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Quoted phrase not found in phrase index: "Nephrotic Syndrome - MEFV Associated"
Page 1
Renal involvement in familial Mediterranean fever in an Algerian population.
Khellaf G, Benziane A, Kaci L, Ait-Idir D, Missoum S, Benabadji M. Khellaf G, et al. Clin Nephrol. 2023 Apr;99(4):172-179. doi: 10.5414/CN110930. Clin Nephrol. 2023. PMID: 36734158
The diagnosis of nephropathy was suspected clinically and biologically and confirmed histologically. All our patients were tested for MEFV mutations. Results: 58 patients, 30 males and 28 females, mean age 31.68 12.71; 3 (5.17%) chronic dialysis patients and 55 (94.82%) re …
The diagnosis of nephropathy was suspected clinically and biologically and confirmed histologically. All our patients were tested for MEF …
Familial Mediterranean fever, inflammation and nephrotic syndrome: fibrillary glomerulopathy and the M680I missense mutation.
Fisher PW, Ho LT, Goldschmidt R, Semerdjian RJ, Rutecki GW. Fisher PW, et al. BMC Nephrol. 2003 Aug 11;4:6. doi: 10.1186/1471-2369-4-6. BMC Nephrol. 2003. PMID: 12908875 Free PMC article.
Further diagnostic studies were unremarkable with clinical workup negative for amyloidosis or other secondary causes of nephrotic syndrome. DISCUSSION: Individuals with FMF are at greater risk for developing nephrotic syndrome. ...Other known renal dis …
Further diagnostic studies were unremarkable with clinical workup negative for amyloidosis or other secondary causes of nephrotic …
Predictors of AA amyloidosis in familial Mediterranean fever.
Mukhin NA, Kozlovskaya LV, Bogdanova MV, Rameev VV, Moiseev SV, Simonyan AKh. Mukhin NA, et al. Rheumatol Int. 2015 Jul;35(7):1257-61. doi: 10.1007/s00296-014-3205-x. Epub 2015 Jan 14. Rheumatol Int. 2015. PMID: 25586652
The diagnosis of amyloidosis that was suspected clinically (new proteinuria or nephrotic syndrome) was confirmed histologically. Screening for MEFV gene mutations was performed in 70 patients. ...AA amyloidosis was diagnosed in 17 (68 %) of 25 patients with h …
The diagnosis of amyloidosis that was suspected clinically (new proteinuria or nephrotic syndrome) was confirmed histologicall …
Phenotype 2 familial mediterranean fever: evaluation of 22 case series and review of the literature on phenotype 2 FMF.
Altunoğlu A, Erten Ş, Canoz MB, Yuksel A, Ceylan GG, Balci S, Dogan HT. Altunoğlu A, et al. Ren Fail. 2013;35(2):226-30. doi: 10.3109/0886022X.2012.745115. Epub 2012 Dec 11. Ren Fail. 2013. PMID: 23228227 Review.
This study included 420 patients who were admitted to the Nephrology and Rheumatology Departments of Ataturk Education and Research Hospital with unexplained proteinuria/nephrotic syndrome. The initial screening test for amyloidosis was the presence of significant p …
This study included 420 patients who were admitted to the Nephrology and Rheumatology Departments of Ataturk Education and Research Hospital …
Familial Mediterranean fever (FMF)-associated amyloidosis in childhood. Clinical features, course and outcome.
Cakar N, Yalçinkaya F, Ozkaya N, Tekin M, Akar N, Koçak H, Misirlioğlu M, Akar E, Tümer N. Cakar N, et al. Clin Exp Rheumatol. 2001 Sep-Oct;19(5 Suppl 24):S63-7. Clin Exp Rheumatol. 2001. PMID: 11760404
At the end of observation period of 4.5 +/- 2.23 years (range 2-12 yrs) on treatment, nephrotic syndrome resolved in 13 patients and proteinuria was lost in 5 of them. ...Colchicine treatment ameliorates the progression of renal disease in the patients who presented …
At the end of observation period of 4.5 +/- 2.23 years (range 2-12 yrs) on treatment, nephrotic syndrome resolved in 13 patien …
Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report.
Peces R, Afonso S, Peces C, Nevado J, Selgas R. Peces R, et al. BMC Med Genet. 2017 Aug 31;18(1):97. doi: 10.1186/s12881-017-0457-9. BMC Med Genet. 2017. PMID: 28859624 Free PMC article.
The recipient had presented recurrent acute febrile episodes of familial Mediterranean fever, developed nephrotic syndrome secondary to amyloidosis and needed bilateral nephrectomy and chronic dialysis. ...CONCLUSIONS: In familial Mediterranean fever, analyses of th …
The recipient had presented recurrent acute febrile episodes of familial Mediterranean fever, developed nephrotic syndrome sec …
Autosomal dominant familial Mediterranean fever in Northern European Caucasians associated with deletion of p.M694 residue-a case series and genetic exploration.
Rowczenio DM, Iancu DS, Trojer H, Gilbertson JA, Gillmore JD, Wechalekar AD, Tekman M, Stanescu HC, Kleta R, Lane T, Hawkins PN, Lachmann HJ. Rowczenio DM, et al. Rheumatology (Oxford). 2017 Feb;56(2):209-213. doi: 10.1093/rheumatology/kew058. Epub 2016 May 5. Rheumatology (Oxford). 2017. PMID: 27150194
METHODS: MEFV gene was analysed in 3500 subjects with suspected FMF referred to a single UK centre between 2002 and 2014. ...The 14% incidence of AA amyloidosis may reflect delay in diagnosis associated with extreme rarity of FMF in this population. The common haplo …
METHODS: MEFV gene was analysed in 3500 subjects with suspected FMF referred to a single UK centre between 2002 and 2014. ...The 14% …
A complex case of renal amyloidosis with a rare co-occurrence of 2 mutations in separate hereditary periodic fever syndrome-related genes.
Cigni A, Ledda F, Satta AE. Cigni A, et al. J Nephrol. 2006 Jul-Aug;19(4):543-9. J Nephrol. 2006. PMID: 17048217
A 41 year-old male was admitted because of nephrotic syndrome associated with renal impairment and arterial hypertension. ...The patient has never complained of the typical features of the Familial Mediterranean fever or of the TNF receptor-associated …
A 41 year-old male was admitted because of nephrotic syndrome associated with renal impairment and arterial hypertensio …