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ugo ramenghi
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Diagnosing and treating Diamond Blackfan anaemia: results of an international clinical consensus conference
A Vlachos, S Ball, N Dahl, BP Alter, S Sheth, U Ramenghi, J Meerpohl, ...
British journal of haematology 142 (6), 859-876, 2008
545*2008
Outcomes 5 years after response to rituximab therapy in children and adults with immune thrombocytopenia
VL Patel, M Mahévas, SY Lee, R Stasi, S Cunningham-Rundles, ...
Blood, The Journal of the American Society of Hematology 119 (25), 5989-5995, 2012
4312012
Rituximab for the treatment of refractory autoimmune hemolytic anemia in children
M Zecca, B Nobili, U Ramenghi, S Perrotta, G Amendola, P Rosito, ...
Blood, The Journal of the American Society of Hematology 101 (10), 3857-3861, 2003
3732003
Multicentre Italian study of SARS-CoV-2 infection in children and adolescents, preliminary data as at 10 April 2020
S Garazzino, C Montagnani, D Donà, A Meini, E Felici, G Vergine, ...
Eurosurveillance 25 (18), 2000600, 2020
3462020
X–linked thrombocytopenia and Wiskott–Aldrich syndrome are allelic diseases with mutations in the WASP gene
A Villa, L Notarangelo, P Macchi, E Mantuano, G Cavagni, D Brugnoni, ...
Nature genetics 9 (4), 414-417, 1995
3261995
Mutations in ribosomal protein S19 gene and diamond blackfan anemia: wide variations in phenotypic expression
TN Willig, N Draptchinskaia, I Dianzani, S Ball, C Niemeyer, U Ramenghi, ...
Blood, The Journal of the American Society of Hematology 94 (12), 4294-4306, 1999
2771999
Chloride Channel ClCN7 Mutations Are Responsible for Severe Recessive, Dominant, and Intermediate Osteopetrosis
A Frattini, A Pangrazio, L Susani, C Sobacchi, M Mirolo, M Abinun, ...
Journal of bone and mineral research 18 (10), 1740-1747, 2003
2712003
Eltrombopag for children with chronic immune thrombocytopenia (PETIT2): a randomised, multicentre, placebo-controlled trial
JD Grainger, F Locatelli, T Chotsampancharoen, E Donyush, ...
The Lancet 386 (10004), 1649-1658, 2015
2492015
The ribosomal basis of Diamond‐Blackfan Anemia: mutation and database update
I Boria, E Garelli, HT Gazda, A Aspesi, P Quarello, E Pavesi, D Ferrante, ...
Human mutation 31 (12), 1269-1279, 2010
2462010
A proportion of patients with lymphoma may harbor mutations of the perforin gene
R Clementi, F Locatelli, L Dupré, A Garaventa, L Emmi, M Bregni, ...
Blood 105 (11), 4424-4428, 2005
2212005
Position of nonmuscle myosin heavy chain IIA (NMMHC‐IIA) mutations predicts the natural history of MYH9‐related disease
A Pecci, E Panza, N Pujol‐Moix, C Klersy, F Di Bari, V Bozzi, P Gresele, ...
Human mutation 29 (3), 409-417, 2008
2192008
Deficiency of the Fas apoptosis pathway without Fas gene mutations in pediatric patients with autoimmunity/lymphoproliferation
U Dianzani, M Bragardo, D DiFranco, C Alliaudi, P Scagni, D Buonfiglio, ...
Blood, The Journal of the American Society of Hematology 89 (8), 2871-2879, 1997
2131997
Stem cell transplantation in patients with severe congenital neutropenia without evidence of leukemic transformation
C Zeidler, K Welte, Y Barak, F Barriga, AA Bolyard, L Boxer, G Cornu, ...
Blood, The Journal of the American Society of Hematology 95 (4), 1195-1198, 2000
1872000
Immunopathological signatures in multisystem inflammatory syndrome in children and pediatric COVID-19
K Sacco, R Castagnoli, S Vakkilainen, C Liu, OM Delmonte, C Oguz, ...
Nature medicine 28 (5), 1050-1062, 2022
1762022
Cyclosporin A response and dependence in children with acquired aplastic anaemia: a multicentre retrospective study with long‐term observation follow‐up
P Saracco, P Quarello, AP Iori, M Zecca, D Longoni, J Svahn, S Varotto, ...
British journal of haematology 140 (2), 197-205, 2008
1592008
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disorders
P Noris, G Biino, A Pecci, E Civaschi, A Savoia, M Seri, F Melazzini, ...
Blood, The Journal of the American Society of Hematology 124 (6), e4-e10, 2014
1462014
Deficiency of the Fas apoptosis pathway without Fas gene mutations is a familial trait predisposing to development of autoimmune diseases and cancer
U Ramenghi, S Bonissoni, G Migliaretti, S DeFranco, F Bottarel, ...
Blood, The Journal of the American Society of Hematology 95 (10), 3176-3182, 2000
1372000
High levels of osteopontin associated with polymorphisms in its gene are a risk factor for development of autoimmunity/lymphoproliferation
A Chiocchetti, M Indelicato, T Bensi, R Mesturini, M Giordano, S Sametti, ...
Blood 103 (4), 1376-1382, 2004
1342004
Molecular basis of Diamond-Blackfan anemia: new findings from the Italian registry and a review of the literature
MF Campagnoli, E Garelli, P Quarello, A Carando, S Varotto, B Nobili, ...
haematologica 89 (4), 480-489, 2004
1342004
RPS19 mutations in patients with Diamond‐Blackfan anemia
MF Campagnoli, U Ramenghi, M Armiraglio, P Quarello, E Garelli, ...
Human mutation 29 (7), 911-920, 2008
1212008
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