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 insomnia
Familial exudative vitreoretinopathy Results of surgical management.
Progressive
familial 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.
Familial 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.
Multiple
familial trichoepithelioma is a relatively infrequent
familial disease.
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.
