net/2318/38814
http://hdl.handle.net/2318/38814
Autor:
Antonella Roetto, Marco De Gobbi, Mario Rizzetto, Claudio Lucetti, Sandra Bosio, Eugenio Leonardo, Gabriella Zecchina, Ubaldo Bonuccelli, Clara Camaschella, Lucia Petrozzi
Aceruloplasminemia is a recessive disorder characterized by anemia, iron overload, and neurodegeneration, caused by the absence of ceruloplasmin (Cp), a multicopper oxidase important for iron export. Few patients homozygous for loss of function mutat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7ee9629f93694f755c773fb82383b8
http://hdl.handle.net/2318/90234
http://hdl.handle.net/2318/90234