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Luigi Porcaro

Showing results (1-10 of 27) with videos related to

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Proteomes|May 14, 2020
Urinary Extracellular Vesicles and Salt-Losing Tubulopathies: A Proteomic ApproachFrancesca Raimondo, Clizia Chinello, Luigi Porcaro, et al.
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Complement System as a New Target for Hematopoietic Stem Cell Transplantation-Related Thrombotic MicroangiopathyGianluigi Ardissino, Valentina Capone, Silvana Tedeschi, et al.
Journal of Nephrology|January 11, 2022
Eculizumab treatment in atypical hemolytic uremic syndrome: correlation between functional complement tests and drug levelsMassimo Cugno, Valentina Capone, Samantha Griffini, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)Dario Degiorgio, Carla Colombo, Manuela Seia, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|April 6, 2026
Exercise-induced vasculitis with histological and genetic evidence of complement involvementMassimo Cugno, Paolo Calzari, Alessandra Di Benedetto, et al.
American Journal of Respiratory Cell and Molecular Biology|January 26, 2013
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator geneLucy Costantino, Damiana Rusconi, Giulia Soldà, et al.
Gene|February 8, 2012
A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) geneAnna Diana, Riccardina Tesse, Angela M Polizzi, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 20, 2011
A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysisLucy Costantino, Damiana Rusconi, Laura Claut, et al.
Clinical Chemistry and Laboratory Medicine|June 6, 2009
High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasmaFrancesca Bruno, Francesco Damin, Vincenza Causarano, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 30, 2010
A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patientsLucy Costantino, Laura Claut, Valentina Paracchini, et al.
Pageof 3

Showing results (1-10 of 27) with videos related to

Sort By:
Pageof 3
Proteomes|May 14, 2020
Urinary Extracellular Vesicles and Salt-Losing Tubulopathies: A Proteomic ApproachFrancesca Raimondo, Clizia Chinello, Luigi Porcaro, et al.
Pharmaceuticals (Basel, Switzerland)|July 27, 2022
Complement System as a New Target for Hematopoietic Stem Cell Transplantation-Related Thrombotic MicroangiopathyGianluigi Ardissino, Valentina Capone, Silvana Tedeschi, et al.
Journal of Nephrology|January 11, 2022
Eculizumab treatment in atypical hemolytic uremic syndrome: correlation between functional complement tests and drug levelsMassimo Cugno, Valentina Capone, Samantha Griffini, et al.
European Journal of Human Genetics : EJHG|August 30, 2007
Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3)Dario Degiorgio, Carla Colombo, Manuela Seia, et al.
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|April 6, 2026
Exercise-induced vasculitis with histological and genetic evidence of complement involvementMassimo Cugno, Paolo Calzari, Alessandra Di Benedetto, et al.
American Journal of Respiratory Cell and Molecular Biology|January 26, 2013
Fine characterization of the recurrent c.1584+18672A>G deep-intronic mutation in the cystic fibrosis transmembrane conductance regulator geneLucy Costantino, Damiana Rusconi, Giulia Soldà, et al.
Gene|February 8, 2012
A large deletion causes apparent homozygosity for the D1152H mutation in the cystic fibrosis transmembrane regulator (CFTR) geneAnna Diana, Riccardina Tesse, Angela M Polizzi, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|August 20, 2011
A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysisLucy Costantino, Damiana Rusconi, Laura Claut, et al.
Clinical Chemistry and Laboratory Medicine|June 6, 2009
High-sensitive microarray substrates specifically designed to improve sensitivity for the identification of fetal paternally inherited sequences in maternal plasmaFrancesca Bruno, Francesco Damin, Vincenza Causarano, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|September 30, 2010
A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patientsLucy Costantino, Laura Claut, Valentina Paracchini, et al.
Pageof 3