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Journal of Separation Science
|
April 2, 2014
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms?
Angelo Minucci, Giulia Canu, Maria De Bonis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 6, 2009
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report
Paola Concolino, Enrica Mello, Vincenzo Toscano, et al.
International Journal of Molecular Sciences
|
July 25, 2019
<i>BRCA1</i> and <i>BRCA2</i> Testing through Next Generation Sequencing in a Small Cohort of Italian Breast/Ovarian Cancer Patients: Novel Pathogenic and Unknown Clinical Significance Variants
Paola Concolino, Gianfranco Gelli, Roberta Rizza, et al.
Clinical Chemistry and Laboratory Medicine
|
June 19, 2012
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis
Enrica Mello, Benedetto Falsini, Cecilia Zuppi, et al.
Metabolism: Clinical and Experimental
|
May 20, 2017
CYP21A2 intronic variants causing 21-hydroxylase deficiency
Paola Concolino, Roberta Rizza, Alessandra Costella, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 4, 2012
Small amplicons high resolution melting analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population
Angelo Minucci, Giulia Canu, Leonarda Gentile, et al.
Clinical Biochemistry
|
December 19, 2007
Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency
Angelo Minucci, Paola Concolino, Francesca Vendittelli, et al.
European Cytokine Network
|
July 9, 2002
Effects of early dexamethasone therapy on pulmonary fibrogenic mediators and respiratory mechanics in preterm infants
Giovanni Vento, Piero G Matassa, Franco Ameglio, et al.
Clinical Chemistry and Laboratory Medicine
|
June 13, 2019
CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
Elisa De Paolis, Giovanni Luca Scaglione, Maria De Bonis, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
February 3, 2015
Evaluation of the diagnostic and predictive power of PCA3 in the prostate cancer. A different best cut-off in each different scenario. Preliminary results
Giuseppe Albino, Ettore Capoluongo, Sandro Rocchetti, et al.
Page
of 20
Search research articles
Search
Showing results (21-30 of 192) with videos related to
Sort By:
Page
of 20
Journal of Separation Science
|
April 2, 2014
Is capillary electrophoresis on microchip devices able to genotype uridine diphosphate glucuronosyltransferase 1A1 TATA-box polymorphisms?
Angelo Minucci, Giulia Canu, Maria De Bonis, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
March 6, 2009
Multiplex ligation-dependent probe amplification (MLPA) assay for the detection of CYP21A2 gene deletions/duplications in congenital adrenal hyperplasia: first technical report
Paola Concolino, Enrica Mello, Vincenzo Toscano, et al.
International Journal of Molecular Sciences
|
July 25, 2019
<i>BRCA1</i> and <i>BRCA2</i> Testing through Next Generation Sequencing in a Small Cohort of Italian Breast/Ovarian Cancer Patients: Novel Pathogenic and Unknown Clinical Significance Variants
Paola Concolino, Gianfranco Gelli, Roberta Rizza, et al.
Clinical Chemistry and Laboratory Medicine
|
June 19, 2012
Rapid detection of CFH (p.Y402H) and ARMS2 (p.A69S) polymorphisms in age-related macular degeneration using high-resolution melting analysis
Enrica Mello, Benedetto Falsini, Cecilia Zuppi, et al.
Metabolism: Clinical and Experimental
|
May 20, 2017
CYP21A2 intronic variants causing 21-hydroxylase deficiency
Paola Concolino, Roberta Rizza, Alessandra Costella, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
December 4, 2012
Small amplicons high resolution melting analysis (SA-HRMA) allows successful genotyping of acid phosphatase 1 (ACP1) polymorphisms in the Italian population
Angelo Minucci, Giulia Canu, Leonarda Gentile, et al.
Clinical Biochemistry
|
December 19, 2007
Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency
Angelo Minucci, Paola Concolino, Francesca Vendittelli, et al.
European Cytokine Network
|
July 9, 2002
Effects of early dexamethasone therapy on pulmonary fibrogenic mediators and respiratory mechanics in preterm infants
Giovanni Vento, Piero G Matassa, Franco Ameglio, et al.
Clinical Chemistry and Laboratory Medicine
|
June 13, 2019
CYP24A1 and SLC34A1 genetic defects associated with idiopathic infantile hypercalcemia: from genotype to phenotype
Elisa De Paolis, Giovanni Luca Scaglione, Maria De Bonis, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica
|
February 3, 2015
Evaluation of the diagnostic and predictive power of PCA3 in the prostate cancer. A different best cut-off in each different scenario. Preliminary results
Giuseppe Albino, Ettore Capoluongo, Sandro Rocchetti, et al.
Page
of 20