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Platelets
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February 8, 2022
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia
Francesca Conti, Francesca Gottardi, Mattia Moratti, et al.
Prenatal Diagnosis
|
September 30, 2006
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndrome
Daniela Turchetti, Elisabetta Razzaboni, Hila Zomer, et al.
Frontiers in Genetics
|
September 27, 2018
Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
Roberta Zuntini, Simona Ferrari, Elena Bonora, et al.
Journal of Medical Genetics
|
December 30, 2023
Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for <i>BRCA1/2</i>
Giovanni Innella, Simona Ferrari, Sara Miccoli, et al.
Frontiers in Immunology
|
November 23, 2020
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis
Bianca Cinicola, Andrea Uva, Lucia Leonardi, et al.
Journal of Immunology Research
|
April 29, 2016
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes
Federica Pulvirenti, Roberta Zuntini, Cinzia Milito, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 17, 2016
Molecular detection and genetic characterization of circulating measles virus in northern Italy
Giulia Piccirilli, Angela Chiereghin, Maria Grazia Pascucci, et al.
Clinical Chemistry
|
January 20, 2007
Simple method for haplotyping the poly(TG) repeat in individuals carrying the IVS8 5T allele in the CFTR gene
Vilma Mantovani, Paolo Garagnani, Paola Selva, et al.
Journal of Clinical Immunology
|
September 15, 2005
Mutational analysis of human BAFF receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency
Claretta Gioia Losi, Antonietta Silini, Claudia Fiorini, et al.
Familial Cancer
|
March 26, 2026
Cascade testing as the missing link in cancer prevention among Lynch syndrome families
Lea Godino, Giulia Erini, Giovanni Innella, et al.
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of 8
Search research articles
Search
Showing results (21-30 of 73) with videos related to
Sort By:
Page
of 8
Platelets
|
February 8, 2022
Refractory immune thrombocytopenia successfully treated with bortezomib in a child with 22q11.2 deletion syndrome, complicated by Evans syndrome and hypogammaglobulinemia
Francesca Conti, Francesca Gottardi, Mattia Moratti, et al.
Prenatal Diagnosis
|
September 30, 2006
Psychological consequences of prenatal diagnosis in a case of familial Angelman syndrome
Daniela Turchetti, Elisabetta Razzaboni, Hila Zomer, et al.
Frontiers in Genetics
|
September 27, 2018
Dealing With BRCA1/2 Unclassified Variants in a Cancer Genetics Clinic: Does Cosegregation Analysis Help?
Roberta Zuntini, Simona Ferrari, Elena Bonora, et al.
Journal of Medical Genetics
|
December 30, 2023
Clinical implications of VUS reclassification in a single-centre series from application of ACMG/AMP classification rules specified for <i>BRCA1/2</i>
Giovanni Innella, Simona Ferrari, Sara Miccoli, et al.
Frontiers in Immunology
|
November 23, 2020
Case Report: A Case of X-Linked Agammaglobulinemia With High Serum IgE Levels and Allergic Rhinitis
Bianca Cinicola, Andrea Uva, Lucia Leonardi, et al.
Journal of Immunology Research
|
April 29, 2016
Clinical Associations of Biallelic and Monoallelic TNFRSF13B Variants in Italian Primary Antibody Deficiency Syndromes
Federica Pulvirenti, Roberta Zuntini, Cinzia Milito, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 17, 2016
Molecular detection and genetic characterization of circulating measles virus in northern Italy
Giulia Piccirilli, Angela Chiereghin, Maria Grazia Pascucci, et al.
Clinical Chemistry
|
January 20, 2007
Simple method for haplotyping the poly(TG) repeat in individuals carrying the IVS8 5T allele in the CFTR gene
Vilma Mantovani, Paolo Garagnani, Paola Selva, et al.
Journal of Clinical Immunology
|
September 15, 2005
Mutational analysis of human BAFF receptor TNFRSF13C (BAFF-R) in patients with common variable immunodeficiency
Claretta Gioia Losi, Antonietta Silini, Claudia Fiorini, et al.
Familial Cancer
|
March 26, 2026
Cascade testing as the missing link in cancer prevention among Lynch syndrome families
Lea Godino, Giulia Erini, Giovanni Innella, et al.
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of 8