Functional analysis from ex-vivo characterization of LDLR exon 13-15 duplication associated to familial hypercholesterolemia. [PDF]
Martínez C +8 more
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Baseline characteristics and response to evinacumab in females and males with homozygous familial hypercholesterolemia in the ELIPSE OLE study. [PDF]
Brisson D +5 more
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Diagnosis of Familial Hypercholesterolemia in Children: From Clinical Features Through Gene Variants to Polygenic Score. [PDF]
Buganza R +6 more
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Awareness and management of pediatric familial hypercholesterolemia: a Polish physician survey. [PDF]
Szeliga K, Gawlik-Starzyk A.
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A de novo LDLR mutation in severe familial hypercholesterolemia: case report, functional characterization, and a personalized gene correction strategy exploration. [PDF]
Zhang S +7 more
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Editorial commentary: From prevalence to practice - implementing familial hypercholesterolemia screening in high-risk clinics using an implementation science framework. [PDF]
Al-Rasadi K, Mehta A.
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The High Price of Interrupted Follow-Up: Catastrophic Progression of Homozygous Familial Hypercholesterolemia-A Case Report and Literature Review. [PDF]
Dastjerdi P +5 more
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[Familial hypercholesterolemia].
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Tendon Pathology in Hypercholesterolemia and Familial Hypercholesterolemia
Current Rheumatology Reports, 2017Hypercholesterolemia (HC), or high cholesterol, is usually caused by diet, other health conditions, or inherited diseases, such as familial hypercholesterolemia (FHC). Studies have shown patients with hypercholesterolemia are more prone to tendon injury and impaired healing.
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