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Clinical and Experimental Rheumatology
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November 18, 2017
Exacerbation of Behçet's syndrome and familial Mediterranean fever with menstruation
Gul Guzelant, Yesim Ozguler, Sinem Nihal Esatoglu, et al.
Rheumatology International
|
January 12, 2018
Rituximab for anti-neutrophil cytoplasmic antibodies-associated vasculitis: experience of a single center and systematic review of non-randomized studies
Gizem Ayan, Sinem Nihal Esatoglu, Gulen Hatemi, et al.
Modern Rheumatology Case Reports
|
August 5, 2023
A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants
Kerem Parlar, Eda Tahir Turanli, Eda Nuhoglu Kantarci, et al.
Annals of the Rheumatic Diseases
|
January 30, 2016
Development and initial validation of international severity scoring system for familial Mediterranean fever (ISSF)
Erkan Demirkaya, Cengizhan Acikel, Philip Hashkes, et al.
Internal Medicine Journal
|
August 21, 2024
Characteristics of arthritis in patients with familial Mediterranean fever
Selcan Yenigun, Ali Yagiz Ayla, Mebrure B Yuzbasioglu, et al.
Pediatrics
|
January 24, 2007
Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement
Tilmann Kallinich, Dieter Haffner, Tim Niehues, et al.
Annals of the Rheumatic Diseases
|
February 27, 2014
FMF50: a score for assessing outcome in familial Mediterranean fever
Seza Ozen, Erkan Demirkaya, Ali Duzova, et al.
Annals of the Rheumatic Diseases
|
June 24, 2020
Long-term efficacy and safety of canakinumab in patients with colchicine-resistant familial Mediterranean fever: results from the randomised phase III CLUSTER trial
Seza Ozen, Eldad Ben-Cherit, Ivan Foeldvari, et al.
Internal and Emergency Medicine
|
July 21, 2017
Recommendations for the inclusion of Fabry disease as a rare febrile condition in existing algorithms for fever of unknown origin
Raffaele Manna, Roberto Cauda, Sandro Feriozzi, et al.
Rheumatology (Oxford, England)
|
June 3, 2022
Frequency of AA amyloidosis has decreased in Behçet's syndrome: a retrospective study with long-term follow-up and a systematic review
Guzin Karatemiz, Sinem Nihal Esatoglu, Mert Gurcan, et al.
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of 5
Search research articles
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Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Clinical and Experimental Rheumatology
|
November 18, 2017
Exacerbation of Behçet's syndrome and familial Mediterranean fever with menstruation
Gul Guzelant, Yesim Ozguler, Sinem Nihal Esatoglu, et al.
Rheumatology International
|
January 12, 2018
Rituximab for anti-neutrophil cytoplasmic antibodies-associated vasculitis: experience of a single center and systematic review of non-randomized studies
Gizem Ayan, Sinem Nihal Esatoglu, Gulen Hatemi, et al.
Modern Rheumatology Case Reports
|
August 5, 2023
A case with febrile attacks and vasculopathy associated with ADA2 and MEFV pathogenic variants
Kerem Parlar, Eda Tahir Turanli, Eda Nuhoglu Kantarci, et al.
Annals of the Rheumatic Diseases
|
January 30, 2016
Development and initial validation of international severity scoring system for familial Mediterranean fever (ISSF)
Erkan Demirkaya, Cengizhan Acikel, Philip Hashkes, et al.
Internal Medicine Journal
|
August 21, 2024
Characteristics of arthritis in patients with familial Mediterranean fever
Selcan Yenigun, Ali Yagiz Ayla, Mebrure B Yuzbasioglu, et al.
Pediatrics
|
January 24, 2007
Colchicine use in children and adolescents with familial Mediterranean fever: literature review and consensus statement
Tilmann Kallinich, Dieter Haffner, Tim Niehues, et al.
Annals of the Rheumatic Diseases
|
February 27, 2014
FMF50: a score for assessing outcome in familial Mediterranean fever
Seza Ozen, Erkan Demirkaya, Ali Duzova, et al.
Annals of the Rheumatic Diseases
|
June 24, 2020
Long-term efficacy and safety of canakinumab in patients with colchicine-resistant familial Mediterranean fever: results from the randomised phase III CLUSTER trial
Seza Ozen, Eldad Ben-Cherit, Ivan Foeldvari, et al.
Internal and Emergency Medicine
|
July 21, 2017
Recommendations for the inclusion of Fabry disease as a rare febrile condition in existing algorithms for fever of unknown origin
Raffaele Manna, Roberto Cauda, Sandro Feriozzi, et al.
Rheumatology (Oxford, England)
|
June 3, 2022
Frequency of AA amyloidosis has decreased in Behçet's syndrome: a retrospective study with long-term follow-up and a systematic review
Guzin Karatemiz, Sinem Nihal Esatoglu, Mert Gurcan, et al.
Page
of 5