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 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
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
Analysis of telomeres in peripheral blood cells from patients with bone marrow failure
2009-01-01 Pavesi E; Avondo F; Aspesi A; Quarello P; Rocci A; Vimercati C; Pigullo S; Dufour C; Ramenghi U; Dianzani I
Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress.
1989-01-01 RAMENGHI U; DAVID O; DIANZANI I; SACCHETTI L; BIASI F; CHIARPOTTO E; POLI G
| 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 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 | |
| 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 | |
| Analysis of telomeres in peripheral blood cells from patients with bone marrow failure | 2009 | Pavesi E; Avondo F; Aspesi A; Quarello P; Rocci A; Vimercati C; Pigullo S; Dufour C; Ramenghi U; Dianzani I | |
| Analysis of the carbonyl compounds produced in beta thalassaemic erythrocytes by oxidative stress. | 1989 | RAMENGHI U; DAVID O; DIANZANI I; SACCHETTI L; BIASI F; CHIARPOTTO E; POLI G |