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Journal of Clinical Immunology
|
December 5, 2022
Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers
Mathilde Labouret, Stefania Costi, Vincent Bondet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 27, 2021
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases
Francis Rossignol, Marvid S Duarte Moreno, Jean-François Benoist, et al.
The Journal of Experimental Medicine
|
August 26, 2018
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency
Nicholas Hernandez, Isabelle Melki, Huie Jing, et al.
Journal of Clinical Immunology
|
January 7, 2021
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies
Lorenzo Lodi, Isabelle Melki, Vincent Bondet, et al.
The Journal of Experimental Medicine
|
April 20, 2017
Detection of interferon alpha protein reveals differential levels and cellular sources in disease
Mathieu P Rodero, Jérémie Decalf, Vincent Bondet, et al.
The New England Journal of Medicine
|
December 20, 2018
Reverse-Transcriptase Inhibitors in the Aicardi–Goutières Syndrome
Gillian I Rice, Candice Meyzer, Naïm Bouazza, et al.
RMD Open
|
November 1, 2022
Tolerance and efficacy of targeted therapies prescribed for off-label indications in refractory systemic autoimmune diseases: data of the first 100 patients enrolled in the TATA registry (TArgeted Therapy in Autoimmune Diseases)
Jacques-Eric Gottenberg, Aurore Chaudier, Yves Allenbach, et al.
Medicine
|
July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey
Marie-Olivia Chandesris, Isabelle Melki, Angels Natividad, 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 Patients
Marie-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 cases
Maud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
Page
of 11
Search research articles
Search
Showing results (91-100 of 102) with videos related to
Sort By:
Page
of 11
Journal of Clinical Immunology
|
December 5, 2022
Juvenile Neuropsychiatric Systemic Lupus Erythematosus: Identification of Novel Central Neuroinflammation Biomarkers
Mathilde Labouret, Stefania Costi, Vincent Bondet, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 27, 2021
Quantitative analysis of the natural history of prolidase deficiency: description of 17 families and systematic review of published cases
Francis Rossignol, Marvid S Duarte Moreno, Jean-François Benoist, et al.
The Journal of Experimental Medicine
|
August 26, 2018
Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency
Nicholas Hernandez, Isabelle Melki, Huie Jing, et al.
Journal of Clinical Immunology
|
January 7, 2021
Differential Expression of Interferon-Alpha Protein Provides Clues to Tissue Specificity Across Type I Interferonopathies
Lorenzo Lodi, Isabelle Melki, Vincent Bondet, et al.
The Journal of Experimental Medicine
|
April 20, 2017
Detection of interferon alpha protein reveals differential levels and cellular sources in disease
Mathieu P Rodero, Jérémie Decalf, Vincent Bondet, et al.
The New England Journal of Medicine
|
December 20, 2018
Reverse-Transcriptase Inhibitors in the Aicardi–Goutières Syndrome
Gillian I Rice, Candice Meyzer, Naïm Bouazza, et al.
RMD Open
|
November 1, 2022
Tolerance and efficacy of targeted therapies prescribed for off-label indications in refractory systemic autoimmune diseases: data of the first 100 patients enrolled in the TATA registry (TArgeted Therapy in Autoimmune Diseases)
Jacques-Eric Gottenberg, Aurore Chaudier, Yves Allenbach, et al.
Medicine
|
July 4, 2012
Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey
Marie-Olivia Chandesris, Isabelle Melki, Angels Natividad, 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 Patients
Marie-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 cases
Maud Tusseau, Samira Khaldi-Plassart, Audrey Labalme, et al.
Page
of 11