colchicine has been researched along with Hereditary Autoinflammation Diseases in 40 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (7.50) | 29.6817 |
| 2010's | 27 (67.50) | 24.3611 |
| 2020's | 10 (25.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bovis, F; Bustaffa, M; Caorsi, R; D'Orsi, C; Gattorno, M; Matarese, S; Matucci-Cerinic, C; Palmeri, S; Papa, R; Penco, F; Prigione, I; Sutera, D; Volpi, S | 1 |
| 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, A | 1 |
| Demir, F; Sözeri, B | 1 |
| Ayaz, NA; Çakan, M; Çakmak, F; Demir, F; Karadağ, ŞG; Sönmez, HE; Sözeri, B; Tanatar, A | 1 |
| Barbosa, A; Borges, T; Silva, S | 1 |
| Antón-Vázquez, V; Corominas, H; Cortes, C; Farré, EG; Hausmann, JS | 1 |
| Adrovic, A; Aliyeva, A; Barut, K; Haslak, F; Kasapcopur, O; Koker, O; Sahin, S; Yildiz, M | 1 |
| Lachmann, HJ; Oldham, J | 1 |
| Anton, J; Belot, A; Berendes, R; Bovis, F; Brogan, PA; Cantarini, L; Cattalini, M; Espada, G; Frenkel, J; Gattorno, M; Hawkins, PN; Hoppenreijs, E; Jansson, AF; Jelusic, M; Lachmann, HJ; Lane, T; Maggio, MC; Masini, M; Minden, K; Nikishina, I; Obici, L; Papa, R; Papadopoulou, C; Remesal, A; Rezk, T; Ruperto, N; Touitou, I; Wolska-Kusnierz, B; Woo, P; Youngstein, T | 1 |
| Demir, S; Ozen, S | 1 |
| Amado, C; Guiote, V; Henrique, M; Kieselova, K; Santiago, F | 1 |
| Argyris, AA; Liantinioti, G; Protogerou, AD; Vlachoyiannopoulos, P | 1 |
| Lachmann, HJ | 1 |
| Abu Rumi, M; Amarilyo, G; Brik, R; Butbul Aviel, Y; Harel, L; Hezkelo, N; Ohana, O | 1 |
| Kavukcu, S; Soylu, A | 1 |
| Bukhari, M; Davies, K; Lonergan, B; Patel, R | 1 |
| Brogan, PA; Cantarini, L; Cimaz, R; Eijkelboom, C; Fingerhutová, S; Frenkel, J; Gattorno, M; Hofer, M; Iagaru, N; Insalaco, A; Jelusic, M; Kone-Paut, I; Licciardi, F; Modesto, C; Nielsen, S; Nikishina, I; Olivieri, AN; Papa, R; Papadopoulou-Alataki, E; Ruperto, N; Stanevica, V; Susic, G; Ter Haar, NM; Uziel, Y; van Gijn, M; Vitale, A | 1 |
| Bovis, F; Caorsi, R; Caroli, F; Castana, C; Ceccherini, I; Gattorno, M; Grossi, A; Musso, V; Obici, L; Papa, R; Picco, P; Ravelli, A; Rusmini, M; Van Gijn, ME; Volpi, S | 1 |
| Cuppen, E; Frenkel, J; Kamphuis, S; Kloosterman, WP; Lachmann, HJ; Netea, MG; Plantinga, TS; Simon, A; Stoffels, M; Szperl, A; van der Meer, JW; van Deuren, M; van Diemen, CC; van Gijn, M; Wijmenga, C | 1 |
| Chiang, VW; Hazen, MM; Koyfman, A; Lovallo, E | 1 |
| Leslie, KS; Tripathi, SV | 1 |
| Aguado-Gil, L; Irarrazaval-Armendáriz, I; Pretel-Irazabal, M | 1 |
| Kawamura, H; Migita, K; Minota, S; Nara, M; Sano, H | 1 |
| Frenkel, J; Ter Haar, NM | 1 |
| Ben-Zvi, I; Livneh, A | 1 |
| Dusser, P; Hentgen, V; Koné-Paut, I; Neven, B | 1 |
| Berkun, Y; Padeh, S | 1 |
| Simon, A; van der Meer, JW | 1 |
| Goldbach-Mansky, R; Lee, CR; Shwin, KW | 1 |
| Aksentijevich, I; McDermott, MF | 1 |
| Goldfinger, S | 1 |
| Aamar, S; Ben-Chetrit, E; Heyman, SN; Peleg, H | 1 |
| Hoffman, HM | 1 |
| Duruöz, MT; Grateau, G | 1 |
| de Socio, G; Fonnesu, C; Gasbarrini, GB; Giovinale, M; Manna, R; Verrecchia, E | 1 |
| Carlucci, JG; Edwards, KM; Wurster, VM | 1 |
| Herlin, T; Sørensen, N; Veirum, J | 1 |
| Barone, L; Brambilla, G; Brizi, MG; Brucato, A; Cantarini, L; Cimaz, R; Cumetti, D; Frediani, B; Galeazzi, M; Iacoponi, F; Imazio, M; Lucherini, OM; Paolazzi, G; Patrosso, MC; Penco, S; Rigante, D; Valesini, G; Vitale, A | 1 |
| Hashkes, PJ; Toker, O | 1 |
| Spalding, SJ; Zeft, AS | 1 |
21 review(s) available for colchicine and Hereditary Autoinflammation Diseases
| Article | Year |
|---|---|
Adult-onset systemic autoinflammatory disorders: a clinical approach.
Topics: Adult; Age of Onset; Anti-Inflammatory Agents, Non-Steroidal; Autoimmune Diseases; Colchicine; Delayed Diagnosis; Female; Fever of Unknown Origin; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Immunosuppressive Agents; Interleukin-1; Male; Steroids; Tumor Necrosis Factor Inhibitors | 2020 |
The systemic autoinflammatory disorders for dermatologists. Part 2: disease examples.
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.
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 |
The Role of Colchicine in the Treatment of Autoinflammatory Diseases.
Topics: Colchicine; Gout Suppressants; Hereditary Autoinflammatory Diseases; Humans | 2018 |
Periodic fever syndromes.
Topics: Child; Child, Preschool; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Infant; Syndrome; Tumor Necrosis Factor-alpha | 2017 |
A taste of periodic fever syndromes.
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 |
Autoinflammatory diseases in dermatology: CAPS, TRAPS, HIDS, FMF, Blau, CANDLE.
Topics: Autoimmune Diseases; Colchicine; Diagnosis, Differential; Hereditary Autoinflammatory Diseases; Humans; Immunosuppressive Agents; Skin Diseases; Syndrome | 2013 |
Advances in the diagnosis and treatment of tumor necrosis factor receptor-associated periodic syndrome.
Topics: Adrenal Cortex Hormones; Age of Onset; Amyloidosis; Antibodies, Monoclonal, Humanized; Colchicine; Comorbidity; DNA Mutational Analysis; Etanercept; Fever; Hereditary Autoinflammatory Diseases; Humans; Immunoglobulin G; Interleukin 1 Receptor Antagonist Protein; Multiple Sclerosis; Pericarditis; Receptors, Tumor Necrosis Factor; Receptors, Tumor Necrosis Factor, Type I; Recurrence; Symptom Assessment; Tumor Necrosis Factor-alpha | 2013 |
Treatment of hereditary autoinflammatory diseases.
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 |
Familial Mediterranean fever.
Topics: Antibodies, Monoclonal; Antibodies, Monoclonal, Humanized; Antirheumatic Agents; Colchicine; Familial Mediterranean Fever; Fever; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Peritonitis; Pleurisy; Pyrin; Recombinant Fusion Proteins; Synovitis; Tubulin Modulators | 2016 |
The challenge of autoinflammatory syndromes: with an emphasis on hyper-IgD syndrome.
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 |
Dermatologic Manifestations of Monogenic Autoinflammatory Diseases.
Topics: Adrenal Cortex Hormones; Anemia, Dyserythropoietic, Congenital; Antirheumatic Agents; Autoimmune Diseases; Colchicine; Hereditary Autoinflammatory Diseases; Humans; Immunologic Deficiency Syndromes; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Interleukin-18; Macrophage Activation Syndrome; Osteomyelitis; Skin Diseases; Tubulin Modulators; Tumor Necrosis Factor-alpha | 2017 |
Lessons from characterization and treatment of the autoinflammatory syndromes.
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.
Topics: Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Mevalonate Kinase Deficiency; Pyoderma Gangrenosum; Receptors, Tumor Necrosis Factor; Syndrome | 2009 |
The spectrum of MEFV clinical presentations--is it familial Mediterranean fever only?
Topics: Adult; Child; Colchicine; Cytoskeletal Proteins; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Humans; Male; Mutation; Pyrin; Skin Diseases, Vascular; Tubulin Modulators; Young Adult | 2009 |
Therapy of autoinflammatory syndromes.
Topics: Antirheumatic Agents; Autoantibodies; Autoimmune Diseases; Autoimmunity; Clinical Trials as Topic; Colchicine; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Interleukin-1beta; Syndrome; Tubulin Modulators; Tumor Necrosis Factor-alpha | 2009 |
Autoinflammatory conditions: when to suspect? How to treat?
Topics: Amyloidosis; Autoimmune Diseases; Colchicine; Familial Mediterranean Fever; Genetic Predisposition to Disease; Hereditary Autoinflammatory Diseases; Humans; Inflammation; Interleukin-1; Syndrome | 2010 |
Periodic Fever syndromes.
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].
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.
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.
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 |
1 trial(s) available for colchicine and Hereditary Autoinflammation Diseases
| Article | Year |
|---|---|
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.
Topics: Antibodies, Monoclonal, Humanized; Colchicine; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Mevalonate Kinase Deficiency | 2022 |
18 other study(ies) available for colchicine and Hereditary Autoinflammation Diseases
| Article | Year |
|---|---|
Clinical characterization, long-term follow-up, and response to treatment of patients with syndrome of undifferentiated recurrent fever (SURF).
Topics: Colchicine; Female; Fever; Follow-Up Studies; Hereditary Autoinflammatory Diseases; Humans; Lymphadenitis; Male; Pharyngitis; Retrospective Studies; Stomatitis, Aphthous; Syndrome | 2022 |
NLRP12-associated autoinflammatory disease: much more than the FCAS phenotype.
Topics: Child; Colchicine; Cryopyrin-Associated Periodic Syndromes; Familial Mediterranean Fever; Hereditary Autoinflammatory Diseases; Humans; Intracellular Signaling Peptides and Proteins; Phenotype; Syndrome | 2023 |
Performance of Tel-Hashomer, Livneh, pediatric and new Eurofever/PRINTO classification criteria for familial Mediterranean fever in a referral center.
Topics: Adolescent; Arthritis; Case-Control Studies; Chest Pain; Child; Child, Preschool; Colchicine; Consanguinity; Drug Resistance; Exons; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Heterozygote; Homozygote; Humans; Male; Mutation; Pyrin; Reproducibility of Results; Retrospective Studies; Severity of Illness Index; Tubulin Modulators | 2020 |
Adult-Onset Autoinflammatory Syndromes.
Topics: Adult; Age of Onset; Antirheumatic Agents; Colchicine; Female; Hereditary Autoinflammatory Diseases; Humans; Immunity, Innate; Immunologic Tests; Interleukin 1 Receptor Antagonist Protein; Interleukin-1; Middle Aged; Mutation; Pyrin; Spain; Symptom Assessment; Symptom Flare Up | 2020 |
Management of childhood-onset autoinflammatory diseases during the COVID-19 pandemic.
Topics: Adalimumab; Adolescent; Antibodies, Monoclonal, Humanized; Betacoronavirus; Biological Products; Child; Child, Preschool; Cohort Studies; Colchicine; Coronavirus Infections; COVID-19; Cryopyrin-Associated Periodic Syndromes; Etanercept; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Humans; Infant; Interleukin 1 Receptor Antagonist Protein; Male; Pandemics; Pneumonia, Viral; SARS-CoV-2; Tubulin Modulators; Tumor Necrosis Factor Inhibitors; Turkey; Young Adult | 2020 |
INSAID Variant Classification and Eurofever Criteria Guide Optimal Treatment Strategy in Patients with TRAPS: Data from the Eurofever Registry.
Topics: Abdominal Pain; Colchicine; Female; Hereditary Autoinflammatory Diseases; Humans; Mutation; Registries | 2021 |
Fever, lipodystrophy and cutaneous lesions.
Topics: Adrenal Cortex Hormones; Adult; Antigens, CD; Antigens, Differentiation, Myelomonocytic; Arthralgia; Colchicine; Diagnosis, Differential; Fatty Liver; Female; Fever; Hereditary Autoinflammatory Diseases; Humans; Lipodystrophy; Mutation; Peroxidase; Proteasome Endopeptidase Complex; Skin Diseases; Treatment Outcome; Tubulin Modulators | 2017 |
Familial Mediterranean Fever Is Commonly Diagnosed in Children in Israel with Periodic Fever Aphthous Stomatitis, Pharyngitis, and Adenitis Syndrome.
Topics: Child; Child, Preschool; Colchicine; Female; Hereditary Autoinflammatory Diseases; Humans; Israel; Male; Mutation; Pyrin; Retrospective Studies; Tubulin Modulators | 2019 |
Could blood products obtained from patients with familial Mediterranean fever have beneficial or harmful effects?
Topics: Blood Transfusion; Colchicine; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Humans; Inflammation; Interleukin-1beta; Leukocytes, Mononuclear; Male | 2019 |
Symptomatic patients with P369S-R408Q mutations: familial Mediterranean fever or mixed auto-inflammatory syndrome?
Topics: Colchicine; Diagnosis, Differential; Familial Mediterranean Fever; Female; Hereditary Autoinflammatory Diseases; Humans; Middle Aged; Mutation; Syndrome; Tubulin Modulators | 2019 |
Clinical characteristics and genetic analyses of 187 patients with undefined autoinflammatory diseases.
Topics: Adolescent; Adrenal Cortex Hormones; Adult; Age of Onset; Antirheumatic Agents; Child; Child, Preschool; Chronic Disease; Colchicine; Europe; Female; Genetic Variation; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Male; Pedigree; Registries; Retrospective Studies; Young Adult | 2019 |
Next generation sequencing panel in undifferentiated autoinflammatory diseases identifies patients with colchicine-responder recurrent fevers.
Topics: Adolescent; Adult; Child; Child, Preschool; Cluster Analysis; Colchicine; Female; Fever; Hereditary Autoinflammatory Diseases; High-Throughput Nucleotide Sequencing; Humans; Male; Mutation; Phenotype; Recurrence; Tubulin Modulators; Young Adult | 2020 |
MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease.
Topics: Cells, Cultured; Child; Colchicine; Cytokines; Cytoskeletal Proteins; DNA Mutational Analysis; Exome; Female; Gene Library; Hereditary Autoinflammatory Diseases; Humans; Inflammasomes; Lipopolysaccharides; Male; Mutation, Missense; Pedigree; Pyrin; Sequence Alignment | 2014 |
[Organ damage in collagen vascular diseases: toward the understanding of the complicated conditions (discussion)].
Topics: Adalimumab; Adult; Antibodies, Monoclonal, Humanized; Antibodies, Monoclonal, Murine-Derived; Antirheumatic Agents; Colchicine; Collagen Diseases; Female; Gastrointestinal Diseases; Hemorrhage; Hereditary Autoinflammatory Diseases; Humans; Hypertension, Pulmonary; Lung Diseases; Lung Diseases, Interstitial; Lupus Erythematosus, Systemic; Lupus Vasculitis, Central Nervous System; Rituximab; Vasculitis; Young Adult | 2013 |
Pearls from the Third Israeli Conference on FMF, other autoinflammatory disorders and AA amyloidosis.
Topics: Amyloidosis; Antirheumatic Agents; Colchicine; Drug Resistance; Familial Mediterranean Fever; Genetic Testing; Glucocorticoids; Hereditary Autoinflammatory Diseases; Humans; Interleukin 1 Receptor Antagonist Protein; Israel | 2014 |
Is colchicine an effective treatment in periodic fever, aphtous stomatitis, pharyngitis, cervical adenitis (PFAPA) syndrome?
Topics: Age Factors; Child, Preschool; Cohort Studies; Colchicine; Confidence Intervals; Female; Hereditary Autoinflammatory Diseases; Humans; Infant; Lymphadenitis; Male; Odds Ratio; Pharyngitis; Prognosis; Retrospective Studies; Risk Assessment; Sex Factors; Statistics, Nonparametric; Stomatitis, Aphthous; Syndrome; Treatment Outcome | 2016 |
Effectiveness of colchicine therapy in 4 cases of retroperitoneal fibrosis associated with autoinflammatory diseases.
Topics: Adult; Aged; Colchicine; Hereditary Autoinflammatory Diseases; Humans; Male; Middle Aged; Retroperitoneal Fibrosis; Tubulin Modulators | 2010 |
Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study.
Topics: Acute Disease; Adrenal Cortex Hormones; Adult; Anti-Inflammatory Agents, Non-Steroidal; Colchicine; DNA Mutational Analysis; Female; Fever; Gene Frequency; Genetic Predisposition to Disease; Hereditary Autoinflammatory Diseases; Humans; Immunosuppressive Agents; Italy; Male; Middle Aged; Mutation; Odds Ratio; Pedigree; Pericarditis; Phenotype; Prospective Studies; Receptors, Tumor Necrosis Factor, Type I; Recurrence; Risk Assessment; Risk Factors | 2012 |