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Ettore Capoluongo

Showing results (11-20 of 192) with videos related to

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Clinical Chemistry and Laboratory Medicine|May 21, 2010
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutationsPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
IUBMB Life|October 23, 2008
Glucose-6-phosphate dehydrogenase laboratory assay: How, when, and why?Angelo Minucci, Bruno Giardina, Cecilia Zuppi, et al.
Blood Cells, Molecules & Diseases|February 3, 2016
Red blood cell PK deficiency: An update of PK-LR gene mutation databaseGiulia Canu, Maria De Bonis, Angelo Minucci, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 26, 2009
Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosisAngelo Minucci, Paola Concolino, Bruno Giardina, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) familyPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|January 9, 2014
Potential usefulness of CTC detection in follow up of prostate cancer patients. A preliminary report obtained by using Adnagene platformGiuseppe Albino, Francesca Vendittelli, Carmela Paolillo, et al.
Clinical Chemistry and Laboratory Medicine|June 9, 2009
A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiencyPaola Concolino, Angelo Minucci, Enrica Mello, et al.
Clinical Biochemistry|March 16, 2011
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: comparison of two methods and implications in molecular diagnosticsAngelo Minucci, Enrica Mello, Domenico Tripodi, et al.
Laboratory Medicine|April 13, 2016
The Hemo One Autoanalyzer for Glycated Hemoglobin AssayKrizia Pocino, Rossana Molinario, Rocco Manieri, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 2013
Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian populationPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Pageof 20

Showing results (11-20 of 192) with videos related to

Sort By:
Pageof 20
Clinical Chemistry and Laboratory Medicine|May 21, 2010
Molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency: an update of new CYP21A2 mutationsPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
IUBMB Life|October 23, 2008
Glucose-6-phosphate dehydrogenase laboratory assay: How, when, and why?Angelo Minucci, Bruno Giardina, Cecilia Zuppi, et al.
Blood Cells, Molecules & Diseases|February 3, 2016
Red blood cell PK deficiency: An update of PK-LR gene mutation databaseGiulia Canu, Maria De Bonis, Angelo Minucci, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 26, 2009
Rapid UGT1A1 (TA)(n) genotyping by high resolution melting curve analysis for Gilbert's syndrome diagnosisAngelo Minucci, Paola Concolino, Bruno Giardina, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) familyPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
Archivio Italiano Di Urologia, Andrologia : Organo Ufficiale [Di] Societa Italiana Di Ecografia Urologica E Nefrologica|January 9, 2014
Potential usefulness of CTC detection in follow up of prostate cancer patients. A preliminary report obtained by using Adnagene platformGiuseppe Albino, Francesca Vendittelli, Carmela Paolillo, et al.
Clinical Chemistry and Laboratory Medicine|June 9, 2009
A new CYP21A2 nonsense mutation causing severe 21-hydroxylase deficiencyPaola Concolino, Angelo Minucci, Enrica Mello, et al.
Clinical Biochemistry|March 16, 2011
Contribution of the TA repeats on melting temperature (T(m)) in a double strand DNA: comparison of two methods and implications in molecular diagnosticsAngelo Minucci, Enrica Mello, Domenico Tripodi, et al.
Laboratory Medicine|April 13, 2016
The Hemo One Autoanalyzer for Glycated Hemoglobin AssayKrizia Pocino, Rossana Molinario, Rocco Manieri, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 2013
Genes, pseudogenes and like genes: the case of 21-hydroxylase in Italian populationPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Pageof 20