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Maria Luisa Tenchini

Showing results (21-30 of 33) with videos related to

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Thrombosis and Haemostasis|March 11, 2008
Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defectIlaria Guella, Giulia Soldà, Silvia Spena, et al.
Blood|April 9, 2004
Missense or splicing mutation? The case of a fibrinogen Bbeta-chain mutation causing severe hypofibrinogenemiaRosanna Asselta, Stefano Duga, Silvia Spena, et al.
European Journal of Gastroenterology & Hepatology|February 16, 2007
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian populationVera Bianchi, Giovanni Maconi, Sandro Ardizzone, et al.
Brain Research Bulletin|September 27, 2005
Two new putative susceptibility loci for ADNFLERomina Combi, Luigi Ferini-Strambi, Arianna Montruccoli, et al.
Haematologica|November 9, 2004
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patientsGiorgia Zadra, Rosanna Asselta, Massimo Malcovati, et al.
Blood|October 24, 2002
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant proteinStefano Duga, Maria Claudia Montefusco, Rosanna Asselta, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
BMC Genomics|April 18, 2008
Non-random retention of protein-coding overlapping genes in MetazoaGiulia Soldà, Mikita Suyama, Paride Pelucchi, et al.
Epilepsia|April 16, 2002
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsyStefano Duga, Rosanna Asselta, Maria Teresa Bonati, et al.
Journal of Neurology|August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated familiesMaria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Thrombosis and Haemostasis|March 11, 2008
Molecular characterization of two novel mutations causing factor XI deficiency: A splicing defect and a missense mutation responsible for a CRM+ defectIlaria Guella, Giulia Soldà, Silvia Spena, et al.
Blood|April 9, 2004
Missense or splicing mutation? The case of a fibrinogen Bbeta-chain mutation causing severe hypofibrinogenemiaRosanna Asselta, Stefano Duga, Silvia Spena, et al.
European Journal of Gastroenterology & Hepatology|February 16, 2007
Association of NOD2/CARD15 mutations on Crohn's disease phenotype in an Italian populationVera Bianchi, Giovanni Maconi, Sandro Ardizzone, et al.
Brain Research Bulletin|September 27, 2005
Two new putative susceptibility loci for ADNFLERomina Combi, Luigi Ferini-Strambi, Arianna Montruccoli, et al.
Haematologica|November 9, 2004
Molecular genetic analysis of severe coagulation factor XI deficiency in six Italian patientsGiorgia Zadra, Rosanna Asselta, Massimo Malcovati, et al.
Blood|October 24, 2002
Arg2074Cys missense mutation in the C2 domain of factor V causing moderately severe factor V deficiency: molecular characterization by expression of the recombinant proteinStefano Duga, Maria Claudia Montefusco, Rosanna Asselta, et al.
Blood|June 21, 2003
Clinical and molecular characterization of 6 patients affected by severe deficiency of coagulation factor V: Broadening of the mutational spectrum of factor V gene and in vitro analysis of the newly identified missense mutationsMaria Claudia Montefusco, Stefano Duga, Rosanna Asselta, et al.
BMC Genomics|April 18, 2008
Non-random retention of protein-coding overlapping genes in MetazoaGiulia Soldà, Mikita Suyama, Paride Pelucchi, et al.
Epilepsia|April 16, 2002
Mutational analysis of nicotinic acetylcholine receptor beta2 subunit gene (CHRNB2) in a representative cohort of Italian probands affected by autosomal dominant nocturnal frontal lobe epilepsyStefano Duga, Rosanna Asselta, Maria Teresa Bonati, et al.
Journal of Neurology|August 27, 2002
Exclusion of linkage of nine neuronal nicotinic acetylcholine receptor subunit genes expressed in brain in autosomal dominant nocturnal frontal lobe epilepsy in four unrelated familiesMaria Teresa Bonati, Romina Combi, Rosanna Asselta, et al.
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