Results 101 to 110 of about 4,476 (134)

Variable phenotype associated with compound LDLR gene mutations in familial hypercholesterolemia patients: Case series and clinical implications. [PDF]

open access: yesMedicine (Baltimore)
Mohd Kasim NA   +12 more
europepmc   +1 more source

A systematic review of ABCG8 mutation and sitosterolemia. [PDF]

open access: yesAm J Blood Res
Parekh D   +4 more
europepmc   +1 more source

Clinical features and genetic analysis of a Brazilian patient with sitosterolemia: a case report. [PDF]

open access: yesArch Endocrinol Metab
Leão FAA   +3 more
europepmc   +1 more source

Correlation between clinical classification and genetic analysis of familial hypercholesterolemia in premature coronary artery disease in a cohort of Egyptian patients. [PDF]

open access: yesHum Genomics
Zahwo RA   +12 more
europepmc   +1 more source

Cholesterol-rich diet exacerbates steatohepatitis in the STAM mouse model. [PDF]

open access: yesSci Rep
Jonas W   +5 more
europepmc   +1 more source

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