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Alexandre Belot

Showing results (221-230 of 251) with videos related to

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Annals of the Rheumatic Diseases|April 24, 2010
EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteriaSeza Ozen, Angela Pistorio, Silvia M Iusan, et al.
The Journal of Experimental Medicine|April 20, 2017
Detection of interferon alpha protein reveals differential levels and cellular sources in diseaseMathieu P Rodero, Jérémie Decalf, Vincent Bondet, et al.
Arthritis and Rheumatism|May 14, 2013
Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferationAlexandre Belot, Paul R Kasher, Eleanor W Trotter, et al.
The New England Journal of Medicine|December 20, 2018
Reverse-Transcriptase Inhibitors in the Aicardi–Goutières SyndromeGillian I Rice, Candice Meyzer, Naïm Bouazza, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Nature Communications|October 22, 2020
Early-onset autoimmunity associated with SOCS1 haploinsufficiencyJérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 20, 2020
Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 PatientsMarie-Louise Frémond, Alice Hadchouel, Laureline Berteloot, et al.
Ebiomedicine|April 3, 2026
Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus casesMaud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
JAMA Network Open|May 31, 2023
Evaluation and Management of Deficiency of Adenosine Deaminase 2: An International Consensus StatementPui Y Lee, Brad A Davidson, Roshini S Abraham, et al.
Pageof 26

Showing results (221-230 of 251) with videos related to

Sort By:
Pageof 26
Annals of the Rheumatic Diseases|April 24, 2010
EULAR/PRINTO/PRES criteria for Henoch-Schönlein purpura, childhood polyarteritis nodosa, childhood Wegener granulomatosis and childhood Takayasu arteritis: Ankara 2008. Part II: Final classification criteriaSeza Ozen, Angela Pistorio, Silvia M Iusan, et al.
The Journal of Experimental Medicine|April 20, 2017
Detection of interferon alpha protein reveals differential levels and cellular sources in diseaseMathieu P Rodero, Jérémie Decalf, Vincent Bondet, et al.
Arthritis and Rheumatism|May 14, 2013
Protein kinase cδ deficiency causes mendelian systemic lupus erythematosus with B cell-defective apoptosis and hyperproliferationAlexandre Belot, Paul R Kasher, Eleanor W Trotter, et al.
The New England Journal of Medicine|December 20, 2018
Reverse-Transcriptase Inhibitors in the Aicardi–Goutières SyndromeGillian I Rice, Candice Meyzer, Naïm Bouazza, et al.
The Lancet. Rheumatology|January 24, 2024
Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus: a large, genetic panel analysis of British and French cohortsAlexandre Belot, Gillian I Rice, Sulliman Ommar Omarjee, et al.
The Journal of Allergy and Clinical Immunology|April 6, 2015
PRKDC mutations associated with immunodeficiency, granuloma, and autoimmune regulator-dependent autoimmunityAnne-Laure Mathieu, Estelle Verronese, Gillian I Rice, et al.
Nature Communications|October 22, 2020
Early-onset autoimmunity associated with SOCS1 haploinsufficiencyJérôme Hadjadj, Carla Noemi Castro, Maud Tusseau, et al.
The Journal of Allergy and Clinical Immunology. in Practice|November 20, 2020
Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 PatientsMarie-Louise Frémond, Alice Hadchouel, Laureline Berteloot, et al.
Ebiomedicine|April 3, 2026
Exome sequencing enables molecular diagnosis in 10% of early-onset or familial systemic lupus erythematosus casesMaud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
JAMA Network Open|May 31, 2023
Evaluation and Management of Deficiency of Adenosine Deaminase 2: An International Consensus StatementPui Y Lee, Brad A Davidson, Roshini S Abraham, et al.
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