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Sfoglia per Autore  FERRARI, MAURIZIO

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Titolo Data di pubblicazione Autore(i) File
Fetal diagnosis of beta-thalassaemia by DNA analysis in Italy 1-gen-1986 Camaschella, Clara; Saglio, G; Serra, A; Cremonesi, L; Travi, M; Ferrari, Maurizio
Meiotic recombination in the beta globin gene cluster causing an error in prenatal diagnosis of beta thalassaemia 1-gen-1988 Camaschella, Clara; Serra, A; Saglio, G; Bertero, Mt; Mazza, U; Terzoli, S; Brambati, B; Cremonesi, L; Travi, M; Ferrari, Maurizio
Sera from patients with IDDM and healthy individuals have antibodies to ICA69 on western blots but do not immunoprecipitate liquid phase antigen 1-gen-1994 Lampasona, V; Ferrari, Maurizio; Bosi, Emanuele; Pastore, Rm; Bingley, Pj; Bonifacio, E.
Identification of protein tyrosine phosphatase-like IA2 (islet cell antigen 512) as the insulin-dependent diabetes-related 37/40K autoantigen and a target of islet cell antibodies 1-gen-1995 Bonifacio, E; Lampasona, V; Genovese, S; Ferrari, Maurizio; Bosi, Emanuele
HLA-DQ screening for risk assessment of insulin-dependent diabetes in Northern Italy 1-gen-1995 Lampasona, V; Ferrari, Maurizio; Bonifacio, E; Pastore, Mr; Carrera, P; Sergi, A; Genovese, S; Trucco, M; Dorman, J; Bosi, Emanuele
HLA DQA1-DQB1-TAP2 haplotypes in IDDM families: no evidence for an additional contribution to disease risk by the TAP2 locus 1-gen-1995 Esposito, L; Lampasona, V; Bosi, Emanuele; Poli, F; Ferrari, Maurizio; Bonifacio, E.
Autoantibodies in insulin-dependent diabetes recognize distinct cytoplasmic domains of the protein tyrosin phosphatase-like IA-2 autoantigen 1-gen-1996 Lampasona, V; Bearzatto, M; Genovese, S; Bosi, Emanuele; Ferrari, Maurizio; Bonifacio, E.
Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the P/Q-type calcium channel alfa 1-subunit gene (CACNL1A4) on chromosome 19p13.1 1-gen-1996 Ophoff, R. A.; Terwindt, G. M.; Vergouwel, M. N.; VAN EIJK, R.; Oefner, P. J.; Hoffman, S. M. G.; Lamerdin, J. E.; Mohrenweiser, H. W.; Bulman, D. E.; Ferrari, Maurizio; Haan, J.; Frants, R. R.
Seven novel additional small mutations and a new alternative splicing in the human dystrophin gene detect by heteroduplex analysis and restricted RT-PCR heteroduplex analysis of illegitimate transcripts 1-gen-1996 A. M., Barbieri; N., Soriani; A., Ferlini; A., Michelato; Ferrari, Maurizio; P., Carrera
Temperature programmed capillary electrophoresis for detection of DNA point mutations 1-gen-1996 C., Gelfi; L., Cremonesi; Ferrari, Maurizio; P. G., Righetti
Lack of association of DMB polymorphism with insulin-dependent diabetes 1-gen-1997 Esposito, L; Lampasona, V; Bonifacio, E; Bosi, Emanuele; Ferrari, Maurizio
Rapid detection of 21-hydroxylase deficiency mutations by allele-specific in vitro amplification and capillary zone electrophoresis 1-gen-1997 P., Carrera; A. M., Barbieri; Ferrari, Maurizio; P. G., Righetti; M., Perego; C., Gelfi
Comparison of clinical-radiological and molecular findings in hypochondroplasia 1-gen-1998 Prinster, C; Carrera, P; DEL MASCHIO, M; Weber, Giovanna; Maghnie, M; Vigone, Mc; Mora, S; Tonini, G; Rigon, F; Beluffi, G; Severi, F; Chiumello, G; Ferrari, Maurizio
Genetic analysis of chromosome 2 in type 1 diabetes. Analysis of putative loci IDDM7, IDDM12 and IDDM13 and candidate genes NRAMP1 and IA-2 and the inteleukin-1 gene cluster 1-gen-1998 Esposito, L; Hill, Nj; Pritchard, Le; Cucca, F; Muxworthy, C; Merriman, Me; Wilson, A; Julier, C; Delepine, M; Tuomilehto, J; Tuomilehto Wolf, E; Ionesco Tirgoviste, C; Nisticò, L; Imdiab, Group; Buzzetti, R; Pozzilli, P; Ferrari, Maurizio; Bosi, Emanuele; Pociot, F; Nerup, J; Bain, Sc; Todd, Ja
Rapid capillary zone electrophoresis in isoelectric histidine buffer for high resolution of the poly-T tract allelic variants in intron 8 of the CFTR gene 1-gen-1998 Gelfi, C.; Perego, M.; Righetti, P. G.; Cainarca, S.; Firpo, S.; Ferrari, Maurizio; Cremonesi, L.
Validation of Double Gradient Denaturing Gradient Gel Electrophoresis through Multigenic Retrospective Analysis 1-gen-1999 Cremonesi, L.; Carrera, P.; Fumagalli, A.; Lucchiari, S.; Cardillo, E.; Ferrari, Maurizio; Righetti, S. C.; Zunino, F.; Righetti, P. G.; Gelfi, C.
A new CACNA1A Gene Mutation in Familial Hemiplegic Migraine Acetazolamide-Responsive and Ataxia 1-gen-1999 Battistini, S.; Stenirri, S.; Piatti, M.; Gelfi, C.; Righetti, P. G.; Rocchi, R.; Giannini, F.; Battistini, N.; Guazzi, G. C.; Ferrari, Maurizio; Carrera, P.
An approach for screening of Hereditary Hyperferritinemia Cataract Syndrome (HHCS) by a new DG-DGGE method for rapid mutational scanning in ferritin L-chain IRE. 1-gen-1999 Cremonesi, L; Fumagalli, A; Soriani, N; Ferrari, Maurizio; Tinazzi, E; Camparini, M; Aldigeri, R; Girelli, D; Arosio, P; Levi, SONIA MARIA ROSA
Genetic Heterogenity in Italian Families with Familial Hemiplegic Migraine 1-gen-1999 Carrera, P.; Piatti, M.; Stenirri, S.; Grimaldi, L. M. E.; Marchioni, E.; Curcio, M.; Righetti, Pg; Ferrari, Maurizio; Gelfi, C.
Involvement of the HLXB9 Homeobox Gene in Currarino Syndrome 1-gen-2000 Belloni, E.; Martucciello, G.; Verderio, D.; Ponti, E.; Seri, M.; Jasonniv, ; Torre, M.; Ferrari, Maurizio; Tsui, L. C.; Scherer, S.
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