Results 141 to 150 of about 8,537 (193)
Canakinumab treatment in patients with colchicine-resistant familial mediterranean fever: a multicenter observational study. [PDF]
Koç E, Pekdiker M, Kara M.
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Dental Age Estimation by Demirjian, Willems, and Cameriere Methods in Children with Familial Mediterranean Fever: A Case-Control Study. [PDF]
Altan H +6 more
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A Case of Familial Mediterranean Fever Diagnosed After Oral Administration of a Gonadotropin-Releasing Hormone (GnRH) Antagonist. [PDF]
Ueno H +4 more
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Scrotal Pain in Familial Mediterranean Fever: A Series of Three Case Reports and Literature Review. [PDF]
Bahaa A +6 more
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Epigenetic and Inflammatory Signatures in Familial Mediterranean Fever: Implication of miR-204-3p and miR-223-3p in Pyrin-Mediated Immune Regulation. [PDF]
Hajiyeva R +8 more
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Lancet, The, 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 ...
Eldad Ben-Chetrit, Micha Levy
exaly +5 more sources
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 ...
Eldad Ben-Chetrit, Micha Levy
exaly +5 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
openaire +2 more sources

