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British Journal of Haematology
|
September 13, 2006
Chromosomal locus 19p13 as potential hotspot for aberrant gene expression in relapsed paediatric acute lymphoblastic leukaemia
Marina Lanciotti, Maria D'Apolito, Paolo Paolucci, et al.
Handbook of Clinical Neurology
|
February 21, 2023
Lessons from immunotherapies in multiple sclerosis
Marianna G Rispoli, Maria D'Apolito, Valeria Pozzilli, et al.
Turk Pediatri Arsivi
|
February 28, 2018
Levels of inflammatory cytokines from peripheral blood mononuclear cells of children with cow's milk protein allergy
Maria D'Apolito, Angelo Campanozzi, Ida Giardino, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
October 2, 2019
Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeability
Maurizio Margaglione, Maria D'Apolito, Rosa Santocroce, et al.
Gene
|
April 12, 2002
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes
Maria D'Apolito, Vito Guarnieri, Marianna Boncristiano, et al.
British Journal of Haematology
|
February 1, 2011
Gene expression profiling: a possible tool in the prediction of outcome in paediatric acute lymphoblastic leukaemia?
Marina Lanciotti, Maria D'Apolito, Paolo Paolucci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 28, 2024
Sporadic hemiplegic migraine with novel missense mutation in the SCN1A gene and positive response to anti-CGRP antibody: a case report
Maria D'Apolito, Marianna Gabriella Rispoli, Paola Ajdinaj, et al.
Journal of Clinical Medicine
|
June 2, 2021
The Genetics of Hereditary Angioedema: A Review
Rosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Blood
|
September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)
Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Haematologica
|
January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia
Maria D'Apolito, Agnese Marrone, Veronica Servedio, et al.
Page
of 8
Search research articles
Search
Showing results (1-10 of 71) with videos related to
Sort By:
Page
of 8
British Journal of Haematology
|
September 13, 2006
Chromosomal locus 19p13 as potential hotspot for aberrant gene expression in relapsed paediatric acute lymphoblastic leukaemia
Marina Lanciotti, Maria D'Apolito, Paolo Paolucci, et al.
Handbook of Clinical Neurology
|
February 21, 2023
Lessons from immunotherapies in multiple sclerosis
Marianna G Rispoli, Maria D'Apolito, Valeria Pozzilli, et al.
Turk Pediatri Arsivi
|
February 28, 2018
Levels of inflammatory cytokines from peripheral blood mononuclear cells of children with cow's milk protein allergy
Maria D'Apolito, Angelo Campanozzi, Ida Giardino, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
October 2, 2019
Hereditary angioedema: Looking for bradykinin production and triggers of vascular permeability
Maurizio Margaglione, Maria D'Apolito, Rosa Santocroce, et al.
Gene
|
April 12, 2002
Cloning of the murine non-muscle myosin heavy chain IIA gene ortholog of human MYH9 responsible for May-Hegglin, Sebastian, Fechtner, and Epstein syndromes
Maria D'Apolito, Vito Guarnieri, Marianna Boncristiano, et al.
British Journal of Haematology
|
February 1, 2011
Gene expression profiling: a possible tool in the prediction of outcome in paediatric acute lymphoblastic leukaemia?
Marina Lanciotti, Maria D'Apolito, Paolo Paolucci, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
June 28, 2024
Sporadic hemiplegic migraine with novel missense mutation in the SCN1A gene and positive response to anti-CGRP antibody: a case report
Maria D'Apolito, Marianna Gabriella Rispoli, Paola Ajdinaj, et al.
Journal of Clinical Medicine
|
June 2, 2021
The Genetics of Hereditary Angioedema: A Review
Rosa Santacroce, Giovanna D'Andrea, Angela Bruna Maffione, et al.
Blood
|
September 15, 2005
Microcytic anemia and hepatic iron overload in a child with compound heterozygous mutations in DMT1 (SCL11A2)
Achille Iolascon, Maria d'Apolito, Veronica Servedio, et al.
Haematologica
|
January 19, 2007
Seven novel mutations of the UGT1A1 gene in patients with unconjugated hyperbilirubinemia
Maria D'Apolito, Agnese Marrone, Veronica Servedio, et al.
Page
of 8