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Correlation of fetal DNA levels in maternal plasma with Doppler status in pathological pregnacies 1-gen-2006 Smid, M; Galbiati, S; Lojacono, A; Valsecchi, L; Platto, C; Cavoretto, P; Calza, S; Ferrari, A; Ferrari, Maurizio; Cremonesi, L.
Duodenal duplication cyst causing severe pancreatitis: Imaging findings and pathological correlation 1-gen-2006 Guarise, A; Faccioli, N; Ferrari, M; Romano, L; Parisi, A; Falconi, M
De novo deletion removes a conserved motif in the C-terminus of ABCA4 and results in cone-rod dystrophy 1-gen-2006 Stenirri, S; Battistella, S; Fermo, I; Manitto, Mp; Martina, E; Brancato, R; Ferrari, Maurizio; Cremonesi, L.
Different approaches for noninvasive prenatal diagnosis of genetic diseases based on PNA-mediated enriched PCR 1-gen-2006 Galbiati, S; Restagno, G; F, ; Bonalumi, S; Travi, M; Piga, A; Sbaiz, L; Chiari, M; Damin, F; Smid, M; Valsecchi, L; Pasi, F; Ferrari, A; Ferrari, Maurizio; Cremonesi, L.
Microelectronic DNA chip for hereditary hyperferritinemia cataract syndrome, a model for large-scale analysis of disorders of iron metabolism 1-gen-2006 Ferrari, F; Foglieni, B; Arosio, P; Camaschella, Clara; Daraio, F; Levi, SONIA MARIA ROSA; García Erce, Ja; Beaumont, C; Cazzola, M; Ferrari, Maurizio; Cremonesi, L.
Skewed X-chromosome inactivation is not associated with premature ovarian failure in a large cohort of Italian patients. 1-gen-2006 Bione, S; Benedetti, S; Goegan, M; Menditto, I; Marozzi, A; Ferrari, Maurizio; Toniolo, D.
The ILAILL study: Iloprost as adjuvant to surgery for acute ischemia of lower limbs - A randomized, placebo-controlled, double-blind study by the Italian Society for Vascular and Endovascular Surgery 1-gen-2006 De Donato, G; Gussoni, G; De Donato, G; Andreozzi, Gm; Bonizzoni, E; Mazzone, A; Odero, A; Paroni, G; Setacci, C; Settembrini, P; Veglia, F; Martini, R; Setacci, F; Palombo, D; The Members of the ILAILL Study, Group; Chiesa, Roberto; Tshomba, Yamume; Ferrari, Maurizio
High-throughput mutation screening for beta-thalassemia by single-nucleotide extension 1-gen-2007 Galbiati, S; Chiari, M; Macellari, M; Ferrari, Maurizio; Cremonesi, L; Cretich, M.
Molecular scanning of the abca4 gene in spanish patients affected by retinitis pigmentosa and stargardt disease: identification of novel mutations 1-gen-2007 Stenirri, S; Battistella, S; Soriani, N; Bernal, S; Baiget, M; Ferrari, Maurizio; Cremonesi, L.
Unexplained Neonatal Respiratory Distress Due to Congenital Surfactant Deficiency 1-gen-2007 Marco, Somaschini; LAWRENCE M., Nogee; Isabella, Sassi; Olivier, Danhaive; Silvia, Presi; Renata, Boldrini; Cristina, Montrasio; Ferrari, Maurizio; SUSAN E., Wert; AND PAOLA, Carrera
Phenotypic clustering of lamin A/C mutations in neuromuscular patients 1-gen-2007 Benedetti, S; Menditto, I; Degano, M; Rodolico, C; Merlini, L; D'Amico, A; Palmucci, L; Berardinelli, A; Pegoraro, E; Trevisan, Cp; Morandi, L; Moroni, I; Galluzzi, G; Bertini, E; Toscano, A; Olive, M; Bonne, G; Mari, F; Caldara, R; Fazio, R; Mammi, I; Carrera, P; Toniolo, D; Comi, Giancarlo; Quattrini, A; Ferrari, Maurizio; Previtali, Sc
Integrated Strategy for Fast and Automated Molecular Characterization of Genes Involved in Craniosynostosis. 1-gen-2007 Stenirri, S; Restagno, G; Ferrero, Gb; Alaimo, G; Sbaiz, L1; Gomez, A1; Mari, C1c; Genitori, L; Ferrari, Maurizio; Cremonesi, L.
An overview of current microarray-based human globin gene mutation detection methods 1-gen-2007 Cremonesi, L; Ferrari, M; Giordano, Pc; Harteveld, Cl; Kleanthous, M; Papasavva, T; Patrinos, Gp; TRAEGER-SYNODINOS, J
Analysis of ferritin genes in Parkinson disease. 1-gen-2007 Foglieni, B; Ferrari, F; Goldwurm, S; Santambrogio, P; Castiglioni, E; Sessa, M; Volontè, Ma; Lalli, S; Galli, C; Wang, Xs; Connor, J; Sironi, F; Canesi, M; Biasiotto, G; Pezzoli, G; Levi, SONIA MARIA ROSA; Ferrari, Maurizio; Arosio, P; Cremonesi, L.
Genomic typing for patient-specific human leukocyte antigen-alleles is an efficient tool for relapse detection of high-risk hematopoietic malignancies after stem cell transplantation from alternative donors 1-gen-2008 Mazzi, B; Clerici, Td; Zanussi, M; Stanghellini, Mtl; Vago, L; Sironi, E; Peccatori, J; Bernardi, M; Carrera, P; Palini, A; Rossini, S; Bordignon, Claudio; Bonini, MARIA CHIARA; Ferrari, Maurizio; Ciceri, Fabio; Fleischhauer, K.
Evaluation of human gene variants detection in amplicon pools by the GS-FLX parallel 1-gen-2008 Bordoni, R; Bonnal, R; Rizzi, E; Carrera, P; Benedetti, S; Cremonesi, L; Stenirri, S; Colombo, A; Montrasio, C; Bonalumi, S; Albertini, A; ROSSI BERNARDI, L; Ferrari, Maurizio; DE BELLIS, G.
A fast microelectronic array for screening and prenatal diagnosis of beta-thalassemia 1-gen-2008 Foglieni, B; Galbiati, S; Ferrari, Maurizio; Cremonesi, L.
Development of new substrates for high sensitive genotyping of minority mutated alleles 1-gen-2008 Galbiati, S; Damin, F; DI CARLO, G; Ferrari, Maurizio; Cremonesi, L; Chiari, M.
Genomic Loss of the Mismatched HLA Locus in Leukemia Is a Major Mechanism of in Vivo Escape from T Cell Immunosurveillance Following Haploidentical HSCT 1-gen-2008 Vago, L; Perna, Sk; Zanussi, M; Mazzi, B; Stanghellini, Mtl; Perrelli, Nf; Forno, B; Corti, C; Bernardi, M; Peccatori, J; Ferrari, Maurizio; Rossini, S; Roncarolo, Mg; Bordignon, Claudio; Bonini, MARIA CHIARA; Ciceri, Fabio; Fleischhauer, K.
Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of ß-thalassemia 1-gen-2008 Galbiati, S; Foglieni, B; Travi, M; Curcio, C; Restagno, G; Sbaiz, L; Smid, M; Pasi, F; Ferrari, A; Ferrari, Maurizio; Cremonesi, L.
Mostrati risultati da 41 a 60 di 192
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