Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Francesca Schena

3PUBLICATIONS

19CO-AUTHORS

AutoimmunityInstrumental methods (excl. immunological and bioassay methods)Respiratory diseases

Featured researcher

Get your video featured.

Publish with JoVE

Featured researcher

Get your video featured.

Publish with JoVE

Publications (3)

Sort by Publication Date:

|Nov 17, 2025

Neurological Phenotypes of SOCS1 Haploinsufficiency: Insights from Functional and Histological Investigations.

Serena Palmeri, Ignazia Prigione, Francesca Schena

|Sep 28, 2021

A Novel LC-MS/MS-Based Method for the Diagnosis of ADA2 Deficiency from Dried Plasma Spot.

Alessia Cafaro, Federica Pigliasco, Sebastiano Barco

|Jul 25, 2020

Dysregulation in B-cell responses and T follicular helper cell function in ADA2 deficiency patients.

Francesca Schena, Federica Penco, Stefano Volpi

Pageof 1

Frequent Collaborators

2 joint publications

Roberta Caorsi

2 joint publications

Stefano Volpi

1 joint publications

Sebastiano Barco

1 joint publications

Serena Palmeri

1 joint publications

Ignazia Prigione

1 joint publications

Arinna Bertoni

1 joint publications

Federica Penco

1 joint publications

Paola Bocca

1 joint publications

Genny Del Zotto

1 joint publications

Sara Massucco

Frequent Collaborators

2 joint publications

Roberta Caorsi

2 joint publications

Stefano Volpi

1 joint publications

Sebastiano Barco

1 joint publications

Serena Palmeri

Top Related Videos

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Published on : Mar 23, 2022

Isolation of CD4<sup>+</sup> T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry

Isolation of CD4<sup>+</sup> T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry

Published on : Jan 07, 2019

See more related videos

Top Related Videos

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and <em>In Utero</em> Electroporation in Rodents to Identify Causative Genes for Brain Malformations

Published on : Dec 01, 2017

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Fingerprinting Cardiolipin in Leukocytes by Mass Spectrometry for a Rapid Diagnosis of Barth Syndrome

Published on : Mar 23, 2022

Isolation of CD4<sup>+</sup> T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry

Isolation of CD4<sup>+</sup> T-cells and Analysis of Circulating T-follicular Helper (cTfh) Cell Subsets from Peripheral Blood Using 6-color Flow Cytometry

Published on : Jan 07, 2019

See more related videos