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Simona Ferrari

Showing results (51-60 of 73) with videos related to

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Blood|August 2, 2003
Functional defects of dendritic cells in patients with CD40 deficiencyStefania Fontana, Daniele Moratto, Surinder Mangal, et al.
Oncotarget|February 11, 2017
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotypeRoberta Zuntini, Laura Cortesi, Daniele Calistri, et al.
Frontiers in Pediatrics|October 4, 2021
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
Frontiers in Pediatrics|July 26, 2021
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
COPD|May 5, 2015
Italian registry of patients with alpha-1 antitrypsin deficiency: general data and quality of life evaluationMaurizio Luisetti, Ilaria Ferrarotti, Luciano Corda, et al.
International Journal of Molecular Sciences|October 2, 2020
An Analysis of Clinical, Surgical, Pathological and Molecular Characteristics of Endometrial Cancer According to Mismatch Repair Status. A Multidisciplinary ApproachGiulia Dondi, Sara Coluccelli, Antonio De Leo, et al.
Molecular Cytogenetics|October 3, 2012
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genesCristina Marletta, Roberto Valli, Barbara Pressato, et al.
Journal of Translational Medicine|July 5, 2024
Interplay between WNT/PI3K-mTOR axis and the microbiota in APC-driven colorectal carcinogenesis: data from a pilot study and possible implications for CRC preventionFloriana Jessica Di Paola, Chiara Alquati, Gabriele Conti, et al.
Clinical Genetics|December 21, 2024
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily PracticeGiovanni Innella, Emanuele Coccia, Carlotta Pia Cristalli, et al.
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
Pageof 8

Showing results (51-60 of 73) with videos related to

Sort By:
Pageof 8
Blood|August 2, 2003
Functional defects of dendritic cells in patients with CD40 deficiencyStefania Fontana, Daniele Moratto, Surinder Mangal, et al.
Oncotarget|February 11, 2017
BRCA1 p.His1673del is a pathogenic mutation associated with a predominant ovarian cancer phenotypeRoberta Zuntini, Laura Cortesi, Daniele Calistri, et al.
Frontiers in Pediatrics|October 4, 2021
Corrigendum: Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
Frontiers in Pediatrics|July 26, 2021
Case Report: Hodgkin Lymphoma and Refractory Systemic Lupus Erythematosus Unveil Activated Phosphoinositide 3-Kinase-δ Syndrome 2 in an Adult PatientFrancesca Conti, Arianna Catelli, Cristina Cifaldi, et al.
COPD|May 5, 2015
Italian registry of patients with alpha-1 antitrypsin deficiency: general data and quality of life evaluationMaurizio Luisetti, Ilaria Ferrarotti, Luciano Corda, et al.
International Journal of Molecular Sciences|October 2, 2020
An Analysis of Clinical, Surgical, Pathological and Molecular Characteristics of Endometrial Cancer According to Mismatch Repair Status. A Multidisciplinary ApproachGiulia Dondi, Sara Coluccelli, Antonio De Leo, et al.
Molecular Cytogenetics|October 3, 2012
Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genesCristina Marletta, Roberto Valli, Barbara Pressato, et al.
Journal of Translational Medicine|July 5, 2024
Interplay between WNT/PI3K-mTOR axis and the microbiota in APC-driven colorectal carcinogenesis: data from a pilot study and possible implications for CRC preventionFloriana Jessica Di Paola, Chiara Alquati, Gabriele Conti, et al.
Clinical Genetics|December 21, 2024
Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily PracticeGiovanni Innella, Emanuele Coccia, Carlotta Pia Cristalli, et al.
Sleep Medicine|April 9, 2014
Polysomnographic and neurometabolic features may mark preclinical autosomal dominant cerebellar ataxia, deafness, and narcolepsy due to a mutation in the DNA (cytosine-5-)-methyltransferase gene, DNMT1Keivan Kaveh Moghadam, Fabio Pizza, Caterina Tonon, et al.
Pageof 8