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Clinical Rheumatology, ISSN 0770-3198, 6/2018, Volume 37, Issue 6, pp. 1683 - 1687
Although familial Mediterranean fever (FMF) is inherited autosomal recessively, some heterozygotes may express disease phenotype and require therapy. To date,... 
Familial Mediterranean fever | Children | Medicine & Public Health | MEFV heterozygotes | Rheumatology | Follow-up | GENE-MUTATIONS | CRITERIA | POPULATION | SUBCLINICAL INFLAMMATION | PREVALENCE | RHEUMATOLOGY | JEWISH ETHNIC-GROUPS | COLCHICINE | HENOCH-SCHONLEIN PURPURA | FREQUENCY | Pediatrics | Colchicine | Analysis | Target marketing | Phenotypes | Pyrin protein | Laboratories | Heterozygotes | Amyloid | Mutation | Fever | Proteinuria
Journal Article
Modern Rheumatology, ISSN 1439-7595, 11/2019, pp. 1 - 6
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2013, Volume 49, Issue 4, pp. 289 - 291
Journal Article
Reumatologia, ISSN 0034-6233, 2017, Volume 55, Issue 6, pp. 323 - 327
Journal Article
Clinical rheumatology, ISSN 0770-3198, 03/2019, Volume 38, Issue 3, pp. 645 - 645
The name of the last author of this article was incorrectly presented as "Cogulu Ozgur" this should have been "Ozgur Cogulu". 
Medicine, Experimental | Medical research | Genetic aspects | MicroRNA | Analysis | Medical genetics | Familial Mediterranean fever
Journal Article
The Journal of Allergy and Clinical Immunology, ISSN 0091-6749, 11/2018, Volume 142, Issue 5, pp. 1589 - 1604.e11
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 02/2018, Volume 38, Issue 3, pp. 1 - 9
Familial Mediterranean fever (FMF) is an inherited autoinflammatory disorder that can result in attacks with accompanying recurrent episodes of fever,... 
MEFV | Familial Mediterranean fever | MicroRNA | PYRIN MUTATIONS | ACTIVATION | MECHANISM | ALPHA | MICRORNAS | RHEUMATOLOGY | LUPUS | AMYLOIDOSIS | KAPPA-B PATHWAY | EXPRESSION | CONTRIBUTES | Medical research | Analysis | Medicine, Experimental | Genetic aspects | Colchicine | Immune response | Serositis | Exanthema | MiRNA | Skin | Patients | Fever
Journal Article
Modern rheumatology, 12/2018, p. 1
Little is known about the long-term efficacy and safety of canakinumab in paediatric FMF patients. To present the single centre experience of... 
Journal Article
Clinical Rheumatology, ISSN 0770-3198, 3/2012, Volume 31, Issue 3, pp. 493 - 501
Journal Article
Molecular and Cellular Pediatrics, ISSN 2194-7791, 12/2016, Volume 3, Issue 1, pp. 1 - 5
Familial Mediterranean fever (FMF) is an autosomal recessive disease characterized by self-limited recurrent attacks of fever and serositis. Patients may... 
Pediatrics | Medicine & Public Health | Oncology | Familial Mediterranean fever | Amyloidosis | Diabetes | Canakinumab | Child | Endocrinology | Amyloidogenesis | Serositis | Monoclonal antibodies | Colchicine | IL-1β | Fever | Proteinuria
Journal Article
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 12/2012, Volume 32, Issue 6, pp. 1165 - 1179
B lymphocyte subpopulations, previously defined classification schemes (Freiburg, Paris, EuroClass), TNFRSF13B (TACI), TNFRSF13C (BAFF-R), TNFSF13 (APRIL) gene... 
Medical Microbiology | Biomedicine | Immunology | Common variable immunodeficiency | childhood | Infectious Diseases | Internal Medicine | B lymphocyte subpopulations | PHENOTYPE | DISORDERS | ANTIBODY-DEFICIENCY | IGA DEFICIENCY | SUBGROUPS | IMMUNOLOGY | CELL SUBSETS | UPDATE | CONSANGUINITY | EXPRESSION | MANIFESTATIONS | Common Variable Immunodeficiency - immunology | B-Lymphocytes - classification | Humans | Male | Splenomegaly - pathology | Case-Control Studies | Young Adult | Inducible T-Cell Co-Stimulator Protein - genetics | Female | B-Lymphocytes - pathology | B-Cell Activation Factor Receptor - genetics | Child | B-Lymphocytes - metabolism | Inducible T-Cell Co-Stimulator Protein - immunology | B-Cell Activation Factor Receptor - immunology | Severity of Illness Index | Tumor Necrosis Factor Ligand Superfamily Member 13 - immunology | Lymphatic Diseases - immunology | Splenomegaly - immunology | Common Variable Immunodeficiency - pathology | CTLA-4 Antigen - genetics | Common Variable Immunodeficiency - genetics | CTLA-4 Antigen - immunology | Polymorphism, Genetic | Transmembrane Activator and CAML Interactor Protein - genetics | B-Lymphocytes - immunology | Common Variable Immunodeficiency - metabolism | Turkey | Adolescent | Immunologic Memory | Lymphatic Diseases - pathology | Tumor Necrosis Factor Ligand Superfamily Member 13 - genetics | Consanguinity | Mutation | Transmembrane Activator and CAML Interactor Protein - immunology
Journal Article
Pediatric Allergy and Immunology, ISSN 0905-6157, 11/2009, Volume 20, Issue 7, pp. 693 - 698
Journal Article
International Journal of Immunopathology and Pharmacology, ISSN 0394-6320, 7/2018, Volume 32, p. 2058738418779458
Common variable immunodeficiency (CVID) and immunoglobulin A deficiency (IgAD) are the most prevalent primary immunodeficiency disorders. High rates of... 
CVID | familial | IgA deficiency | screening | MANAGEMENT | PHENOTYPE | DISORDERS | IMMUNOLOGY | PATHOLOGY | SELECTIVE IGA DEFICIENCY | PHARMACOLOGY & PHARMACY | UPDATE | LINKAGE | Immunoglobulins | Inheritances
Journal Article
ITALIAN JOURNAL OF PEDIATRICS, ISSN 1720-8424, 03/2012, Volume 38, Issue 1, pp. 8 - 8
Background: Severe combined immunodeficiency is within a heterogeneous group of inherited defects throughout the development of T and/or B lymphocytes.... 
SEVERE COMBINED IMMUNODEFICIENCY | RAG MUTATIONS | DEFECTS | Recombinase-activating genes | DNA | Immunodeficiency | BCG | OMENN SYNDROME | PEDIATRICS | PATIENT | REARRANGEMENTS | VARIANT | Genes, RAG-1 - genetics | Epigenesis, Genetic | Humans | Severe Combined Immunodeficiency - therapy | Genotyp