SIMONI, GIUSEPPE
SIMONI, GIUSEPPE
DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)
Unusual detection of lathosterol in amniotic fluids investigated for the determination of cholesterol and 7-dehydrocholesterol for suspected Smith-Lemli-Opitz Syndrome
2014 V. Gambaro, F. Farè, A. Barlocco, F. Maggi, G. Simoni, L. Dell’Acqua, C. Rusconi, G. Roda
The size of juxtaluminal hypoechoic area in ultrasound images of asymptomatic carotid plaques predicts the occurrence of stroke
2013 S.K. Kakkos, M.B. Griffin, A.N. Nicolaides, E. Kyriacou, M.M. Sabetai, T. Tegos, G.C. Makris, D.J. Thomas, G. Geroulakos, R. Adovasio, B. Ziani, F.P. Alo, C.G. Cicilioni, G. Ambrosio, A. Andreev, G.M. Andreozzi, F. Verlato, G. Camporese, E. Arosio, E. Barkauskas, A.A.B. Barros D'Sa, P. Brannigan, V. Batchvarova, A. Dramov, P. Belardi, G.P. Novelli, G. Simoni, P. Bell, G.M. Biasi, P. Mingazzini, N.M. Bornstein, D. Bouchier-Hayes, P. Fitzgerald, M.A. Cairols, P.G. Cao, P. Derango, G.P. Carboni, C. Geoffredo, M. Catalano, B. Chambers, M. Goetzmann, A. Dickinson, D. Clement, M. Bobelyn, S. Coccheri, E. Conti, E. Diamantopoulos, E.A. Andreadis, P.B. Dimakakos, T. Kotsis, B. Eikelboom, L. Entz, A. Ferrari-Bardile, T. Aloi, M. Salerno, J. Fernandes E Fernandes, L. Pedro, D.E. Fitzgerald, A.M. O'Shaughnessy, J. Fletcher, S. Forconi, R. Cappeli, M. Bicchi, S. Arrigucci, V. Gallai, G. Cardaiolli, G. Geroulakos, S. Kakkos, L.F. Gomez-Isaza, G. Gorgoyannis, N. Liasis, M. Graf, P. Guarini, S. Hardy, P. Harris, S. Aston, G. Iosa, A. Katsamouris, A. Giannoukas, M. Krzanowski, G. Ladurner, J. Leal-Monedero, B.B. Lee, C. Liapis, P. Galanis, W. Liboni, E. Pavanelli, E. Mannarino, G. Vaudo, P. Mccollum, R. Levison, G. Micieli, D. Bosone, L. Middleton, M. Pantziaris, T. Tyllis, E. Minar, A. Willfort, L. Moggi, P. Derango, G. Nenci, S. Radicchia, A. Nicolaides, S. Kakkos, D. Thomas, L. Norgren, E. Ribbe, S. Novo, R. Tantillo, D. Olinic, W. Paaske, A. Pagnan, P. Pauletto, V. Pagliara, G. Pettina, C. Pratesi, S. Matticari, J. Polivka, P. Sevcik, P. Poredos, A. Blinc, V. Videcnik, A. Pujia, A. Raso, P. Rispoli, M. Conforti, T. Robinson, M.S.J. Dennis, S. Rosfors, G. Rudofsky, T. Schroeder, M.L. Gronholdt, G. Simoni, C. Finocchi, G. Rodriguez, C. Spartera, M. Ventura, P. Scarpelli, M. Sprynger, B. Sadzot, C. Hottermans, M. Moonen, P.R. Taylor, A. Tovar-Pardo, J. Negreira, M. Vayssairat, J.M. Faintuch, J. Valaikiene, M.G. Walker, A.R. Wilkinson
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi
2006 F.R. Grati, B. Grimi, G. Frascoli, A.M. Di Meco, R. Liuti, S. Milani, A. Trotta, F. Dulcetti, E. Grosso, M. Miozzo, F. Maggi, G. Simoni
Detection of human immunodeficiency virus-1 RNA and DNA by extractive and in situ PCR in unprocessed semen and seminal fractions isolated by semen washing procedure
2006 T. Persico, V. Savasi, E. Ferrazzi, M. Oneta, A.E. Semprini, G. Simoni
Ruolo di ESX1L nella spermatogenesi umana
2005 E. Bonaparte, F.R. Grati, S.M. Sirchia, F. Rossella, G. Contalbi, F. Nerva, G.M. Colpi, G. Simoni, M. Miozzo
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST
2005 L. Ramoscelli, R. Azzimonti, M. Marsoni, G. Porta, G. Simoni, M. Miozzo, S.M. Sirchia
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva
2005 B. Gentilin, F.R. Grati, P. Invernizzi, C. Selmi, P. Busatto, S.M. Sirchia, F. Rossella, G. Simoni, M. Miozzo
Three cases with de novo 6q imbalance and variable prenatal phenotype
2005 FR Grati ,F Lalatta ,L Turolla ,U Cavallari ,B Gentilin ,F Rossella ,I Cetin ,P Antonazzo ,M Bellotti ,F Dulcetti ,D Baldo,R Tenconi,G Simoni,M Miozzo
X chromosome monosomy : a common mechanism for autoimmune diseases
2005 P. Invernizzi, M. Miozzo, C. Selmi, L. Persani, P.M. Battezzati, M. Zuin, S. Lucchi, P.L. Meroni, B. Marasini, S. Zeni, M. Watnik, F.R. Grati, G. Simoni, M.E. Gershwin, M. Podda
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells
2005 S.M. Sirchia, L. Ramoscelli, F.R. Grati, F. Barbera, D. Coradini, F. Rossella, G. Porta, E. Lesma, A. Ruggeri, P. Radice, G. Simoni, M. Miozzo
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies
2005 F.R. Grati, M. Miozzo, B. Cassani, F. Rossella, P. Antonazzo, B. Gentilin, S.M. Sirchia, L. Mori, S. Rigano, G. Bulfamante, I. Cetin, G. Simoni
Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations
2004 A. Ruggeri, F. Dulcetti, M. Miozzo, F.R. Grati, B. Grimi, S. Bellato, F. Natacci, F. Maggi, G. Simoni
Frequency of monosomy X in women with primary biliary cirrhosis
2004 P. Invernizzi, M. Miozzo, P.M. Battezzati, I. Bianchi, F.R. Grati, G. Simoni, C. Selmi, M. Watnik, M.E. Gershwin, M. Podda
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes
2004 E. Sironi, A. Cerri, D.Tomasini, S.M. Sirchia, G. Porta, F. Rossella, F.R. Grati, G. Simoni
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies
2004 F.R. Grati, S.M. Sirchia, B. Gentilin, F. Rossella, L. Ramoscelli, P. Antonazzo, U. Cavallari , G. Bulfamante, I. Cetin , G. Simoni, M. Miozzo
The role of imprinted genes in fetal growth
2002 M. Miozzo, G. Simoni
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries
2001 F.R. Grati, G. Ghilardi, S.M. Sirchia, F. Massaro, B. Cassani, R. Scorza, C. De Andreis, E. Sironi, G. Simoni
Post-zygotic origin of complete maternal chromosome 7 isodysomy and consequent loss of placental PEG1/MEST expression
2001 M. Miozzo, F. Grati, G. Bulfamante, F. Rossella, M. Cribiu, T. Radaelli, B. Cassani, T. Persico, E. Ferrazzi, I. Cetin, G. Pardi, G. Simoni
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas
2000 E. Sironi, S. Sirchia, A. Cerri, F. Rossella, F. Grati, R. Calcaterra, D. Tomasini, G. Simoni
Detection of maternal DNA in cord blood at birth after elective caesarean section or vaginal delivery
2000 A.E. Semprini, C. De Andreis, S. Fiore, I. Garagiola, S.M. Sirchia, V. Savasi, M.L. Newell, G. Simoni