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Year Number of Results
1979 1
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1990 1
1992 1
1993 1
1994 2
1995 2
2000 3
2003 2
2005 1
2006 1
2007 1
2012 1
2013 3
2016 4
2017 3
2019 1
2020 1
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29 results

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Page 1
Current trends in diagnosis and management of cardiac amyloidosis.
Esplin BL, Gertz MA. Esplin BL, et al. Curr Probl Cardiol. 2013 Feb;38(2):53-96. doi: 10.1016/j.cpcardiol.2012.11.002. Curr Probl Cardiol. 2013. PMID: 23337445 Review.
Amyloidosis is a rare disease in which insoluble extracellular protein fibrils in beta-pleated sheets infiltrate multiple organs, causing organ dysfunction and failure. Amyloidoses are generally classified into light chain or primary systemic amyloidosis, hereditary …
Amyloidosis is a rare disease in which insoluble extracellular protein fibrils in beta-pleated sheets infiltrate multiple organs, cau …
Amyloidosis: prognosis and treatment.
Gertz MA, Kyle RA. Gertz MA, et al. Semin Arthritis Rheum. 1994 Oct;24(2):124-38. doi: 10.1016/s0049-0172(05)80006-x. Semin Arthritis Rheum. 1994. PMID: 7839154 Review.
The objective of this study was to review (1) the factors that have been linked to prediction of clinical outcome and survival in amyloidosis and (2) the available studies on the therapy for localized and systemic forms of amyloidosis. ...Advances have been m …
The objective of this study was to review (1) the factors that have been linked to prediction of clinical outcome and survival in amyloid …
Auto inflammatory syndromes: Diagnosis and treatment.
Stankovic K, Grateau G. Stankovic K, et al. Joint Bone Spine. 2007 Dec;74(6):544-50. doi: 10.1016/j.jbspin.2007.07.005. Epub 2007 Sep 20. Joint Bone Spine. 2007. PMID: 17950649 Review.
New pathophysiological insights have led to the development of promising maintenance treatments designed to reduce the number and severity of the inflammatory attacks and to diminish the risk of secondary amyloidosis....
New pathophysiological insights have led to the development of promising maintenance treatments designed to reduce the number and severity o …
Amyloidosis in Inflammatory Bowel Disease: A Systematic Review of Epidemiology, Clinical Features, and Treatment.
Tosca Cuquerella J, Bosca-Watts MM, Anton Ausejo R, Tejedor Alonso S, Mora De Miguel F, Minguez Perez M. Tosca Cuquerella J, et al. J Crohns Colitis. 2016 Oct;10(10):1245-53. doi: 10.1093/ecco-jcc/jjw080. Epub 2016 Apr 7. J Crohns Colitis. 2016. PMID: 27056947 Review.
BACKGROUND AND AIMS: Amyloidosis is a rare complication of inflammatory bowel disease [IBD]; its low prevalence has hindered both descriptive and therapeutic studies. The aim of this study was to estimate the prevalence of amyloidosis in IBD and the risk fact …
BACKGROUND AND AIMS: Amyloidosis is a rare complication of inflammatory bowel disease [IBD]; its low prevalence has hindered both des …
Tocilizumab in the treatment of twelve cases with aa amyloidosis secondary to familial mediterranean fever.
Ugurlu S, Hacioglu A, Adibnia Y, Hamuryudan V, Ozdogan H. Ugurlu S, et al. Orphanet J Rare Dis. 2017 May 30;12(1):105. doi: 10.1186/s13023-017-0642-0. Orphanet J Rare Dis. 2017. PMID: 28558744 Free PMC article. Review.
Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent may be effective in AA amyloidosis resistant to conventional treatments. We report our data on the effect of TCZ in patients with FMF complicated with AA amyloidosis. ...Further st …
Recently there are few reports pointing out that tocilizumab(TCZ), an anti IL-6 agent may be effective in AA amyloidosis resistant to …
Advances in the diagnosis and treatment of tumor necrosis factor receptor-associated periodic syndrome.
Aguado-Gil L, Irarrazaval-Armendáriz I, Pretel-Irazabal M. Aguado-Gil L, et al. Actas Dermosifiliogr. 2013 Sep;104(7):617-22. doi: 10.1016/j.adengl.2012.11.020. Epub 2013 Jul 23. Actas Dermosifiliogr. 2013. PMID: 23891452 Free article. Review.
The diagnosis is reached using gene analysis and prognosis depends on the appearance of amyloidosis secondary to the recurrent episodes of inflammation. Tumor necrosis factor inhibitors and corticosteroids are the most widely used treatments. ...
The diagnosis is reached using gene analysis and prognosis depends on the appearance of amyloidosis secondary to the recurrent …
A survey of resistance to colchicine treatment for French patients with familial Mediterranean fever.
Corsia A, Georgin-Lavialle S, Hentgen V, Hachulla E, Grateau G, Faye A, Quartier P, Rossi-Semerano L, Koné-Paut I. Corsia A, et al. Orphanet J Rare Dis. 2017 Mar 16;12(1):54. doi: 10.1186/s13023-017-0609-1. Orphanet J Rare Dis. 2017. PMID: 28302131 Free PMC article. Review.
Physicians considered colchicine resistance with > 6 attacks/year (n = 21/51, 42%), > 4 attacks in the last 6 months (n = 13/51, 26%), persistent inflammation (n = 23/51, 45%), renal amyloidosis in (n = 6/28, 22%) of adult patients and intolerance to an increase in c …
Physicians considered colchicine resistance with > 6 attacks/year (n = 21/51, 42%), > 4 attacks in the last 6 months (n = 13/51, 26%), …
Colchicine, Biologic Agents and More for the Treatment of Familial Mediterranean Fever. The Old, the New, and the Rare.
Portincasa P. Portincasa P. Curr Med Chem. 2016;23(1):60-86. doi: 10.2174/0929867323666151117121706. Curr Med Chem. 2016. PMID: 26572612 Review.
The MEFV gene mutations on chromosome 16p13.3 encodes the abnormal pyrin (marenostrin), a protein expressed in granulocytes, monocytes, serosal and synovial fibroblasts and involved in the activation of caspase-1 and the processing and release of active pro-inflammatory IL-1beta. …
The MEFV gene mutations on chromosome 16p13.3 encodes the abnormal pyrin (marenostrin), a protein expressed in granulocytes, monocytes, sero …
The M694I/M694I genotype: A genetic risk factor of AA-amyloidosis in a group of Algerian patients with familial Mediterranean fever.
Ait-Idir D, Djerdjouri B, Bouldjennet F, Taha RZ, El-Shanti H, Sari-Hamidou R, Khellaf G, Benmansour M, Benabadji M, Haddoum F. Ait-Idir D, et al. Eur J Med Genet. 2017 Mar;60(3):149-153. doi: 10.1016/j.ejmg.2016.12.003. Epub 2016 Dec 10. Eur J Med Genet. 2017. PMID: 27956278
The data about the renal AA-amyloidosis secondary to FMF are scarce in North African countries and non-existent in Algeria. ...Molecular analysis included 28 unrelated Algerian FMF patients with ascertained amyloidosis, 23 of them were symptomatic and 5 were …
The data about the renal AA-amyloidosis secondary to FMF are scarce in North African countries and non-existent in Algeria. .. …
The most recent advances in pathophysiology and management of tumour necrosis factor receptor-associated periodic syndrome (TRAPS): personal experience and literature review.
Magnotti F, Vitale A, Rigante D, Lucherini OM, Cimaz R, Muscari I, Granados Afonso de Faria A, Frediani B, Galeazzi M, Cantarini L. Magnotti F, et al. Clin Exp Rheumatol. 2013 May-Jun;31(3 Suppl 77):141-9. Epub 2013 Jul 24. Clin Exp Rheumatol. 2013. PMID: 23899820 Review.
Most reported cases of TRAPS involve patients of European ancestry and diagnosis can be formulated by the combination of genetic analysis and a compatible phenotype. Its prognosis is strictly dependent on the appearance of amyloidosis, secondary to uncontrolled rela …
Most reported cases of TRAPS involve patients of European ancestry and diagnosis can be formulated by the combination of genetic analysis an …
29 results