SIMONI, GIUSEPPE

SIMONI, GIUSEPPE  

DIPARTIMENTO DI MEDICINA, CHIRURGIA E ODONTOIATRIA (attivo dal 01/01/1999 al 26/04/2012)  

Mostra records
Risultati 1 - 20 di 34 (tempo di esecuzione: 0.0 secondi).
Titolo Data di pubblicazione Autori Tipo File Abstract
Unusual detection of lathosterol in amniotic fluids investigated for the determination of cholesterol and 7-dehydrocholesterol for suspected Smith-Lemli-Opitz Syndrome 2014 V. GambaroF. FarèG. SimoniL. Dell’AcquaC. RusconiG. Roda + Article (author) -
The size of juxtaluminal hypoechoic area in ultrasound images of asymptomatic carotid plaques predicts the occurrence of stroke 2013 Ambrosio G.Arosio E.Simoni G.Catalano M.Salerno M.Thomas D.Simoni G. + Article (author) -
Confirmation of mosaicism and uniparental disomy in amniocytes, after detection of mosaic chromosome abnormalities in chorionic villi 2006 M. MiozzoG. Simoni + Article (author) -
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. PersicoV. SavasiE. FerrazziA.E. SempriniG. Simoni + Article (author) -
Ruolo di ESX1L nella spermatogenesi umana 2005 F.R. GratiS. M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Analisi dell'inattivazione del cromosoma X in donne affette da cirrosi biliare primitiva 2005 B. GentilinF.R. GratiP. InvernizziC. SelmiS.M. SirchiaF. RossellaG. SimoniM. Miozzo + Book Part (author) -
Ruolo di BRCA1 nella regolazione dell’espressione del gene XIST 2005 RAMOSCELLI, LISETTAG. SimoniM. MiozzoS.M. Sirchia + Book Part (author) -
Loss of the inactive X chromosome and replication of the active X in BRCA1-defective and wild-type breast cancer cells 2005 S.M. SirchiaL. RamoscelliF.R. GratiF. RossellaE. LesmaG. SimoniM. Miozzo + Article (author) -
X chromosome monosomy : a common mechanism for autoimmune diseases 2005 P. InvernizziM. MiozzoC. SelmiL. PersaniP.M. BattezzatiM. ZuinP.L. MeroniMARASINI, BIANCAF.R. GratiG. SimoniM. Podda + Article (author) -
Fetal and placental chromosomal mosaicism revealed by QF-PCR in severe IUGR pregnancies 2005 F.R. GratiM. MiozzoF. RossellaP. AntonazzoB. GentilinS.M. SirchiaS. RiganoG. BulfamanteI. CetinG. Simoni + Article (author) -
Three cases with de novo 6q imbalance and variable prenatal phenotype 2005 FR GratiB GentilinF RossellaI CetinG SimoniM Miozzo + Article (author) -
Biparental expression of ESX1L gene in placentas from normal and intrauterine growth-restricted pregnancies 2004 F.R. GratiS.M. SirchiaB. GentilinF. RossellaL. RamoscelliG. BulfamanteI. CetinG. SimoniM. Miozzo + Article (author) -
Loss of heterozygosity on chromosome 4q32-35 in sporadic basal cell carcinomas: evidence for the involvement of p33ING2/ING1L and SAP30 genes 2004 A. CerriS.M. SirchiaF. RossellaF.R. GratiG. Simoni + Article (author) -
Prenatal search for UPD 14 and UPD 15 in 83 cases of familial and de novo heterologous Robertsonian translocations 2004 M. MiozzoG. Simoni + Article (author) -
Frequency of monosomy X in women with primary biliary cirrhosis 2004 P. InvernizziM. MiozzoP.M. BattezzatiF.R. GratiG. SimoniC. SelmiM. Podda + Article (author) -
The role of imprinted genes in fetal growth 2002 M. MiozzoG. Simoni Article (author) -
Loss of heterozygosity of the NOS3 dinucleotide repeat marker in atherosclerotic plaques of human carotid arteries 2001 F.R. GratiG. GhilardiS.M. SirchiaR. ScorzaG. Simoni + Article (author) -
Post-zygotic origin of complete maternal chromosome 7 isodysomy and consequent loss of placental PEG1/MEST expression 2001 M. MiozzoT. RadaelliT. PersicoE. FerrazziI. CetinG. PardiG. Simoni + Article (author) -
Loss of heterozigosity of chromosomal region 4q32-35 in basal cell carcinomas 2000 S. SirchiaA. CerriF. RossellaF. GratiG. Simoni + Article (author) -
Losses of heterozygosity in oral and oropharyngeal epithelial carcinomas 2000 F.R. GratiS.M. SirchiaI. GaragiolaE. SironiF. RossellaR. BrusatiG. Simoni + Article (author) -