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Concolino

Showing results (111-120 of 347) with videos related to

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European Journal of Medical Genetics|July 1, 2008
Precocious puberty in Sanfilippo IIIA disease: diagnosis and follow-up of two new casesD Concolino, G Muzzi, L Pisaturo, et al.
Molecular Genetics and Metabolism|September 29, 2023
c.376A>G, (p.Ser126Gly) Alpha-Galactosidase A mutation induces ER stress, unfolded protein response and reduced enzyme trafficking to lysosome: Possible relevance in the pathogenesis of late-onset forms of Fabry DiseaseConcetta Riillo, Giuseppe Bonapace, Maria Teresa Moricca, et al.
Hormone Research|January 1, 1977
Prolactinemia during hemodialysis: lack of correlation with sodium, potassium and renin-aldosterone systemF Sciarra, F Sparano, G Giaquinto, et al.
Pediatric Blood & Cancer|May 8, 2009
A prolonged neonatal jaundice associated with a rare G6PD mutationAngelo Minucci, Paola Concolino, Daniele De Luca, et al.
Pediatric Nephrology (Berlin, Germany)|April 30, 2021
Fabry disease and kidney involvement: starting from childhood to understand the futureRoberto Chimenz, Valeria Chirico, Caterina Cuppari, et al.
Inorganic Chemistry|January 16, 2003
Synthesis of Cl2InN3, Br2InN3, and related adductsC Steffek, J McMurran, B Pleune, et al.
Urology|February 1, 1993
Acquired cystic kidney disease: the hormonal hypothesisG Concolino, C Lubrano, M Ombres, et al.
Clinical Chemistry and Laboratory Medicine|March 28, 2014
Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detectionPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|June 25, 2004
High seroprevalence of Helicobacter pylori infection in non-institutionalised children with mental retardationF Luzza, D Concolino, M Imeneo, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
GAPO syndrome associated with vestibular dysfunction and hearing lossM Rapsomaniki, G Chiarella, I Mascaro, et al.
Pageof 35

Showing results (111-120 of 347) with videos related to

Sort By:
Pageof 35
European Journal of Medical Genetics|July 1, 2008
Precocious puberty in Sanfilippo IIIA disease: diagnosis and follow-up of two new casesD Concolino, G Muzzi, L Pisaturo, et al.
Molecular Genetics and Metabolism|September 29, 2023
c.376A>G, (p.Ser126Gly) Alpha-Galactosidase A mutation induces ER stress, unfolded protein response and reduced enzyme trafficking to lysosome: Possible relevance in the pathogenesis of late-onset forms of Fabry DiseaseConcetta Riillo, Giuseppe Bonapace, Maria Teresa Moricca, et al.
Hormone Research|January 1, 1977
Prolactinemia during hemodialysis: lack of correlation with sodium, potassium and renin-aldosterone systemF Sciarra, F Sparano, G Giaquinto, et al.
Pediatric Blood & Cancer|May 8, 2009
A prolonged neonatal jaundice associated with a rare G6PD mutationAngelo Minucci, Paola Concolino, Daniele De Luca, et al.
Pediatric Nephrology (Berlin, Germany)|April 30, 2021
Fabry disease and kidney involvement: starting from childhood to understand the futureRoberto Chimenz, Valeria Chirico, Caterina Cuppari, et al.
Inorganic Chemistry|January 16, 2003
Synthesis of Cl2InN3, Br2InN3, and related adductsC Steffek, J McMurran, B Pleune, et al.
Urology|February 1, 1993
Acquired cystic kidney disease: the hormonal hypothesisG Concolino, C Lubrano, M Ombres, et al.
Clinical Chemistry and Laboratory Medicine|March 28, 2014
Advanced tools for BRCA1/2 mutational screening: comparison between two methods for large genomic rearrangements (LGRs) detectionPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Clinical Microbiology and Infection : the Official Publication of the European Society of Clinical Microbiology and Infectious Diseases|June 25, 2004
High seroprevalence of Helicobacter pylori infection in non-institutionalised children with mental retardationF Luzza, D Concolino, M Imeneo, et al.
American Journal of Medical Genetics. Part A|June 25, 2013
GAPO syndrome associated with vestibular dysfunction and hearing lossM Rapsomaniki, G Chiarella, I Mascaro, et al.
Pageof 35