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- W2044002092 abstract "Introduction Familial Mediterranean fever (FMF) is a disease characterized by recurrent episodes of fever, peritonitis, or pleuritis, 1 which is probably inherited as an autosomal recessive disorder. 2 Most of the patients reported with FMF have been of Armenian 3 or Sephardic Jewish ancestry. 1 Although the etiology of FMF is unknown, it has been suggested it may be an inborn error of metabolism 4 or probably a manifestation of a hypersensitive state. 5 It was recently reported that some FMF patients excreted increased amounts of urinary histidine as measured by two-dimensional paper chromatography. 4,6,7 On the basis of these reports, aminoaciduria has been suggested as a differential diagnostic criterion for FMF. 8 We have studied the amino acid excretion with ion-exchange chromatography in five FMF patients both while they were afebrile and pain free and also during spontaneous episodes of fever and peritonitis. The results of these studies demonstrate" @default.
- W2044002092 created "2016-06-24" @default.
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- W2044002092 date "1964-03-01" @default.
- W2044002092 modified "2023-09-26" @default.
- W2044002092 title "Amino Acid Excretion in Familial Mediterranean Fever" @default.
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- W2044002092 doi "https://doi.org/10.1001/archinte.1964.00280090095015" @default.
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