RAMENGHI, Ugo
RAMENGHI, Ugo
SCIENZE DELLA SANITA' PUBBLICA E PEDIATRICHE
A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease?
2020-01-01 Quarello, Paola; Garelli, Emanuela; Carando, Adriana; Cillario, Rebecca; Brusco, Alfredo; Giorgio, Elisa; Ferrante, Daniela; Corti, Paola; Zecca, Marco; Luciani, Matteo; Pierri, Filomena; Putti, Maria C; Cantarini, Maria E; Farruggia, Piero; Barone, Angelica; Cesaro, Simone; Russo, Giovanna; Fagioli, Franca; Dianzani, Irma; Ramenghi, Ugo
A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood
2004-01-01 L. Farinasso; L. Garbarini; F. Timeus; M.E. Basso; S. Aschero; A. Iavarone; A. Linari; E. Gottardi; U. Ramenghi; P. Saracco
A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia
2018-01-01 Aspesi, Anna*; Betti, Marta; Sculco, Marika; Actis, Chiara; Olgasi, Cristina; Wlodarski, Marcin W.; Vlachos, Adrianna; Lipton, Jeffrey M.; Ramenghi, Ugo; Santoro, Claudio; Follenzi, Antonia; Ellis, Steven R.; Dianzani, Irma
A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation
2015-01-01 Clemente, N; Boggio, E.; Gigliotti, C.L.; Orilieri, E.; Cappellano, G.; Toth, E.; Valletti, P.A.; Santoro, C.; Quinti, I.; Pignata, C.; Notarangelo, L.D.; Dianzani, C.; Dianzani, I.; Ramenghi, U.; Dianzani, U.; Chiocchetti, A.
A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia
2008-01-01 Ilenia Boria; Paola Quarello; Federica Avondo; Emanuela Garelli; Anna Aspesi; Adriana Carando; Maria Francesca Campagnoli; Irma Dianzani; Ugo Ramenghi
A practical approach to diagnosis and treatment of symptomatic thromboembolic events in children with acute lymphoblastic leukemia: Recommendations of the "coagulation defects" AIEOP Working Group
2007-01-01 Giordano P, Del Vecchio GC, Saracco P, Zecca M, Molinari AC, De Mattia D; Cougulation Defects AIEOP Working Group. Collaboration Group: Del Principe D, Jankovic M, Nobili B, Nardi Mh, Ramenghi U, Russo G, Santoro Nk.
A proportion of patients with lymphoma may harbor mutations of the perforin gene
2005-01-01 CLEMENTI R; LOCATELLI F; DUPRÉ L; GARAVENTA A; EMMI L; BREGNI M; CEFALO G; MORETTA A; DANESINO C; COMIS M; PESSION A; RAMENGHI U; MACCARIO R; ARICÒ M; RONCAROLO MG
A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome
2020-01-01 Cesaro S.; Pegoraro A.; Sainati L.; Lucidi V.; Montemitro E.; Corti P.; Ramenghi U.; Nasi C.; Menna G.; Zecca M.; Danesino C.; Nicolis E.; Pasquali F.; Perobelli S.; Tridello G.; Farruggia P.; Cipolli M.
Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia
2016-01-01 Parodi, Emilia; Giraudo, Maria Teresa; Ricceri, Fulvio; Aurucci, Maria Luigia; Mazzone, Raffaela; Ramenghi, Ugo
Acquired aplastic anaemia in children: Diagnostic-therapeutic recommendations
2014-01-01 Barone A; Lucarelli A; Onofrillo D; Verzegnassi F; Bonanomi S; Longoni D; Cesaro S; Cugno C; Zecca M; Fioredda F; Svahn J; Dufour C; Iori AP; Ladogana S; Maruzzi M; Locasciulli A; Lanciotti M; Macaluso A; Mandaglio R; Marra N; Menna G; Martire B; Notarangelo LD; Palazzi G; Pillon M; Ramenghi U; Saracco P; Russo G; Timeus F; Tucci F; Farruggia P.
ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia
2018-01-01 Faleschini M.; Melazzini F.; Marconi C.; Giangregorio T.; Pippucci T.; Cigalini E.; Pecci A.; Bottega R.; Ramenghi U.; Siitonen T.; Seri M.; Pastore A.; Savoia A.; Noris P.
ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization.
2015-01-01 Bottega R; Marconi C; Faleschini M; Baj G; Cagioni C; Pecci A; Pippucci T; Ramenghi U; Pardini S; Ngu L; Baronci C; Kunishima S; Balduini CL; Seri M; Savoia A; Noris P.
Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica.
2000-01-01 De Mattia D; Del Principe D; Del Vecchio GC; Jankovic M; Arrighini A; Giordano P; Menichelli A; Mori P; Zecca M; Pession A. Collaboration group: Schettini F; Masera G; Macchia P; Amendola G; Baligan M; Baronci C; Biddau P; Borgna C; Crupi S; De Santis R; Felici L; Laffranchi M; Mancuso G; Massolo F; Nespoli L; Nobili B; Ramenghi U; Russo G; Tucci F.
Acute non-lymphatic leukemia in children
1983-01-01 Pastore G; Miniero R; Cordero di Montezemolo L; Besenzon L; Saracco P; Fiandino G; Grazia G; Ramenghi U; Nicola P; Madon E.
Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor.
1992-01-01 MINIERO R ;MADON E ;ARTESANI L ;BUSCA A ;SANDRI A ;AGLIETTA M ;RAMENGHI U
Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival.
1984-01-01 MINIERO R ;DAVID O ;GHIGO D ;LUZZATTO L ;RAMENGHI U ;SARACCO P ;MORICI G ;NICOLA P
Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent Neuropsychiatry
2024-01-01 Calcaterra, Valeria; Tornese, Gianluca; Zuccotti, Gianvincenzo; Staiano, Annamaria; Cherubini, Valentino; Gaudino, Rossella; Fazzi, Elisa Maria; Barbi, Egidio; Chiarelli, Francesco; Corsello, Giovanni; Esposito, Susanna Maria Roberta; Ferrara, Pietro; Iughetti, Lorenzo; Laforgia, Nicola; Maghnie, Mohamad; Marseglia, Gianluigi; Perilongo, Giorgio; Pettoello-Mantovani, Massimo; Ruggieri, Martino; Russo, Giovanna; Salerno, Mariacarolina; Striano, Pasquale; Valerio, Giuliana; Wasniewska, Malgorzata; null, null; Agosti, Massimo; Agostoni, Carlo Virginio; Aiuti, Alessandro; Azzari, Chiara; Badolato, Raffaele; Balduzzi, Adriana; Baraldi, Eugenio; Canani, Roberto Berni; Biffi, Alessandra; Biondi, Andrea; Bisogno, Gianni; Pierri, Nicola Brunetti; Carnielli, Virginio; Cianfarani, Stefano; Cogo, Paola; Corvaglia, Luigi; Dani, Carlo; Di Salvo, Giovanni; Fagioli, Franca; Fanos, Vassilios; Ferrero, Giovanni Battista; Francavilla, Ruggiero; Galli, Luisa; Gazzolo, Diego; Giaquinto, Carlo; Giordano, Paola; Gitto, Eloisa; Grosso, Salvatore; Guarino, Alfredo; Indrio, Flavia; Lanari, Marcello; Lionetti, Paolo; Locatelli, Franco; Lombardo, Fortunato; Maffeis, Claudio; Marino, Bruno; Midulla, Fabio; Del Giudice, Emanuele Miraglia; Del Giudice, Michele Miraglia; Montini, Giovanni; Parenti, Giancarlo; Parisi, Pasquale; Peroni, Diego; Perrotta, Silverio; Piacentini, Giorgio; Pietrobelli, Angelo; Raimondi, Francesco; Ramenghi, Ugo; Ravelli, Angelo; Romano, Claudio; Rossi, Francesca; Rossi, Paolo; Damiano, Vincenzo Salpietro; Spalice, Alberto; Suppiej, Agnese; Troncone, Riccardo; Verrotti, Alberto
Alteration of liver enzymes is a feature of the MYH9-related disease syndrome.
2012-01-01 Pecci, A; Biino, G; Fierro, T; Bozzi, V; Mezzasoma, A; Noris, P; Ramenghi, U; Loffredo, G; Fabris, F; Momi, S; Magrini, U; Pirastu, M; Savoia, A; Balduini, C; Gresele, P; Italian Registry for MYH9-releated diseases.
Altered regulatory mechanisms governing cell survival in children affected with clustering of autoimmune disorders.
2012-01-01 Palamaro L; Giardino G; Santamaria F; Ramenghi U; Dianzani U; Pignata C.
Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients
2010-01-01 Ramenghi U ;Quarello P ;Garelli E ;Carando A;Lorenzati A ;Ansaldi G;Davitto M ;Boria I; Aspesi A ;Dianzani I
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A 20-year long term experience of the Italian Diamond-Blackfan Anaemia Registry: RPS and RPL genes, different faces of the same disease? | 2020 | Quarello, Paola; Garelli, Emanuela; Carando, Adriana; Cillario, Rebecca; Brusco, Alfredo; Giorgio, Elisa; Ferrante, Daniela; Corti, Paola; Zecca, Marco; Luciani, Matteo; Pierri, Filomena; Putti, Maria C; Cantarini, Maria E; Farruggia, Piero; Barone, Angelica; Cesaro, Simone; Russo, Giovanna; Fagioli, Franca; Dianzani, Irma; Ramenghi, Ugo | |
| A comprehensive diagnostic surveillance protocol for idiopathic (de novo) and secondary myelodisplastic syndromes in childhood | 2004 | L. Farinasso; L. Garbarini; F. Timeus; M.E. Basso; S. Aschero; A. Iavarone; A. Linari; E. Gottardi; U. Ramenghi; P. Saracco | |
| A functional assay for the clinical annotation of genetic variants of uncertain significance in Diamond–Blackfan anemia | 2018 | Aspesi, Anna*; Betti, Marta; Sculco, Marika; Actis, Chiara; Olgasi, Cristina; Wlodarski, Marcin W.; Vlachos, Adrianna; Lipton, Jeffrey M.; Ramenghi, Ugo; Santoro, Claudio; Follenzi, Antonia; Ellis, Steven R.; Dianzani, Irma | |
| A mutation in caspase-9 decreases the expression of BAFFR and ICOS in patients with immunodeficiency and lymphoproliferation | 2015 | Clemente, N; Boggio, E.; Gigliotti, C.L.; Orilieri, E.; Cappellano, G.; Toth, E.; Valletti, P.A.; Santoro, C.; Quinti, I.; Pignata, C.; Notarangelo, L.D.; Dianzani, C.; Dianzani, I.; Ramenghi, U.; Dianzani, U.; Chiocchetti, A. | |
| A new database for ribosomal protein genes which are mutated in Diamond-Blackfan Anemia | 2008 | Ilenia Boria; Paola Quarello; Federica Avondo; Emanuela Garelli; Anna Aspesi; Adriana Carando; Maria Francesca Campagnoli; Irma Dianzani; Ugo Ramenghi | |
| A practical approach to diagnosis and treatment of symptomatic thromboembolic events in children with acute lymphoblastic leukemia: Recommendations of the "coagulation defects" AIEOP Working Group | 2007 | Giordano P, Del Vecchio GC, Saracco P, Zecca M, Molinari AC, De Mattia D; Cougulation Defects AIEOP Working Group. Collaboration Group: Del Principe D, Jankovic M, Nobili B, Nardi Mh, Ramenghi U, Russo G, Santoro Nk. | |
| A proportion of patients with lymphoma may harbor mutations of the perforin gene | 2005 | CLEMENTI R; LOCATELLI F; DUPRÉ L; GARAVENTA A; EMMI L; BREGNI M; CEFALO G; MORETTA A; DANESINO C; COMIS M; PESSION A; RAMENGHI U; MACCARIO R; ARICÒ M; RONCAROLO MG | |
| A Prospective Study of Hematologic Complications and Long-Term Survival of Italian Patients Affected by Shwachman-Diamond Syndrome | 2020 | Cesaro S.; Pegoraro A.; Sainati L.; Lucidi V.; Montemitro E.; Corti P.; Ramenghi U.; Nasi C.; Menna G.; Zecca M.; Danesino C.; Nicolis E.; Pasquali F.; Perobelli S.; Tridello G.; Farruggia P.; Cipolli M. | |
| Absolute reticulocyte count and reticulocyte hemoglobin content as predictors of early response to exclusive oral iron in children with iron deficiency anemia | 2016 | Parodi, Emilia; Giraudo, Maria Teresa; Ricceri, Fulvio; Aurucci, Maria Luigia; Mazzone, Raffaela; Ramenghi, Ugo | |
| Acquired aplastic anaemia in children: Diagnostic-therapeutic recommendations | 2014 | Barone A; Lucarelli A; Onofrillo D; Verzegnassi F; Bonanomi S; Longoni D; Cesaro S; Cugno C; Zecca M; Fioredda F; Svahn J; Dufour C; Iori AP; Ladogana S; Maruzzi M; Locasciulli A; Lanciotti M; Macaluso A; Mandaglio R; Marra N; Menna G; Martire B; Notarangelo LD; Palazzi G; Pillon M; Ramenghi U; Saracco P; Russo G; Timeus F; Tucci F; Farruggia P. | |
| ACTN1 mutations lead to a benign form of platelet macrocytosis not always associated with thrombocytopenia | 2018 | Faleschini M.; Melazzini F.; Marconi C.; Giangregorio T.; Pippucci T.; Cigalini E.; Pecci A.; Bottega R.; Ramenghi U.; Siitonen T.; Seri M.; Pastore A.; Savoia A.; Noris P. | |
| ACTN1-related thrombocytopenia: identification of novel families for phenotypic characterization. | 2015 | Bottega R; Marconi C; Faleschini M; Baj G; Cagioni C; Pecci A; Pippucci T; Ramenghi U; Pardini S; Ngu L; Baronci C; Kunishima S; Balduini CL; Seri M; Savoia A; Noris P. | |
| Acute childhood idiopathic thrombocytopenic purpura: AIEOP consensus guidelines for diagnosis and treatment. Associazione Italiana di Ematologia e Oncologia Pediatrica. | 2000 | De Mattia D; Del Principe D; Del Vecchio GC; Jankovic M; Arrighini A; Giordano P; Menichelli A; Mori P; Zecca M; Pession A. Collaboration group: Schettini F; Masera G; Macchia P; Amendola G; Baligan M; Baronci C; Biddau P; Borgna C; Crupi S; De Santis R; Felici L; Laffranchi M; Mancuso G; Massolo F; Nespoli L; Nobili B; Ramenghi U; Russo G; Tucci F. | |
| Acute non-lymphatic leukemia in children | 1983 | Pastore G; Miniero R; Cordero di Montezemolo L; Besenzon L; Saracco P; Fiandino G; Grazia G; Ramenghi U; Nicola P; Madon E. | |
| Acute pulmonary failure after the first administration of recombinant human granulocyte-macrophage colony-stimulating factor. | 1992 | MINIERO R ;MADON E ;ARTESANI L ;BUSCA A ;SANDRI A ;AGLIETTA M ;RAMENGHI U | |
| Administration of vitamin E in heterozygous beta-thalassaemia: the effect on red blood cell survival. | 1984 | MINIERO R ;DAVID O ;GHIGO D ;LUZZATTO L ;RAMENGHI U ;SARACCO P ;MORICI G ;NICOLA P | |
| Adolescent gender dysphoria management: position paper from the Italian Academy of Pediatrics, the Italian Society of Pediatrics, the Italian Society for Pediatric Endocrinology and Diabetes, the Italian Society of Adolescent Medicine and the Italian Society of Child and Adolescent Neuropsychiatry | 2024 | Calcaterra, Valeria; Tornese, Gianluca; Zuccotti, Gianvincenzo; Staiano, Annamaria; Cherubini, Valentino; Gaudino, Rossella; Fazzi, Elisa Maria; Barbi, Egidio; Chiarelli, Francesco; Corsello, Giovanni; Esposito, Susanna Maria Roberta; Ferrara, Pietro; Iughetti, Lorenzo; Laforgia, Nicola; Maghnie, Mohamad; Marseglia, Gianluigi; Perilongo, Giorgio; Pettoello-Mantovani, Massimo; Ruggieri, Martino; Russo, Giovanna; Salerno, Mariacarolina; Striano, Pasquale; Valerio, Giuliana; Wasniewska, Malgorzata; null, null; Agosti, Massimo; Agostoni, Carlo Virginio; Aiuti, Alessandro; Azzari, Chiara; Badolato, Raffaele; Balduzzi, Adriana; Baraldi, Eugenio; Canani, Roberto Berni; Biffi, Alessandra; Biondi, Andrea; Bisogno, Gianni; Pierri, Nicola Brunetti; Carnielli, Virginio; Cianfarani, Stefano; Cogo, Paola; Corvaglia, Luigi; Dani, Carlo; Di Salvo, Giovanni; Fagioli, Franca; Fanos, Vassilios; Ferrero, Giovanni Battista; Francavilla, Ruggiero; Galli, Luisa; Gazzolo, Diego; Giaquinto, Carlo; Giordano, Paola; Gitto, Eloisa; Grosso, Salvatore; Guarino, Alfredo; Indrio, Flavia; Lanari, Marcello; Lionetti, Paolo; Locatelli, Franco; Lombardo, Fortunato; Maffeis, Claudio; Marino, Bruno; Midulla, Fabio; Del Giudice, Emanuele Miraglia; Del Giudice, Michele Miraglia; Montini, Giovanni; Parenti, Giancarlo; Parisi, Pasquale; Peroni, Diego; Perrotta, Silverio; Piacentini, Giorgio; Pietrobelli, Angelo; Raimondi, Francesco; Ramenghi, Ugo; Ravelli, Angelo; Romano, Claudio; Rossi, Francesca; Rossi, Paolo; Damiano, Vincenzo Salpietro; Spalice, Alberto; Suppiej, Agnese; Troncone, Riccardo; Verrotti, Alberto | |
| Alteration of liver enzymes is a feature of the MYH9-related disease syndrome. | 2012 | Pecci, A; Biino, G; Fierro, T; Bozzi, V; Mezzasoma, A; Noris, P; Ramenghi, U; Loffredo, G; Fabris, F; Momi, S; Magrini, U; Pirastu, M; Savoia, A; Balduini, C; Gresele, P; Italian Registry for MYH9-releated diseases. | |
| Altered regulatory mechanisms governing cell survival in children affected with clustering of autoimmune disorders. | 2012 | Palamaro L; Giardino G; Santamaria F; Ramenghi U; Dianzani U; Pignata C. | |
| Analysis of seven ribosomal protein genes in Italian Diamond Blackfan anemia patients | 2010 | Ramenghi U ;Quarello P ;Garelli E ;Carando A;Lorenzati A ;Ansaldi G;Davitto M ;Boria I; Aspesi A ;Dianzani I |