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European Cytokine Network
|
November 4, 2005
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation
Ettore Capoluongo, Giovanni Vento, Concetta Santonocito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 5, 2014
Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients
Concetta Santonocito, Margherita Scapaticci, Donatella Guarino, et al.
The International Journal of Biological Markers
|
January 7, 2017
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population
Concetta Santonocito, Margherita Scapaticci, Bojan Nedovic, et al.
Clinical Biochemistry
|
October 14, 2018
Additional molecular and clinical evidence open the way to definitive IARC classification of the BRCA1 c.5332G > A (p.Asp1778Asn) variant
Angelo Minucci, Maurizio Lalle, Rossella De Leo, et al.
Frontiers in Endocrinology
|
August 4, 2018
Medullary Thyroid Carcinoma With Exon 2 p.L56M RET Variant: Clinical Particular Features in Two Patients
Rosa M Paragliola, Rosa M Lovicu, Giampaolo Papi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 11, 2014
A preliminary Quality Control (QC) for next generation sequencing (NGS) library evaluation turns out to be a very useful tool for a rapid detection of BRCA1/2 deleterious mutations
Paola Concolino, Alessandra Costella, Angelo Minucci, et al.
Molecular Biology Reports
|
May 30, 2020
High resolution melting profiles (HRMPs) obtained by magnetic induction cycler (MIC) have been used to monitor the BRCA2 status highlighted by next generation tumor sequencing (NGTS): a combined approach in a diagnostic environment
Giorgia Mazzuccato, Maria De Bonis, Vittoria Carboni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 21, 2005
Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: a genetic study of Sardinian family
Paola Concolino, Maria Antonia Satta, Concetta Santonocito, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 9, 2012
The first case of association between postpartum thyroiditis and thyroid hormone resistance in an Italian patient showing a novel p.V283A THRB mutation
Rosa Maria Paragliola, Paola Concolino, Annapina De Rosa, et al.
Blood
|
September 20, 2002
Role for granulocyte colony-stimulating factor in the generation of human T regulatory type 1 cells
Sergio Rutella, Luca Pierelli, Giuseppina Bonanno, et al.
Page
of 20
Search research articles
Search
Showing results (81-90 of 192) with videos related to
Sort By:
Page
of 20
European Cytokine Network
|
November 4, 2005
Comparison of serum levels of seven cytokines in premature newborns undergoing different ventilatory procedures: high frequency oscillatory ventilation or synchronized intermittent mandatory ventilation
Ettore Capoluongo, Giovanni Vento, Concetta Santonocito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
October 5, 2014
Lactose intolerance genetic testing: is it useful as routine screening? Results on 1426 south-central Italy patients
Concetta Santonocito, Margherita Scapaticci, Donatella Guarino, et al.
The International Journal of Biological Markers
|
January 7, 2017
XRCC1 Arg399Gln gene polymorphism and hepatocellular carcinoma risk in the Italian population
Concetta Santonocito, Margherita Scapaticci, Bojan Nedovic, et al.
Clinical Biochemistry
|
October 14, 2018
Additional molecular and clinical evidence open the way to definitive IARC classification of the BRCA1 c.5332G > A (p.Asp1778Asn) variant
Angelo Minucci, Maurizio Lalle, Rossella De Leo, et al.
Frontiers in Endocrinology
|
August 4, 2018
Medullary Thyroid Carcinoma With Exon 2 p.L56M RET Variant: Clinical Particular Features in Two Patients
Rosa M Paragliola, Rosa M Lovicu, Giampaolo Papi, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
July 11, 2014
A preliminary Quality Control (QC) for next generation sequencing (NGS) library evaluation turns out to be a very useful tool for a rapid detection of BRCA1/2 deleterious mutations
Paola Concolino, Alessandra Costella, Angelo Minucci, et al.
Molecular Biology Reports
|
May 30, 2020
High resolution melting profiles (HRMPs) obtained by magnetic induction cycler (MIC) have been used to monitor the BRCA2 status highlighted by next generation tumor sequencing (NGTS): a combined approach in a diagnostic environment
Giorgia Mazzuccato, Maria De Bonis, Vittoria Carboni, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
September 21, 2005
Linkage between I172N mutation, a marker of 21-hydroxylase deficiency, and a single nucleotide polymorphism in Int6 of CYP21B gene: a genetic study of Sardinian family
Paola Concolino, Maria Antonia Satta, Concetta Santonocito, et al.
Thyroid : Official Journal of the American Thyroid Association
|
November 9, 2012
The first case of association between postpartum thyroiditis and thyroid hormone resistance in an Italian patient showing a novel p.V283A THRB mutation
Rosa Maria Paragliola, Paola Concolino, Annapina De Rosa, et al.
Blood
|
September 20, 2002
Role for granulocyte colony-stimulating factor in the generation of human T regulatory type 1 cells
Sergio Rutella, Luca Pierelli, Giuseppina Bonanno, et al.
Page
of 20