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The Pharmacogenomics Journal
|
January 17, 2019
A single nucleotide polymorphism of IL6-receptor is associated with response to tocilizumab in rheumatoid arthritis patients
Cécile Luxembourger, Adeline Ruyssen-Witrand, Chayma Ladhari, et al.
Clinical and Experimental Rheumatology
|
July 20, 2023
TNFRSF1A-pR92Q variant identifies a subset of patients more similar to systemic undifferentiated recurrent fever than TNF receptor-associated periodic syndrome
Anna M Gerritsma, Diana Sutera, Luca Cantarini, et al.
Arthritis and Rheumatism
|
May 1, 2007
Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever
Isabelle Touitou, Tamara Sarkisian, Myrna Medlej-Hashim, et al.
Cell Death & Disease
|
March 25, 2023
Mutations in the B30.2 and the central helical scaffold domains of pyrin differentially affect inflammasome activation
Daria Chirita, Pauline Bronnec, Flora Magnotti, et al.
Journal of the American Academy of Dermatology
|
April 14, 2020
Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational study
François Chasset, Antoine Fayand, Philippe Moguelet, et al.
Journal of Immunology Research
|
March 9, 2017
<i>TMEM187-IRAK1</i> Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin
Olfa Khalifa, Nathalie Balandraud, Nathalie Lambert, et al.
The Journal of Allergy and Clinical Immunology
|
November 30, 2019
PSMB10, the last immunoproteasome gene missing for PRAAS
Guillaume Sarrabay, Déborah Méchin, Aicha Salhi, et al.
European Journal of Human Genetics : EJHG
|
May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability
Frederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
Pediatrics
|
June 29, 2011
Mevalonate kinase deficiency: a survey of 50 patients
Brigitte Bader-Meunier, Benoit Florkin, Jean Sibilia, et al.
Seminars in Arthritis and Rheumatism
|
September 27, 2021
DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French cases
Antoine Fayand, François Chasset, David Boutboul, et al.
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of 13
Search research articles
Search
Showing results (91-100 of 121) with videos related to
Sort By:
Page
of 13
The Pharmacogenomics Journal
|
January 17, 2019
A single nucleotide polymorphism of IL6-receptor is associated with response to tocilizumab in rheumatoid arthritis patients
Cécile Luxembourger, Adeline Ruyssen-Witrand, Chayma Ladhari, et al.
Clinical and Experimental Rheumatology
|
July 20, 2023
TNFRSF1A-pR92Q variant identifies a subset of patients more similar to systemic undifferentiated recurrent fever than TNF receptor-associated periodic syndrome
Anna M Gerritsma, Diana Sutera, Luca Cantarini, et al.
Arthritis and Rheumatism
|
May 1, 2007
Country as the primary risk factor for renal amyloidosis in familial Mediterranean fever
Isabelle Touitou, Tamara Sarkisian, Myrna Medlej-Hashim, et al.
Cell Death & Disease
|
March 25, 2023
Mutations in the B30.2 and the central helical scaffold domains of pyrin differentially affect inflammasome activation
Daria Chirita, Pauline Bronnec, Flora Magnotti, et al.
Journal of the American Academy of Dermatology
|
April 14, 2020
Clinical and pathological dermatological features of deficiency of adenosine deaminase 2: A multicenter, retrospective, observational study
François Chasset, Antoine Fayand, Philippe Moguelet, et al.
Journal of Immunology Research
|
March 9, 2017
<i>TMEM187-IRAK1</i> Polymorphisms Associated with Rheumatoid Arthritis Susceptibility in Tunisian and French Female Populations: Influence of Geographic Origin
Olfa Khalifa, Nathalie Balandraud, Nathalie Lambert, et al.
The Journal of Allergy and Clinical Immunology
|
November 30, 2019
PSMB10, the last immunoproteasome gene missing for PRAAS
Guillaume Sarrabay, Déborah Méchin, Aicha Salhi, et al.
European Journal of Human Genetics : EJHG
|
May 16, 2013
Expanding the phenotype of IQSEC2 mutations: truncating mutations in severe intellectual disability
Frederic Tran Mau-Them, Marjolaine Willems, Beate Albrecht, et al.
Pediatrics
|
June 29, 2011
Mevalonate kinase deficiency: a survey of 50 patients
Brigitte Bader-Meunier, Benoit Florkin, Jean Sibilia, et al.
Seminars in Arthritis and Rheumatism
|
September 27, 2021
DADA2 diagnosed in adulthood versus childhood: A comparative study on 306 patients including a systematic literature review and 12 French cases
Antoine Fayand, François Chasset, David Boutboul, et al.
Page
of 13