Results 181 to 190 of about 848,404 (232)
Cachexia as an unusual presentation of familial Mediterranean fever: A case report. [PDF]
World J Clin CasesSira AM, Shoeir SA, Sira MM.
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Clinically Probable Late-Onset Familial Mediterranean Fever Presenting as Recurrent Pericarditis and Suggestive of Evolving Constrictive Physiology. [PDF]
CureusGovil D, Ather A, Patel K.
europepmc +1 more source
Modulation of Inflammasome Activity by miR-197-3p in Familial Mediterranean Fever Mouse Macrophages. [PDF]
Arch RheumatolAkkaya-Ulum YZ +3 more
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Archives of Dermatology, 1998
A 33-year-old moderately mentally handicapped man who was living in a group home presented to our clinic with a 1-week history of pain, swelling, and erythema of the lower portion of the right leg and foot. The patient was of Roman Catholic, Italian origin, although the history of his distant family revealed that some of his relatives had emigrated ...
C Y, Muhn +4 more
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A 33-year-old moderately mentally handicapped man who was living in a group home presented to our clinic with a 1-week history of pain, swelling, and erythema of the lower portion of the right leg and foot. The patient was of Roman Catholic, Italian origin, although the history of his distant family revealed that some of his relatives had emigrated ...
C Y, Muhn +4 more
openaire +4 more sources
Familial Mediterranean fever—A review [PDF]
Genetics in Medicine, 2011 Familial Mediterranean fever is inherited in an autosomal recessive manner. There are two phenotypes: types 1 and 2. Familial Mediterranean fever type 1 is characterized by recurrent short episodes of inflammation and serositis, including fever, peritonitis, synovitis, pleuritis, and, rarely, pericarditis.
Tamy Shohat
exaly +3 more sources
Archives of Internal Medicine, 1958
I. Introduction The purpose of this communication is to describe a disease which we define as a heredofamilial syndrome of undetermined pathogenesis in persons of Mediterranean stock, becoming manifest as a rule in infancy or adolescence and characterized by short recurrent bouts of fever accompanied by pain in the abdomen or chest or one or multiple ...
H, HELLER, E, SOHAR, L, SHERF
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I. Introduction The purpose of this communication is to describe a disease which we define as a heredofamilial syndrome of undetermined pathogenesis in persons of Mediterranean stock, becoming manifest as a rule in infancy or adolescence and characterized by short recurrent bouts of fever accompanied by pain in the abdomen or chest or one or multiple ...
H, HELLER, E, SOHAR, L, SHERF
openaire +2 more sources
Current Opinion in Rheumatology, 2016
Purpose of review Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary
Shai, Padeh, Yackov, Berkun
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Purpose of review Familial Mediterranean fever (FMF) is the oldest and most common of the hereditary autoinflammatory diseases (AIDs). A large body of information has been accumulated over recent years on the pathophysiology, diagnosis and treatment of these diseases. The purpose of this review is to bring an up-to-date summary
Shai, Padeh, Yackov, Berkun
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Update in familial Mediterranean fever
Current Opinion in Rheumatology, 2021Purpose of review Familial Mediterranean fever (FMF) is the prototypic autoinflammatory disease. Although the gene associated with the disease was identified 24 years ago, we still have to learn about the pathogenesis of its inflammation and the variation in the phenotype. In this review, we discuss some recent findings in FMF,
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