The myths we believed in familial
Mediterranean fever: what have we learned in the past years?
The cutaneous manifestations in children with familial
Mediterranean fever (recurrent hereditary polyserositis).
Suggestive features and probable fatal familial
exudative vitreoretinopathy Results of surgical management.
intrahepatic cholestasis type 1 and extrahepatic features: no catch-up of stature growth, exacerbation of diarrhea, and appearance of liver steatosis after liver transplantation.
Goren et al., "A rare cause of ascites: familial
Mediterranean fever," Turkish Journal of Gastroenterology, vol.
Yavuzcen et al., "Clinical and subclinical inflammation in patients with familial
Mediterranean fever and in heterozygous carriers of MEFV mutations," Rheumatology, vol.
hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society.
Temel aramada (basic search) "Title" secilerek, "Familial
Mediterranean Fever" kullanilarak ve more settings'te "Science Citation Index Expanded (SCI-E)" kabul edilerek yayinlar Nisan 2016 tarihinde, retrospektif olarak tarandi.
trichoepithelioma is a relatively infrequent familial
Mediterranean fever (FMF) is a hereditary autoinflammatory disease characterized by repeated attacks of fever abdominal pain, pleuritic chest pain, and arthritis.
"This case is more reason for anybody opposed to (familial
DNA searching) to rethink their position and get onboard," Phil said.