Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Gloria Colarusso"'
Autor:
Giovanna Graziadei, Lucia De Franceschi, Laura Sainati, Donatella Venturelli, Nicoletta Masera, Piero Bonomo, Aurora Vassanelli, Maddalena Casale, Gianluca Lodi, Vincenzo Voi, Paolo Rigano, Valeria Maria Pinto, Alessandra Quota, Lucia D. Notarangelo, Giovanna Russo, Massimo Allò, Rosamaria Rosso, Domenico D'Ascola, Elena Facchini, Silvia Macchi, Francesco Arcioni, Federico Bonetti, Enza Rossi, Antonella Sau, Saveria Campisi, Gloria Colarusso, Fiorina Giona, Roberto Lisi, Paola Giordano, Gianluca Boscarol, Aldo Filosa, Sarah Marktel, Paola Maroni, Mauro Murgia, Raffaella Origa, Filomena Longo, Marta Bortolotti, Raffaella Colombatti, Rosario Di Maggio, Raffaella Mariani, Alberto Piperno, Paola Corti, Carmelo Fidone, Giovanni Palazzi, Luca Badalamenti, Barbara Gianesin, Frédéric B. Piel, Gian Luca Forni
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Sickle cell disease (SCD) is a worldwide distributed hereditary red cell disorder characterized by recurrent acute vaso-occlusive crises (VOCs and anemia). Gold standard treatments are hydroxycarbamide (HC) and/or different red blood cell (RBC) trans
Externí odkaz:
https://doaj.org/article/398e4c9f5e034cb4a3d5f9a863a7b433
Autor:
Gloria Colarusso, Eleonora Gambineri, Elisabetta Lapi, Tommaso Casini, Fabio Tucci, Francesca Lippi, Chiara Azzari
Publikováno v:
Pediatric Reports, Vol 2, Iss 2, Pp e13-e13 (2010)
We report a case of an 8-year-old male patient with Evans syndrome and severe hypogammaglobulinemia, subsequently in whom the 22q11.2 deletion syndrome (22q11.2 DS) was diagnosed. No other clinical sign of 22q11.2 DS was present with the exception of
Externí odkaz:
https://doaj.org/article/99807840cc9e4d73b7ba82126bd29593
Autor:
Giovanna, Graziadei, Laura, Sainati, Pietro, Bonomo, Donatella, Venturelli, Nicoletta, Masera, Maddalena, Casale, Aurora, Vassanelli, Gianluca, Lodi, Frédéricb, Piel, Vincenzo, Voi, Lucia, Defranceschi, Paolo, Rigano, Alessandra, Quota, Luciadora, Notarangelo, Russo, MARIA GIOVANNA, Rosamaria, Rosso, Massimo, Allò, Domenico, D'Ascola, Elena, Facchini, Silvia, Macchi, Francesco, Arcioni, Alberto, Piperno, Federico, Bonetti, Giovanni, Palazzi, Mariagrazia, Bisconte, Antonella, Sau, Roberto, Lisi, Giona, Fiorina, Saveria, Campisi, Gloria, Colarusso, Paola, Giordano, Gianluca, Boscariol, Sarah, Marktel, Aldo, Filosa, Raffaella, Origa, Mauro, Murgia, Paola, Maroni, Barbara, Gianesin, Luca Badalamenti and Gian Luca, Forni.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3686::4d01110a86303b44aff6bd12d3b42514
http://hdl.handle.net/11573/1277725
http://hdl.handle.net/11573/1277725
Autor:
Frédéric B. Piel, Saveria Campisi, A. Vassanelli, Gianluca Boscariol, Giovanni Palazzi, Aldo Filosa, Gianluca Lodi, Vincenzo Voi, Roberto Lisi, Paola Giordano, Luca Badalamenti, Alberto Piperno, Barbara Gianesin, Gian Luca Forni, Maria Grazia Bisconte, Massimo Allò, Rosamaria Rosso, Lucia Dora Notarangelo, Giovanna Russo, Alessandra Quota, Lucia De Franceschi, Silvia Macchi, Giovanna Graziadei, Maddalena Casale, Elena Facchini, Fiorina Giona, Donatella Venturelli, Mauro Murgia, Paolo Rigano, Nicoletta Masera, Francesco Arcioni, Federico Bonetti, Paola Maroni, Laura Sainati, Raffaella Origa, Antonella Sau, Domenico Giuseppe D'Ascola, Sarah Marktel, Gloria Colarusso, Pietro Bonomo
Introduction. Despite the increasing of number of patients with Sickle Cell Disease (SCD) in Italy, due to multi-ethnic migratory phenomena, a large percentage of Caucasian sickle population is already present in Italy mainly with b-thal/HbS genotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7c5e0b8d294fa6e26920a3009d6c9bfd
http://hdl.handle.net/20.500.11769/371083
http://hdl.handle.net/20.500.11769/371083
Autor:
Maurizio de Martino, Chiara Azzari, Eleonora Gambineri, Stefano Stagi, Roberto Salti, Rita Jenuso, Elisabetta Lapi, Maurizio Genuardi, Francesco Chiarelli, Gloria Colarusso, Camilla Conti
Publikováno v:
Clinical Endocrinology. 72:839-844
Summary Introduction Monoallelic microdeletion of chromosome 22q11 (22q11DS) is considered to be the commonest human microdeletion syndrome. Abnormalities of thyroid function are sporadically reported in this syndrome, but very few studies have speci
Autor:
Sara Ciullini Mannurita, Eleonora Gambineri, Marina Vignoli, Stefano Frenos, Maurizio Aricò, Fabio Tucci, Claudio Favre, Gloria Colarusso, Matthew Collin, Veronica Tintori, Venetia Bigley, Marinella Veltroni
Publikováno v:
Journal of Allergy and Clinical Immunology. 138:1480-1483.e4
Autor:
Chiara Azzari, Francesca Lippi, Gloria Colarusso, Elisabetta Lapi, Eleonora Gambineri, Tommaso Casini, Fabio Tucci
Publikováno v:
Pediatric Reports
Pediatric Reports, Vol 2, Iss 2, Pp e13-e13 (2010)
Volume 2
Issue 2
Pediatric Reports, Vol 2, Iss 1, Pp e13-e13 (2010)
Pediatric Reports, Vol 2, Iss 2, Pp e13-e13 (2010)
Volume 2
Issue 2
Pediatric Reports, Vol 2, Iss 1, Pp e13-e13 (2010)
We report a case of an 8-year-old male patient with Evans syndrome and severe hypogammaglobulinemia, subsequently in whom the 22q11.2 deletion syndrome (22q11.2 DS) was diagnosed. No other clinical sign of 22q11.2 DS was present with the exception of
Autor:
Elisabetta Lapi, Gloria Colarusso, Francesco Chiarelli, Chiara Azzari, Eleonora Gambineri, Stefano Stagi, Maurizio Genuardi, Cristina Manoni, Camilla Conti, Maurizio de Martino
Publikováno v:
European journal of endocrinology. 163(2)
IntroductionAlthough hypoparathyroidism with hypocalcaemia is one of the most frequent clinical features of monoallelic microdeletion of chromosome 22q11 (22q11DS), bone mass and metabolism have not yet been assessed in these patients.DesignThis stud
Autor:
Stefano, Stagi, Elisabetta, Lapi, Eleonora, Gambineri, Roberto, Salti, Maurizio, Genuardi, Gloria, Colarusso, Camilla, Conti, Rita, Jenuso, Francesco, Chiarelli, Chiara, Azzari, Maurizio, de Martino
Publikováno v:
Clinical endocrinology. 72(6)
Monoallelic microdeletion of chromosome 22q11 (22q11DS) is considered to be the commonest human microdeletion syndrome. Abnormalities of thyroid function are sporadically reported in this syndrome, but very few studies have specifically assessed this