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HLA
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December 15, 2025
Biological Effects of F(ab')2 Fragments Generated by Imlifidase From Anti-HLA IgG Antibodies From Transplant Patients
Magali Devriese, Ilaria Carelli, Lisa Giraldo, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2025
DDOST-Congenital Disorder of Glycosylation: Defining the Clinical Spectrum and First Report of a Structural Variant
Giuseppe Reynolds, Ilaria Carelli, Federico Rondot, et al.
European Journal of Medical Genetics
|
May 17, 2026
VPS35L-Related Ritscher-Schinzel Syndrome: Expanding Genotype-Phenotype Correlations
Ilaria Carelli, Federico Rondot, Maria Luca, et al.
Genes
|
June 26, 2026
<i>TRAPPC9</i>-Related Intellectual Developmental Disorder: A Systematic Review and a Novel Case of a Complex Structural Variant
Marta Calvo, Giuseppe Reynolds, Maria Luca, et al.
Genes
|
October 29, 2025
Expanding Clinical and Genetic Landscape of <i>SATB2</i>-Associated Syndrome
Verdiana Pullano, Federico Rondot, Ilaria Carelli, et al.
Human Immunology
|
April 30, 2026
HLA DRB1*01:02 allele is associated with anti-AT1R antibodies production in kidney transplanted patients
Ilaria Carelli, Alessandro Romano, Angelo Corso Faini, et al.
European Journal of Human Genetics : EJHG
|
January 8, 2026
Domain-specific phenotypic profiles in RAF1-related Noonan syndrome
Andrea Gazzin, Marta Calvo, Federico Rondot, et al.
Page
of 1
Search research articles
Search
Showing results (1-10 of 7) with videos related to
Sort By:
Page
of 1
HLA
|
December 15, 2025
Biological Effects of F(ab')2 Fragments Generated by Imlifidase From Anti-HLA IgG Antibodies From Transplant Patients
Magali Devriese, Ilaria Carelli, Lisa Giraldo, et al.
American Journal of Medical Genetics. Part A
|
December 15, 2025
DDOST-Congenital Disorder of Glycosylation: Defining the Clinical Spectrum and First Report of a Structural Variant
Giuseppe Reynolds, Ilaria Carelli, Federico Rondot, et al.
European Journal of Medical Genetics
|
May 17, 2026
VPS35L-Related Ritscher-Schinzel Syndrome: Expanding Genotype-Phenotype Correlations
Ilaria Carelli, Federico Rondot, Maria Luca, et al.
Genes
|
June 26, 2026
<i>TRAPPC9</i>-Related Intellectual Developmental Disorder: A Systematic Review and a Novel Case of a Complex Structural Variant
Marta Calvo, Giuseppe Reynolds, Maria Luca, et al.
Genes
|
October 29, 2025
Expanding Clinical and Genetic Landscape of <i>SATB2</i>-Associated Syndrome
Verdiana Pullano, Federico Rondot, Ilaria Carelli, et al.
Human Immunology
|
April 30, 2026
HLA DRB1*01:02 allele is associated with anti-AT1R antibodies production in kidney transplanted patients
Ilaria Carelli, Alessandro Romano, Angelo Corso Faini, et al.
European Journal of Human Genetics : EJHG
|
January 8, 2026
Domain-specific phenotypic profiles in RAF1-related Noonan syndrome
Andrea Gazzin, Marta Calvo, Federico Rondot, et al.
Page
of 1