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  • Theresa M Marteau, V. Oravec Senior, +16 authors Richard Wray
  • Biology, Medicine
  • American journal of medical genetics. Part A
  • 2004 (First Publication: 30 July 2004)
  • This trial tests the hypothesis that confirming a clinical diagnosis of familial hypercholesterolemia (FH) by finding a genetic mutation reduces patients' perceptions of control over the disease andExpand
  • Ewan R. Pearson, Stepanka Pruhova, +10 authors Andrew T. Hattersley
  • Medicine, Biology
  • Diabetologia
  • 2005 (First Publication: 1 May 2005)
  • Aims/hypothesisHeterozygous mutations in the gene of the transcription factor hepatocyte nuclear factor 4α (HNF-4α) are considered a rare cause of MODY with only 14 mutations reported to date. TheExpand
  • Dimitri P. Mikhailidis, Moses Elisaf, +15 authors Evangelos N. Liberopoulos
  • Medicine
  • Current vascular pharmacology
  • 2011 (First Publication: 31 August 2011)
  • Aim of the present Consensus Statement is to provide a comprehensive and up to-date document on the pathophysiology, atherogenicity and clinical significance of low density liproproteins (LDL)Expand