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Page last updated: 2024-08-17

colchicine and Hyper IgD Syndrome

colchicine has been researched along with Hyper IgD Syndrome in 14 studies

Research

Studies (14)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (7.14)29.6817
2010's10 (71.43)24.3611
2020's3 (21.43)2.80

Authors

AuthorsStudies
Benseler, S; De Benedetti, F; Jansson, A; Karadag, O; Koné-Paut, I; Kuemmerle-Deschner, JB; Levy, J; McCreddin, S; Migliaccio, M; Murias, S; Piram, M; Rosner, I; Tommasini, A1
Blais, J; Bonneville-Roussy, D; Elfassy, HL; Lanthier, S1
Lachmann, HJ; Oldham, J1
Demir, S; Ozen, S1
Chiang, VW; Hazen, MM; Koyfman, A; Lovallo, E1
Devlin, LA; Edgar, JD; Shendi, HM1
Frenkel, J; Ter Haar, NM1
Simon, A; van der Meer, JW1
Aksentijevich, I; McDermott, MF1
Goldfinger, S1
Carlucci, JG; Edwards, KM; Wurster, VM1
Herlin, T; Sørensen, N; Veirum, J1
Hashkes, PJ; Toker, O1
Spalding, SJ; Zeft, AS1

Reviews

11 review(s) available for colchicine and Hyper IgD Syndrome

ArticleYear
The systemic autoinflammatory disorders for dermatologists. Part 2: disease examples.
    Clinical and experimental dermatology, 2020, Volume: 45, Issue:8

    Topics: Amyloidosis; Anti-Inflammatory Agents, Non-Steroidal; Biological Products; Colchicine; Cryopyrin-Associated Periodic Syndromes; Dermatologists; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Immune System Diseases; Immunity, Innate; Inflammation; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Mevalonate Kinase Deficiency; Receptors, Interleukin-1; Receptors, Interleukin-6; Schnitzler Syndrome; Skin Diseases, Genetic; Steroids; Tubulin Modulators

2020
Monogenic Periodic Fever Syndromes: Treatment Options for the Pediatric Patient.
    Paediatric drugs, 2017, Volume: 19, Issue:4

    Topics: Antibodies, Monoclonal; Child; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Interleukin-1; Mevalonate Kinase Deficiency; Treatment Outcome

2017
A taste of periodic fever syndromes.
    Pediatric emergency care, 2013, Volume: 29, Issue:7

    Topics: Amyloidosis; Anti-Inflammatory Agents, Non-Steroidal; Carrier Proteins; Colchicine; Cold Temperature; Cryopyrin-Associated Periodic Syndromes; Emergencies; Etanercept; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunoglobulin G; Lymphadenitis; Mevalonate Kinase Deficiency; NLR Family, Pyrin Domain-Containing 3 Protein; Periodicity; Pharyngitis; Prednisone; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Stomatitis, Aphthous

2013
Treatment of hereditary autoinflammatory diseases.
    Current opinion in rheumatology, 2014, Volume: 26, Issue:3

    Topics: Biological Products; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Interleukin-1; Mevalonate Kinase Deficiency; Severity of Illness Index

2014
The challenge of autoinflammatory syndromes: with an emphasis on hyper-IgD syndrome.
    Rheumatology (Oxford, England), 2016, Volume: 55, Issue:suppl 2

    Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antirheumatic Agents; Colchicine; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Interleukin-1beta; Mevalonate Kinase Deficiency; Molecular Targeted Therapy; Phosphotransferases (Alcohol Group Acceptor); Tubulin Modulators

2016
Lessons from characterization and treatment of the autoinflammatory syndromes.
    Current opinion in rheumatology, 2017, Volume: 29, Issue:2

    Topics: Antirheumatic Agents; Arthritis, Juvenile; Colchicine; Endopeptidases; Familial Mediterranean Fever; Haploinsufficiency; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Intracellular Signaling Peptides and Proteins; Mevalonate Kinase Deficiency; Phosphotransferases (Alcohol Group Acceptor); Proteins; Pyrin; Tubulin Modulators; Tumor Necrosis Factor alpha-Induced Protein 3

2017
The inherited autoinflammatory syndrome: a decade of discovery.
    Transactions of the American Clinical and Climatological Association, 2009, Volume: 120

    Topics: Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Mevalonate Kinase Deficiency; Pyoderma Gangrenosum; Receptors, Tumor Necrosis Factor; Syndrome

2009
Periodic Fever syndromes.
    Pediatric annals, 2011, Volume: 40, Issue:1

    Topics: Anti-Bacterial Agents; Anti-Inflammatory Agents; Anti-Inflammatory Agents, Non-Steroidal; Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antirheumatic Agents; Child; Colchicine; Cryopyrin-Associated Periodic Syndromes; Cytokines; Diagnosis, Differential; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Hydroxymethylglutaryl-CoA Reductase Inhibitors; Immunosuppressive Agents; Lymphadenitis; Mevalonate Kinase Deficiency; Neutropenia; Pharyngitis; Prednisone; Recombinant Fusion Proteins; Recurrence; Simvastatin; Stomatitis, Aphthous; Syndrome

2011
[Hereditary periodical fever syndromes].
    Ugeskrift for laeger, 2011, Mar-28, Volume: 173, Issue:13

    Topics: Antibodies, Monoclonal; Antirheumatic Agents; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunologic Factors; Mevalonate Kinase Deficiency; Tubulin Modulators

2011
Autoinflammatory syndromes.
    Pediatric clinics of North America, 2012, Volume: 59, Issue:2

    Topics: Anti-Inflammatory Agents; Child; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Immunosuppressive Agents; Interleukin 1 Receptor Antagonist Protein; Mevalonate Kinase Deficiency; Osteomyelitis; Receptors, Interleukin-1 Type I; Treatment Outcome; Tubulin Modulators

2012
Autoinflammatory syndromes: fever is not always a sign of infection.
    Cleveland Clinic journal of medicine, 2012, Volume: 79, Issue:8

    Topics: Colchicine; Diagnosis, Differential; Gout Suppressants; Hereditary Autoinflammatory Diseases; Humans; Male; Mevalonate Kinase Deficiency; Mutation; Prognosis; Quality of Life; Risk; Syndrome; Tubulin Modulators; Young Adult

2012

Trials

1 trial(s) available for colchicine and Hyper IgD Syndrome

ArticleYear
Use of the Auto-inflammatory Disease Activity Index to monitor disease activity in patients with colchicine-resistant Familial Mediterranean Fever, Mevalonate Kinase Deficiency, and TRAPS treated with canakinumab.
    Joint bone spine, 2022, Volume: 89, Issue:6

    Topics: Antibodies, Monoclonal, Humanized; Colchicine; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Mevalonate Kinase Deficiency

2022

Other Studies

2 other study(ies) available for colchicine and Hyper IgD Syndrome

ArticleYear
Ischemic stroke is a potential complication of uncontrolled inflammation in mevalonate kinase deficiency - A case report.
    Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association, 2022, Volume: 31, Issue:12

    Topics: Adult; Canada; Child; Colchicine; Exanthema; Fever; Humans; Infant; Inflammation; Ischemic Stroke; Lymphadenopathy; Male; Mevalonate Kinase Deficiency

2022
Interleukin 6 blockade for hyperimmunoglobulin D and periodic fever syndrome.
    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 2014, Volume: 20, Issue:2

    Topics: Adolescent; Antibodies, Monoclonal, Humanized; Colchicine; Etanercept; Female; Humans; Immunoglobulin G; Interleukin 1 Receptor Antagonist Protein; Interleukin-6; Mevalonate Kinase Deficiency; Receptors, Tumor Necrosis Factor; Treatment Failure; Treatment Outcome

2014