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Items: 1 to 20 of 93

1.

An atypical familial Mediterranean fever patient who developed ulcers in the terminal ileum and recurrent abscess-like lesions in multiple organs.

Takahashi T, Tsukuda H, Itoh H, Kimura H, Yoshimoto M, Tsujisaki M.

Intern Med. 2012;51(16):2239-44. Epub 2012 Aug 15.

2.

Hereditary periodic fever.

Hull KM, Kastner DL, Balow JE.

N Engl J Med. 2002 May 2;346(18):1415-6; author reply 1415-6. No abstract available.

3.

Successful treatment with infliximab of a patient with tumor necrosis factor-associated periodic syndrome (TRAPS) who failed to respond to etanercept.

Krelenbaum M, Chaiton A.

J Rheumatol. 2010 Aug 1;37(8):1780-2. doi: 10.3899/jrheum.091094. No abstract available.

PMID:
20675856
4.

Familial Mediterranean fever successfully treated with etanercept.

Mor A, Pillinger MH, Kishimoto M, Abeles AM, Livneh A.

J Clin Rheumatol. 2007 Feb;13(1):38-40.

PMID:
17278949
5.
6.

Usefulness of Small Intestinal Endoscopy in a Case of Adult-onset Familial Mediterranean Fever Associated with Jejunoileitis.

Kitade T, Horiki N, Katsurahara M, Totoki T, Harada T, Tano S, Yamada R, Hamada Y, Inoue H, Tanaka K, Gabazza EC, Hayashi H, Tanaka M, Takei Y.

Intern Med. 2015;54(11):1343-7. doi: 10.2169/internalmedicine.54.3690. Epub 2015 Jun 1.

7.

Successful treatment with infliximab and low-dose methotrexate in a Japanese patient with familial Mediterranean fever.

Nakamura A, Matsuda M, Tazawa K, Shimojima Y, Ikeda S.

Intern Med. 2007;46(15):1247-9. Epub 2007 Aug 2.

8.

[Fever of unknown origin and colchicine-sensitive amyloidosis: familial Mediterranean fever?].

Schneider W, Wehmeier A.

Dtsch Med Wochenschr. 1989 Jun 16;114(24):951-4. German.

PMID:
2731480
9.

Anti-interleukin 1 treatment for patients with familial Mediterranean fever resistant to colchicine.

Ozen S, Bilginer Y, Aktay Ayaz N, Calguneri M.

J Rheumatol. 2011 Mar;38(3):516-8. doi: 10.3899/jrheum.100718. Epub 2010 Dec 15.

PMID:
21159830
10.

[Familial Mediterranean fever. Case of a 48-year-old patient with recurrent abdominal pain].

Hofer JF, Franz B, Holzinger G.

Wien Klin Wochenschr. 1992;104(7):208-10. German.

PMID:
1381854
11.

Recurrent bullous lesions associated with familial Mediterranean fever: a case report.

Akman A, Cakcak DS, Coban E, Ozbudak HI, Ciftcioglu MA, Alpsoy E, Yilmaz E.

Clin Exp Dermatol. 2009 Mar;34(2):216-8. doi: 10.1111/j.1365-2230.2008.02884.x.

PMID:
19187302
12.

[A three-year-old girl with abdominal pain and fever].

Olbjørn C, Fjaerli HO.

Tidsskr Nor Laegeforen. 2010 Mar 11;130(5):494-5. doi: 10.4045/tidsskr.09.0692. Norwegian.

13.

Familial Mediterranean fever at the millennium. Clinical spectrum, ancient mutations, and a survey of 100 American referrals to the National Institutes of Health.

Samuels J, Aksentijevich I, Torosyan Y, Centola M, Deng Z, Sood R, Kastner DL.

Medicine (Baltimore). 1998 Jul;77(4):268-97. Review.

14.

[Familial Mediterranean Fever (FMF): from diagnosis to treatment].

Medlej-Hashim M, Loiselet J, Lefranc G, Mégarbané A.

Sante. 2004 Oct-Dec;14(4):261-6. Review. French.

15.

[Turkish children with recurrent abdominal pain and fever: familial Mediterranean fever].

Hulsmann AR, Hofstra WB, Brinkman JG, van der Wielen MJ, Bakker E, Oudesluys-Murphy AM.

Ned Tijdschr Geneeskd. 2003 Jun 7;147(23):1097-100. Dutch.

PMID:
12822516
16.

Malignant nephrosclerosis in a patient with familial Mediterranean fever.

Yamanouchi M, Ubara Y, Imafuku A, Kawada M, Koki M, Sumida K, Hiramatsu R, Hasegawa E, Hayami N, Suwabe T, Hoshino J, Sawa N, Ohashi K, Fujii T, Matsuda M, Takaichi K.

Intern Med. 2015;54(20):2643-6. doi: 10.2169/internalmedicine.54.4937. Epub 2015 Oct 15.

17.

Hereditary periodic fever syndrome sans fever or distinct periodicity presenting with psychosis.

Hurst M, Hull K, Nicholls D, Ameratunga R.

J Clin Rheumatol. 2005 Dec;11(6):329-30.

PMID:
16371805
18.
19.

[Unusual cutaneous lesions of familial Mediterranean fever].

Bafounta ML, Doumat-Batch F, Vasseur E, Staroz F, Clerici T, Saiag P.

Ann Dermatol Venereol. 2004 Feb;131(2):183-6. French.

PMID:
15026746
20.

Two familial cases with tumor necrosis factor receptor-associated periodic syndrome caused by a non-cysteine mutation (T50M) in the TNFRSF1A gene associated with severe multiorganic amyloidosis.

Kallinich T, Briese S, Roesler J, Rudolph B, Sarioglu N, Blankenstein O, Keitzer R, Querfeld U, Haffner D.

J Rheumatol. 2004 Dec;31(12):2519-22.

PMID:
15570662

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