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Amphotericin B FDA Label
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Demeclocycline FDA Label
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Doxycycline FDA Label
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A standard database for drug repositioning. Sci Data. 2017 Mar 14;4:170029.
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Minocycline FDA Label
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Oxytetracycline FDA Label
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Tetracycline FDA Label
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An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist. N Engl J Med. 2009 Jun 4;360(23):2426-37. doi: 10.1056/NEJMoa0807865.
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Association of mutations in the NALP3/CIAS1/PYPAF1 gene with a broad phenotype including recurrent fever, cold sensitivity, sensorineural deafness, and AA amyloidosis.Arthritis Rheum. 2002 Sep;46(9):2445-52. doi: 10.1002/art.10509.
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A novel point mutation affecting the tyrosine kinase domain of the TRKA gene in a family with congenital insensitivity to pain with anhidrosis.J Invest Dermatol. 1999 May;112(5):810-4. doi: 10.1046/j.1523-1747.1999.00569.x.
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A novel mutation (T61I) in the gene encoding tumour necrosis factor receptor superfamily 1A (TNFRSF1A) in a Japanese patient with tumour necrosis factor receptor-associated periodic syndrome (TRAPS) associated with systemic lupus erythematosus.Rheumatology (Oxford). 2004 Oct;43(10):1292-9. doi: 10.1093/rheumatology/keh320. Epub 2004 Jul 27.
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Genome-wide analysis of Borrelia turcica and 'Candidatus Borrelia tachyglossi' shows relapsing fever-like genomes with unique genomic links to Lyme disease Borrelia.Infect Genet Evol. 2018 Dec;66:72-81. doi: 10.1016/j.meegid.2018.09.013. Epub 2018 Sep 18.
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Compound heterozygous LPIN2 pathogenic variants in a patient with Majeed syndrome with recurrent fever and severe neutropenia: case report.BMC Med Genet. 2019 Nov 14;20(1):182. doi: 10.1186/s12881-019-0919-3.
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A novel insertion mutation identified in exon 10 of the MEFV gene associated with Familial Mediterranean Fever.BMC Med Genet. 2014 Jul 1;15:74. doi: 10.1186/1471-2350-15-74.
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The clinical phenotype and genotype of NLRP12-autoinflammatory disease: a Chinese case series with literature review.World J Pediatr. 2020 Oct;16(5):514-519. doi: 10.1007/s12519-019-00294-8. Epub 2019 Dec 9.
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