PIETROGRANDE, MARIA CRISTINA
PIETROGRANDE, MARIA CRISTINA
Dipartimento di Scienze Cliniche e di Comunità
Long-term follow-up in common variable immunodeficiency: the pediatric-onset and adult-onset landscape
2023 M. Carrabba, M. Salvi, L.A. Baselli, S. Serafino, M. Zarantonello, E. Trombetta, M.C. Pietrogrande, G. Fabio, R.M. Dellepiane
Invasive meningococcal disease in three siblings with hereditary deficiency of the 8th component of complement: Evidence for the importance of an early diagnosis
2016 R.M. Dellepiane, L. Dell'Era, P. Pavesi, P. Macor, M. Giordano, L. De Maso, M.C. Pietrogrande, M. Cugno
Nutritional Status in Agammaglobulinemia : An Italian Multicenter Study
2015 R.M. Dellepiane, L. Dell’Era, L.V. Beilis, P. Pavesi, M. Raimondi, A. Soresina, V. Lougaris, M. Carrabba, B. Martire, S. Martino, G. Russo, G. Patuzzo, C. Pignata, G. Spadaro, R. Gallizzi, M. Duse, F.G. Specchia, V. Moschese, G.L. Marseglia, M.C. Pietrogrande, G. Bedogni, C. Agostoni
Intra-erythrocyte infusion of dexamethasone reduces neurological symptoms in ataxia teleangiectasia patients : results of a phase 2 trial
2014 L. Chessa, V. Leuzzi, A. Plebani, A. Soresina, R. Micheli, D. D'Agnano, T. Venturi, A. Molinaro, E. Fazzi, M. Marini, P. Ferremi Leali, I. Quinti, F.M. Cavaliere, G. Girelli, M.C. Pietrogrande, A. Finocchi, S. Tabolli, D. Abeni, M. Magnani
Clinical features and follow-up in patients with 22q11.2 deletion syndrome
2014 C. Cancrini, P. Puliafito, M.C. Digilio, A. Soresina, S. Martino, R. Rondelli, R. Consolini, E.M. Ruga, F. Cardinale, A. Finocchi, M.L. Romiti, B. Martire, R. Bacchetta, V. Albano, A. Carotti, F. Specchia, D. Montin, E. Cirillo, G. Cocchi, A. Trizzino, G. Bossi, O. Milanesi, C. Azzari, G. Corsello, C. Pignata, A. Aiuti, M.C. Pietrogrande, B. Marino, A.G. Ugazio, A. Plebani, P. Rossi
Does NADPH oxidase deficiency cause artery dilatation in humans?
2013 L. Loffredo, R. Carnevale, V. Sanguigni, A. Plebani, P. Rossi, C. Pignata, D. De Mattia, A. Finocchi, B. Martire, M.C. Pietrogrande, S. Martino, E. Gambineri, G. Giardino, A.R. Soresina, F. Martino, P. Pignatelli, F. Violi
Non invasive assessment of lung disease in ataxia telangiectasia by high-field magnetic resonance imaging
2013 S. Montella, C. Mollica, A. Finocchi, A. Pession, M.C. Pietrogrande, A. Trizzino, G. Ranucci, M. Maglione, G. Giardino, M. Salvatore, F. Santamaria, C. Pignata
Anti-infective prophylaxis for primary immunodeficiencies : what is done in Italian Primary Immunodeficiency Network centers (IPINet) and review of the literature
2013 V. Moschese, B. Martire, A. Soresina, L. Chini, S. Graziani, E. Monteferrario, R. Bacchetta, C. Cancrini, M. Fiorilli, E. Gambineri, A. Pession, C. Pignata, I. Quinti, R. Rondelli, P. Rossi, A.G. Ugazio, A. Plebani, M.C. Pietrogrande
Cardiopulmonary Exercise Testing in CVID and X-LA patients
2012 M. Carrabba, A. Pierini, M.C. Pietrogrande, R.M. Dellepiane, G. Fabio
Hyper-IgE syndrome : dental implications
2012 L. Esposito, L. Poletti, C. Maspero, A. Porro, M.C. Pietrogrande, P. Pavesi, R.M. Dellepiane, G. Farronato
A randomized trial of oral betamethasone to reduce ataxia symptoms in ataxia telangiectasia
2012 R. Zannolli, S. Buoni, G. Betti, S. Salvucci, A. Plebani, A. Soresina, M.C. Pietrogrande, S. Martino, V. Leuzzi, A. Finocchi, R. Micheli, L.N. Rossi, A. Brusco, F. Misiani, A. Fois, J. Hayek, C. Kelly, L. Chessa
Ruolo della tonsillectomia nella PFAPA syndrome
2010 M.C. Pietrogrande, R.M. Dellepiane, S. Torretta, P. Pavesi, L. Beilis, L. Pignataro
Hyper IgE syndrome (HIES): associazione genotipo-fenotipo
2010 R.M. Dellepiane, P. Pavesi, C. Woellner, M. Raimondi, L. Beilis, B. Grimbacher, M.C. Pietrogrande
Sindrome di Giobbe. Le nuove scoperte sull'associazione genotipo-fenotipo
2010 M. Raimondi, R.M. Dellepiane, P. Pavesi, L. Beilis, M.C. Pietrogrande
Centrally randomized, double-blind, crossover, multicenter phase 2 trial of betamethasone versus placebo in children with ataxia teleangiectasia
2010 R. Zannolli, S. Buoni, A. Plebani, A. Soresina, M.C. Pietrogrande, S. Martino, V. Leuzzi, A. Finocchi, A. Brusco, L. Chessa
Hyper-IgE syndrome: fatal progressive multifocal leukoencephalopathy in an Italian child with DOCK8 mutation
2010 R.M. Dellepiane, K. Engelhardt, D. Pfeifer, L. Beilis, M. Raimondi, P. Pavesi, L. Graham, M.C. Pietrogrande
Respiratory diseases in primary immunodeficienzies: severity assessment
2010 P. Pavesi, M. Carrabba, R.M. Dellepiane, M.F. Patria, N. Bonelli, S. Torretta, L. Beilis, G. Fabio, M.C. Pietrogrande
Mutations in STAT3 and diagnostic guidelines for hyper-IgE syndrome
2010 C. Woellner, E.M. Gertz, A.A. Schäffer, M. Lagos, M. Perro, E.O. Glocker, M.C. Pietrogrande, F. Cossu, J.L. Franco, N. Matamoros, B. Pietrucha, E. Heropolitanska Pliszka, M. Yeganeh, M. Moin, T. Español, S. Ehl, A.R. Gennery, M. Abinun, A. Breborowicz, T. Niehues, S. Sebnem Kilic, A. Junker, S.E. Turvey, A. Plebani, B. Sánchez, B.Z. Garty, C. Pignata, C. Cancrini, J. Litzman, Ö. Sanal, U. Baumann, R. Bacchetta, A.P. Hsu, J.N. Davis, L. Hammarström, E.G. Davies, E. Eren, P.D. Arkwright, J.S. Moilanen, D. Viemann, S. Khan, L. Maródi, A.J. Cant, A.F. Freeman, J.M. Puck, S.M. Holland, B. Grimbacher
Implicazione dei geni dell'immunità adattativa nella malattia di Kawasaki in pazienti residenti in Italia
2010 G. Bossi, S. Mannarino, G. Corana, M.C. Pietrogrande, P. Salice, R.M. Dellepiane, G.P. Noè, S. Grassidonio, F. Garlaschelli, A.L. Cremaschi, L. Salvaneschi, M. Martinetti, M. Stronati
Valutazione standardizzata delle complicanze polmonari in 15 pazienti con deficit primitivo dell'immunità umorale
2010 P. Pavesi, M. Carrabba, R.M. Dellepiane, M.F. Patria, N. Bonelli, L. Beilis, M. Raimondi, G. Fabio, M.C. Pietrogrande